Summary
IMPPAT Phytochemical identifier: IMPHY000351
Phytochemical name: Calycopterone
Synonymous chemical names:calycopterone
External chemical identifiers:CID:10100323, ChEMBL:CHEMBL34316, ZINC:ZINC000029250488
Chemical structure information
SMILES:
CO[C@H]1C[C@@H](Oc2c1c1O[C@]34[C@@](c1c(c2OC)O)(OC)C(=C(C(=O)C4=CC[C@@H](O3)c1ccccc1)OC)OC)c1ccccc1InChI:
InChI=1S/C35H34O10/c1-38-24-18-23(20-14-10-7-11-15-20)43-30-25(24)29-26(28(37)31(30)39-2)34(42-5)33(41-4)32(40-3)27(36)21-16-17-22(44-35(21,34)45-29)19-12-8-6-9-13-19/h6-16,22-24,37H,17-18H2,1-5H3/t22-,23-,24+,34+,35-/m1/s1InChIKey:
CRTQTCGLSVSTRI-ZXTJMZMPSA-NDeepSMILES:
CO[C@H]C[C@@H]Occ6cO[C@@][C@@]c5cc9OC)))O)))OC))C=CC=O)C6=CC[C@@H]O%10)cccccc6)))))))))))OC)))OC))))))))))cccccc6Functional groups:
COC, cO, cOC, cO[C@@]12CC(OC)=C(OC)C(=O)C1=CCCO2
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1C=CC2c3ccc4c(c3OC23OC(c2ccccc2)CC=C13)CCC(c1ccccc1)O4Scaffold Graph/Node level:
OC1CCC2C3CCC4OC(C5CCCCC5)CCC4C3OC23OC(C2CCCCC2)CCC13Scaffold Graph level:
CC1CCC2C3CCC4CC(C5CCCCC5)CCC4C3CC23CC(C2CCCCC2)CCC13
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Flavonoids
ClassyFire Subclass: Flavans
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Flavonoids
NP Classifier Class: Flavandiols (Leucoanthocyanidins)
NP-Likeness score: 2.212
Chemical structure download