Summary
IMPPAT Phytochemical identifier: IMPHY007014
Phytochemical name: (+)-13alpha-Hydroxylupanine
Synonymous chemical names:(+)-13alpha-hydroxylupanine, (+)-13α-hydroxylupanine
External chemical identifiers:CID:439768, ZINC:ZINC000100153567, MolPort-000-737-142
Chemical structure information
SMILES:
O[C@H]1CCN2[C@@H](C1)[C@@H]1C[C@@H](C2)[C@@H]2N(C1)C(=O)CCC2InChI:
InChI=1S/C15H24N2O2/c18-12-4-5-16-8-10-6-11(14(16)7-12)9-17-13(10)2-1-3-15(17)19/h10-14,18H,1-9H2/t10-,11+,12-,13+,14-/m0/s1InChIKey:
JVYKIBAJVKEZSQ-VJTDZRGJSA-NDeepSMILES:
O[C@H]CCN[C@@H]C6)[C@@H]C[C@@H]C6)[C@@H]NC6)C=O)CCC6Functional groups:
CC(=O)N(C)C, CN(C)C, CO
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CCCC2C3CC(CN12)C1CCCCN1C3Scaffold Graph/Node level:
OC1CCCC2C3CC(CN12)C1CCCCN1C3Scaffold Graph level:
CC1CCCC2C3CC4CCCCC4C(C3)CC12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Alkaloids and derivativesClassyFire Class: Lupin alkaloids
ClassyFire Subclass: Sparteine, lupanine, and related alkaloids
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Lysine alkaloids
NP Classifier Class: Quinolizidine alkaloids
NP-Likeness score: 1.357
Chemical structure download