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WO/2023/173016A1 |
The present disclosure relates to diaryl compounds targeting KRAS, pharmaceutical compositions containing the compounds, and methods of using such compounds to treat disease, such as cancer.
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WO/2023/169436A1 |
Disclosed in the present invention are a benzo bicyclic compound, and a preparation method and application thereof. Specifically disclosed is a compound, which is a compound as shown in formula (X), or a stereoisomer, geometric isomer, t...
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WO/2023/169438A1 |
The invention relates to nitrogen-containing heterocyclic compounds as well as a preparation method therefor and the use thereof, in particular to a nitrogen-containing heterocyclic compound represented in general formula (I), or a pharm...
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WO/2023/169547A1 |
A nitrogen-containing heterocyclic compound represented by formula (I-c), or a stereoisomer, a deuterated compound or a pharmaceutically acceptable salt, and a pharmaceutical composition thereof. Also provided is a use of the compound in...
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WO/2023/165504A1 |
Described herein are DGKalpha inhibitors and pharmaceutical compositions comprising said inhibitors. The subject compounds and compositions are useful for the treatment of a disease or disorder associated with DGKalpha.
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WO/2023/165509A1 |
Described herein are DGKalpha inhibitors and pharmaceutical compositions comprising said inhibitors. The subject compounds and compositions are useful for the treatment of a disease or disorder associated with DGKalpha.
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WO/2023/168378A1 |
The present disclosure provides compounds, compositions, and methods useful for inhibiting PI3Ka, and/or treating a disease, disorder, or condition associated with PI3Ka, and/or treating cancer. (Formula I)
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WO/2023/167279A1 |
The present invention provides a method for controlling harmful arthropods or harmful nematodes. Compounds represented by formula (I) [in the formula, R1 represents a hydrogen atom, etc., R2 represents ORA2, R3, R7, R14, R17, R19, and R2...
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WO/2023/166450A1 |
The present invention relates to a compound represented by chemical formula I, a stereoisomer thereof, a pharmaceutically acceptable salt thereof, a hydrate or a solvate thereof, and a pharmaceutical composition comprising same.
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WO/2023/165079A1 |
The present invention relates to a dipyridinophenazine thermally activated delayed fluorescent material doped white electroluminescent device, which is obtained by sequentially carrying out vacuum evaporation on a hole injection layer, a...
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WO/2023/167475A1 |
The present invention relates to an improved preparation method for rucaparib, enabling excellent synthesis yield and reproducibility to be achieved. More particularly, the present invention relates to: an improved preparation method for...
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WO/2023/165525A1 |
Provided are DGKalpha inhibitors and pharmaceutical compositions comprising said inhibitors. The compounds and compositions are useful for the treatment of a disease or disorder associated with DGKalpha.
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WO/2023/165493A1 |
Disclosed are a naphthyridine derivative and use thereof. The naphthyridine derivative can well inhibit ATR kinase activity and can be used in the preparation of an ATR kinase inhibitor, particularly in the preparation of a medicament ag...
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WO/2023/165077A1 |
The present invention relates to a thermally activated delayed fluorescent material based on a dipyridino[3,2-a:2',3'-c]phenazine acceptor and a preparation method therefor. The thermally activated delayed fluorescent material is 11-(9,9...
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WO/2023/167234A1 |
The present invention provides a compound which is represented by formula (1) (wherein each of R1 to R6 independently represents a hydrogen atom, a halogen atom, a linear, branched or cyclic alkyl group, or the like).
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WO/2023/165570A1 |
The present invention relates to a compound of formula (I) or a tautomer, stereoisomer, prodrug, crystal form, pharmaceutically acceptable salt, hydrate, or solvate thereof, a pharmaceutical composition thereof, and a use of the compound...
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WO/2023/165501A1 |
The present application relates to the field of chemical synthesis of pharmaceutics. Specifically, the present application relates to a crystal form of AZD5305, a preparation method therefor, and use thereof. The crystal form provided by...
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WO/2023/165438A1 |
The present invention relates to a substituted tricyclic derivative, a preparation method therefor, and pharmaceutical use of a pharmaceutical composition comprising same. Specifically, the present invention relates to a substituted tric...
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WO/2023/165574A1 |
Disclosed are a compound used as a TYK2 inhibitor, a preparation method therefor, and pharmaceutical use thereof. Specifically, the compound has a structure represented by formula (I), wherein the definitions of the groups and substituen...
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WO/2023/165078A1 |
The present invention relates to a red-light electroluminescent device based on a bipyridine phenazine thermally activated delayed fluorescent material. A hole injection layer, a hole transport layer, a barrier layer, a light-emitting la...
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WO/2023/165581A1 |
Disclosed are a pyridine derivative represented by formula I and use thereof. The compound has a significant inhibitory effect on KRAS and PI3K protein activities and can be used as a KRAS and/or PI3K protein inhibitor and in preparing a...
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WO/2023/160652A1 |
Provided are a substituted fused ring compound represented by formula (I), a pharmaceutical composition thereof, a preparation method therefor and the uses thereof. The compound has a good LRRK2 kinase regulation/inhibition effect, and t...
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WO/2023/164237A1 |
The disclosure relates to compounds of Formula I or a pharmaceutically acceptable salt thereof, wherein, m, R1-R5, R5A, and L are defined herein. These compounds are useful in methods for stabilizing a mutant PAH protein or reducing bloo...
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WO/2023/160527A1 |
A pyrimido aromatic ring compound and a use thereof in a drug, especially a use thereof as a TLR8 agonist. Specifically, the present invention relates to a compound represented by general formula (I), or a stereoisomer, tautomer, nitroge...
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WO/2023/164358A1 |
The present application describes GLP-IR modulating compounds that are useful for treating GLP-IR-mediated diseases or conditions.
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WO/2023/163140A1 |
The purpose of the present invention is to provide a compound that exhibits an H-PGDS inhibitory activity. The present invention relates to a compound expressed by formula [I] or a pharmaceutically acceptable salt thereof (in the formula...
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WO/2023/164680A1 |
Provided are compounds of Formula (I): and pharmaceutically acceptable salts and compositions thereof, which are useful for treating a variety of conditions associated with STAT3 and/or STAT6, such as e.g. cancer and inflammatory conditi...
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WO/2023/164233A1 |
The disclosure relates to compounds of Formula I or a pharmaceutically acceptable salt thereof, wherein, m, R1-R5, R5A, and L are defined herein. These compounds are useful in methods for stabilizing a mutant PAH protein or reducing bloo...
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WO/2023/164063A1 |
Provided are compounds of the Formula (I): or pharmaceutically acceptable salts thereof, which are useful for the inhibition of EBP and in the treatment of a variety of EBP mediated conditions or diseases, such as multiple sclerosis.
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WO/2023/160577A1 |
The present application relates to the field of pharmaceutical chemistry, relates to a fused bicyclic compound containing pyrrolinone, and in particular relates to a compound represented by formula (II), a stereoisomer or a pharmaceutica...
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WO/2023/163479A1 |
The present invention relates to a novel compound with excellent carrier transport ability, light-emitting ability, and thermal stability, and an organic electroluminescent device that includes the compound in at least one organic materi...
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WO/2023/161316A1 |
The invention provides novel imidazole pyrazole derivatives having the general formula (I), and pharmaceutically acceptable salts thereof, wherein A, X, R1-R9, R12 and R13 are as described herein (I). Further provided are pharmaceutical ...
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WO/2023/164612A1 |
Disclosed herein are compounds (I) and compositions having potency in the modulation of Myc family proteins. Such compounds and compositions can be used in the treatment of proliferative diseases, such as cancer, or in the treatment of d...
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WO/2023/161317A1 |
A compound of formula (I): (I) wherein R3, R4, R5, R6, Z1, Z2 and T are as defined in the description. Medicaments.
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WO/2023/160552A1 |
Disclosed in the present invention are a spiro-compound and the use thereof, and in particular, disclosed are a compound as shown in a formula (III), and a stereoisomer or a pharmaceutically acceptable salt thereof.
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WO/2023/164236A1 |
The disclosure relates to compounds of Formula I or a pharmaceutically acceptable salt thereof, wherein, m, R1-R5, R5A, and L are defined herein. These compounds are useful in methods for stabilizing a mutant PAH protein or reducing bloo...
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WO/2023/163553A1 |
The present invention relates to a compound bearing a photosensitizer and an imidazopyridine derivative, a liposome including the compound, and a photodynamic therapeutic composition containing the compound or liposome. According to exem...
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WO/2023/160572A1 |
Disclosed are a pyrazole derivative, a pharmaceutical composition, and use. The pyrazole derivative has a structure represented by formula (I). The pyrazole derivative has a good selectivity for inhibiting the activity of CDK2.
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WO/2023/160187A1 |
A derivative of a naphthyl carbazole or naphthyl carboline structure, the use thereof respectively as a luminescent material layer, a hole transport layer, a hole barrier layer or an encapsulation layer material in an organic electrolumi...
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WO/2023/164025A1 |
A method of regenerating a symmetrical redox flow battery includes: a first discharge process having a duration in which a capacity of the redox flow battery in a first polarity and comprising a membrane decreases from a first to a secon...
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WO/2023/155866A1 |
The present invention relates to the compound shown in general formula (I) or to a stereoisomer, tautomer, deuterated substance, solvate, prodrug, metabolite, pharmaceutically-acceptable salt or eutectic crystal thereof, and to an interm...
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WO/2023/155841A1 |
A salt form and a crystalline form of a pyrimidine fused-ring compound and a preparation method therefor. Specifically, use of a salt form and a crystalline form of the compound of formula (II) in the preparation of treatment-related med...
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WO/2023/155892A1 |
Described herein are PKMYT1 (Myt1) inhibitors and pharmaceutical compositions comprising said inhibitors. The subject compounds and compositions are useful for the treatment of a disease or disorder associated with PKMYT1.
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WO/2023/155710A1 |
The present invention belongs to the field of medicinal chemistry, and relates to an IKZF2 degradation agent, a pharmaceutical composition comprising same and use thereof. Specifically, the IKZF2 degradation agent has a structure represe...
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WO/2023/159155A1 |
Disclosed herein are compounds of Formulae 1A, 1B, 1C and 1D, (1A), (1B), (1C) and (1D) and methods of making and methods of using the same.
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WO/2023/159154A1 |
Disclosed are compounds of Formulas (I): (Formulas (I)) or a salt thereof, wherein X, Y, Q, G, R1, and R5a are defined herein. Also disclosed are methods of using such compounds as inhibitors of TLR9, and pharmaceutical compositions comp...
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WO/2023/157891A1 |
The present invention addresses the problem of providing a drug for use in the treatment of triple-negative breast cancer, providing a blood marker for triple-negative breast cancer, and providing a drug for use in the treatment of infla...
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WO/2023/158862A2 |
The invention provides novel modulators of STING (Stimulator of Interferon Genes) and pharmaceutical compositions thereof, as well as methods of their preparation and use, in therapy of various diseases and conditions, such as cancer, in...
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WO/2023/157862A1 |
Provided is a method for producing α-fluoroether starting from an inactivated chloride. Disclosed is a method for producing a compound represented by formula (3), the method comprising step A in which a compound represented by formula (...
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WO/2023/159153A1 |
Disclosed are compounds of Formulas (I) or a salt thereof, wherein Q, G, R1, R5a, and R5b are defined herein. Also disclosed are methods of using such compounds as inhibitors of TLR9, and pharmaceutical compositions comprising such compo...
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