389122-01-4
Chemical Structure
3,29-O-Dibenzoyloxykarounidiol
Synonym(s): Karounidiol dibenzoate
- CAS No.: 389122-01-4
- Formula:C44H56O4
- Molecular Weight:648.91
IUPAC Name: ((2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-10-(benzoyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydropicen-2-yl)methyl benzoate
InChIKey: RTSZUVCSDUONDF-GJSTXJOSSA-N
SMILES: CC1(C)[C@H](OC(C2=CC=CC=C2)=O)CC[C@]3(C)C4=CC[C@@]5(C)[C@]6([H])C[C@](C)(COC(C7=CC=CC=C7)=O)CC[C@@](C)6CC[C@@](C)5C4=CC[C@@]13[H]
Biological Activity: 3,29-O-Dibenzoyloxykarounidiol (Karounidiol dibenzoate) is a multiflorane-type triterpene benzoate that inhibits Phorbol 12-myristate 13-acetate (TPA) (HY-18739)-induced Epstein-Barr virus early antigen activation and exhibits tumor-promotion inhibitory activity. 3,29-O-Dibenzoyloxykarounidiol is used in cancer-related research[1][2].
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3,29-O-Dibenzoyloxykarounidiol | 99.79% | 3,29-O-Dibenzoyloxykarounidiol (Karounidiol dibenzoate) is a multiflorane-type triterpene benzoate that inhibits Phorbol 12-myristate 13-acetate (TPA) (HY-18739)-induced Epstein-Barr virus early antigen activation and exhibits tumor-promotion inhibitory activity. 3,29-O-Dibenzoyloxykarounidiol is used in cancer-related research. | ||||||||||||||||||||
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References
- [1]. Ukiya M, et al. Inhibitory effects of cucurbitane glycosides and other triterpenoids from the fruit of Momordica grosvenori on epstein-barr virus early antigen induced by tumor promoter 12-O-tetradecanoylphorbol-13-acetate. Journal of agricultural and food chemistry. 2002 Nov 06;50(23):6710-5. [Content Brief]
- [2]. Akihisa T, et al. Anti-tumor promoting effects of multiflorane-type triterpenoids and cytotoxic activity of karounidiol against human cancer cell lines. Cancer letters. 2001 Nov 08;173(1):9-14. [Content Brief]
