Formula: C15H10O5

MW: 270.24

CAS: 548-83-4

TNP NUMBER: TNP00099

MDL NUMBER: MFCD00006833

IUPAC: 3,5,7-trihydroxy-2-phenylchromen-4-one

Smiles: c1(c(c2c(cc(cc2oc1c1ccccc1)O)O)=O)O

THERAPEUTIC CATEGORY: Antioxidant, Antinflammotary

REFERENCE: 10. Cipak L, Berczeliova E, Paulikova H. Effects of Flavonoids on Glutathione and Glutathione Related Enzymes in Cisplatin Treated L1210 Leukemia Cells. Neoplasma 2003;50(6):443-6. 11. Kaneko T, Baba N. Protective effects of Flavonoids on Endothelial Cells Against Linoleic Acid Hydro-peroxide Induced Toxicity. Biosci Biotechnol Biochem. 1999 Feb;63(2):323-8. 12. Evans WC, Trease and Evans Pharmacognosy 15th ed. 2002 WB Saunders London pg. 47. 13. Janssen AM, Scheffer JJ. Acetoxychavicol acetate, an antifungal component of Alpinia galangal. Planta Med, 1985 Dec. (6):507-11.

SOURCE: From Galanga Root, Alpninia officinarum,

ACCEPTORS: 5

DONORS: 3

ROTATION BONDS: 3

N+O: 5

Chiral Centers: 0

LogP: 1.39

LogS: -3.3

LIPINSKI: 4

Synonyms: 3,5,7-trihydroxy-2-phenyl-4h-benzopyran-4-on;3,5,7-trihydroxy-flavon;NORIZALPININ;GALANGIN;3,5,7-trihydroxy-2-phenyl-chromen-4-one;3,5,7-TRIHYDROXYFLAVONE;3,5,7-trihydroxy-2-phenyl-4-benzopyrone;3,5,7-Trihydroxyflavone (Galangin)

CAS:548-83-4

MF:C15H10O5

MW:270.24

EINECS:208-960-4

Product Categories:Flavanols Galangin

Chemical Properties: mp 214-215 C(lit.) Merck 14,4339 BRN 272179

CAS DataBase Reference: 548-83-4(

CAS DataBase Reference: ) Xi Risk Statements 36/37/38 Safety Statements 26-37/39 WGK Germany 3 RTECS LK9275500 F 10 Galangin

Usage And Synthesis: Galangin

< Prev		Next >

Chemical Compounds - BioActive Compounds