IMPPAT Phytochemical information:
Bullatine B
Summary
IMPPAT Phytochemical identifier: IMPHY011445
Phytochemical name: Bullatine B
Synonymous chemical names:neoline
External chemical identifiers:CID:10003218, ChEBI:132629, SureChEMBL:SCHEMBL2127034, MolPort-002-526-188
Chemical structure information
SMILES:
COC[C@]12CC[C@@H]([C@@]34[C@@H]2[C@@H](OC)[C@@H](C3N(C1)CC)[C@@]1([C@@H]2[C@H]4C[C@@H]([C@@H]2O)[C@H](C1)OC)O)OInChI:
InChI=1S/C24H39NO6/c1-5-25-10-22(11-29-2)7-6-15(26)24-13-8-12-14(30-3)9-23(28,16(13)18(12)27)17(21(24)25)19(31-4)20(22)24/h12-21,26-28H,5-11H2,1-4H3/t12-,13-,14+,15+,16-,17+,18+,19+,20-,21?,22+,23-,24+/m1/s1InChIKey:
XRARAKHBJHWUHW-QVUBZLTISA-NDeepSMILES:
COC[C@@]CC[C@@H][C@@][C@@H]6[C@@H]OC))[C@@H]C5NC%11)CC))))[C@@][C@@H][C@H]7C[C@@H][C@@H]5O))[C@H]C7)OC)))))))O))))))OFunctional groups:
CN(C)C, CO, COC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1CC2CNC3C4CC2C3(C1)C1CC2CCC4C1C2Scaffold Graph/Node level:
C1CC2CNC3C4CC2C3(C1)C1CC2CCC4C1C2Scaffold Graph level:
C1CC2CCC3C4CC2C3(C1)C1CC2CCC4C1C2
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Prenol lipids
ClassyFire Subclass: Diterpenoids
NP Classifier Biosynthetic pathway: Alkaloids, Terpenoids
NP Classifier Superclass: Pseudoalkaloids
NP Classifier Class: Terpenoid alkaloids
NP-Likeness score: 3.732
Chemical structure download