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Details

Stereochemistry ACHIRAL
Molecular Formula C21H13N
Molecular Weight 279.3346
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIBENZ(A,H)ACRIDINE

SMILES

C1=CC2=C(C=C1)C3=CC4=C(N=C3C=C2)C5=CC=CC=C5C=C4

InChI

InChIKey=JNCSIWAONQTVCF-UHFFFAOYSA-N
InChI=1S/C21H13N/c1-3-7-17-14(5-1)11-12-20-19(17)13-16-10-9-15-6-2-4-8-18(15)21(16)22-20/h1-13H

HIDE SMILES / InChI

Molecular Formula C21H13N
Molecular Weight 279.3346
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cytotoxicity and aryl hydrocarbon receptor-mediated activity of n-heterocyclic polycyclic aromatic hydrocarbons: structure-activity relationships.
2006-05
A computational study of carbocations from oxidized metabolites of dibenzo[a,h]acridine and their fluorinated and methylated derivatives.
2005-12
Comparative metabolism of the aza polynuclear aromatic hydrocarbon dibenz[a,h]acridine by recombinant human and rat cytochrome P450s.
2004-05
Aryl hydrocarbon receptor-mediated and estrogenic activities of oxygenated polycyclic aromatic hydrocarbons and azaarenes originally identified in extracts of river sediments.
2001-12
Tumorigenicity of racemic and optically pure bay region diol epoxides and other derivatives of the nitrogen heterocycle dibenz[a,h]acridine on mouse skin.
2001-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:44:39 GMT 2025
Edited
by admin
on Mon Mar 31 18:44:39 GMT 2025
Record UNII
I64KK77PZY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2,5,6-DIBENZACRIDINE
Preferred Name English
DIBENZ(A,H)ACRIDINE
HSDB  
Systematic Name English
DB(A,H)AC
Common Name English
7-AZADIBENZ(A,H)ANTHRACENE
Systematic Name English
1,2:5,6-DIBENZACRIDINE
Common Name English
1,2,5,6-DIBENZOACRIDINE
Common Name English
DIBENZ(A,H)ACRIDINE [HSDB]
Common Name English
DIBENZ(A,H)ACRIDINE [IARC]
Common Name English
Code System Code Type Description
CAS
226-36-8
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID3059761
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
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HSDB
4038
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
PRIMARY
MESH
C022289
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
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FDA UNII
I64KK77PZY
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
PRIMARY
PUBCHEM
9183
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
PRIMARY
NCI_THESAURUS
C44367
Created by admin on Mon Mar 31 18:44:39 GMT 2025 , Edited by admin on Mon Mar 31 18:44:39 GMT 2025
PRIMARY