Inventor

YU YOUNONG

US39 patents

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

YU YOUNONG

MERCK SHARP & DOHME

Aminopyrazine compounds with A2A antagonist properties

Indazole and azaindazole Btk inhibitors

Substituted aminoquinazoline compounds as A2A antagonist

Factor XIa inhibitors

Heterobicyclo-substituted [1,2,4]triazolo[1,5-c]quinazolin-5-amine compounds with A2A anatagonist properties

BTK Inhibitors

Piperazine-substituted [1,2,4]triazolo[1,5-C]quinazolin-5-amine compounds with A2A antagonist properties

Tricyclic substituted thiadiazine dioxide compounds as BACE inhibitors, compositions and their use

Tricyclic substituted thiadiazine dioxide compounds as BACE inhibitors, compositions and their use

Substituted benzamides and substituted pyridinecarboxamides as Btk inhibitors

Biaryl-spiroaminooxzaoline analogues as alpha 2C adrenergic receptor modulators

Biaryl spiroaminooxazoline analogues as Alpha2C adrenergic receptor modulators

BTK inhibitors

Processes for making substituted quinazoline compounds using hydrogen bonding catalysts

BTK inhibitors

SCHERING CORP

3,4-di-substituted pyridazinediones as CXC chemokine receptor antagonists

Functionally selective ALPHA2C adrenoreceptor agonists

Phenoxypiperidines and analogs thereof useful as histamine H3 antagonists

3,4-DI-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands

3,4-di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands

α2C adrenoreceptor agonists

Thiadiazoles AS CXC- and CC- chemokine receptor ligands

Thiadiazoledioxides and thiadiazoleoxides as CXC- and CC-chemokine receptor ligands

Isothiazole dioxides as CXC- and CC-chemokine receptor ligands

Treatment of chemokine mediated diseases

Functionally selective ALPHA2C adrenoreceptor agonists

Thiadiazoles as CXC- and CC- chemokine receptor ligands

MERCK SHARP & DOHME LLC

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

4-amino or 4-alkoxy-substituted aryl sulfonamide compounds with selective activity in voltage-gated sodium channels

PHARMACOPEIA DRUG DISCOVERY

3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands

ALPHA2C adrenoreceptor agonists

UNIV RUTGERS

Heterocyclic cytotoxic agents

WU WEN-LIAN

5-substituted iminothiazines and their mono- and dioxides as BACE inhibitors, compositions, and their use

ASLANIAN ROBERT G

Quinazolinone-type compounds as CRTH2 antagonists

BOYCE CHRISTOPHER W

Quinoxalines and AZA-quinoxalines as CRTH2 receptor modulators

HU MENGWEI

Crystalline polymorphs of a CXC-chemokine receptor ligand

ZHENG JUNYING

Derivatives and analogs of chroman as functionally selective ALPHA2C adrenoreceptor agonists

DE LERA RUIZ MANUEL

Functionally selective alpha2C adrenoreceptor agonists