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AIM-102
go.drugbank.com/drugs/DB16176InvestigationalAIM-102 is under investigation in clinical trial NCT01501942 (Efficacy, Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of Oral Administration of AIM-102 in Patients With Mild to Moderate Allergic
Brivanib
go.drugbank.com/drugs/DB11958InvestigationalBrivanib is under investigation for the treatment of HepatoCellular Carcinoma. … Brivanib has been investigated for the treatment of Solid Tumors, Hepato Cellular Carcinoma (HCC), and Metastatic Colorectal Cancer (MCRC).
Indusatumab vedotin
go.drugbank.com/drugs/DB12413InvestigationalIndusatumab vedotin has been used in trials studying the treatment of Pancreatic Adenocarcinoma, Adenocarcinoma of the Stomach, Recurrent Gastric Adenocarcinoma, Metastatic Gastric Adenocarcinoma, and
ATL-104
go.drugbank.com/drugs/DB05670InvestigationalATL-104 is a potent mitogen for epithelial cells of the gastrointestinal tract. In animal models, ATL-104 aids regeneration of the gastrointestinal tract after treatment with chemotherapeutic agents.
Aetiocholanolone
go.drugbank.com/drugs/DB02854ExperimentalThe 5-beta-reduced isomer of androsterone. Etiocholanolone is a major metabolite of testosterone and androstenedione in many mammalian species including humans. It is excreted in the urine. [PubChem]
Urolithin A
go.drugbank.com/drugs/DB15464ExperimentalUrolithin A is a metabolite of ellagic acid. It has been demonstrated to stimulate mitophagy and improve muscle health in old animals and in preclinical models of aging.[A179494]
N-acetyl-alpha-D-glucosamine
go.drugbank.com/drugs/DB03740ExperimentalThe N-acetyl derivative of glucosamine.
Itopride
go.drugbank.com/drugs/DB04924InvestigationalItopride is a dopamine D2 antagonist with acetylcholinesterase inhibitory actions.
Products: DOIZ 50 MG FC TABLET, Itomed 50 mg FilmtablettenMonoxerutin
go.drugbank.com/drugs/DB13764ExperimentalMonoxerutin is a flavonol, a type of flavonoid.
Synonyms: O-(beta-Hydroxyethyl)rutinSacubitrilat
go.drugbank.com/drugs/DB14127ExperimentalA metabolite of LCZ696 with neprilysin inhibitory activity.