Summary
IMPPAT Phytochemical identifier: IMPHY011602
Phytochemical name: 9H-Pyrido[3,4-B]indole
Synonymous chemical names:9h-pyrido[3,4-b]indole, beta-carboline, harman, nor, norharman, norharmane, β-carboline
External chemical identifiers:CID:64961, ChEMBL:CHEMBL275224, ChEBI:109895, ZINC:ZINC000000066039, FDASRS:94HMA1I78O, SureChEMBL:SCHEMBL25834, MolPort-000-141-389
Chemical structure information
SMILES:
c1ccc2c(c1)[nH]c1c2ccnc1InChI:
InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10/h1-7,13HInChIKey:
AIFRHYZBTHREPW-UHFFFAOYSA-NDeepSMILES:
cccccc6)[nH]cc5ccnc6Functional groups:
c[nH]c, cnc
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc2c(c1)[nH]c1cnccc12Scaffold Graph/Node level:
C1CCC2C(C1)NC1CNCCC12Scaffold Graph level:
C1CCC2C(C1)CC1CCCCC12
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Organoheterocyclic compoundsClassyFire Class: Indoles and derivatives
ClassyFire Subclass: Pyridoindoles
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tryptophan alkaloids
NP Classifier Class: Carboline alkaloids
NP-Likeness score: -0.131
Chemical structure download