IMPPAT Phytochemical information: 
9H-Pyrido[3,4-B]indole

9H-Pyrido[3,4-B]indole
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]c1c2ccnc1

InChI:
InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10/h1-7,13H

InChIKey:
AIFRHYZBTHREPW-UHFFFAOYSA-N

DeepSMILES:
cccccc6)[nH]cc5ccnc6

Functional groups:
c[nH]c, cnc
Molecular scaffolds

Scaffold Graph/Node/Bond level:
c1ccc2c(c1)[nH]c1cnccc12

Scaffold Graph/Node level:
C1CCC2C(C1)NC1CNCCC12

Scaffold Graph level:
C1CCC2C(C1)CC1CCCCC12
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Organoheterocyclic compounds

ClassyFire 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