Cas No.: | 58546-34-2 |
Chemical Name: | Cucurbitacin IIa |
Synonyms: | Cucurbitacin A;CUCURBITACIN IIA;23,24-Dihydrocucurbitacin F-25-O-acetate;25-Acetoxy-23,24-dihydrocucurbitacin F;25-O-Acetyl-23,24-dihydrocucurbitacin F;Dihydrocucurbitacin F 25-O-acetate;Dihydrocucurbitacin Q1;[(6R)-6-hydroxy-2-methyl-5-oxo-6-[(2S,3S,8S,9R,10R,13R,14S,16R,17R)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-11-oxo-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]heptan-2-yl] aceta;Hemslecin A;Cucurbitacin?IIa;Curcurbitacin Q1;X1160;Curcurbitacin IIa;C32H50O8 |
SMILES: | O([H])[C@]1([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@]3([H])C([H])([H])C([H])=C4C(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])([C@]([H])(C([H])([H])[C@@]4([H])[C@]3(C([H])([H])[H])C(C([H])([H])[C@]2(C([H])([H])[H])[C@@]1([H])[C@@](C(C([H])([H])C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])OC(C([H])([H])[H])=O)=O)(C([H])([H])[H])O[H])=O)O[H])O[H] |
Formula: | C32H50O8 |
M.Wt: | 562.7346 |
Purity: | >98% |
Sotrage: | 4°C for 1 year, -20°C for more than 2 years |
Description: | Cucurbitacin IIa is a triterpene isolated from Hemsleya amalils Diels, induces apoptosis of cancer cells, reduces expression of survivin, reduces phospho-Histone H3 and increases cleaved PARP in cancer cells[1]. |
References: | [1]. Boykin C, et al. Cucurbitacin IIa: a novel class of anti-cancer drug inducing non-reversible actin aggregation and inhibiting survivin independent of JAK2/STAT3 phosphorylation. Br J Cancer. 2011 Mar 1;104(5):781-9. |