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WO/2024/064316A1 |
Described herein are compounds and conjugates of Formula II and their pharmaceutically acceptable salts, solvates, or stereoisomers, as well as their uses (e.g., as SMARCA2 or SMARCA4 inhibitors or degraders).
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WO/2024/060966A1 |
The present invention relates to a pan-KRAS inhibitor compound represented by formula (I), a pharmaceutical composition comprising the compound, and use of the compound of formula (I) in preventing and/or treating cancers, tumors, inflam...
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WO/2024/062250A1 |
The present invention relates to compounds of Formula (I) that may act as inhibitors of checkpoint kinase 1 (Chk1). The invention also relates to pharmaceutical compositions comprising those compounds, and to their use in the treatment o...
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WO/2024/061118A1 |
The present invention provides a macrocyclic nitrogen-containing crown ether compound represented by formula (I) and use thereof as a protein kinase inhibitor.
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WO/2024/061333A1 |
Provided are a compound of formula I having KRas inhibitory activity, a pharmaceutical composition comprising the compound, a preparation method therefor, and use thereof. The compound has remarkable selectivity, inhibitory activity, and...
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WO/2024/064328A1 |
Described herein are compounds of Formula II and their pharmaceutically acceptable salts, solvates, or stereoisomers, as well as their uses (e.g., as SMARCA2 or SMARCA4 degraders).
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WO/2024/060672A1 |
The present application belongs to the technical field of organic electroluminescence, and relates to an organic compound, an organic electroluminescent device using same, and an electronic apparatus. The organic compound has a structure...
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WO/2024/057013A1 |
Disclosed are compounds, compositions and methods for treating disease, syndromes, conditions and disorders that are affected by the modulation of NLRP3 and/or the NLRP3 inflammasome. Such compounds are represented by Formula (I), wherei...
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WO/2024/056016A1 |
The present invention relates to a free base crystal form of a polycyclic compound of a nitrogen-containing heterocycle, and a preparation method therefor. Specifically, the present invention provides a free base crystal form of a compou...
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WO/2024/055879A1 |
Provided are a class of fused bicyclic compounds, a method for preparing same, and use thereof. Particularly, provided are a compound represented by formula (I) or a pharmaceutically acceptable salt, ester, stereoisomer, tautomer, polymo...
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WO/2024/056625A1 |
The invention relates to a method for producing indolo[3,2,1-jk]carbazole and derivatives by reacting a compound of formula (1) and at least one nitrosyl cation source.
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WO/2024/057021A1 |
The present disclosure relates to a novel class of bifunctional molecules that are useful in a targeted or selective degradation of a protein.
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WO/2024/056090A1 |
Disclosed are a pyrrolopyrimidine derivative as an RSK inhibitor and use thereof. Specifically, disclosed are a compound represented by formula I, a pharmaceutical composition containing the compound of formula I, and use of the compound...
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WO/2024/059808A1 |
Compounds of general Formula (I) are provided herein. Such compounds, as well as pharmaceutically acceptable salts and compositions thereof, are useful for treating diseases or conditions, including conditions characterized by excessive ...
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WO/2024/057001A1 |
The present invention relates to compounds of Formula (I) that may act as agonists of retinoic acid receptor alpha (RAR-α) and/or retinoic acid receptor beta (RAR-β). The invention also relates to pharmaceutical compositions comprising...
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WO/2024/059249A1 |
The present disclosure provides compounds of Formula I: (I), or an N- oxide thereof, or a pharmaceutically acceptable salt of the compound or the N-oxide, wherein: A, Y, m, n, p, R1, R2, R3, R3a, R4, R5, R6, R7, and Z are as described he...
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WO/2024/059010A1 |
The present application relates to compounds of Formula (A), as defined herein, and pharmaceutically acceptable salts thereof, as well as processes for preparing compounds of Formula (A), and pharmaceutically acceptable salts thereof. Th...
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WO/2023/159307A9 |
Disclosed are compounds and pharmaceutically acceptable salts of formula (I), which feature either a N-(1H-pyrazol-3-yl)pyridin-2-amine or a N-(1H-pyrazol-3-yl)pyrimidin-4-amine core structure. These compounds may be used in the treatmen...
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WO/2024/059806A1 |
The disclosure is directed to compounds of Formula (I). Pharmaceutical compositions comprising compounds of Formula (I), as well as methods of their use and preparation, are also described.
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WO/2024/059200A1 |
Compounds having activity as inhibitors of NEK7 are provided. The compounds have Structure (I): (I) or a stereoisomer, tautomer, or salt thereof, wherein A, W, X, Y, Z, R1, and R2 are as defined herein. Methods associated with preparatio...
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WO/2024/059163A1 |
The present invention relates to highly pure and crystalline compounds as starting materials and intermediates to make maralixibat and the processes of making highly pure maralixibat. The invention also relates to an amorphous form of ma...
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WO/2024/059607A1 |
The present disclosure relates to physical forms of a PRC2 inhibitor compound, pharmaceutical compositions comprising the physical forms of the compound, and methods of treating subjects having cancer by administering the physical forms,...
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WO/2024/059524A1 |
The invention provides pyrazolylcarboxamide compounds, pharmaceutical compositions, their use for inhibiting mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT1), and their use in the treatment of a disease or condi...
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WO/2024/059186A1 |
The present invention provides compounds and compositions thereof which are useful as inhibitors of plasma kallikrein and which exhibit desirable characteristics for the same.The present invention provides isoquinoline derivatives of for...
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WO/2024/054919A1 |
Disclosed are compounds having enhanced potency in the modulation of NMDA receptor activity. Such compounds can be useful in the treatment of conditions such as depression and related disorders. Orally available formulations and other ph...
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WO/2024/054602A1 |
The invention provides heterobifunctional compounds, pharmaceutical compositions, and their use in treating disease, such as cancer.
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WO/2024/051749A1 |
Provided are a polymorph of a GLP-1R agonist compound I, a preparation method therefor, and use thereof. Compared with the free state of the compound I, the polymorph has higher stability and better processability, and is more suitable f...
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WO/2024/050635A1 |
A method for fabricating an ionic liquid electrolyte such as a spiro-based ionic liquid electrolyte, the method has the steps of: synthesizing an intermediate spiro-based product, and applying an ionic exchange process to the intermediat...
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WO/2024/051631A1 |
Disclosed are a macrocyclic imidazo[1,2-b]pyridazine compound represented by formula (I) or an isotopically labeled compound thereof, or an optical isomer thereof, a geometric isomer, a tautomer thereof or an isomer mixture thereof, or a...
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WO/2024/051816A1 |
Provided is a bicyclic PRMT5 inhibitor, which is a compound having a structure represented by formula (I). Further provided are a preparation method for the compound and use of the compound in regulating PRMT5 activity or treating PRMT5-...
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WO/2024/054851A1 |
The present disclosure includes, among other things, macrocyclic CFTR modulators of formula I, pharmaceutical compositions, and methods of making and using the same.
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WO/2024/050742A1 |
Providing certain bifunctional compounds that cause degradation of K-ras G12D via ubiquitin proteasome pathway and are therefore useful for the treatment of diseases mediated by K-ras G12D. Also provided are pharmaceutical compositions c...
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WO/2024/054952A1 |
The invention provides heterobifunctional compounds, pharmaceutical compositions, and their use in treating disease, such as cancer.
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WO/2024/051664A1 |
Provided are a novel compound having a binding effect with an E3 ligase protein (CRBN), and a use of the compound in the preparation of a drug for treating abnormal cell proliferation diseases.
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WO/2024/054647A1 |
Provided are small molecule inhibitors of the KRAS(G12D) mutant oncoprotein having the structural formula (I) and pharmaceutically acceptable salts and compositions thereof, which are useful for treating cancers and related conditions.
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WO/2024/054512A1 |
Provided herein are inhibitors of AKT1, pharmaceutical compositions comprising the inhibitory compounds, and methods for using the AKT1 inhibitory compounds for the treatment of disease.
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WO/2024/051795A1 |
The present disclosure relates to a substituted purinone derivative used as a ubiquitin-specific protease inhibitor, and in particular to a compound represented by formula (I), an isomer thereof, or a pharmaceutically acceptable salt the...
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WO/2024/051308A1 |
Disclosed are a pemetrexed near-infrared fluorescent molecule targeting an α-type folate receptor, a preparation method therefor, and use thereof. The structural formula of the pemetrexed near-infrared fluorescent molecule is: . The pem...
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WO/2024/050694A1 |
Disclosed herein are a natural porphin salt and use thereof as a plant growth regulator and an immune resistance inducer. The porphin salt comprises a salt of porphin or a salt of chlorin. Compared with the prior art, the porphin salt of...
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WO/2024/052801A1 |
Method for preparing amidines or derivatives thereof, comprising the step of subjecting N-(amino-alkyl) lactams to dehydration in the presence of a heterogeneous catalyst chosen from a Lewis acid, Lewis acids with Bronsted acid or Bronst...
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WO/2024/051727A1 |
The present invention relates to a pyrazole derivative, a pharmaceutical a composition, and a use. The pyrazole derivative has a structure as represented by formula (I). The pyrazole derivative has good activity inhibition selectivity wi...
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WO/2024/051778A1 |
Provided herein are compounds having a Formula II-4, or a pharmaceutically acceptable salt thereof. Also provided herein are methods of preparing the compounds and methods of using the compounds in inhibiting PI3K in a cell, or in treati...
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WO/2024/051784A1 |
Provided are a nitrogen-containing heterocyclic compound, a pharmaceutical composition thereof, and use thereof. The structure of the nitrogen-containing heterocyclic compound is represented by formula I. The nitrogen-containing heterocy...
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WO/2024/054956A1 |
The invention provides heterobifunctional compounds which may bind to both an androgen receptor and BRD4 (bromodomain- containing protein 4). Also provided are pharmaceutical compositions comprising the same and their use in treating dis...
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WO/2024/054955A1 |
The invention provides heterobifunctional compounds, pharmaceutical compositions, and their use in treating disease, such as cancer.
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WO/2024/051702A1 |
The present invention relates to a compound used as an inhibitor of a CDK4 kinase and use thereof. Specifically, the compound of the present invention has a structure represented by formula (I), wherein the definitions of each group and ...
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WO/2024/054954A1 |
The invention provides heterobifunctional compounds, pharmaceutical compositions, and their use in treating disease, such as cancer.
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WO/2024/054624A1 |
Novel compounds, compositions, and methods of using and preparing the same, which may be useful for treating alpha-1 antitrypsin deficiency (AATD). (Formula (I))
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WO/2024/051668A1 |
Provided are a compound having a binding effect with an E3 ligase protein (CRBN) as represented by formula I and a use of the compound in the preparation of a drug for treating abnormal cell proliferation diseases.
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WO/2024/054540A1 |
The invention provides pyrazolo[1,5-a][1,3,5]benzotriazepinyl, pyrazolo[1,5-a]pyrido[3,4-f][1,3,5]triazepinyl and related tricyclic compounds that inhibit the activity of one or more kinases, more particularly the protein kinase leucine ...
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