Summary
IMPPAT Phytochemical identifier: IMPHY003414
Phytochemical name: (E,6R)-2-methyl-6-[(1R,3R,6S,8R,11S,12S,13S,15R,16R,18R)-6,13,18-trihydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]hept-2-enoic acid
Synonymous chemical names:ananasic acid, ananasic acid (3β, 11α, 15α-trihydroxy-cycloart-24-en-26-oic acid), ananasic-acid
External chemical identifiers:CID:42608287
Chemical structure information
SMILES:
C[C@@H]([C@H]1C[C@@H]([C@@]2([C@]1(C)C[C@@H](O)[C@@]13[C@H]2CC[C@@H]2[C@]3(C1)CC[C@@H](C2(C)C)O)C)O)CC/C=C(/C(=O)O)CInChI:
InChI=1S/C30H48O5/c1-17(8-7-9-18(2)25(34)35)19-14-23(32)28(6)21-11-10-20-26(3,4)22(31)12-13-29(20)16-30(21,29)24(33)15-27(19,28)5/h9,17,19-24,31-33H,7-8,10-16H2,1-6H3,(H,34,35)/b18-9+/t17-,19-,20+,21+,22+,23+,24-,27-,28-,29-,30+/m1/s1InChIKey:
ITIWNCJDHYQADX-MYPSPUFHSA-NDeepSMILES:
C[C@@H][C@H]C[C@@H][C@@][C@]5C)C[C@@H]O)[C@][C@H]6CC[C@@H][C@]6C7)CC[C@@H]C6C)C))O)))))))))))))C))O))))CC/C=C/C=O)O))CFunctional groups:
C/C=C(C)C(=O)O, CO
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1CC2CCC34CC35CCCCC5CCC4C2C1Scaffold Graph/Node level:
C1CC2CCC34CC35CCCCC5CCC4C2C1Scaffold Graph level:
C1CC2CCC34CC35CCCCC5CCC4C2C1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Steroids and steroid derivatives
ClassyFire Subclass: Cycloartanols and derivatives
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Triterpenoids
NP Classifier Class: Cycloartane triterpenoids
NP-Likeness score: 3.227
Chemical structure download