Summary
IMPPAT Phytochemical identifier: IMPHY000962
Phytochemical name: Cucurbitacin P
Synonymous chemical names:cucurbitacin p
External chemical identifiers:CID:441822, ChEBI:3951, ZINC:ZINC000004097807, SureChEMBL:SCHEMBL10307359
Chemical structure information
SMILES:
O[C@@H]1C[C@@H]2C(=CC[C@@H]3[C@@]2(C)C(=O)C[C@]2([C@@]3(C)C[C@H]([C@@H]2[C@](C(=O)CCC(O)(C)C)(O)C)O)C)C([C@@H]1O)(C)CInChI:
InChI=1S/C30H48O7/c1-25(2,36)12-11-21(33)30(8,37)23-19(32)14-27(5)20-10-9-16-17(13-18(31)24(35)26(16,3)4)29(20,7)22(34)15-28(23,27)6/h9,17-20,23-24,31-32,35-37H,10-15H2,1-8H3/t17-,18-,19-,20+,23+,24-,27+,28-,29+,30+/m1/s1InChIKey:
VVBWBGOEAVGFTN-SYJGCRHZSA-NDeepSMILES:
O[C@@H]C[C@@H]C=CC[C@@H][C@@]6C)C=O)C[C@][C@@]6C)C[C@H][C@@H]5[C@]C=O)CCCO)C)C)))))O)C)))O))))C))))))))C[C@@H]6O))C)CFunctional groups:
CC(C)=O, CC=C(C)C, CO
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CC2CCCC2C2CC=C3CCCCC3C12Scaffold Graph/Node level:
OC1CC2CCCC2C2CCC3CCCCC3C12Scaffold Graph level:
CC1CC2CCCC2C2CCC3CCCCC3C12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Steroids and steroid derivatives
ClassyFire Subclass: Cucurbitacins
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Triterpenoids
NP Classifier Class: Cucurbitane triterpenoids
NP-Likeness score: 2.994
Chemical structure download