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TRV-120027
go.drugbank.com/drugs/DB12199InvestigationalTRV120027 has been used in trials studying the treatment of Heart Failure and Kidney Disease.
GDC-0917
go.drugbank.com/drugs/DB12336InvestigationalCUDC-427 has been used in trials studying the treatment of LYMPHOMA and Solid Cancers.
Zamicastat
go.drugbank.com/drugs/DB12389InvestigationalZamicastat has been used in trials studying the treatment of Hypertension and Chronic Heart Failure.
Decernotinib
go.drugbank.com/drugs/DB12566InvestigationalDecernotinib has been used in trials studying the treatment of Drug Interactions and Rheumatoid Arthritis.
Piperine
go.drugbank.com/drugs/DB12582InvestigationalBioperine has been used in trials studying the treatment of Multiple Myeloma and Deglutition Disorders.
Salirasib
go.drugbank.com/drugs/DB12681InvestigationalSalirasib has been used in trials studying the diagnostic of Carcinoma, Non-Small-Cell Lung.
UK-432097
go.drugbank.com/drugs/DB12691InvestigationalUK-432,097 has been used in trials studying the treatment of Pulmonary Disease, Chronic Obstructive.
Vintafolide
go.drugbank.com/drugs/DB05168InvestigationalVintafolide is a folate-targeted chemotherapeutic conjugate (folate vitamin + vinca alkaloid) in clinical stage development as a treatment for folate-receptor positive cancers.
Navitoclax
go.drugbank.com/drugs/DB12340InvestigationalNavitoclax has been used in trials studying the treatment and basic science of Solid Tumors, Non-Hodgkin's Lymphoma, EGFR Activating Mutation, Chronic Lymphoid Leukemia, and Hematological Malignancies, … Navitoclax is an orally bioavailable small molecule inhibitor of Bcl-2 family proteins. It is a substance being studied in the treatment of lymphomas and other types of cancer.
Synonyms: (R)-4-(3-Morpholin-4-Yl-1-Phenylsulfanylmethyl-Propylamino)-N-(4-{4-[2-(4-Chlorophenyl)-5,5-Dimethylcyclohex-1-Enylmethyl]-Piperazin-1-Yl}-Benzoyl)-3-TrifluoromethanesulfonylbenzenesulfonamidePadoprazan
go.drugbank.com/drugs/DB21689ExperimentalThe usage of the INN stem '-prazan' in the name indicates that Padoprazan is a proton pump inhibitor, not dependent on acid activation. Padoprazan has a monoisotopic molecular weight of 405.12 Da.