IMPPAT Phytochemical information:
Bullatacinone
Summary
IMPPAT Phytochemical identifier: IMPHY013954
Phytochemical name: Bullatacinone
Synonymous chemical names:bullatacinone
External chemical identifiers:CID:441557, ChEBI:3212, ZINC:ZINC000008221139
Chemical structure information
SMILES:
CCCCCCCCCC[C@@H]([C@H]1CC[C@@H](O1)[C@H]1CC[C@@H](O1)[C@@H](CCCCCCCCCC[C@@H]1C[C@H](C(=O)O1)CC(=O)C)O)OInChI:
InChI=1S/C37H66O7/c1-3-4-5-6-7-11-14-17-20-31(39)33-22-24-35(43-33)36-25-23-34(44-36)32(40)21-18-15-12-9-8-10-13-16-19-30-27-29(26-28(2)38)37(41)42-30/h29-36,39-40H,3-27H2,1-2H3/t29-,30-,31+,32-,33-,34-,35-,36-/m1/s1InChIKey:
KGGVWMAPBXIMEM-ZRTAFWODSA-NDeepSMILES:
CCCCCCCCCC[C@@H][C@H]CC[C@@H]O5)[C@H]CC[C@@H]O5)[C@@H]CCCCCCCCCC[C@@H]C[C@H]C=O)O5))CC=O)C))))))))))))))))O))))))))))OFunctional groups:
CC(=O)OC, CC(C)=O, CO, COC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CCC(CCCCCCCCCCCC2CCC(C3CCCO3)O2)O1Scaffold Graph/Node level:
OC1CCC(CCCCCCCCCCCC2CCC(C3CCCO3)O2)O1Scaffold Graph level:
CC1CCC(CCCCCCCCCCCC2CCC(C3CCCC3)C2)C1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Fatty acyls
ClassyFire Subclass: Fatty alcohols
NP Classifier Biosynthetic pathway: Polyketides
NP Classifier Superclass: Linear polyketides
NP Classifier Class: Acetogenins
NP-Likeness score: 1.527
Chemical structure download