| Identification | Back Directory | [Name]
9α,13α-Epidioxyabiet-8(14)-en-18-oic acid | [CAS]
116499-73-1 | [Synonyms]
9Α,13Α-EPIDIOXYABIET-8(14)-EN-18 9α,13α-Epidioxyabiet-8(14)-en-18-oicacid 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid 9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid 3H-3,10b-Ethanonaphtho[1,2-c]-1,2-dioxin-7-carboxylic acid, 5,6,6a,7,8,9,10,10a-octahydro-7,10a-dimethyl-3-(1-methylethyl)-, (3R,6aR,7R,10aS,10bR)- | [Molecular Formula]
C20H30O4 | [MDL Number]
MFCD23103694 | [MOL File]
116499-73-1.mol | [Molecular Weight]
334.45 |
| Chemical Properties | Back Directory | [Boiling point ]
437.8±45.0 °C(Predicted) | [density ]
1.17±0.1 g/cm3(Predicted) | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
Powder | [pka]
4.68±0.60(Predicted) |
| Hazard Information | Back Directory | [Description]
9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid shows potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumor promoter 12-O-tetradecanoylphorbol 13-acetate. | [Uses]
9α,13α-Epidioxyabiet-8(14)-en-18-oic acid (9,13α-Epidioxy-8(14)-abieten-18-oic acid) is a Sesquiterpenoids product that can be isolated from the rhizomes of Carpesium abrotanoides[1]. |
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