Investigational Drug Details

Drug ID: D092
Drug Name: Curcumin
Synonyms: Turmeric
Type: Chemical drug
DrugBank ID: DB11672
DrugBank Description: Curcumin, also known as diferuloylmethane, is an active component in the golden spice turmeric (Curcuma longa) and in . It is a highly pleiotropic molecule that exhibits antibacterial, anti-inflammatory, hypoglycemic, antioxidant, wound-healing, and antimicrobial activities . Due to these properties, curcumin has been investigated for the treatment and supportive care of clinical conditions including proteinuria, breast cancer, multiple myeloma, depression, and Non Small Cell Lung Cancer (NSCLC). Despite proven efficacy against numerous experimental models, poor bioavailability due to poor absorption, rapid metabolism, and rapid systemic elimination have been shown to limit the therapeutic efficacy of curcumin . Curcumin is under investigation for the treatment and supportive care of various clinical conditions including mucositis, rectal cancer, prostate cancer, chronic schizophrenia, and Mild Cognitive Impairment (MCI) .
PubChem ID: 969516
CasNo: 458-37-7
Repositioning for NAFLD: Yes
SMILES: C(=C\C(=O)CC(=O)/C=C/c1cc(OC)c(cc1)O)/c1cc(OC)c(cc1)O
Structure:
InChiKey: VFLDPWHFBUODDF-FCXRPNKRSA-N
Molecular Weight: 368.385
DrugBank Targets: Peroxisome proliferator-activated receptor gamma; Vitamin D3 receptor; Multidrug resistance-associated protein 5 inhibitor; Carbonyl reductase [NADPH] 1; Glutathione S-transferase P
DrugBank MoA: Curcumin acts as a scavenger of oxygen species, such as hydroxyl radical, superoxide anion, and singlet oxygen and inhibit lipid peroxidation as well as peroxide-induced DNA damage . Curcumin mediates potent anti-inflammatory agent and anti-carcinogenic actions via modulating various signalling molecules. It suppresses a number of key elements in cellular signal transduction pathways pertinent to growth, differentiation, and malignant transformation; it was demonstrated _in vitro_ that curcumin inhibits protein kinases, c-Jun/AP-1 activation, prostaglandin biosynthesis, and the activity and expression of the enzyme cyclooxygenase (COX)-2 .
DrugBank Pharmacology: Intravenous application of 25 mg/kg bw curcumin to rats resulted in an increase in bile flow by 80 and 120% . In the rat model of inflammation, curcumin was shown to inhibit edema formation. In nude mouse that had been injected subcutaneously with prostate cancer cells, administration of curcumin caused a marked decrease in the extent of cell proliferation, a significant increase of apoptosis and micro-vessel density . Curcumin may exert choleretic effects by increasing biliary excretion of bile salts, cholesterol, and bilirubin, as well as increasing bile solubility . Curcumin inhibited arachidonic acid-induced platelet aggregation _in vitro_ .
DrugBank Indication: No approved therapeutic indications.
Targets: PPARG; COX inhibitor
Therapeutic Category: Anticancer agent; NSAID
Clinical Trial Progress: Phase 2 on-going (NCT04315350)
Latest Progress: Under clinical trials

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