U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C13H9N
Molecular Weight 179.2173
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZO(F)QUINOLINE

SMILES

C1=CC=C2C(C=CC3=C2C=CC=N3)=C1

InChI

InChIKey=HCAUQPZEWLULFJ-UHFFFAOYSA-N
InChI=1S/C13H9N/c1-2-5-11-10(4-1)7-8-13-12(11)6-3-9-14-13/h1-9H

HIDE SMILES / InChI

Molecular Formula C13H9N
Molecular Weight 179.2173
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A domino synthesis of benzoquinolinamide in the presence of iodine.
2010-11-07
Assessment of azaarenes and azaarones (oxidized azaarene derivatives) in the Dutch coastal zone of the North Sea.
2009-08
Structurally constrained hybrid derivatives containing octahydrobenzo[g or f]quinoline moieties for dopamine D2 and D3 receptors: binding characterization at D2/D3 receptors and elucidation of a pharmacophore model.
2008-12-25
Automatic extraction of structural alerts for predicting chromosome aberrations of organic compounds.
2006-11
Nitrogen-substitution effect on in vivo mutagenicity of chrysene.
2005-09-05
4-Chlorobenzo[F]isoquinoline (CBIQ), a novel activator of CFTR and DeltaF508 CFTR.
2005-06-01
Fungal biotransformation of benzo[f]quinoline, benzo[h]quinoline, and phenanthridine.
2005-05
Theoretical study of aza-polycyclic aromatic hydrocarbons (aza-PAHs), modelling carbocations from oxidized metabolites and their covalent adducts with representative nucleophiles.
2005-04-07
In vivo mutagenicity of benzo[f]quinoline, benzo[h]quinoline, and 1,7-phenanthroline using the lacZ transgenic mice.
2004-04-11
Estimation of kinetic parameter for the biotransformation of three-ring azaarenes by the phenanthrene-degrading strain Sphingomonas sp. LH128.
2004-02
Spectroscopic and computational investigations of stable radical anions of triosmium benzoheterocycle clusters.
2003-12-05
Mechanisms of anion secretion in Calu-3 human airway epithelial cells by 7,8-benzoquinoline.
2003-09
Benzoquinolines and chloride secretion in murine colonic epithelium.
2003-04
Activation of the human Ah receptor by aza-polycyclic aromatic hydrocarbons and their halogenated derivatives.
2003-04
[Antimicrobial action of ammonium salts of fused heterocycles containing ortho-nitrogen].
2003
Controlled photocyclization, photodimerization, and photoisomerization of stilbazole salts within Nafion membranes.
2002-04-04
A concise total synthesis of the azaphenanthrene alkaloid eupolauramine.
2001-11-30
Degradation of phenanthrene-analogue azaarenes by Mycobacterium gilvum strain LB307T under aerobic conditions.
2001-08
Drug metabolizing enzyme induction by benzoquinolines, acridine, and quinacrine; tricyclic aromatic molecules containing a single heterocyclic nitrogen.
1996
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:31 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:31 GMT 2025
Record UNII
525476DTML
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZO(F)QUINOLINE
MI  
Systematic Name English
NSC-9850
Preferred Name English
BENZO(F)QUINOLINE [MI]
Common Name English
5,6-BENZOQUINOLINE
Common Name English
BENZO(F)QUINOLONE
Systematic Name English
.BETA.-NAPHTHOQUINOLINE
Common Name English
NAPHTHOPYRIDINE
Systematic Name English
Code System Code Type Description
MESH
C039108
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
PUBCHEM
6796
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
NSC
9850
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
MERCK INDEX
m2378
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY Merck Index
CAS
85-02-9
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID2024585
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
FDA UNII
525476DTML
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-582-0
Created by admin on Mon Mar 31 18:34:31 GMT 2025 , Edited by admin on Mon Mar 31 18:34:31 GMT 2025
PRIMARY
Related Record Type Details
METABOLITE -> PARENT