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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,J)ACRIDINE

SMILES

C1=CC2=C(C=C1)C3=CC4=C(C=CC5=C4C=CC=C5)N=C3C=C2

InChI

InChIKey=ANUCHZVCBDOPOX-UHFFFAOYSA-N
InChI=1S/C21H13N/c1-3-7-16-14(5-1)9-11-20-18(16)13-19-17-8-4-2-6-15(17)10-12-21(19)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
Induction of micronuclei and sister chromatid exchanges by polycyclic and N-heterocyclic aromatic hydrocarbons in cultured human lymphocytes.
1995
Development of an analytical method for the simultaneous determination of 15 carcinogenic polycyclic aromatic hydrocarbons and polycyclic aromatic nitrogen heterocyclic compounds. application to diesel particulates.
2001 Dec
trans-3,4-dihydroxy-anti-1,2-epoxy-1,2,3,4-tetrahydrodi- benz[a,j]acridine involvement in dibenz[a,j]acridine DNA adduct formation in mouse skin consistent with Ha-ras mutation patterns in tumors.
2001 Jul
Dose-response studies on the induction of liver cytochromes P4501A1 and 1B1 by polycyclic aromatic hydrocarbons in arylhydrocarbon-responsive C57BL/6J mice.
2003 Sep
Inhibition of human cytochrome P450 1A1-, 1A2-, and 1B1-mediated activation of procarcinogens to genotoxic metabolites by polycyclic aromatic hydrocarbons.
2006 Feb
Cytotoxicity and aryl hydrocarbon receptor-mediated activity of n-heterocyclic polycyclic aromatic hydrocarbons: structure-activity relationships.
2006 May
Determination of basic azaarenes in aviation kerosene by solid-phase extraction and HPLC-fluorescence detection.
2009 Jun
Polycyclic aromatic hydrocarbons: 15 Listings - benz[a]anthracene, benzo[b]fluoranthene, benzo[j]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenz[a,h]acridine, dibenz[a,j]acridine, dibenz[a,h]anthracene, 7H-dibenzo[c,g]carbazole, dibenzo[a,e]pyrene, dibenzo[a,h]pyrene, dibenzo[a,i]pyrene, dibenzo[a,l]pyrene, indeno[1,2,3-cd]pyrene, 5-methylchrysene.
2011
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:19:37 GMT 2023
Edited
by admin
on Fri Dec 15 17:19:37 GMT 2023
Record UNII
088X9K64S8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBENZ(A,J)ACRIDINE
HSDB  
Systematic Name English
7-AZADIBENZ(A,J)ANTHRACENE
Systematic Name English
1,2:7,8-DIBENZACRIDINE
Common Name English
DIBENZ(A,J)ACRIDINE [HSDB]
Common Name English
NSC-114903
Code English
DIBENZ(A,J)ACRIDINE [IARC]
Common Name English
Code System Code Type Description
FDA UNII
088X9K64S8
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
PRIMARY
PUBCHEM
9177
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
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NCI_THESAURUS
C44368
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
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NSC
114903
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
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CAS
224-42-0
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
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EPA CompTox
DTXSID4059758
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
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HSDB
4036
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
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MESH
C022289
Created by admin on Fri Dec 15 17:19:37 GMT 2023 , Edited by admin on Fri Dec 15 17:19:37 GMT 2023
PRIMARY