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WO/2023/122938A1 |
Disclosed herein are compounds of formula (I), and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt or solvate thereof; and therapeutic uses of these compounds, which are inhibitors of SHP2, potentially useful i...
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WO/2023/125102A1 |
The present invention provides a method for synthesizing a 1H-furo[3,2-b]imidazo[4,5-d]pyridine compound, the method comprising the following steps: reacting a compound 1 with a compound 2 in a solvent in the presence of a base to obtain...
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WO/2023/130054A2 |
The present disclosure relates to the field of medicinal chemistry, and specifically relates to a compound with interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitory activity, and pharmaceutical compositions and applications ther...
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WO/2023/125707A1 |
Disclosed in the present disclosure are a compound as shown in formula I, a racemate, a stereoisomer, a tautomer, an isotope label, a solvate, a pharmaceutically acceptable salt or a prodrug thereof, and a composition thereof, a preparat...
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WO/2023/122859A1 |
Disclosed are an S-(+)-pranoprofen derivative, a preparation method therefor, a pharmaceutical composition thereof, and a use thereof. The provided S-(+)-pranoprofen derivative has excellent salt formability, so that solubility is improv...
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WO/2023/120062A1 |
This compound represented by the general formula below is useful as an electron barrier material. R1-R21 each represent H, a deuterium atom, and a substituent other than a cyano group, and X represents O or S.
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WO/2023/120696A1 |
The present invention provides a compound that exhibits an anticancer effect based on Checkpoint Kinase 1 (CHK1) inhibition. It is discovered that a compound represented by formula (1) or a pharmaceutically acceptable salt thereof has a ...
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WO/2023/116390A1 |
Provided are a pyrimidine-2(1H)-one-fused bicyclic compound having an MAT2A inhibitory activity and the use thereof. Specifically, provided are a compound of formula (I) having an MAT2A inhibitory activity, a stereoisomer thereof, a phar...
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WO/2023/115142A1 |
This invention relates to compounds of formula (I) and salts, solvates, tautomers, N-oxides, stereoisomers, polymorphs and/or prodrugs thereof. Also disclosed is the use of the compounds of formula (I) to treat necroptosis and/or inhibit...
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WO/2023/122140A1 |
The present disclosure provides compounds, compositions, and methods useful for inhibiting PARP1, and/or treating a disease, disorder, or condition associated with PARP1, and/or treating cancer.
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WO/2023/122662A1 |
Described herein, inter alia, are GTPase inhibitors and uses thereof.
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WO/2023/115166A1 |
The present disclosure relates generally to compounds, their methods of synthesis, and their use in the treatment of mental illness or central nervous system disorders.
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WO/2023/116884A1 |
The present disclosure provides a compound represented by structural formula (I) : or a pharmaceutically acceptable salt, or a stereoisomer thereof and their use in, e.g. treating a disease or disorder associated with CDK2. This disclosu...
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WO/2023/116822A1 |
Disclosed herein are a solid Form of a TYK2 inhibitor N- (5- (2, 2-dimethyl-2, 3-dihydro- [1, 4] dioxino [2, 3-b]pyridin-6-yl) -4- ( (6- (methylsulfonyl) -4- (tetrahydro-2H-pyran-4-yl) pyridin-2-yl) amino) pyridin-2-yl) acetamide per se ...
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WO/2023/121413A1 |
The present invention relates to: a novel bicyclic heterocyclyl compound which has an SOS1 inhibitory activity and thus may be utilized for preventing, relieving or treating various carcinomas or RASopathy; a stereoisomer thereof; a solv...
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WO/2023/120452A1 |
This SREBP-1 inhibitor has inhibitory activity against SREBP-1 and does not have inhibitory activity against SREBP-2, the SREBP-1 inhibitor containing, as an active ingredient, one or more compounds from among compounds represented by fo...
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WO/2023/122260A2 |
Described herein are compounds, and methods for the treatment of coronavirus infection.
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WO/2023/119098A1 |
The present invention relates to PKCθ inhibitors of formula I and pharmaceutically acceptable salts thereof and uses of such compounds. Compound uses include inhibiting PKCθ activity in a subject in need of such treatment, treating T-c...
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WO/2023/115203A1 |
Disclosed are compounds of formula (I), wherein ring A is an 8-10 membered aromatic or partially aromatic bicyclic ring having 1-4 heteroatoms compositions thereof, wherein L1, L2, R1 to R4 and m are as defined in claim 1; and methods of...
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WO/2023/114954A1 |
Provided herein are compounds and pharmaceutical compositions thereof for modulating SHP2 and their use in the treatment of disease.
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WO/2023/111799A1 |
The present disclosure provides for a compound according to formula (I) or a pharmaceutically acceptable salt thereof as Cav1.2 activators for the treatment of schizophrenia, bipolar disorder, major depressive disorder, substance use dis...
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WO/2023/115002A1 |
The present disclosure relates to compound Formula (I) methods for making the compounds and methods for their use.
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WO/2023/111996A1 |
Embodiments of the instant disclosure relate to novel compounds, compositions, and methods for treating health conditions. In certain embodiments, methods of treating cancers can include administering an effective amount of at least one ...
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WO/2023/110664A1 |
Compounds of Formula (I) wherein the substituents are as defined in claim 1. The invention further relates to herbicidal compositions which comprise a compound of Formula (I) and to the use of compounds of Formula (I) for controlling wee...
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WO/2023/114858A1 |
Disclosed herein are compounds, compositions, and methods for promoting neuronal growth and/or improving neuronal structure with the compounds and compositions disclosed herein. Also described are methods of treating diseases or disorder...
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WO/2023/110700A1 |
The invention relates to compounds of formula (I) inhibiting Rho Kinase that are dihydrofuropyridine derivatives, methods of preparing such compounds, pharmaceutical compositions containing them and therapeutic use thereof. Particularly ...
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WO/2023/109965A1 |
Provided is a camptothecin compound, which is a compound represented by structural formula I or a pharmaceutically acceptable salt, stereoisomer, solvate or prodrug thereof. An antibody-drug conjugate comprising the camptothecin compound...
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WO/2023/114822A1 |
The disclosure relates to compounds of Formula (I), which are RXFP1 receptor agonists, compositions containing them, and methods of using them, for example, in the treatment of heart failure, fibrotic diseases, and related diseases such ...
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WO/2023/110394A1 |
The present invention is directed to a process for C-H insertion by the gem-hydrogenation of an internal alkyne.
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WO/2023/109471A1 |
Provided are a compound as represented in general formula (I), and a cis-trans isomer, an enantiomer, a diastereoisomer, a racemate, a solvate, a hydrate or a pharmaceutically acceptable salt or a precursor drug thereof, and a preparatio...
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WO/2023/114539A1 |
The present invention provides novel amino chromen-2-one compounds that are inhibitors of mitochondrial RNA polymerase for treating various diseases such as cancer and others associated with metabolic disorders and mitochondrial dysfunct...
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WO/2023/114428A1 |
The disclosure provides heterocycle derivatives of Formula (I) for the inhibition of the oligosaccharyltransferase complex and the treatment of disease.
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WO/2023/104051A1 |
Disclosed is the combined use of an indole substituted tetrahydroisoquinoline compound and a statin compound. Specifically, a safe and non-interaction pharmaceutical composition or pharmaceutical combination. The composition contains an ...
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WO/2023/107722A1 |
This disclosure provides compounds of formula (I) and pharmaceutically acceptable salts thereof, that inhibit Dual specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A). These chemical entities are useful, e.g., for treating ...
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WO/2023/107356A1 |
The present invention provides methods of treating malaria comprising administration of compounds of Formula (I) or a pharmaceutically acceptable salt thereof, to a subject in need thereof, wherein the variables are as defined herein. Th...
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WO/2023/107606A1 |
Provided herein are compounds (e.g., compounds of Formula (I) or Formula (II)), their mechanism of action, and methods of modulating proliferation activity, and methods of treating diseases and disorders using the compounds provided here...
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WO/2023/104178A1 |
A series of compounds for regulating activity of a protein kinase, in particular a compound for inhibiting activity of PLK1. Further provided are a pharmaceutical composition containing the compound, and a use of the compound and the pha...
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WO/2023/104213A1 |
The present invention provides a cyclic bisbenzyl tetrahydroisoquinoline compound as represented by formula (I), and a pharmaceutically acceptable salt, an enantiomer, a diastereoisomer, a racemate, a crystalline hydrate, and a solvate t...
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WO/2023/106625A1 |
The present invention relates to: a heterocyclic compound represented by chemical formula 1; and an organic light-emitting device comprising same.
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WO/2023/099072A1 |
Compounds of formula (I) wherein Y, n, R1, R2 and R3 have the meanings indicated herein, or a pharmaceutically acceptable solvate or salt thereof, are disclosed. The compounds are useful as inhibitors of protein or lipid kinases (in part...
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WO/2023/102162A1 |
Described herein are novel compounds, compositions and methods for treatment of diseases including cancer using such compounds, compositions, and methods. The compounds include those of Formula (I):
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WO/2023/098515A1 |
Provided in the present application is a method for preparing a drug-linker conjugate. Specifically, provided in the present application is a method for preparing compound IM2, the method comprising the following steps: adding compound S...
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WO/2023/102378A1 |
The present invention relates to macrocyclic compounds of any one of Formula (I), or a pharmaceutically acceptable form thereof, pharmaceutical compositions comprising the same, methods of preparing the same, and methods of treating canc...
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WO/2023/101981A1 |
The disclosure provides at least one compound, tautomer, deuterated derivative, or pharmaceutically acceptable salt chosen from compounds of Formula I, tautomers thereof, deuterated derivatives of those compounds or tautomers, and pharma...
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WO/2023/102228A1 |
Described herein are compounds of Formula l-A that are inhibitors of GCN2 kinase or PERK kinase, and methods of treating diseases, including diseases associated with GCN2 kinase or PERK kinase, with said compounds.
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WO/2023/102231A1 |
The present disclosure relates to compounds of Formula (I): and to their prodrugs, pharmaceutically acceptable salts, pharmaceutical compositions, methods of use, and methods for their preparation. The compounds of the present disclosure...
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WO/2023/097194A2 |
This disclosure relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.
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WO/2023/094304A1 |
Compounds of Formula (I), wherein the substituents are as defined in claim 1, useful as pesticides, especially as fungicides.
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WO/2023/096225A1 |
The present specification relates to a heterocyclic compound of chemical formula 1, and an organic light-emitting device and a composition for forming an organic material layer, comprising same.
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WO/2023/097204A1 |
Microsphere formulations comprising asenapine are provided. Methods for making and using the microsphere formulations are also provided.
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