IMPPAT Phytochemical information:
Tabersonine
Summary
IMPPAT Phytochemical identifier: IMPHY005481
Phytochemical name: Tabersonine
Synonymous chemical names:tabersonine
External chemical identifiers:CID:20485, ChEMBL:CHEMBL2011511, ChEBI:16776, ZINC:ZINC000056871302, SureChEMBL:SCHEMBL829379, MolPort-020-005-961
Chemical structure information
SMILES:
COC(=O)C1=C2Nc3c([C@@]42[C@@H]2[C@@](C1)(CC)C=CCN2CC4)cccc3InChI:
InChI=1S/C21H24N2O2/c1-3-20-9-6-11-23-12-10-21(19(20)23)15-7-4-5-8-16(15)22-17(21)14(13-20)18(24)25-2/h4-9,19,22H,3,10-13H2,1-2H3/t19-,20-,21-/m0/s1InChIKey:
FNGGIPWAZSFKCN-ACRUOGEOSA-NDeepSMILES:
COC=O)C=CNcc[C@]5[C@@H][C@@]C9)CC))C=CCN6CC9)))))))))cccc6Functional groups:
CC=CC, CN(C)C, cNC(C)=C(C)C(=O)OC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1=CC2CC=C3Nc4ccccc4C34CCN(C1)C24Scaffold Graph/Node level:
C1CCC2C(C1)NC1CCC3CCCN4CCC12C34Scaffold Graph level:
C1CCC2C(C1)CC1CCC3CCCC4CCC12C34
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Alkaloids and derivativesClassyFire Class: Plumeran-type alkaloids
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tryptophan alkaloids
NP Classifier Class: Aspidosperma type
NP-Likeness score: 2.434
Chemical structure download