Description
Actinidic acid isolated from the leaves of Eucalyptus maideni. It possesses the highest inhibitory activity on PL, with an IC(50) of 14.95 microM.
Synonyms
(2alpha,3beta,4alpha)-2,3,23-Trihydroxyursa-12,20(30)-dien-28-oic acid
IUPAC Name
(1R,4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,6a,6b,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
Molecular Formula
C30H46O5
Canonical SMILES
CC1C2C3=CCC4C(C3(CCC2(CCC1=C)C(=O)O)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C
InChI
InChI=1S/C30H46O5/c1-17-9-12-30(25(34)35)14-13-28(5)19(23(30)18(17)2)7-8-22-26(3)15-20(32)24(33)27(4,16-31)21(26)10-11-29(22,28)6/h7,18,20-24,31-33H,1,8-16H2,2-6H3,(H,34,35)/t18-,20+,21+,22+,23-,24-,26-,27-,28+,29+,30-/m0/s1
InChIKey
FFMVHFPLIIYYNC-QXIFDOFRSA-N