Document |
Document Title |
WO/2014/002106A1 |
The present invention relates to compounds of the general formula (I), their tautomeric forms, their stereoisomers, their pharmaceutically acceptable salts, pharmaceutical compositions containing them, methods for their preparation, use ...
|
WO/2013/191188A1 |
This fused heterocyclic compound represented in formula (1) has excellent effectiveness in pest control. (In the formula, A1 represents -NR4-, etc., A2 represents a nitrogen atom, etc., R1 represents an ethyl group, a cyclopropyl group, ...
|
WO/2013/191986A1 |
Provided are compounds which are useful for controlling microorganisms in aqueous or water-containing systems or in systems which are exposed to moisture, including at elevated temperature. The antimicrobial compounds are of the formula ...
|
WO/2013/185976A1 |
The present invention is related to a new process for the preparation of 4-methyloxazole-5-carboxylic ester, which is a valuable intermediate in the synthesis of pyridoxine (vitamin B6). The present invention is also related to a new int...
|
WO/2013/182993A1 |
The present invention relates to a method for preparing nitrogen compounds using carbon dioxide, and to the use of said method in the production of vitamins, pharmaceutical products, adhesives, acrylic fibres, synthetic leathers, pestici...
|
WO/2013/182070A1 |
Disclosed in the present invention is a drug for preventing or treating mycobacterial diseases. In particular, disclosed is the use of a compound represented by the following general formula (I) or pharmaceutically acceptable salts, hydr...
|
WO/2013/183642A1 |
Provided is a pyridine derivative represented by general formula (1) or a salt thereof, by which an optically active form can be obtained with favorable enantioselectivity. (In the formula, R1 to R6 and R1' to R6' each independently are ...
|
WO/2013/178451A1 |
The invention relates to a method for the synthesis of a compound according to formula I comprising the following steps: a) reacting a N-carboxyanhydride according to formula II and a N-carboxy- anhydride according to formula III with a ...
|
WO/2013/178362A1 |
The invention provides modulators for the orphan nuclear receptor RORy and methods for treating RORy mediated diseases by administering these novel RORy modulators to a human or a mammal in need thereof. Specifically, the present inventi...
|
WO/2013/174508A1 |
The present invention relates to a novel class of 1,3-benzoxazol-2(3H) -ones of formula (1) and their use as a medicament, preferably as a dermatologic agent, and as a cosmetic. These novel compounds are particularly useful in treating a...
|
WO/2013/173218A1 |
Disclosed are compounds of Formula 1, N-oxides, and salts thereof, wherein Q is and Z1, Z2, J1, J2, M, R1a, R1b, R2a, R2b, R2c, R2d, R14 and R14a are as defined in the disclosure. Also disclosed are compositions containing the compounds ...
|
WO/2013/167737A1 |
This invention relates to pharmaceutical compositions comprising 5-(ethylsulfonyl)-2-(naphthalen-2-yl)benzo[d]oxazole (C1100), to processes for preparing the compositions, and to various therapeutic uses of the combinations. Also provide...
|
WO/2013/168014A1 |
The invention relates to the compounds of formula (I) or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amoun...
|
WO/2013/163889A1 |
Provided is a new intermediate compound for preparing vitamin B6, which can be used to synthesize the known intermediate compound for preparing vitamin B6, 4-methyloxazole-5-carboxyLate. Further provided is a process for preparing the ne...
|
WO/2013/160322A1 |
The present invention provides a novel process for synthesis of 4-methyl-oxazole-5- carboxamide (OXA) which comprises reacting a compound of formula (I) with a high concentration of aqueous ammonia: (I) Wherein R1 is H or C1-10 alkyl.
|
WO/2013/161851A1 |
The present invention pertains to a benzamide derivative represented by formula (I), or a pharmaceutically acceptable salt thereof.
|
WO/2013/153873A1 |
A photosensitive compound represented by formula (1) or formula (2). (Chemical formula 1) (In formula (1) and formula (2), n is an integer of 1-3; R1 is a linear or branched alkyl group having 1-6 carbon atoms or an alkylene group having...
|
WO/2013/147629A1 |
The present invention relates to the new chemical compounds containing (Z)-1,2- diphenylethene moiety in the structures, particularly the new derivatives of cis-stilbene, the new derivatives of 4,5-diphenyl-1,3-oxazole, the new derivativ...
|
WO/2013/144101A1 |
The present invention relates to a novel process for preparing cis-alkoxy-substituted spirocyclic phenylacetylamino acid esters and cis-alkoxy-substituted spirocyclic 1-H-pyrrolidine-2,4-dione derivatives and also novel intermediates and...
|
WO/2013/147118A1 |
The present invention provides: a salt of a 2-(oxazol-2-yl)phenol derivative which is an intermediate for use in a process for producing an N-phenyl-N'-phenylsulfonylpiperazine derivative; a crystal of the salt; a method for producing th...
|
WO/2013/142712A1 |
The invention provides compounds of formual (I): wherein R1-R7 and W have any of the values defined in the specification, and salts thereof. The compounds have good solubility and are useful for treating bacterial infections.
|
WO/2013/131409A1 |
Disclosed are phenyl-oxazolyl derivatives having a general formula (I), a preparation method thereof, and an application of the phenyl-oxazolyl derivatives as an inosine monophosphate dehydrogenase (IMPDH) inhibitor.
|
WO/2013/133343A1 |
The purpose of the present invention is to provide a fluorine-containing α,β-unsaturated aldehyde, a method for producing same, an optically active fluorine-containing compound using the fluorine-containing α,β-unsaturated aldehyde, ...
|
WO/2013/134079A1 |
Compounds of Formula (I) and Formula (II) are useful inhibitors of tankyrase. Compounds of Formula (I) and Formula (II) have the following structure: where the definitions of the variables are provided herein.
|
WO/2013/128421A1 |
The present invention relates to a compound of formula (1-1 ) in free form or in pharmaceutically acceptable salt form in which the substituents are as defined in the specification; to its preparation, to its use as a medicament and to m...
|
WO/2013/123634A1 |
Disclosed is a process for the production of a compound of formula (ΙΠ). The process comprises a step of reacting a compound of formula (I) with an excess amount of a compound of formula (II) in absence of aromatic solvent:wherein - n ...
|
WO/2013/121449A1 |
The present invention regards compositions and methods for the modulation of amidases capable of hydrolysing N-acylethanolamines useable in the therapy of inflammatory diseases. In particular, the present invention regards a compound of ...
|
WO/2013/120448A1 |
Disclosed is a new method for preparing a methyl substitute of a linezolid intermediate, (S)-2-((3-(3-Fluoro-4-Morpholine phenyl)-2-oxy-5-oxazoline)) (I), wherein the intermediate (I) is obtained by the cyclisation of a 3-Fluoro-4-morpho...
|
WO/2013/120496A1 |
The present invention relates to a process for the preparation of Linezolid, in particular a process for large scale production of a stable Linezolid crystalline form and pharmaceutically acceptable salts thereof, without any contaminati...
|
WO/2013/111048A1 |
The invention relates to a substantially pure linezolid hydroxide having R-isomer content more than about 99.9% relative to its S-isomer. Further aspect of invention provides the ambient moisture condition, which is critical for enantiom...
|
WO/2013/108800A1 |
Provided are: a compound having an excellent hypoglycemic activity and an excellent protective activity for a β cell or the pancreas, or a pharmaceutically acceptable salt thereof; and a pharmaceutical composition having an excellent th...
|
WO/2013/107283A1 |
Disclosed are compound of formula (I) and pharmaceutically accepted salts and prodrugs thereof, wherein each of R1, R2, R3, R4, R5, R6, X1 and X2 is as defined in the description. These compounds are protein kinases inhibitors, especiall...
|
WO/2013/103297A1 |
The present invention relates to functionalized ploy(2-oxazoline) polymers, which are very suitable as a carrier and/or delivery vehicle (conjugate) of drugs, such as small therapeutic molecules and bio-pharmaceuticals. These polymers ar...
|
WO/2013/097773A1 |
The invention provides novel ethylene derivatives represented by Formula I, which may be used as selective estrogen receptor modulators (SERMs) and useful in the prophylaxis and/or treatment of estrogen-dependent conditions or conditions.
|
WO/2013/093751A1 |
Provided is a stable microcrystalline form of Linezolid and a processes for preparation thereof. Also provided is a multiple packing and vacuum sealed pack comprising Linezolid, or stable microcrystalline form of Linezolid and optionally...
|
WO/2013/091082A1 |
The present disclosure relates to novel bis-(aryl/heteroaryl)-methylene compounds of formula (I) having vitamin D receptor agonist and histone deacetylase (HDAC) inhibitory efficacy as well as to methods for reducing or inhibiting the pr...
|
WO/2013/096771A1 |
Compounds of structure (I), or a stereoisomer, tautomer, pharmaceutically acceptable salt or prodrug thereof, wherein R1, R2, R3, R4, R8, R9, R10, R11, R12, A1, A2, X, Y and Z are as defined herein. Uses of such compounds as TGR5 antagon...
|
WO/2013/092711A1 |
The invention relates to compounds acting as selective antagonists of Transient Receptor Potential cation channel subfamily M member 8 (TRPM8), and having formula (I). Said compounds are useful in the treatment of diseases associated wit...
|
WO/2013/091696A1 |
The present invention relates to the field of organic chemistry, more specifically to the synthesis of intermediate compounds which can be used in the synthesis of pharmaceutically active agents such as anacetrapib or derivatives thereof.
|
WO/2013/090454A2 |
The invention relates to compounds that modulate the glucagon-like peptide 1 (GLP-1) receptor, methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds are act as modulators or potentiators of ...
|
WO/2013/084013A1 |
The present invention relates to compounds of formula 1 that are useful as an active ingredient of a medicament for preventive and/or therapeutic treatment of diseases caused by abnormal activation of CXCR3 chemokines. The invention rela...
|
WO/2013/080999A1 |
Provided is an agent for treating and/or preventing obesity. An agent for inhibiting expression of NPC1L1 (Niemann-Pick disease, type C1, gene-like 1) and/or LIPG (Lipase, endothelial) mRNA, comprising a compound having CETP inhibitory a...
|
WO/2013/081372A1 |
The present invention provides a pharmaceutical composition for preventing or treating hyperlipidemia comprising (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-({2-[4-fluoro-2
-methoxy-5-(propan-2-yl)phenyl]-5-(trifluoromethyl)phenyl}me
th...
|
WO/2013/081373A1 |
The present invention provides a pharmaceutical composition for preventing or treating hyperlipidemia comprising (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-({2-[4-fluoro-2
-methoxy-5-(propan-2-yl)phenyl]-5-(trifluoromethyl)phenyl}me
th...
|
WO/2013/076227A1 |
The present invention relates to novel heterocyclic alkanol derivatives, to a method for producing said compounds, to agents comprising said compounds, and to the use thereof as biologically active compounds, in particular for controllin...
|
WO/2013/078441A1 |
Heterocyclic entities that modulate PI3 kinase activity, pharmaceutical compositions containing the heterocyclic entities, and methods of using these chemical entities for treating diseases and conditions associated with PI3 kinase activ...
|
WO/2013/072923A1 |
The present invention discloses a stable crystalline Form-I of linesolid process for preparation thereof.
|
WO/2013/073596A1 |
An optically active bisoxazoline compound represented by formula (1) (wherein R1, R2 and R3 independently represent an alkyl group having 1 to 8 carbon atoms, a phenyl group or a benzyl group; n represents an integer of 0 to 3; and * rep...
|
WO/2013/069545A1 |
Provided is a complex compound which is composed of a compound represented by formula (I), a metal and at least one kind of ion that is selected from the group consisting of ions obtained by adding one or more protons to amines, ammonium...
|
WO/2013/067578A1 |
Heterocyclic compounds that modulate C3a receptors and their use in the treatment or prevention of inflammatory diseases, infectious diseases, cancers, metabolic disorders, obesity, type 2 diabetes, metabolic syndrome and associated card...
|