Inventor

YU WENSHENG

CN52 patents

⚠️ This page may combine multiple inventors who share the name “YU WENSHENG”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

YU WENSHENG

MERCK SHARP & DOHME

Heterocycle-substituted tetracyclic compounds and methods of use thereof for the treatment of viral diseases

Inhibitors of IRAK4 activity

Fused tetracyclic heterocyclic compounds and methods of use thereof for the treatment of viral diseases

Substituted cyclobutylbenzene compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted phenyl compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted cyclobutylpyridine and cyclobutylpyrimidine compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted pyridinyl compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted N′-hydroxycarbamimidoyl-1,2,5-oxadiazole compounds as indoleamine 2,3-dioxygenase IDO inhibitors

Substituted n′-hydroxycarbamimidoyl-1,2,5-oxadiazole compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted sulfoximine compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted benzamides and substituted pyridinecarboxamides as Btk inhibitors

Spiro-imidazolone derivatives as glucagon receptor antagonists

Substituted biaryl compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Benzamide imidazopyrazine Btk inhibitors

Heterocycle-substituted tetracyclic compounds and methods of use thereof for the treatment of viral diseases

Chromane-substituted tetracyclic compounds and uses thereof for the treatment of viral diseases

BTK inhibitors

Hepatitis C virus inhibitors

SCHERING CORP

Amine-linked pyridyl and phenyl substituted piperazine-piperidines with CXCR3 antagonist activity

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Piperazine-piperidines with CXCR3 antagonist activity

Compounds for the treatment of inflammatory disorders

Pyrazinyl substituted piperazine-piperidines with CXCR3 antagonist activity

Heteroaryl substituted pyrazinyl-piperazine-piperidines with CXCR3 antagonist activity

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

Compounds for the treatment of inflammatory disorders

MERCK SHARP & DOHME LLC

Arylalkyl pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors

Substituted pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors

Inhibitors of histone deacetylase useful for the treatment or prevention of HIV infection

Aryloxypiperidine pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors

Inhibitors of histone deacetylase useful for the treatment or prevention of HIV infection

Inhibitors of histone deacetylase-3 useful for the treatment of cancer, inflammation, neurodegeneration diseases and diabetes

Substituted piperazine amide compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors

Inhibitors of histone deacetylase useful for the treatment or prevention of HIV infection

LAVEY BRIAN J

Compounds for the treatment of inflammatory disorders

TONG LING

Compounds for the treatment of inflammatory disorders

NAIR ANILKUMAR GOPINADHAN

Fused tricyclic silyl compounds and methods of use thereof for the treatment of viral diseases

KOZLOWSKI JOSEPH A

Compounds for the treatment of inflammatory disorders

INST PHARM & TOXICOLOGY AMMS

Endothelin antagonist

UNIV IOWA RES FOUNDATION INC

Process for preparing saponin compounds

SHANGHAI HANSOH BIOMEDICAL CO LTD

Nitrogen-containing heterocyclic derivative inhibitor, preparation method therefor and use thereof