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Details

Stereochemistry ACHIRAL
Molecular Formula C17H11N
Molecular Weight 229.2759
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZ(C)ACRIDINE

SMILES

C1=CC2=C(C=C1)C3=NC4=CC=CC=C4C=C3C=C2

InChI

InChIKey=OAPPEBNXKAKQGS-UHFFFAOYSA-N
InChI=1S/C17H11N/c1-3-7-15-12(5-1)9-10-14-11-13-6-2-4-8-16(13)18-17(14)15/h1-11H

HIDE SMILES / InChI

Molecular Formula C17H11N
Molecular Weight 229.2759
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Base-base recognition of nonionic dinucleotide analogues in an apolar environment studied by low-temperature NMR spectroscopy.
2010-03-24
Assessment of azaarenes and azaarones (oxidized azaarene derivatives) in the Dutch coastal zone of the North Sea.
2009-08
Disposition of sanguinarine in the rat.
2007-05
Metabolism of sanguinarine: the facts and the myths.
2007-02
A liquid chromatographic-mass spectrometric evidence of dihydrosanguinarine as a first metabolite of sanguinarine transformation in rat.
2006-01-02
Aryl hydrocarbon receptor-mediated and estrogenic activities of oxygenated polycyclic aromatic hydrocarbons and azaarenes originally identified in extracts of river sediments.
2001-12
Phototoxicity of azaarene isomers to the marine flagellate Dunaliella tertiolecta.
2001-07
Surface changes and hormone production in pituitary cells during tumorigenesis.
1999-12
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:45:41 GMT 2025
Edited
by admin
on Mon Mar 31 18:45:41 GMT 2025
Record UNII
BV4376Y90X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-89261
Preferred Name English
BENZ(C)ACRIDINE
HSDB  
Systematic Name English
BENZ(C)ACRIDINE [IARC]
Common Name English
BENZ(C)ACRIDINE [HSDB]
Common Name English
3,4-BENZOACRIDINE
Common Name English
12-AZABENZ(A)ANTHRACENE
Systematic Name English
Code System Code Type Description
PUBCHEM
9181
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY
CAS
225-51-4
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-930-2
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY
FDA UNII
BV4376Y90X
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY
NSC
89261
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY
MESH
C035985
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
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HSDB
5094
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID9059759
Created by admin on Mon Mar 31 18:45:41 GMT 2025 , Edited by admin on Mon Mar 31 18:45:41 GMT 2025
PRIMARY