Aligos Therapeutics Inc. has disclosed programmed cell death protein 1 (PD-1; PDCD1; CD279), PD-1 ligand 1 (PD-L1; CD274) and/or PD-1/PD-L1 interaction inhibitors reported to be useful for the treatment of hepatocellular carcinoma and hepatitis B virus (HBV).
Corcept Therapeutics Inc. has described piperazine indazole glucocorticoid receptor (GR) antagonists reported to be useful for the treatment of obesity, Cushing syndrome, Alzheimer’s disease, amyotrophic lateral sclerosis, nonalcoholic steatohepatitis and cancer, among others.
Sato Pharmaceutical Co. Ltd. has divulged azaindole derivatives acting as hematopoietic prostaglandin D synthase (HPGDS) inhibitors reported to be useful for the treatment of amyotrophic lateral sclerosis, asthma, chronic obstructive pulmonary disease, cystic fibrosis, myocardial infarction, rheumatoid arthritis, sarcopenia and thromboangiitis obliterans (Buerger’s disease), among others.
Delix Therapeutics Inc. has identified pyrrolidine psychoplastogens acting as 5-HT2A receptor modulators reported to be useful for the treatment of neurodegeneration, substance abuse and dependence, impulse control, mood, sleep, anxiety, eating and personality disorders, among others.
3M Innovative Properties Co. has synthesized immune response modifiers (IRMs) and their conjugates reported to be useful for the treatment of cancer and viral infections.
Novartis AG has described pyridine-3-carboxylate compounds acting as voltage-dependent L-type calcium channel subunit α-1C channel (Cav1.2) activators reported to be useful for the treatment of schizophrenia, major depression, attention deficit hyperactivity disorder, autism spectrum disorder, multiple sclerosis, frontotemporal dementia, Alzheimer’s disease and Brugada syndrome.
National Institute of Pharmaceutical R&D Co. Ltd. has divulged heterocyclic compounds acting as RAC-α serine/threonine-protein kinase (AKT1; PKB α), AKT2 (PKB β) and AKT3 (PKB γ) inhibitors reported to be useful for the treatment of cancer.
Beigene Co. Ltd. has identified 3, 4-dihydroisoquinolin-1 (2h)-ones derivatives acting as stimulator of interferon genes protein (STING; TMEM173) antagonists reported to be useful for the treatment of systemic lupus erythematosus (SLE).
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