All
Chemical Reagents
Biomedicine
Organic raw materials
Inorganic chemical industry
intermediate
Agricultural chemicals
Auxiliaries and catalysts
Fragrances and Flavors
Dyes and Pigments
Daily chemical industry

Ankaflavin

CAS number:50980-32-0    molecular formula:C23H30O5

overview

compound introduction

Ankaflavin, isolated from Monascus-Fermented red rice, is an orally active PPARγ agonist. Ankaflavin exhibits selective cytotoxic effect and induces cell death through apoptosis on cancer cells. Ankaflavin has anti-inflammatory, anti-cancer, antiatherosclerotic, and hypolipidemic effects In Vitro Ankaflavin (0-50 µg/mL, 48 h) shows cytotoxicity against cancer cells with no significant toxicity toward normal cells. Ankaflavin (0-30 µg/mL, 0-48 h) arrests Hep G2 cell cycle at sub-G1 phase in a dose- and time-dependent manner. Ankaflavin (25 µg/mL, 48 h) induces Hep G2 cell apoptosis. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Cytotoxicity AssayCell Line: A549, Hep G2, MRC-5 and WI-38 Concentration: 1, 10, 25, and 50 µg/mL Incubation Time: 48 h Result: Showed cytotoxicity against A549 and Hep G2 cells in a dose-dependent manner with no significant toxicity toward normal cells (MRC-5 and WI-38). Cell Cycle AnalysisCell Line: Hep G2 cells Concentration: 15, 20, 25, and 30 µg/mL Incubation Time: 12, 24, 36, and 48 h Result: Induced a distinct sub-G1 peak in Hep G2 cells in a dose- and time-dependent manner. Apoptosis AnalysisCell Line: Hep G2 cells Concentration: 25 µg/mL Incubation Time: 48 h Result: Exhibited significant chromatin condensation (fluorescent spot) through Hoechst staining. In Vivo Ankaflavin (10 mg/kg; p.o.; daily for 28 days) shows antidiabetic and anti-inflammatory activity, improves liver function and pancreatic function. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Wistar rats (4 weeks of age), diabetes was induced by treating them with Methylglyoxal (MG) (600 mg/kg; oral) for 4 weeksDosage: 10 mg/kg Administration: Oral administration for 28 days Result: Exerted PPARγ agonist activity. Effectively reduced AGE (advanced glycation end-products) levels in serum, liver, and pancreas of MG-induced rats. Form:Solid IC50& Target:PPARγ

Specs

Chinese alias安卡黄素
English alias-
CAS number50980-32-0molecular formulaC23H30O5
molecular weight386.48 g/molExact mass≥98%
PSA69.700 Ųlogp4.300

numbering system

No numbering system information yet

physicochemical properties

No physical and chemical property information yet

Safety information

No safety information yet

Production methods and uses

No production method and use information yet

Related

upstream information

No upstream information yet

downstream information

No downstream information yet

MSDS

Found 0 shareMSDS