PeptideDB

Gossypin

CAS No.: 652-78-8

Gossypin has antidiabetic, antioxdiant, anticonvulsant, anti-allergic, antiinflammatory, antinociceptive, cytotoxic and
Sales Email:peptidedb@qq.com

This product is for research use only, not for human use. We do not sell to patients.

Description Gossypin has antidiabetic, antioxdiant, anticonvulsant, anti-allergic, antiinflammatory, antinociceptive, cytotoxic and antibacterial activities; it inhibits the NF-kappaB activation pathway, which may explain its role in the suppression of inflammation, carcinogenesis, and angiogenesis.
In vitro Gossypin is a flavone extracted from Hibiscus vitifolius, which has been reported to exhibit anti-inflammatory, antioxidant, and anticancer activities.?However, the anticancer properties of gossypin and its molecular mechanism of action against gastric cancer have not been fully investigated.?gossypin is an Aurora kinase A (AURKA) and RSK2 inhibitor that suppresses gastric cancer growth.?Gossypin attenuated anchorage-dependent and anchorage-independent gastric cancer cell growth as well as cell migration.?Based on the results of in vitro screening and cell-based assays, gossypin directly binds to and inhibits AURKA and RSK2 activities and their downstream signaling proteins.?Gossypin decreased S phase and increased G2/M phase cell cycle arrest by reducing the expression of cyclin A2 and cyclin B1 and the phosphorylation of the CDC protein.?Additionally, gossypin also induced intrinsic apoptosis by activating caspases and PARP and increasing the expression of cytochrome c. Gossypin is an AURKA and RSK2 inhibitor that could be useful for treating gastric cancer[2].
molecular weight 480.38
Molecular formula C21H20O13
CAS 652-78-8
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility DMSO: 25 mg/mL (52.04 mM)
References 1. Gossypin protects primary cultured rat cortical cells from oxidative stress- and beta-amyloid-induced toxicity.Arch Pharm Res. 2004 Apr;27(4):454-9. 2. Wang L , Wang X , Chen H , et al. Gossypin inhibits gastric cancer growth by direct targeting of AURKA and RSK2[J]. Phytotherapy Research, 2019, 33(4).