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WO/2023/221022A1 |
Disclosed in the present invention are intermediate I and intermediate II which have structural formulas as represented by formula (I) and formula (II), respectively, and can be used for preparing galantamine, and a preparation method th...
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WO/2023/217230A1 |
The present invention provides a KIF18A inhibitor and a method for synthesizing same. The compound of the present invention can regulate KIF18A protein to influence the cell cycle and the cell proliferation process, so as to treat cancer...
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WO/2023/216956A1 |
The present invention relates to a camptothecin compound with anti-tumor activity, a preparation method therefor and use thereof. In particular, the present invention relates to a compound of the following formula or a pharmaceutically a...
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WO/2023/220439A1 |
Described herein are compounds that modulate splicing of a pre-mRNA, encoded by genes, and methods of treating diseases and conditions associated with gene expression or activity of proteins encoded by genes.
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WO/2023/220433A1 |
Described herein are compounds that modulate splicing of a pre-mRNA, encoded by genes, and methods of treating diseases and conditions associated with gene expression or activity of proteins encoded by genes.
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WO/2023/218245A1 |
The present invention relates to heteroaryl derivative compounds and a pharmaceutical composition comprising thereof. Specifically, the present invention relates to heteroaryl derivative compounds having RAF inhibitory activity.
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WO/2023/217227A1 |
The present disclosure relates to a ligand-drug conjugate of a novel structure or a pharmaceutically acceptable salt thereof. Specifically, the present disclosure provides a ligand-drug conjugate having a structural general formula repre...
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WO/2023/217064A1 |
The present invention belongs to the field of pharmaceutical chemistry, and relates to a camptothecin derivative, an antibody-drug conjugate and pharmaceutical composition based on same, and the use thereof. The derivative has a structur...
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WO/2023/217906A1 |
The present disclosure relates to compounds of Formula (I) that inhibit NIK and pharmaceutical compositions comprising such compounds and methods of using the same. These compounds and pharmaceutical compositions are useful for preventin...
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WO/2023/220541A1 |
Tetrahydropyrido[3,4-d]pyrimidine compounds are provided that are potent HPK1 inhibitors. The compounds are useful to treat or prevent cancer and/or inflammatory and/or autoimmune diseases or symptoms thereof in mammals, particularly hum...
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WO/2023/220435A1 |
Described herein are compounds that modulate splicing of a pre-mRNA, encoded by genes, and methods of treating diseases and conditions associated with gene expression or activity of proteins encoded by genes.
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WO/2023/214651A1 |
The present invention relates to: a heterocyclic compound represented by chemical formula 1; and an organic light-emitting element comprising same.
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WO/2023/214650A1 |
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/2023/215238A1 |
Described herein are new 8,9-dialoxy-7-azaindenoisoquinoline compounds (I), processes for their preparation, and methods of their use in the treatment of diseases responsive to inhibition of topoisomerase 1 and/or binding to the c-MYC G-...
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WO/2023/214836A1 |
The present invention relates to a novel berberine analogue CD1-410. It has been identified that the novel berberine analogue promotes the activity of mitophagy, and thus can reduce mitochondria with a damaged structure and/or function. ...
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WO/2023/207991A1 |
Disclosed in the present invention are a fused quinazoline compound and the use thereof. Specifically, the present invention relates to a compound as represented by formula (IV) and a pharmaceutically acceptable salt thereof.
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WO/2023/212219A1 |
Described herein are tricyclic PARP1 inhibitors and pharmaceutical compositions comprising said inhibitors. The subject compounds and compositions are useful for the treatment of cancer.
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WO/2023/206274A1 |
The present disclosure provides an organic electroluminescent diode and a display panel, belonging to the technical field of display. The organic electroluminescent diode comprises an anode, a luminescent layer, a hole blocking layer, an...
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WO/2023/207773A1 |
Provided are conjugates of novel camptothecin analogs with a cell binding molecule of formula (I). It also provides methods of making the conjugates of camptothecin analogs to a cell-binding agent, as well as methods of application the c...
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WO/2023/212240A1 |
The present disclosure relates generally to inhibitors of KIF18A, compositions thereof, and methods of using said compounds and compositions thereof. More specifically, the present disclosure relates to inhibitors of KIF18A and methods o...
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WO/2023/210623A1 |
The present invention is a novel haloalkyl sulfone anilide compound or a salt thereof, an herbicide composition including said compound or salt thereof, an herbicide method including a step for applying the herbicide composition, and a m...
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WO/2023/210192A1 |
This compound, represented by a general formula, is useful in a light-emitting device. Ar1 is a benzene ring, a naphthalene ring, a phenanthrene ring, or the like; D is a 5H-benzofuro[3,2-c]carbazol-5-yl group, or the like; A is a cyano ...
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WO/2023/211990A1 |
Provided herein are compounds of formula (I), pharmaceutical compositions comprising the compounds, methods of preparing the compounds, and methods of using the compounds and compositions in treating conditions associated with voltage-ga...
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WO/2023/201421A1 |
The present application relates to indoline derivatives of general Formula (I), to processes for their preparation, to compositions comprising them and to their use in activation of a serotonin receptors in a cell, as well as to treating...
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WO/2023/201429A1 |
The present application relates to combination treatments for breast cancer. For example, the application relates to the use of homoharringtonine and paclitaxel for the treatment of breast cancer including, for example, triple negative b...
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WO/2023/204631A1 |
The present invention relates to: (a) an active camptothecin derivative represented by chemical formula 1, which is designed to bind to a DDX5 protein or E3 ligase; (b) a prodrug thereof designed to release the active camptothecin deriva...
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WO/2023/201780A1 |
Provided is a method for preparing a quinolone compound and an intermediate thereof, particularly, a method for preparing quinolone and a pharmaceutical quinolinone intermediate. Specifically, provided are a method for preparing a compou...
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WO/2023/205251A1 |
Disclosed are compounds of formula (I) which modulate bromodomains, pharmaceutical compositions containing said compounds and use of said compounds in therapy.
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WO/2023/205468A1 |
Compounds, and pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels are provided. Also provided are pharmaceutical compositions comprising the compounds or pharmaceutically acceptable salts and methods of us...
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WO/2023/198114A1 |
An ALK2 kinase inhibitor as represented by general formula (I), a pharmaceutical composition thereof, a preparation method therefor, and use of the ALK2 kinase inhibitor in preparing a drug for the prevention and/or treatment of indicati...
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WO/2023/200441A1 |
The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: Formula (I) which inhibit Human Respiratory Syncytial Virus (HRSV) or Human Metapneumo virus (HMPV) inhibitors. ...
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WO/2023/198078A1 |
The present invention provides compounds as KRAS G12D inhibitors. Specifically, the present invention provides compounds having a structure represented by formula (I), or optical isomers, pharmaceutically acceptable salts, prodrugs, deut...
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WO/2023/201012A1 |
Described herein are compounds of Formulae I' and their pharmaceutically acceptable salts, solvates, or stereoisomers, as well as their uses (e.g., as IKZF2 degraders).
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WO/2023/200964A1 |
Provided herein are compounds, compositions, and methods useful for inhibiting protein tyrosine phosphatase, e.g., protein tyrosine phosphatase non-receptor type 2 (PTPN2) and/or protein tyrosine phosphatase non-receptor type 1 (PTPN1), ...
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WO/2023/196538A1 |
Substituted benzofuran, benzothiophene, and indole carboxamide compounds, conjugates, and pharmaceutical compositions for use as immunotherapeutics in the treatment of cancer, such as solid tumors, are disclosed herein. The disclosed com...
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WO/2023/195530A1 |
The present invention provides a compound showing coronavirus 3CL protease inhibitory activity or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition containing the same. A compound represented by formula (I) [in...
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WO/2023/196875A1 |
The present disclosure relates generally to compounds, of Formula I: Also disclosed are pharmaceutical compositions comprising said compounds and methods of making said compounds. The compounds of the disclosure are useful in treating or...
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WO/2023/195529A1 |
The present invention provides: a compound that exhibits a coronavirus 3CL protease inhibitory activity or a pharmaceutically acceptable salt thereof; and a pharmaceutical composition containing the same. The compound is represented by f...
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WO/2023/194964A1 |
Disclosed are compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein α, β, m, R5, R6, R7, R9, R10, R11, Ra, Rb, X1, X2, X3, X4 and X8 are defined in the specification. This disclosure also relates to materials...
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WO/2023/191536A1 |
The present invention relates to a thiobenzimidazole derivative or a pharmaceutically acceptable salt thereof, and a composition for preventing or treating cancer, the composition comprising the derivative as an active ingredient. The th...
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WO/2023/191533A1 |
The present invention relates to a thiobenzimidazole derivative preparation method, a novel intermediate therefor, and the like. The present invention uses an intermediate containing O-ethyl carbonodithioate or an intermediate containing...
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WO/2023/192328A1 |
The present disclosure features compounds (e.g., oxaziridine-based compounds), as well as related compositions and methods of use thereof, e.g., for selectively labeling a methionine residue in a target peptide or protein.
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WO/2023/187099A1 |
The invention relates to morphinan-derivatives, processes for their preparation, medicaments containing them and the use of these morphinan-derivatives for the preparation of medicaments.
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WO/2023/192112A1 |
Provided herein are methods for preparing a SHP2 inhibitor and intermediates useful therein.
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WO/2023/192801A1 |
The present disclosure provides certain sulfonamido derivatives that are Cyciin-dependent kinase 2 (CDK2) inhibitors of Formula (I): for the treatment of diseases treatable by inhibition of CDK2. Also provided are pharmaceutical composit...
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WO/2023/192653A1 |
The present disclosure provides photocleavable rhodamine probes that facilitate live- and fixed-cell immunofluorescence. The ultra-fast spirocyclization of the dye following cleavage depletes the fluorescence signal, enabling cyclic mult...
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WO/2023/183520A1 |
Disclosed herein are inhibitors of TACC and methods of treating certain diseases and disorders (e.g., diseases and disorders related to TACC).
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WO/2023/183607A1 |
Described herein are compounds or conjugates of Formula II and their pharmaceutically acceptable salts, solvates, or stereoisomers thereof, as well as their uses (e.g., as cereblon-binding agents or bifunctional degraders for degrading c...
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WO/2023/181952A1 |
This compound is represented by formula (1). [In the formula, Ar1 represents an aromatic hydrocarbon ring or an aromatic heterocycle. Ring Ar2 and ring Ar3 each independently represent an aromatic hydrocarbon ring or an aromatic heterocy...
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WO/2023/179275A1 |
Disclosed in the present invention are a fused ring unit based on a quinoxaline derivative, a small molecule containing same, a polymer, and preparation methods therefor and the use thereof. In the present invention, a new aromatic unit ...
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