Backaround to the Invention The art of diagnostic imaging exploits contrasting agents that in binding or localizing a site selectively within the body, help to resolve the image of diagnostic interest. 67Gallium salts, for example, have an affinity for tumours and infected tissue and, with the aid of scanning tomography, can reveal affiicted body regions to the physician. Other contrasting agents include the metal radionuclides such as 99mtechnetium and '86/'88rhenium, and these have been used to label targeting molecules, such as proteins, peptides and antibodies that localize at desired regions of the human body.

Metal ions such as Gd are useful in diagnostic imaging as contrasting agents in magnetic resonance imaging (MRI). MRI is a currently used technique for the in vivo imaging of biological processes and offers non-ionizing radiation, modest magnetic fields, and is non invasive. In addition, it offers superb spatial resolution (of the order of 1-3mm). In order to enhance the sometimes weak signals of MRI contrasting agents, such as Gd, agents are used to improve the signal to noise ratio for the purpose of imaging designated areas or processes of the body. These are known as MRI contrast agents and have the potential to allow aquisition of data over shorter time periods and the ability to image regions that currently have poor image contrast.

Metal complexes have applications in the treatment, management or diagnosis of diseases. 9 Examples include the use of Pt complexes in cancer

therapy,4J the use of Au complexes in rheumatoid arthritis therapy and the applications of Ga, In, Tc, Re, and Sm complexes in nuclear medicine.3 '5-'7 Previously, difficulties have been encountered in attaching diagnostically useful metals and radionuclide metals to targeting agents. Targeting agents such as proteins and other macromolecules can offer the tissue specificity required for diagnostic accuracy. However, labeling of these agents with metal radionuclides is made difficult by their physical structure. Particularly, protein and peptide targeting agents present numerous sites at which radionuclide binding can occur, resulting in a product that is labeled heterogeneously. Also, and despite their possibly large size, proteins rarely present the structural configuration most appropriate for high affinity radionuclide binding, i.e. a region incorporating four or more donor atoms that form five-membered rings. As a result, radionuclides are bound typically at the more abundant low-affinity sites, forming unstable complexes.

We have found that a promising alternative to the direct labeling of targeting agents is an indirect approach, in which targeting agent and radionuclide are coupled using a chelating agent. Candidates for use as chelators are those compounds that bind tightly to the chosen metal radionuclide and also have a reactive functional group for conjugation with the targeting molecule.

However, it is difficult to identify suitable targeting agents that retain their targeting ability when coupled to a chelator complexed with a metal or a radionuclide metal. A major problem affecting radiopharmaceutical development arises from difficulties in incorporating diagnostically useful metal complexes such as 99mtechnebum complexes into a targeting molecule without drastically reducing the affinity of the targeting molecule for the receptor and adequate pharmacokinetics.

With targeting molecules that are small peptides or small organic compounds, the addition of a chelated metal compound can double the molecular weight of the overall radiopharmaceutical and thereby radically alter the ability of the molecule to bind the receptor with comparable affinity.

To identify suitable labeled targeting agents according to the traditional approach, it is necessary to screen thousands of compounds in biological assays to provide a lead compound having the desired biological activity. This initial lead compound is then optimized to provide an agent having improved pharmacological properties. This approach is very time consuming and expensive.

The problems inherent in the traditional approach have been overcome for the development of some pharmaceuticals through the use of combinatorial chemistry.

Combinatorial chemistry is a methodology by which large numbers of compounds or libraries can be prepared and screened rapidly and concurrently in an efficient manner.

While the use of combinatorial library techniques has been applied to the development of drugs that are organic molecules, it has never been applied to the development of metallodrugs. This is most likely due to the greater considerations involved in the chemistry of metallodrugs. In addition to the usual considerations, the oxidation state and the coordination chemistry of the metal, and the stability of the resulting metal complexes must also be considered when combinatorial library techniques are applied to metallodrug development. As the combinatorial library consists of a series of metal complexes, the site of metal coordination is of great importance. This site of metal coordination may be incorporated as part of the whoie molecule or as a separate group or entity attached to the biologically active component of the molecule. In either case, the site of coordination affects the oxidation state of the metal, and vice versa. As the library of molecules will be evaluated in solution, the metal complexes must also resist decomplexation when they are cleaved from the solid support.

Attempts to overcome these problems have been made through the attachment of bifunctional chelators to moieties of potential biological activities. The use of bifunctional chelators permits control of the type of metal coordination, the oxidation state of the coordinated metal, the stability and the conformation of the

resulting metal complex. A variety of bifunctional chelators are available. Examples of bifunctional chelators include polyamino polycarboxylates, polyamino polyphenolates, polyaza macrocycles with or without pendent coordination groups, tetradentate NxS4-x ligands, polyamino polyphosphates, polyamino polysulphides, polyamino polyheterocyclics and derivatives or combinations of the above mentioned chelators.2294 A number of techniques have been developed for attaching chelators to molecules of interest.25~32 However, problems in attaching stable metal complexes have not been adequately overcome because of the inability to produce chelators that provide for the stability necessary for the development of metallodrugs. As a result, the practice in this field has previously been to attach metal complexes to targeting molecules only after these molecules have been screened. As discussed above, the attachment of the metal complexes will often affect the binding of the lead targeting molecule to its receptor. This results in increased time and expense in searching for further lead molecules that do not lose their binding ability upon attachment to the chelated metal complex in question.

There is therefore a need for a method of producing a combinatorial library for isolating labeled radiopharmaceutical compounds that will bind to an appropriate receptor. There is a need for such a method that employs a suitable chelating agent that will permit the targeting molecule to be labeled prior to screening so that the labeled radiopharmaceutical compounds can be evaluated rapidly and efficiently to identify lead molecules. Such a method would significantly reduce the research and development effort required to identify new lead molecules.

Summarv of the invention The present invention provides combinatorial library compounds which are effective for binding to a biological target in a rapid and cost effective manner, as well as a method of synthesizing the compounds.

The present invention provides a combinatorial library of targeting agents that are labelled with a metal or radionuclide metal complexed to a chelating agent. A large number of labelled targeting agents can be quickly screened for their ability to bind to a biological target.

The present invention provides a combinatorial library of targeting compounds which have attached non-radioactive metal complexes which are isostructural with radiactive compounds for imaging applications or reactive Re complexes for radiotherapy.

According to one aspect of the present invention, there is provided a library comprising one or more sets of compounds, each set comprising a mixture of compounds of formula (1): A-(B)n-C (1) wherein: A is a chelator moiety capable of complexing a metal; B is a spacer group; n is selected from the integers 0 and 1; and C comprises one of a plurality of potential targeting molecules.

According to another aspect of the present invention there is provided a library comprising one or more sets of compounds, each set comprising a mixture of compounds of formula (11): (W)m-x-(y)n-z (11) wherein: W is selected from a group comprising: a) a metal binding moiety; b) a chelator moiety capable of binding a metal selected from polyamino polycarboxylates, polyamino polyphenolates, polyazamacrocycles with or without pendent coordination groups, tetradentate NXS4-X ligands,

polyamino polysulfides, polyamino polyphosphates, polyamino polyheterocyclics and derivatives or combinations of the above; c) a metal chelator of the general formula; X is a linear or branched, saturated or unsaturated C16 alkyl chain that is optionally interrupted by one or two heteroatoms selected from N, O, and S; and is optionally substituted by at least one group selected from hydroxyl, amino, carboxyl, C, 6 alkyl, aryl and C(O)Z; Y is H or a substituent defined by X; Z is the position of attachment for the targeting portion of the library; <BR> <BR> <BR> <BR> R' through R4 are selected independently from H; carboxyl; C, 4 alkyl; C,, alkyl substituted with a group selected from hydroxyl, amino, sulfhydryl, halogen, carboxyl, C14 alkoxycarbonyl and aminocarbonyl; an alpha carbon side chain of a D- or L- amino acid other than proline; and C(O)Z; R5 is selected from H and a sulphur protecting group; and T is carbonyl or CH2. d) a metal chelator selected from N,N-dimethyglycine-ser- cys-gly or N, N-dimethylglycine-tertbutylglycine-cys-g iy; and e) a chelator complexed to a metal or metal radionuclide; X is a multiple chelator binding moiety capable of coupling to at least one metal binding moiety; Y is a spacer group is selected from the integers 0 and 1; Z comprises a mixture of potential targeting moieties;

m is greater than or equal to 1; and n is selected from the integers 0 and 1.

According to another aspect of the present invention there is provided a method for the synthesis of a library comprising one or more sets of compounds, each set comprising a mixture of compounds of formula (1): A-(B)n-C (1) wherein: A is a chelator moiety capable of complexing a metal; B is a spacer group; n is selected from the integers 0 and 1; and C comprises one of a plurality of potential targeting molecules. comprising of the steps of: (1) Preparing a mixture of potential targeting molecules using combinatorial synthesis; (11) Attaching to the mixture a metal chelating moiety capable of complexing a metal; and (111) Complexing the mixture with a solution of the metal in a suitable solvent.

According to another aspect of the present invention, there is provided a method for the synthesis of a library comprising one or more sets of compounds, each set comprising a mixture of compounds of formula (1): A-(B)n-C (1) wherein: A is a chelator moiety capable of complexing a metal; B is a spacer group; n is selected from the integers 0 and 1; and C comprises one of a plurality of potential targeting molecules. comprising the steps of:

(1) Preparing a mixture of potential targeting molecules using combinatorial synthesis; and (11) Attaching to the mixture a preformed metal complex as an activated reagent in a suitable solvent.

According to yet another aspect of the present invention, there is provided a method of obtaining a compound having a desired targeting property comprising the steps of: (1) providing a mixture which comprises a set of candidate compounds of formula (1): A-(B)r-C (1) wherein: A is a chelator complexed to a metal or metal nuclide B is a spacer group n is selected from the integers 0 and 1 C is one of a plurality of potential targeting molecules; and (11) selecting from amongst the set of candidate compounds a compound having the desired property by exposing the mixture of candidate compounds to a substance to which the compound having the desired targeting property will preferentially bind.

According to another aspect of the present invention there is provided a method of obtaining a labeled compound for the purposes of diagnostic imaging having a desired targeting property comprising the steps of: (1) providing one or more sets of mixtures which comprise a mixture of candidate compounds of formula (1): A-(B)n-C (1) wherein: A is a chelator compiexed to a metal or metal nuclide B is a spacer group n is selected from the integers 0 and 1

C is one of a plurality of potential targeting molecules; and (11) selecting from among the set of candidate compounds a compound having the desired property by exposing the mixture of candidate compounds to a substance to which the compound having the desired targeting property will preferentially bind.

According to another aspect of the present invention there is provided a method of obtaining a labeled compound for the purposes of therapy or radiotherapy having a desired targeting property comprising the steps of; (1) providing one or more sets of mixtures which comprise a mixture of candidate compounds of formula (1): A-(B)n-C (1) Wherein: A is a chelator complexed to a metal or metal nuclide B is a spacer group n is selected from the integers 0 and 1; and C is one of a plurality of potential targeting molecules; and (11) selecting from among the set of candidate compounds a compound having the desired property by exposing the mixture of candidate compounds to a substance to which the compound having the desired targeting property will preferentially bind.

According to yet another aspect of the present invention, there is provided a method of obtaining a compound having a desired targeting property comprising the steps of; (1) providing a mixture or set of mixtures which comprise a set of candidate compounds of formula (11): (W)m-X-(Y)n-Z (11)

wherein: W is a metal binding moiety X is a multiple chelator binding moiety capable of coupling to at least one metal binding moiety Y is a spacer group is selected from the integers 0 and 1; and Z comprises a mixture of potential targeting moieties m is greater than or equal to 1; and n is selected from the integers 0 and 1; and (11) selecting from among the set of compounds a compound having the desired targeting property by exposing the mixture of compounds to a substance to which the compound having a desired targeting property will preferentially bind.

According to another aspect of the present invention, there is provided a method of obtaining a molecule having a desired targeting property comprising the steps of: (1) preparing a mixture or set of mixtures of candidate compounds of general formula (1): A-(B)n-C (1) Wherein: A is a chelator complexed to a non-radioactive metal which is isostructural with an analogous complex of a radioactive metal B is a spacer group n is selected from the integers 0 and 1; and C is one of a plurality of potential targeting molecules; (11) selecting from among the set of candidates a compound having the desired targeting property by exposing the mixture of candidate compounds to a substance to which the compound will preferentially bind; and (111) preparing the isostructural radioactive analogue of the selected candidate having the desired targeting property

According to another aspect of the present invention, there is provided a method for the synthesis of a library comprising one or more sets of compounds, each set comprising a mixture of compounds of formula (1): A-(B)n-C (1) Wherein: A is a chelator complexed to a non-radioactive metal which is isostructural with an analogous complex of a radioactive metal; B is a spacer group; n is selected from the integers 0 and 1; and C is one of a plurality of potential targeting molecules; comprising the steps of: (1) Preparing a mixture of potential targeting molecules using solid phase combinatorial synthesis; and (11) Attaching to the mixture a preformed metal complex as an activated reagent in a suitable solvent.

According to another aspect of the present invention there is provided a method for the synthesis of a library comprising one or more sets of compounds comprising the steps of: (I) Selecting a suitable targeting molecule for binding a biological target; (II) Preparing a library of non-radioactive rhenium-targeting molecule conjugates; (III) Dividing mixtures of the conjugates into separate wells; (IV) Assaying the mixtures for binding affinity to the biological target; (V) Deconvoluting the mixtures having a high a binding affinity for said biological target; and (Vl) Isolating a series of discrete compounds having a high a binding affinity for said biological target.

Descrintion The invention provides an iterative approach of library synthesis followed by biological testing and subsequent deconvolution to provide final compounds.

Following initial selection of a suitable target molecule, a moderately sized focused library of non-radioactive rhenium compounds is prepared as mixtures of up to 25 compounds. Typically, a large library of rhenium targeting moiety conjugates is delivered as equimolar mixtures of 9-25 compounds in 96 well microtiter plates (1 mg/well) for in vitro testing. These are then tested in the relevant assays and the most promising mixtures are segregated for deconvolution. Depending on the number of promising molecules, discovered, a second round of testing may then be undertaken using a smaller subset of the rhenium containing molecules together with a second set of biological tests to further reduce the number of molecules. The final iteration will provide a series of discrete compounds as both the rhenium complex and a free chelate ready for labeling with radioactive 99mtechnetium which is isostructural to the non-radioactive rhenium isotope used. The potential imaging lead candidates (preferably about 10 compounds) are delivered as pure chelator targeting moiety conjugates for radiolabeling development in in vivo studies. This process provides labeled compounds that are effective for binding a biological target in a rapid and cost effective manner.

The targeting moiety of the present invention is a molecule that can selectively deliver a chelated metal or radionuclide or MRI contrasting agent to a desired location in a mammal. Preferred targeting molecules selectively target cellular receptors, transport systems, enzymes, glycoproteins and processes such as fluid pooling. Examples of targeting molecules suitable for coupling to the chelator include, but are not limited to: steroids, proteins, peptides, antibodies, nucleotides and saccharides. Preferred targeting molecules include proteins and peptides, particularly those capable of binding with specificity to cell surface receptors characteristic of a particular pathology. For instance, disease states associated with over-expression of particular protein receptors can be imaged by labeling that protein or a receptor

binding fragment thereof coupled to a suitable chelator. Most preferably, targeting molecules are peptides capable of specifically binding to target sites and have three or more amino acid residues. The targeting moiety can be synthesized either on a solid support or in solution and is coupled to the next portion of the chelator-targeting moiety conjugates using known chemistry.

The second portion of the molecule, the optional linker, serves the purpose of separating the targeting portion from the imaging portion of the conjugate.

In the case of MRI agents, in order to increase the number of gadolinium (Gd) units attached to the biological target and for the purpose of increasing the relaxivity of the system, a multiple chelator coupling unit is attached to the targeting moiety (optionally via a linker subunit). This is of oligomeric or dendrimeric construction and is capable of coupling multiple chelator units to the conjugate. Preferably, this multiple chelator coupling unit is a dendrimer containing a functionality to which suitable chelators can be attached. Preferably, the multiple chelator coupling unit is a branched lysine dendrimer.

The metal chelators used for the purposes of the present invention have the following general formula:

wherein, X is a linear or branched, saturated or unsaturated C, 6 alkyl chain that is optionally interrupted by one or two heteroatoms selected from N, O,and S; and is optionally substituted by at least one group selected from hydroxyl, amino, carboxyl, C1-6 alkyl, aryl and C(O)Z; Y is H or a substituent defined by X; Z is the position of attachment for the targeting portion of the library; R' through R4 are selected independently from H; carboxyl; C,4 alkyl; C,4 alkyl substituted with a group selected from hydroxyl, amino, sulfhydryl, halogen, carboxyl, C14 alkoxycarbonyl and aminocarbonyl; an alpha carbon side chain of a D- or L- amino acid other than proline; and C(O)Z; R5 is selected from H and a sulphur protecting group; and T is carbonyl or CH2 Where a chelator is complexed to a metal or a metal radionuclide, the complex has the following general formula:

X is a linear or branched, saturated or unsaturated C1.6 alkyl chain that is optionally interrupted by one or two heteroatoms selected from N, O, and S; and is optionally substituted by at least one group selected from hydroxyl, amino, carboxyl, C1-6 alkyl, aryl and C(O)Z; Y is H or a substituent defined by X; Z is the position of attachment for the targeting portion of the library; R' through R4 are selected independently from H; carboxyl; CiA alkyl; C1-4 alkyl substituted with a group selected from hydroxyl, amino, sulfhydryl, halogen, carboxyl, CiA alkoxycarbonyl and aminocarbonyl; an alpha carbon side chain of a D- or L- amino acid other than proline; and C(O)Z; T is carbonyl or CH and M is metal The preferred chelators for 99mtechnetium radiopharmaceuticals are RP414 and RP455. The structures of RP414 and RP455 are as follows: R=CH2OH RP414 R = C(CH3)3 RP455 Re and Tc complexes of these chelators are isostructural. Also, these chelators are advantageous because the chemistry of these compounds is well understood and they form neutral Re and 99mTc complexes. It is possible to label these chelators with Re or 99mTc in one easy step. In addition these chelators have

the advantage of being applicable for conjugation to a variety of targeting molecules, being compatible with solid phase synthesis.

Labeling of RP414 with 99mTc can be carried out either at ambient or elevated temperature, rapidly, and with quantities of chelator approaching stoichiometric amounts. The complex is stable to both acidic and basic conditions and remains unchanged in-vivo.

Other chelators may be used to carry out the invention. The invention is not limited to the preferred chelators listed above.

With MRI agents, the chelator comprises a functionality chosen from the known Gd chelators and is attached to the remainder of the conjugate by either solid phase or solution chemistry.

The following examples illustrate further this invention. Abbreviations used in the examples include Acm: acetoamidomethyl; Arg: arginine; Boc: tert- butyioxycarbonyl; Cys: cysteine; DIEA: diisopropylethylamine; Dimethylgly: N,N- dimethylglycine; DMF: N,N-dimethylformamide; ES-MS: Electron Spray Mass Spectrometry; Fmoc: 9-fluorenylmethyloxycarbonyl; Gly: glycine; HBTU: 2-(1 H- benzotriazol-1 -yl)-1 , 1 ,3,3-tetramethyl-uronium hexafluorophosphate; HOBT: 1- hydroxybenzotriazole; HPLC: high performance liquid chromatography; Leu: leucine; Lys: lysine; mL: millilitre(s); mmol: millimole(s); mol: mole(s); Mott: 4-methoxytrityl; NMP: N-methylpyrrolidone; Phe: phenylalanine; Pmc: 2,2,5,7,8- pentamethylchroman-6-sulfonyl; Rt: retention time; sasrin: 2-methoxy-4-alkoxybenzyl alcohol (super acid sensitive resin); Ser: serine; t-Bu: tert-butyl; TFA: trifluoroacetic acid; Thr: threonine; Trt: trityl; Tyr: tyrosine; Ye-R: protection group R is attached to the peptide chain via the atom, Y, on the amino acid side chain (Y is N, O or S and R is Acm, Boc, Mott, t-Bu or Trt). N-methylpyrrolidone, dimethylformamide, 2-(1H- benzotriazol-1-yl)-1, 1 ,3,3-tetramethyl-uronium hexafluorophosphate, 1- hydroxybenzotriazole, diisopropylethyl-amine, dichloromethane and trifluoroacetic

acid were purchased from Applied Biosystems Inc. Triethylamine and tert-butyl methyl ether were purchased from Aldrich Chemical Inc. Fmoc amino acids and Sasrin resin were purchased from Bachem Bioscience Inc. All chemicals were used as received. tReO2(en)2]Cl and ReOCl3(PPh3)2 were prepared according to literature methods (Rouschias, G. Chem. Rev. 1974, 74, 531; Fergusson, J. E. Coord. Chem.

Rev. 1966,1, 459). Mass spectra (electrospray) were obtained on a Sciex API&num 3 mass spectrometer in the positive ion detection mode. HPLC analyses and purifications were made on a Beckman System Nouveau Gold chromatographic system with a Waters 4 mm radial pak C-18 column. During analytical HPLC analysis, the mobile phase was changed from 100% 0.1% aqueous trifluoroacetic acid to 100% acetonitrile containing 0.1% trifluoroacetic acid over 20 minutes at a flow rate of 2 mL/min. The HPLC analyses of the RP487 peptide mixture and the Re complexes of the peptide mixture were performed by changing the mobile phase from 100% 0.1% aqueous trifluoroacetic acid to 60% acetonitrile containing 0.1% trifluoroacetic acid over 20 minutes at a flow rate of 2 ml/min. All HPLC analyses were monitored with a UV detector set at 215 and 254 nm. Solid phase peptide syntheses were performed on an ABI Peptide Synthesizer model 433A using FastMoc chemistry and sasrin resin (User' Manual of Peptide Synthesizer Model 433A, Applied BioSystems, Philadelphia. 1993).

Example 1: Preparation of a Re or Tc receptor specific radiopharmaceutical In preparing a combinatorial library of Re or 99Inc receptor specific radiopharmaceuticals, a set of potentially receptor specific structurally distinct molecules are placed on a solid support. A bifunctional chelator such as dimethylglycine-serine-cysteine-glycine is attached to the library of molecules using tetrafluorophenol and 1-[3-(dimethylamino)-propyl]3-ethylcarbodiimide chloride. The resulting solid phase library is then heated in a solution of ReOCI3(PPh3)2 or [ReO2(en)2]CI to produce a library of Re complexes. The library of 99etc complexes can be prepared by reacting the library with pertechnetate in the presence of tin (II) chloride and sodium gluconate. Alternatively, the library of Re and 99etc complexes

can be prepared by reacting the set of potentially receptor specific molecules with the tetrafluorophenol esters of Re and Tc dimethg lycine-serine-cysteine-g lycine complexes. The libraries of Re and 99Inc complexes are then cleaved off the solid support and evaluated in biological assay or in imaging studies.

Example 2: Synthesis of Gd complex as a receptor specific MRI contrasting agent.

Upon deciding on a particular receptor, a series of potentially receptor specific structurally distinct molecules are attached to solid phase support. Using diethylenetriaminetetraacetic acids dianhydride, the chelator diethylenetriaminetetraacetic acid (DTPA) is attached to the set of potentially receptor specific molecules. The resulting solid phase library is then placed in a solution of Gd acetate to produce a solid phase library of potentially receptor specific Gd complexes. The Gd is coordinated to the DTPA chelator. The library of Gd complexes is then cleaved off the solid support and evaluated in a biological assay.

Example 3: Development of a magnetic resonance imaging agent.

Some current attempts to produce efficient relaxation have resulted in the preparation of molecules having a number of gadolinium chelator molecules attached to one targeting molecule, often by way of a linker moiety to allow space between the target and the chelation parts of the molecule37~39 The molecule can be divided into four parts; the targeting moiety, an optional suitable linker, a multiple chelator coupling unit capable of coupling multiple chelator moieties, and the chelator moieties coupled to the multiple chelator coupling unit.

The targeting moiety is a molecule that can selectively deliver a chelated radionuclide or MRI contrasting agent to a desired location in a mammal.

The second portion of the molecule, the optional linker, serves the purpose of separating the targeting portion from the imaging portion of the conjugate.

In order to increase the number of gadolinium units attached to the biological target and for the purpose of increasing the relaxivity of the system a multiple chelator coupling unit is attached to the targeting moiety (optionally via a linker subunit). This is of oligomeric or dendrimeric construction and is capable of coupling multiple chelator units to the conjugate. Preferably, this multiple chelator coupling unit is a dendrimer containing a functionality to which suitable chelators can be attached. Preferably, the multiple chelator coupling unit is a branched lysine dendrimer.

The final portion of the conjugate will consist of the chelator units. This comprises a functionailty chosen from the known Gd chelators and is attached to the remainder of the conjugate by either solid phase or solution chemistry.

In order to synthesize the combinatorial libraries, mixtures of compounds in any or all of the above subsections of the agent are prepared. In addition, the preparation of a combination of libraries having a mixture in one of the sections, together with a series of related libraries produced by the alteration of the previous or subsequent parts of the agent is carried out in a parallel fashion. Hence, a library of targeting molecules would be split and each part attached to a single linker- dendrimer-chelator subunit. Such a route provides a parallel series of libraries each having a single linker-dendrimer-chelator unit in order to optimize the targeting of the molecules. Producing a mixture of compounds based on the dendrimer and single targeting-linker and chelator units allows for variation of the relaxivity of the system.

Example 4: Synthesis of Peptides Attached to a Solid Polymer Resin.

Peptides of various amino acid sequences and with varying side chain protection groups were prepared via a solid phase peptide synthesis method on an

automated peptide synthesizer using FastMoc 1.0 mmole chemistry.3 Preloaded Fmoc amino acid sasrin resin and Fmoc amino acid derivatives were used. Prior to the addition of each amino acid residue to the N-terminus of the peptide chain, the FMOC group was removed with 20% piperidine in NMP. Each Fmoc amino acid residue was activated with 0.50 M HBTU/ HOBt/ DMF, in the presence of 2.0M DIEA/ NMP. The C-terminus of the completed peptide was attached to the resin via the sasrin linker. The peptidyl resin was washed with dichloromethane and dried under vacuum for 20-24 hours. This method was used to prepare the following peptidyl resin of varying amino acid sequences containing side chain protection groups: 1)RP414-resin: Dimethylgly-Ser(Oe-t-Bu)-Cys(Se-Acm)-Gly-[resin] 2)RP440-resin: Dimethylgly-Ser(Oe-t-Bu)-Cys(Se-Trt)-Gly-[resin] 3)RP441-resin: Dimethylgly-Ser(Oe-Trt)-Cys(Se-Mott)-Gly-Thr-Lys(Ne- Boc)-Pro-Pro-Arg(Ne-Pmc)-[resin] 4)RP442-resin: Dimethylgly-Ser(Oe-Trt)-Cys(Se-Trt)-Gly-[resin] 5)RP443-resin: Dimethylg ly-Ser(O"-Trt)-Cys(S"-Mott)-Gly-[resin] 6)RP478-resin: Dimethylgly-Ser(Oe-Trt)-Cys(Se-Mott)-Gly-Gly-Lys(Ne- Boc)-Lys(Ne-Boc)-Leu-Leu-Lys(Ne-Boc)-Lys(Ne-Boc)-Leu Lys(Ne-Boc)-Lys(Ne-Boc)-Leu-Leu-Lys(Ne-Boc)-Lys(Ne- Boc)-Leu-NH2-[resin] Example 5: Synthesis of RP487 peptide mixture-resin, Dimethylgly-Ser(Oe-Trt)- Cys(Se-Mott)-Gly-X-Tyr(Oe-t-bu)-Gly-Z-Gly-[resin] (where X are Leu, Arg(Ne Pmc) or Phe and Z are Lys(Ne-Boc), Ser(Oe-Trt) or Tyr(Oe-t-bu)).

The synthesis of the RP487 peptide mixture resin was performed using FastMoc 0.25 mmol chemistry on an automated synthesizer.35 Fmoc-Gly sasrin- resin (0.7 mmol/ g, 0.25 mmol, 357 mg) was placed in the reaction vessel. Amino acid cartridges 2, 3, 5, 6, and 7 counted from the C-terminus contained 1 mmol of each Fmoc amino acid derivatives, Gly, Tyr(Oe-t-Bu), Gly, Cys(Se-Mott), and

Ser(Oe-Trt), respectively. Cartridge I had Fmoc amino acid derivatives of Lys(Ne- Boc), Ser(Oe-Trt), and Tyr(Oe-t-Bu) (0.33 mmol / amino acid). Meanwhile, cartridge 4 carried Fmoc amino acids of Arg(Ne-Pmc), Leu, and Phe (0.33 mmol/ amino acid).

N,N-Dimethylglycine (1mmol) in cartridge 8 was pre-treated with 0.50 M HBTU/ HOBt/ DMF (0.8 mL) before it was inserted on the synthesizer. After completion of the automatic synthesis, the resulting product was removed from the synthesizer, and dried under vacuum for 2 hours to afford the titled RP487 peptide mixture-resin (610 mg).

Example 6: Synthesis of RP487 peptide mixture, Dimethylgly-Ser-Cys-Gly-X- Tyr-Gly-Z-Gly (where X is Leu, Arg or Phe and Z is Lys, Ser or Tyr).

The RP487 peptide mixture-resin (120 mg 0.05 mmol) was added to a cleavage composition of 82.5% TFA/ 5% phenol/ 5% thioanisole/ 2.5% 1,2-ethane dithioll 5% mili-Q water (1 mL) at o °C.36 The reaction suspension was then stirred at room temperature for 5 hours. The cleavage suspension was filtered by vacuum after 5 hours, and the filtrate was allowed to add in cold tert-butyl methyl ether (20 mL) at 5°C. The precipitated residue was subsequently washed with tert-butyl methyl ether (2 x 30 mL). The resulting residue was then dissolved in milli-Q water (2 mL), frozen and lyophilized (22 hours) to give the titled RP487 peptide mixture as an off-white pellet (52 mg). Mass spectrum (electrospray): m/z = 828 (MH+, [C34H54N9O13S1]), (X is Leu and Z is Ser); m/z = 862 (MH+, [C37H52N9O13S1]), (X is Phe and Z is Ser};. m/z = 869 (MH+, [C37H61N10O12S1]), (X is Leu and Z is Lys); m/z = 871 (MH+, [C34H55N12O13S1]), (X is Arg and Z is Ser}; m/z = 903 (MH+, [C40H59N10012S1]), {X is Phe and Z is Lys}; m/z = 904 (MH+, [C40H58N9O13S1]), (X is Leu and Z is Tyr); m/z = 912 (MH+, [C37H62N13O12S1]), (X is Arg and Z is Lys); m/z = 938 (MH+, [C43H56N9013S1]), (X is Phe and Z is Tyr }; m/z = 947 (MH+, [C40H59N12O13S1j), {X is Arg and Z is Tyr). HPLC retention time: Rt = 7.18 minutes (broad peak); Rt = 9.0-9.9 minutes (overlapping broad peak); Rt = 11.0-11.5 minutes (overlapping broad peak); Rt = 16.5-16.8 minutes (broad overlapping peaks); Rt = 17.9 minutes (broad peaks).

Example 7: Synthesis of Re oxo complex of Dimethylgly-Ser-Cys-Gly using RP442-resin.

RP442-resin (0.1055 g) was swollen in 3 mL of NMP. ReOCl3(PPh3)2 (0.3793 g, 0.000456 moles) and 1 mL of triethylamine were added to the NMP resin mixture.

The ReOCl3(PPh3)2 dissolved to give a purple mixture. The mixture was heated at 40-50 "C for 4 hours. The resin was then collected by vacuum filtration. The resin was washed with 3 x 10 mL NMP, followed by 3 x 10 mL CH2CI2. The resin was dried under vacuum overnight. To cleave the Re complex off the solid support, the resin was placed in 90 % aqueous trifluoroacetic acid and stirred for 4 hours. The resin was removed by vacuum filtration and the supernatant was added dropwise to tert-butyl methyl ether at 0 "C. Red-brown precipitate formed. The precipitate was collected by centrifugation and analyzed by HPLC and electrospray mass spectrometry. The syn and anti isomers of the Re complex were observed in the HPLC chromatogram. This is consistent with other known Re complexes with N4.XSx chelators. The coordination of the peptide to the Re metal caused the displacement of the cysteine sulfur trityl protection group but did not cause the peptide to be cleaved off the resin. The cleavage of the peptidic complex off the resin in acidic medium removed all remaining side chain protection groups but did not cause the metal complex to undergo decomplexation.. Mass spectrum (electrospray): m/z = 550 (MH+, [C12H20N407Re,S1]) HPLC retention time: Rt = 5.98 minutes (isomer A); R, = 6.22 minutes (isomer B).

Example 8: Synthesis of Re oxo complex of Dimethylgly-Ser-Cys-Gly using RP443-resin.

RP443-resin (0.1621 g) was swollen in 3 mL of NMP. ReOCl3(PPh3)2 (0.4023 g, 0.000483 moles) and 1 mL of triethylamine were added to the NMP resin mixture.

The ReOCl3(PPh3)2 dissolved to give a purple mixture. The mixture was heated at 40-50 "C for 4 hours. The resin was then collected by vacuum filtration. The resin

was washed with 3 x 10 mL NMP, followed by 3 x 10 mL CH2CI2. The resin was dried under vacuum overnight. To cleave the Re complex off the solid support, the resin was placed in 90 % aqueous trifluoroacetic acid and stirred for 4 hours. The resin was removed by vacuum filtration and the supernatant was added dropwise to tert-butyl methyl ether at 0 "C. Red-brown precipitate formed. The precipitate was collected by centrifugation and analyzed by HPLC and electrospray mass spectrometry. The syn and anti isomers of the Re complex was observed in the HPLC chromatogram. The coordination of the peptide to the Re metal caused the displacement of the cysteine sulfur trityl protection group but did not cause the peptide to be cleaved off the resin. The cleavage of the peptidic complex off the resin in acidic medium removed all remaining side chain protection groups but did not cause the metal complex to undergo decomplexation. Mass spectrum (electrospray): m/z = 550 (MH+, [C12H20N407Re,S,]). HPLC retention time: Rt = 5.53 minutes (isomer A); R, = 6.13 minutes (isomer B).

ExamPle 9: Synthesis of Re oxo complex of Dimethylgly-Ser-Cys-Gly-Thr-Lys- Pro-Pro-Arg using RP441-resin.

RP441-resin (0.0799 g) was swollen in 3 mL of NMP. ReOCI3(PPh3)2 (0.3983 g, 0.000478 moles) and 1 mL of triethylamine were added to the NMP resin mixture.

The ReOCl3(PPh3)2 dissolved to give a purple mixture. The mixture was heated at 40-50 "C for 8 hours. The resin was then collected by vacuum filtration. The resin was washed with 3 x 10 mL NMP, followed by 3 x 10 mL CH2CI2. The resin was dried under vacuum overnight. To cleave the Re complexes off the solid support, the resin was placed in 90 % aqueous trifluoroacetic acid and stirred for 4 hours.

The resin was removed by vacuum filtration and the supernatant was added dropwise to tert-butyl methyl ether at 0 "C. Red-brown precipitate formed. The precipitate was collected by centrifugation and analyzed by HPLC and electrospray mass spectrometry. The syn and anfi isomers of the Re complex were observed in the HPLC chromatogram. The coordination of the peptide to the Re metal caused the displacement of the cysteine sulfur trityl protection group but did not cause the

peptide to be cleaved off the resin. The cleavage of the peptidic complex off the resin in acidic medium removed all remaining side chain protection groups but did not cause the metal complex to undergo decomplexation. Mass spectrum (electrospray): m/z = 1129 (MH+, [C36H65N13O13Re1S1]). HPLC retention time: Rt = 6.18 minutes (isomer A); R, = 6.70 minutes (isomer B).

Example 10: TKPPR+ReORP455-TP-P ester: To a slurry of sasrin-Arg-Pro-Pro-Lys-Thr resin (15mg) in ethyl acetate (0.5mL) was added a solution of ReO-N,Ndimethylglycine-ser-cys-gly-Offp (prepared from 10mg of ReO-N,N-dimethyglycine-ser-cys-gly-OH) in ethyl acetate (0.5mL) and the resulting solution shaken intermittently at room temperature for 2h.

The resulting colourless solution was filtered off from the now pink/brown resin and the resin washed with ethyl acetate followed by dichloromethane and then dried in vacua. The peptide-chelate conjugate was then liberated from the resin by treatment with 0.5mL 95% trifluoroacetic acid at room temperature for 1.5h. The solution was then filtered off and the volatiles removed under reduced pressure. Presence of ReORP128 was confirmed by co-injection of the product with an authentic sample of ReORP128 prepared by solution chemistry (retention time 9.15 using a gradient elution of 0 to 100% acetonitrile in water buffered with 0. 1% trifluoroacetic acid over 20 mins) Example 11: Synthesis of Re oxo complex of Dimethylgly-Ser-Cys-Gly-Gly-Lys- Lys-Leu-Leu-Lys-Lys-Leu-Lys-Lys-Leu-Leu-Lys-Lys-Leu-N H2 using RP478- resin.

RP478-resin (0.1125 g) was swollen in 3 mL of NMP. ReOCl3(PPh3)2 (0.6351 g, 0.000763 moles) and 1 mL of triethylamine were added to the NMP resin mixture.

The ReOCl3(PPh3)2 dissolved to give a purple mixture. The mixture was heated at 40-50 "C for 8 hours. The resin was then collected by vacuum filtration. The resin was washed with 3 x 10 mL NMP, followed by 3 x 10 mL CH2CI2. The resin was

dried under vacuum overnight. To cleave the Re complex off the solid support, the resin was placed in 90 % aqueous trifluoroacetic acid and stirred for 8 hours. The resin was removed by vacuum filtration and the supernatant was added dropwise to tert-butyl methyl ether at 0 "C. Red-brown precipitate formed. The precipitate was collected by centrifugation and analyzed by HPLC and electrospray mass spectrometry. The syn and anti isomers of the Re complex was observed in the HPLC chromatogram. The coordination of the peptide to the Re metal caused the displacement of the cysteine sulfur trityl protection group but did not cause the peptide to be cleaved off the resin. The cleavage of the peptidic complex off the resin in acidic medium removed all remaining side chain protection groups but did not cause the metal complex to undergo decomplexation. Mass spectrum (electrospray): m/z = 2310 (MH+, [Cg8H,88N2802,Re,S]). HPLC retention time: Rt = 11.17 minutes (broad peak).

Example 12: Synthesis of Re oxo complex of Dimethylgly-Ser-Cys-Gly-X-Tyr- Gly-Z-Gly (where X is Leu, Arg or Phe and Z is Lys, Ser or Tyr) using RP487- resin.

RP487-resin (0.0618 g) was swollen in 3 mL of NMP. ReOCl3(PPh3)2 (0.9210 g, 0.00111 moles) and 1 mL of triethylamine were added to the NMP resin mixture.

The ReOCl3(PPh3)2 dissolved to give a purple mixture. The mixture was heated at 40-50 OC for 12 hours. The resin was then collected by vacuum filtration. The resin was washed with 3 x 10 mL NMP, followed by 3 x 10 mL CH2Cl2. The resin was dried under vacuum overnight. To cleave the Re complexes off the solid support, the resin was placed in 90 % aqueous trifluoroacetic acid and stirred for 4 hours.

The resin was removed by vacuum filtration and the supernatant was added dropwise to tert-butyl methyl ether at 0 "C. Red-brown precipitate formed. The precipitate was collected by centrifugation and analyzed by HPLC and electrospray mass spectrometry. Since the Re complex of each peptide sequence exists as the syn and anti isomers, the total number of compounds prepared was 18. Mass spectrum (electrospray): m/z = 1027 (MH+, [C34H51N9O14Re1S1j), (X is Leu and Z is

Ser); m/z = 1062 (MH+, [C37H50N9O14Re1S1]), (X is Phe and Z is Ser};. m/z = 1069 (MH+, [C37H59N10O13Re1S1]), (X is Leu and Z is Lys}; m/z = 1071 (MH+, [C34H53N12O14Re1S1]), {X is Arg and Z is Ser); m/z = 1103 (MH+, [C40H57N10O13Re1S1]), (Xis Phe and Z is Lys}; m/z = 1104 (MH+, [C40H56N9O14Re1S1]), (Xis Leu and Z is Tyr}; m/z = 1112 (MH+, [C37H60N13O13Re1S1]), (X is Arg and Z is Lys }; m/z = 1138 (MH+, [C43H54N9O14Re1S1]), (X is Phe and Z is Tyr); m/z = 1147 (MH+, C40H57N12O14Re1S1]), (X is Arg and Z is Tyr }. HPLC retention time: R, = 8.40 minutes; Rt = 8.99 minutes; R, = 9.62 minutes; R = 9.90 minutes; Rt = 10.14 minutes; Rt= 11.0-12.7 minutes (overlapping peaks); Rt = 15.1 minutes (broad peak); R, = 15.4 minutes (broad peak).

Example 13: Synthesis of Re oxo complex of Dimethylgly-Ser-Cys-Gly-X-Tyr- Gly-Z-Gly (where Xare Leu, Arg or Phe and Z are Lys, Ser or Tyr) in aqueous solution.

[ReO2(en)2]Cl (0.0434 g, 0.000116 moles) was dissolved in 1.5 mL of milli-Q water. The mixture of the 9 peptides (0.0436 g) was dissolved in 2 mL of milli-Q water. The two solutions were combined to give a light green solution. The pH of the solution was adjusted to 6 using 1 M NaOH. The solution was refluxed under Ar for 2 hours, during which time the solution changed from green to red. The solution was frozen and lyophilized overnight, yielding a red solid. The solid was analyzed by HPLC and electrospray mass spectrometry. Mass spectrum (electrospray): m/z = 1027 (MH+, [C34N51N9O14Re1S1]), (X is Leu and Z is Ser); m/z = 1061 (MH+, C37H49N9O14Re1S1]), (X is Phe and Z is Ser);. m/z = 1068 (MH+, [C37H58N10C13Re1S1j), (X is Leu and Z is Lys}; m/z = 1071 (MH+, [C34H53N12O14Re1S1]), (X is Arg and Z is Ser); m/z = 1103 (MH+, [C40H57N10O13Re1S1]), (Xis Phe and Z is Lys}; m/z = 1104 (MH+, [C40H56N9O14Re1S1]), (X is Leu and Z is Tyr}; m/z = 1112 (MH+, [C37H60N13O13Re1S1]), (X is Arg and Z is Lys); m/z = 1138 (MH+, [C43H53N9C14Re1S1]) (X is Phe and Z is Tyr); m/z = 1146 (MH+, [C40H56N12O14Re1S1]), (X is Arg and Z is Tyr). HPLC retention time: R, = 8.45 minutes; Rt = 9.02 minutes; Rt = 9.67 minutes;

Rt = 9.95 minutes; Rt = 10.27 minutes; R, = 11.0-12.8 minutes (overlapping peaks); Rt = 15.2 minutes (broad peak); Rt = 15.7 minutes (broad peak).

Example 14: Use of multiple discrete loaded resins in one reactor vessel to provide a combinatorial library The various peptide sequences containing varying side chain protecting groups in these examples were synthesized via a solid phase synthesis method on an automated synthesizer using FastMoc chemistry on scales varying from 0.1 to 1.0mmol. Prior to the addition of each amino acid residue to the N-terminus of the peptide chain the FMOC group was removed with 20% piperidine in NMP. Each FMOC amino acid was activated with 0.5M HOBT/HBTU/DMF in the presence of 2.0M DIEA/NMP. The C-terminus was attached to the solid phase via the sasrin iinker. After completion of the synthesis the resin was washed with NMP followed by dichloromethane and dried under vacuum for up to 24 hours.

Example 15: Synthesis of a library of peptides on solid phase having the sequence Dimethylglycine-Ser(O-Trt)-Cys(S-Acm)-Gly-X-Tyr(O-t-Bu)-Gly- Z-Y (Where X is Leu, Arg(N-Pmc), or Phe, Z is Lys(N-Boc), Ser(O-Trt), or Tyr(o~t- Bu), and Y is Gly, Phe, Leu, Arg(N-Pmc), or Lys(N-Boc)) The reactor vessels employed in the peptide synthesizer were loaded with a mixture of 5 MicroKans (supplied by IRORI ) each containing 30mg of Tenta gel TGA resin having the following amino acids preloaded; glycine, Phenylalanine, Leucine, Arginine, Lysine. This mixture was then subjected to the conditions described above to synthesize the following amino acid sequence onto each of the resins; <BR> <BR> <BR> <BR> <BR> <BR> RPLl B6G-resin: Dimethylg Iy-ser(O-t-bu)-Cys(S-Acm)-Gly-X-Tyr(O-t-Bu)-Gly-Z- Gly-Resin

RPLl B6F-resin Dimethylg ly-ser(O-t-bu)-Cys(S-Acm)-Gly-X-Tyr(O-t-Bu)-Gly-Z Phe-Resin RP LI B6L-resin: Dimethylg ly-ser(O-t-bu)-Cys(S-Acm)-G ly-X-Tyr(O-t-Bu)-Gly-Z- Leu-Resin <BR> <BR> <BR> <BR> <BR> <BR> RP LI B6R-resin: Dimethylg Iy-ser(O-t-b u )-Cys(S-Acm)-G Iy-X-Tyr(O-t-B u)-G Iy-Z- Arg-Resin RPLIB6K-resin: Dimethylgly-ser(O-t-bu)-Cys(S-Acm)-Gly-X-Tyr(O-t-Bu)-Gly-Z- Lys-Resin Where X consists of a mixture of FMOC amino acid derivatives of Leu, Arg (N-Pmc), or Phe, and Z consists of a mixture of FMOC amino acid derivatives of Lys(N-boc), Ser(O-trt) or Tyr(O-t-Bu). These mixture are incorporated into the peptide synthesis using the method outlined In example 2 Example 16: Synthesis of a series of peptides having the sequence Dimethylglycine-Ser-Cys-Gly-X-Tyr-Gly-Z-Y (Where X is Leu, Arg, or Phe, Z is Lys, Ser, or Tyr, and Y is Gly, Phe, Leu, Arg, or Lys) The RPLIB6 mixtures prepared in example 15 above (30mg) were added to a cleavage mixture consisting of 95% TFA in water (300 L). The reaction suspensions were then shaken at room temperature for 3hours. The mixtures were then filtered and added to tert-butyl methyl ether (1mL). The resulting solid was collected and dried under vacuum then analysed by HPLC using a method of 0 to 100% acetonitrile in water buffered with 0.1% trifluoroacetic acid. Comparison of the particular peptide sequence where Y is Gly with that peptide synthesized in example 6 by HPLC showed formation of the required compounds.

Example 17: Investigation of the effect of amide capping group (CG)NH on the agonistlantagonist functioning ability of peptide CG-NH-Nle-Leu-Leu-Phe-Lys Gly-COOH The N-terminal amine of the above peptide attached to sasrin resin (100mg) is deprotected of its Fmoc group under standard Fmoc deprotection conditions. The amine is then capped with a suitably reactive reagent (see list below). The resin is placed in a solution of NMP (500uL) for the resin to swell. To this solution is added DIEA (25uL, 2M) and one of the capping agents (0.5mmol). The reaction is shaken for 2 to 18 hours at room temperature. The reaction is filtered and the resin is washed with NMP (3x5mL) then dichloromethane (3x5mL) and the resin is dried in vacua. The capped peptide is removed from the resin by shaking in the presence of 95% Trifluoroacetic acid (0.5-lmL) at room temperature for 4 hours. After the cleavage is complete the resin is filtered off and then washed with further trifluoroacetic acid (0.5mL). The combined trifluoroacetic acid solutions are then combined and concentrated under reduced pressure. The capped peptide is then purified by reverse phase HPLC on C18 silica gel using a gradient of 0-100% acetonitrile in water over a period of 20 mins The cuts containing the relevant compound are then lyophilized and the peptide analyzed by electrospray mass spectroscopy. The peptides display the properties shown in the table below.

RP# Capping Group # Retention Time Molecular Weight 522-2 2 11.31 592 522-3 3 12.07 614 522-4 4 13.24 670 522-6 6 12.69 619 522-7 7 12.92 618 522-10 10 13.06 653 522-12 12 11.76 738

522-13 13 14.50 682 522-14 14 12.89 676 522-15 15 13.23 650 522-16 16 14.96 742 522-17 17 11.70 588 522-18 18 14.13 715 A list of the amine capping agents (and the associated capping group number) includes but is not limited to: Example 18: Synthesis of a library of 324 potential chemotactic peptides using a combination of parallel synthesis and split and mix technologies Libraries are based on the following peptide sequence:

RP# Mixture A,B,C Mixture D,E,F Capping Group 552-6 Phe, Asp, Leu Trp, Ser, Tyr N,N-diethycarbamyl 552-10 Phe, Asp, Leu Trp, Ser, Tyr N-phenyl,N-methylcarbamyl 552-13 Phe, Asp, Leu Trp, Ser, Tyr Adamantylcarbonyl 552-16 Phe, Asp, Leu Trp, Ser, Tyr Fluorenylmethylcarbonyl 552-17 Phe, Asp, Leu Trp, Ser, Tyr Cyclopropylcarbonyl 552-18 Phe, Asp, Leu Trp, Ser, Tyr N,N-diphenylcarbamyl 553-6 Glu, His, Lys Trp, Ser, Tyr N,N-diethycarbamyl 553-10 Glu, His, Lys Trp, Ser, Tyr N-phenyl,N-methylcarbamyl 553-13 Giu, His, Lys Trp, Ser, Tyr Adamantylcarbonyl 553-16 Glu, His, Lys Trp, Ser, Tyr Fluorenylmethylcarbonyl 553-17 Glu, His, Lys Trp, Ser, Tyr Cyclopropylcarbonyl 553-18 Glu, His, Lys Trp, Ser, Tyr N,N-diphenylcarbamyl 554-6 Asn, Arg, Val Glu, His, Lys N,N-diethycarbamyl 554-10 Asn, Arg, Val Glu, His, Lys N-phenyl,N-methylcarbamyl 554-13 Asn, Arg, Val Glu, His, Lys Adamantylcarbonyl 554-16 Asn, Arg, Val Glu, His, Lys Fluorenylmethylcarbonyl 554-17 Asn, Arg, Val Glu, His, Lys Cyclopropylcarbonyl 554-18 Asn, Arg, Val Glu, His, Lys N,N-diphenylcarbamyl 555-6 Phe, Asp, Leu Asn, Arg, Val N,N-diethycarbamyl 555-10 Phe, Asp, Leu Asn, Arg, Val N-phenyl,N-methylcarbamyl 555-13 Phe, Asp, Leu Asn, Arg, Val Adamantylcarbonyl 555-16 Phe, Asp, Leu Asn, Arg, Val Fluorenylmethylcarbonyl 555-17 Phe, Asp, Leu Asn, Arg, Val Cyclopropylcarbonyl 555-18 Phe, Asp, Leu Asn, Arg, Val N,N-diphenylcarbamyl 556-6 Trp, Ser, Tyr Asn, Arg, Val N,N-diethycarbamyl 556-10 Trp, Ser, Tyr Asn, Arg, Val N-phenyl,N-methylcarbamyl 556-13 Trp, Ser, Tyr Asn, Arg, Val Adamantylcarbonyl 556-16 Trp, Ser, Tyr Asn, Arg, Val Fluorenylmethylcarbonyl 556-17 Trp, Ser, Tyr Asn Arg, Val Cyclopropylcarbonyl 556-18 Trp, Ser, Tyr Asn Arg, Val N,N-diphenylcarbamyl 557-6 lie, Gln, Thr Asn. Arg Val N,N-diethycarbamyl 557-10 lle, Gln, Thr Asn Arg Val N-phenyl,N-methylcarbamyl 557-13 lle, Gln, Thr Asn. Arg. Val Adamantylcarbonyl 557-16 lle, Gln, Thr Asn, Arg, Val Fluorenylmethylcarbonyl 557-17 lle, Gln, Thr Asn Arg, Val Cyclopropylcarbonyl 557-18 lle, Gln, Thr Asn, Arg, Val zN,N-diphenylcarbamyl The various peptide sequences (that is the sequence Gly-Lys(DDE)-(mixture A,B,C)-(mixture D,E,F)-Phe-Leu-Nle-NH2 and numbered RP552 through RP557) containing varying side chain protecting groups in these examples were synthesised via a solid phase synthesis method on an automated synthesizer using FastMoc chemistry on 1.0 mmol scale. Prior to the addition of each amino acid residue (or mixture of acids as described above) to the N-terminus of the peptide chain the FMOC group was removed with 20% piperidine in NMP. Each FMOC amino acid

was activated with 0.5M HOBT/HBTU/DMF in the presence of 2.0M DIEA/NMP. The C-terminus was attached to the solid phase via the sasrin linker. After completion of the synthesis the resin was washed with NMP followed by dichloromethane and dried under vacuum for up to 24 hours. Where mixture of amino acids were employed the three amino acids were added as equimolar mixtures of suitably side chain protected FMOC acid residues in a single coupling step and otherwise treated as a single amino acid residue.

Example 19: Capping the terminal amino group of peptide mixtures (RP552- 557) The N-terminal amino group of each mixture of 9 compounds is deprotected of its Fmoc group under standard fmoc deprotection conditions. The amine is then capped with a suitably reactive reagent (see list). Each microkan is placed in a solution of NMP (500uL) for the resin to swell. To this solution is added DIEA (25uL, 2M) and one of the capping agents (0.5mmol). The reaction is shaken for 2 to 18 hours at room temperature. Completion of the capping was confirmed by treatment of a small portion of the resin with 3% ninhydrin-EtOH. Lack of blue/purple colour indicated a complete reaction. The reaction is filtered and the resin is washed with NMP (3x5mL) then dichloromethane (3x5mL) and the resin is dried in vacuo.

Each of the peptides was liberated from the support in 95% TFA: 5% water (1mL) after 4 hours shaking at room temperature, followed by filtration. The products were concentrated in vacua. The residue was redissolved in trifluoroacetic acid (150uL) and dripped into t-butyl-methyl ether (5mL) to precipitate. Each was centrifuged to a pellet, the solvent decanted and the pellets dried in vacuo. The products were dissolved in water and acetontrile (~5my) and lyophilized to pale beige powders. The products were then purified by reverse phase HPLC (C18 silica Gel using a gradient system of 0-to 100% acetonitrile in water buffered with 0.1% trifluoroacetic acid), the products having the retention times and mass spectra as described below in the table.

A list of such amine capping agents might include but is not limited to: List of Capping Groups for Chemotactic Peptide Example 20: Routes for the introduction of the rhenium complexes to each mixture (RP552-557) Two routes to the introduction of a rhenium complex to the mixtures can be envisaged.

Route A: This route requires that the lysine side chain first be deprotected and one of the chelators (RP414 or RP455) be attached to the sequence as a single residue or stepwise. Each of these can be accomplished by standard synthesizer chemistry.

The cysteine residue must be sulphur protected with a labile group which is lost

during rhenium coordination such as Mott as described in example 7 of the original patent filing.

Each mixture containing the rhenium chelator is placed in a solution of NMP (3mL) and the resin is allowed to swell. To each is added ReOCI3(PPh3)2 (0.5mmol) and triethylamine (1mL). The reaction is heated at 40-500C for 8 hours. The reaction is filtered and the resin is washed with NMP (3x5mL) then dichloromethane (3x5mL) and dried in vacuo.

Route B: This route requires that the lysine side chain be deprotected on the resin and the entire rhenium complex (RP414 or RP455) be attached as a single residue Each microkan was placed in NMP (lmL) to swell the resin. To the solution was added ReO-RP414 (20mg, 0.037mmol) or ReO-RP455 (0.037mmol), then tetrafluorophenol (10mg, 0.O6mmol) and EDC (20mg, 0.1mmol). The reaction is shaken for 24 hr in a 45"C bath. The reaction is filtered and the resin is washed with NMP (3x5mL) then dichloromethane (3x5mL) and dried in vacua Alternately, several mikrocans can be reacted at the same time in a larger reaction volume in the same stoichiometric ratios.

Example 21: Synthesis of ReO-Dimethylglycine-t-butyl-glycine-S Acetamidomethyl-Cysteine-Glycine(ReO-RP455) The title product was synthesized by the literature methods of E. Wong et al.

Inorganic Chemistry 36: 5799-5808 (1997).

Example 22: Synthesis of ReO-Dimethylglycine-t-butyl-glycine-S- Acetamidomethyl-Cysteine-Glycine(ReO-RP455) tetrafluorophenyl ester To ReO-RP455 (60mg) in 1:1 acetonitrile:water (1mL) was added tetrafluorophenol (100mg). The solution was diluted with acetonitrile (2mL). The pH

was measured at 2. To the solution was added 1 (3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride. The reaction was swirled to dissolve and the pH measured at 5. The reaction was allowed sit at room temperature for 15 minutes followed by concentrating to a dark oil in vacua. The product was purified on a Supelco supelclean LC-18 column. The column was first washed with a 5% acetonitrile: 95% water solution acidified to pH2 with 3N HCI. The product was eluted in a 50% acetonitrile: 50% water solution acidified to pH2 with 3N HCI. The appropriate pure fractions were identified by silica TLC (t-butanol:water:methanol, 10:3:2, rf: 0.85) followed by KMnO4 staining. The correct fractions were pooled and concentrated in vacuo to a red-brown glass (58mg, % yield).

Example 23: Synthesis of ReORP455 libraries RP552 to RP557 (N-terminus amino group capped with capping groups 6,10, 13, 16,17, 18) on sasrin resin Each of the N-terminus capped libraries on sasrin resin (20 mg) was placed in a Biorad disposable column. The Dde epsilon amino group protection on C-terminus Lysine was first removed with three washes of 2% hydrazine in N-methylpyrrolidone (3x1mL). The resin was thoroughly washed with N-methylpyrrolidone then dichloromethane, and dried in vacuo. To each vessel was added ReO- <BR> <BR> <BR> Dimethylglycine-t-butyl-glycine-S-Acetamidomethyl-Cysteine-G lycine(ReO-RP455) tetrafluorophenyl ester (10mg) in ethyl acetate (1mL). The reactions were capped and shaken 20 hours at room temperature, followed by filtration, washing with copious ethyl acetate, N-methylpyrrolidone, dichloromethane. The red-brown resins were dried in vacuo.

Example 24: Cleavage of ReO-RP455-RP552 to RP557 with N-terminus amino capping groups attached Each of the ReO libraries were liberated from the supports in 95% TFA: 5% water (lmL) after 4 hours shaking at room temperature, followed by filtration. The products were concentrated in vacua. The residue was redissolved in trifluoroacetic

acid (150uL) and dripped into t-butyl-methyl ether (5mL) to precipitate. Each was centrifuged to a pellet, the solvent decanted and the pellets dried in vacuo. The products were dissolved in water and acetontrile (~5my) and lyophilized to pale pink powders.

Example 25: Deconvolution of Peptide Mixture ReORP552 with N-terminus capping goups attached.

Following assay of the above mixtures of compounds using the method detailed below the following series of peptides was prepared as single molecules using the following method. The various peptide sequences containing varying side chain protecting groups in these examples were synthesized via a solid phase synthesis method on an automated synthesizer using FastMoc chemistry on scales varying from 0.1 to 1.0mmol. Prior to the addition of each amino acid residue to the N-terminus of the peptide chain the FMOC group was removed with 20% piperidine in NMP. Each FMOC amino acid was activated with 0.5M HOBT/HBTU/DMF in the presence of 2.0M DIEA/NMP. The C-terminus was attached to the solid phase via the sasrin linker. After completion of the synthesis the resin was washed with NMP followed by dichloromethane and dried under vacuum for up to 24 hours.

The following peptides were prepared and used still attached to sasrin resin: Resin-gly-lys(DDE)-glu-trp-phe-leu-Nle Resin-g ly-lys(DDE)-g lu-ser-phe-leu-N le Resin-gly-lys(DDE)-glu-tyr-phe-leu-Nle Resin-g ly-lys(DDE)-his-trp-phe-leu-N le <BR> <BR> <BR> <BR> Resin-g Iy-lys(DDE)-his-ser-phe-leu-N le <BR> <BR> <BR> <BR> <BR> Resin-g Iy-lys(DDE)-his-tyr-phe-leu-N le Resin-gly-lys(DDE)-lys-trp-phe-leu-Nle Resin-g Iy-lys(DDE)-iys-ser-phe-ieu-N le Resin-gly-lys(DDE)-lys-tyr-phe-leu-Nle

Each of the following resins containing the peptides was then capped with a cyclopropylcarbonyl group as follows: Each resin is placed in a solution of NMP (500uL) for the resin to swell. To this solution is added DIEA (25uL, 2M) and cyclopropane carbonyl chloride (0.5mmol). The reaction is shaken for 18 hours at room temperature. The reaction is filtered and the resin is washed with NMP (3x5mL) then dichloromethane (3x5mL) and the resin is dried in vacuo. Completion of the reaction is ensured by the use of a ninhydrin test to indicate complete reaction of amino groups.

Having attached the capping group to the amino terminus of the peptide attached to the resin the rhenium complex was introduced as follows: The Dde epsilon amino group protection on C-terminus Lysine was first removed with three, five minute washes of 2% hydrazine in N-methylpyrrolidone (3x1mL). The resin was then thoroughly washed with N-methylpyrrolidone then dichloromethane, and dried in vacua. To each vessel was added ReO-Dimethylglycine-t-butyl-glycine-S- Acetamidomethyl-Cysteine-Glycine(ReO-RP455) tetrafluorophenyl ester (1 Omg) in ethyl acetate (1mL). The reactions were capped and shaken 20 hours at room temperature, followed by filtration, washing with copious ethyl acetate, N- methylpyrrolidone, dichloromethane. The red-brown resins were dried in vacua.

Liberation of the rhenium complex of the peptide from the resin was carried out as follows: Each of the ReO complexes were liberated from the supports in 95% TFA: 5% water (1mL) after 4 hours shaking at room temperature, followed by filtration.

The products were concentrated in vacua. The residue was redissolved in trifluoroacetic acid (150uL) and dripped into t-butyl-methyl ether (5mL) to precipitate.

Each was centrifuged to a pellet, the solvent decanted and the pellets dried in vacuo. The products were dissolved in water and acetontrile (~5my) and lyophilized to pale pink powders. The single compounds were then purified by reverse phase HPLC using vydac C18 protein and peptide column and a graded eluent system using water and acetonitrile buffered with 0.1% trifluoroacetic acid, the gradient increasing from 0% acetonitrile to 55% acetonitrile in water over a period of 20

minutes. The fractions containing the peptide were then lyophilized and analyzed by mass spectroscopy.

Compounds prepared as their rhenium oxo complex <BR> <BR> <BR> <BR> <BR> <BR> ReO-Gly-lys(Dimethylg Iy-t-Butyig Iy-cys-gly)-g lu-trp-phe-leu-N le-NHCOcyclopropyl HPLC retention time:22min; ESMS (1518, M+H), expected 1518 ReO-Gly-lys(Dimethylgly-t-Butylgly-cys-gly)-glu-ser-phe-leu- Nle-NHCOcyclopropyl RP553-17-0 HPLC retention time: 19.8min <BR> <BR> <BR> <BR> <BR> <BR> ReO-Gly-lys(Dimethylgly-t-Butylgly-cys-9 iy)-g lu-tyr-phe-leu-l\l le-N HCOcyclopropyl RP553-17-0 HPLC retention time: 20.lmin ReO-Gly-lys(Dimethylgly-t-Butylgly-cys-gly)-his-trp-phe-leu- Nle-NHCOcyclopropyl RP553-17-0 HPLC retention time: 21.0min ReO-Gly-lys(Dimethylg ly-t-Butylg Iy-cys-g Iy)-h is-ser-phe-leu-N le-N HCOcyclopropyl RP553-17-0 HPLC retention time: 19.2min ReO-Gly-lys(Dimethylg Iy-t-Butylg ly-cys-g Iy)-his-tyr-phe-leu-N le-N HCOcyclopropyl RP553-17-0 HPLC retention time: 19.3min

ReO-Gly-iys(Dimethylg ly-t-Butylg ly-cys-g ly)-lys-trp-phe-leu-N le-N HCOcyclopropyl RP553-17-0 HPLC retention time: 20.5 min ReO-G Iy-lys(Dimethylg Iy-t-Butylg Iy-cys-g ly)-lys-ser-phe-leu-N le-N H COcyclopropyl RP553-17-0 HPLC retention time: 18.8min ReO-Gly-lys(Dimethylgly-t-Butylgly-cys-gly)-glu-tyr-phe-leu- Nle-NHCOcyclopropyl RP553-17-0 HPLC retention time: Example 26: Small Molecule Re Complex Conjugate Using the methods described above the following peptide was prepared and used attached to the sasrin resin: Resin-Gly-Lys(DDE) Following the procedure described In Journal of the American Chemical Society 1992, 114, 10646 this peptide was treated with bromoacetic acid as follows: To a slurry of the resin (0.5mmol/gram loading, 100mg) in dimethyformamide (0.5mL) was added bromoacetic acid (70mg, 0.5mmol) followed by dicyclohexyicarbodiimide (123mg, 0.6mmol). The resulting mixture was shaken at room temperature for 35 minutes and was then filtered. The resin was washed with dimethylformamide (3 x 2mL) followed by washing with dichloromethane (3 x 2mL) and was then dried in vacuo prior to further use. Ninhydrin test on this resin proved negative for free amino groups.

A portion of the above resin (20mg) was slurried in dimethysulfoxide (200 L) and to this slurry was added 1-phenylpiperazine (32mg, 30 L) and the whole mixture was agitated at room temperature for 4 hours. The mixture was filtered and the resin washed with N-methylpyrrolidinone (3 x 2mL) then dichloromethane (5 x 2mL) and

dried in vacuo. A small portion of this resin (7mg) was liberated from the resin using three successive five minute washes with 500 L of 2% hydrazine in N- methylpyrrolidinone (to remove the DDE protecting group) followed by 95% trifluoroacetic acid (1mL). Filtration of the TFA solution followed by removal of the volatiles under reduced pressure gave glycyl-lysyl-N-(4-phenylpiperazinylcarbonyl).

The remainder of the resin was treated with 2% hydrazine as above (to remove the DDE group) and after washing and drying was then treated with a solution of ReO- <BR> <BR> Dimethylg lycine-t-butyl-g lycine-S-Acetamidomethyl-Cysteine-Glycine(ReQ-RP455) tetrafluorophenyl ester (10mg) (prepared as described above) in ethylacetate (1mL) and the mixture shaken overnight. The resin was filtered and washed with N- methypyrrolidinone (3 x 2mL) followed by dichloromethane (3 x 2 mL) and then dried in vacua. The rhenium complex was liberated from the resin using 95% trifluoroacetic acid (500 L) for 1.5h at room temperature. Filtration of the solution and removal of the trifluoroacetic acid under reduced pressure gave glycyl-lysine( -Re oxo Dimethylglycyl-t-Butylglycyl-cysteinyl-glycyl)-N-(4-phenylpi perazin-1 - ylacetamide):ESMS 963 (M+H+), expected 963.

Example 27: Preparation of libraries of small molecules Using the method described above for the preparation of glycyl-lysine( -Re oxo Dimethylg Iycyl-t-Butylg Iycyl-cysteinyl-g lycyl)-N-(4-phenylpiperazin- 1 -ylacetam ide) libraries of small molecules have been prepared as follows. Equimolar mixtures of eight variously substituted piperazines were substituted for the phenylpiperazine in the above sequence to provide a final mixture of eight compounds. These mixtures are detailed below.

Mixture 1: 1-phenylpiperazine, 2-(1-piperazinyl)pyridine, 2-(1- piperazinyl)pyrimidine, 1 -cyclohexylpiperazine, 1- (pyrrolidinocarbonylmethyl)piperazine, 1-(morpholinocarbonylmethyl)piperazine, 1- bis(4-fluorophenyl)methylpiperazine, 1-piperonylpiperazine Mixture 2: -(2,3dimethylphenyl)piperazine, 1 -(o-tolyl)piperazine, 1-(4- fluorophenyl)piperazine, 1 -(4-nitrophenyl)piperazine, 1-(2-(2- hydroxyethoxy)ethyl)piperazine, 1 -(4-chlorobenzhydryl)piperazine, 1 -(4,4-bis(4- fluorophenyl)butyl)piperazine, 1 -(diphenylmethyl)piperazine, 1-(2- hydroxyethyl)piperazine Example 28: Large Random Library of Re complex-peptide-conjugates Using the peptide synthesis method described previously, 6,859 peptides were synthesized with the following composition: Sasrin-AA1 -AA2-AA3-Q-Ala Nineteen Sasrin resins with one amino acid attached (AA1) were combined in the reaction vessel of the peptide synthesizer. The nineteen amino acids (AA2) included all of the natural amino acids except Cys. The synthesis was done on a 0.1 mmol scale. Therefore, 0.005 mmol of each resin-bound amino acid was added to the reaction vessel. The gram equivalents are listed in Table 1. Nineteen free amino acids were combined in equimolar amounts in each of two cartridges (AA2 and AA3). A 1 04old excess of each of the amino acids was used so that each cartridge contained 1 mmol of amino acids. Therefore, there were 0.05 mmol of each amino acid in each of the cartridges.

The last amino acid to be added to the sequence was -Ala. This acted as a linker for the Re oxo complex. The amount used was 1 mmol which is 0.311g. Sasrin-AA1 Mass (mg) AA2 Mass (mg) AA3 Mass (mg) Gly 7.2 Gly 15.0 Gly 15.0 His(Trt) 12.5 His(Trt) 31.0 His(Trt) 31.0 Val 9.1 Val 17.0 Val 17.0 Tyr (tBu) 8.3 Tyr (tBu) 23.0 Tyr (tBu) 23.0 Trp (Boc) 8.3 Trp (Boc) 26.0 Trp (Boc) 26.0 Ala 7.3 Ala 16.0 Ala 16.0 Arg (Pmc) 11.0 Arg (Pmc) 33.0 Arg (Pmc) 33.0 Leu 8.3 Leu 18.0 Leu 18.0 Met 6.9 Met 18.0 Met 18.0 Phe 7.7 Phe 19.0 Phe 19.0 Pro 7.8 Pro 17.0 Pro 17.0 Ser (Trt) 8.3 Ser (Trt) 28.0 Ser (Trt) 28.0 Asn (Trt) 17.0 Asn (Trt) 30.0 Asn (Trt) 30.0 Thr (tBu) 11.0 Thr (tBu) 20.0 Thr (tBu) 20.0 Lys (Boc) 8.3 Lys (Boc) 23.0 Lys (Boc) 23.0 Ile 8.3 Ile 18.0 Ile 18.0 Glu (OtBu) 8.3 Glu (OtBu) 21.0 Glu (OtBu) 21.0 Gln (Trt) 12.5 Gln (Trt) 31.0 Gln (Trt) 31.0 Asp(OtBu) 8.8 Asp(OtBu) 21.0 Asp(OtBu) 21.0

ReO-Dimethylglycine-serine-S-Acetamidomethyl-Cysteine-Glycin e(ReO- RP414) tetrafluorophenyl ester (10mg) (prepared as described above for ReO- Dimethyiglycine-serine-S-Acetamidomethyl-Cysteine-Glycine ReQ RP455) ester was synthesized as described above and added as an ethyl acetate solution (in 1mL ethyl acetate) to the resin-bound peptide (10 mg). The reaction was allowed to mix overnight then was filtered and washed with ethyl acetate (3 times), water (3 times) and dichloromethane (3 times). The resin was dried on the aspirator and then cleaved with 95% trifluoroacetic acid in water (3 hours). The trifluoroacetic

acid/peptide solution was filtered into tert-butyl methyl ether (10 mL) and centrifuged.

The ether was decanted. This washing process was repeated 3 times. After the final wash the ether was decanted leaving behind the peptide which had precipitated. The peptide was dissolved in water (1 mL), frozen with liquid nitrogen and lyophilized.

Example29: Library of Rhenium compounds based on glycosides Compounds contained in this library rely on the structural constraints inherent in the carbohydrate structure to impart directionality into the compounds. Thus decoration of the carbohydrate skeleton with suitable functional groups, one of which consists of a rhenium chelating agent such as RP414 or RP455 as described above will allow the preparation of structurally diverse libraries of rhenium containing molecules. Hence treatment of glucose with a suitable alcohol (for example tertiary butanol or methanol) in acid catalyzed conditions (most preferably using Dowex 50W-X8 in benzene) following the procedure of Lin et. al. Journal of the American Chemical Society 1992, 114, 10138 gives the glucose substituted at C-i. Treatment of this substituted glucose with a mixtures up to 20 diversity functionalities containing reactive leaving groups (for example iodide, triflate or tosylate) in an inert solvent (for example benzene or dichloromethane) results in a glucose having diversity attached at four points (i.e. C-2, C-3, C-4, C-5) around the periphery of the glucose ring. The rhenium containing moiety is then introduced by removal of the methoxy group at C-I using water in acidic conditions. Application of the above glycosidation conditions with Re oxo d imethyg lycyl-t-butylg lycyl-cysteinyl-g lycyl-4- hydroxypropyl produces a library of rhenium containing glycosides. These are then tested in biological assays and the most promising mixtures deconvoluted by the parallel synthesis of each of the single compounds in the mixture.

Example 30: Construction of a solid phase library of 1,000 metallocarbohydrates for use as imaging agents Where R represents diversity groups as outlined in the procedure Well established methods for organic synthesis are used to obtain a library of molecules having restrained conformation by virtue of a carbohydrate backbone.

Hence glucosamine is protected as its Fmoc derivative by treatment with Fmoc-CI and sodium bicarbonate in aqueous dioxane. The resulting protected amine is then treated with 3-hydroxypropionic acid and Dowex 50W-X8 in benzene according to the procedure of Lin et. al. Journal of the American Chemical Society 1992, 114, 10138 to give 2-fluorenylmethylcarbamoyl- 1 -(3-carboxypropyloxy)-glucosamine.

This amino acid is then attached to sasrin resin using standard chemistry by coupling with HOBT/HBTU and N,N-diisopropylethylamine in NMP to provide a resin having the glucose attached via a propyl group at C-i. According to the procedure of M. J. Sofia, Journal of Organic Chemistry, 1998, 63, 2802 the resin so prepared is then treated with sodium hydride in tetrahydrofurn in the presence of the following to prepare a library of molecules substituted at C-3, C-4, and C-S by ether linkages; 3- iodopropane, benzyliodide, 3-iodopropanol, 3-bromopropylamine, propargyl bromide, 2-bromomethylnaphthalene, 5-bromo-2-methyl-2-pentene, perfluoropropyl iodide, bromomethylcyclopropane, and 2-(2-bromoethyl)-2,5,5-trimethyl-i ,3-dioxane.

This solid phase library is then treated with 20% piperidine in NMP to remove the Fmoc group from the C-2 amino functionality and the resulting resin treated with a solution of ReO-N,N,-d imethylg lyci ne-ser-cys-g ly-tetrafl u orop henyl ester to provide

the solid phase library. This library is then liberated from the solid support by treatment with 50% TFA in dichloromethane. Removal of the TFA and dichloromethane under vacuum followed by lyophilisation provides the metallocarbohydrate library.

Example 31 Biological assays MATERIALS AND METHODS: Animals and Reagents. Sprague-Dawley rats weighing 300-350 g were purchased from Charles River-Bausch & Lomb Laboratories (St.Constant, Quebec).

Procedures followed standard Animal Care Committee protocols. The following drugs were used in this study: fMLP, N-t-BOC-methionyl-leucyl-phenylalanine (N-t- BOC-MLP), cytochalasin B, oyster shell glycogen, polyethyienimine, o- phenylenediamine (OPD), H202 and H2SO4 (Sigma Chemical Corp., St. Louis, MO) and 3H-fMLP (New England Nuclear, Boston, MA). Peptide fMLP derivatives, N- formyl-norleucyl-tyrosyl-lysine (For-Nle-LP-Nle-YK) and iso-boc-MLFK were synthesized in-house by Resolution Pharmaceuticals Inc. (Mississauga, ON).

Neutrophil isolation. Animals were sacrificed via administration of CO2 4 hours after injection of 10 mL of 0.5% oyster glycogen. Leukocytes were harvested by performing peritoneal lavage using 30 mL of Hanks' buffered salt solution (HBSS-) containing 10 mM ethylene-diaminetetra-acetic acid (EDTA) disodium salt. The volume of fluid recovered from each rat was approximately 20-25 mL and bloody lavages were discarded.

Neutrophils isolated by peritoneal lavage were washed twice in HBSS- (without calcium chloride, magnesium chloride and magnesium sulfate). A cold H20 RBC lysis was then performed with the addition of 9 mL of sterile ice-cold H20 and 1 mL of phosphate buffered saline (PBS) solution containing 0.1 M phosphate buffer, 0.027 M KCI and 1.37 M NaCI. White blood cell differential stain was used to

identify neutrophils and viability of cells was confirmed on the basis of trypan blue exclusion.

Neutrophil fMLP receptor binding assays. fMLP saturation binding experiments used to determine KD values were carried out with 2.5 X 105 PMNs per sample suspended in a final volume of 150 uL of fMLP, 3H-fMLP and/or HBSS+.

Samples were done in quadruplicate and non-specific binding was assessed in the presence of 10 uM fMLP and 3H-fMLP in the range of 1 nM to 150 nM. Total binding was evaluated following the addition of 3H-fMLP in the concentration range of 1 nM to 150 nM.

Competition assays were conducted with 6 nM 3H-fMLP in addition to the nonradioactive competing ligand added at 10 uM and 1.0 uM. Total binding in the competition assays was assessed in the presence of 1.0 x 106 PMNs per sample while non-specific binding was determined in the absence of cells.

After a 1 hour incubation period on ice, the samples were vacuum aspirated onto 1.0 um Skatron filter mats which had been pre-treated with polyethylenimine for approximately 24 hours. Sample wells received two consecutive 12 second washes with 0.9 % saline solution and collected filters were counted for 2 minutes in 5 mL of liquid scintillation fluid.

Measurement of Myeloperoxidase release. 0.5 x 106 PMNs per sample were incubated in 96-well Millipore Multiscreen 0.65 um filter plates. In a final volume of 150 uL, 50 uL of the respective fMLP analogues (10 uM to 1pM) and/or fMLP (10 uM to 1.0 uM) were incubated with isolated PMNs pretreated with cytochalasin B (5 ug/mL) for 10 minutes. Following a 30 minute incubation period at room temperature, the supernatant was collected into a standard polypropylene plate with the Millipore vacuum apparatus. Supernatant samples were subsequently incubated with 50 uL o-phenylenediamine (OPD) containing H202 and HBSS+ for 2 minutes

followed by the addition of 2.5M H2SO4. O.D.490values were obtained with the Thermomax Microplate Reader.

Graph Showing % fMLP remaining after challenge with mixtures of compounds prepared in Examples 18-24 Competition Binding of Libraries with fMLP % fMLP Binding According to the above assays, library RP553-capped-17 was selected for further deconvolution.

Although the invention has been described with preferred embodiments, it is to be understood that modifications may be resorted to as will be apparent to those skilled in the art. Such modifications and variations are to be considered within the purview and scope of the present invention.

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