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Details

Stereochemistry ACHIRAL
Molecular Formula C22H14
Molecular Weight 278.3466
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-BENZOTRIPHENYLENE

SMILES

C1=CC2=CC3=C(C=C2C=C1)C4=C(C=CC=C4)C5=CC=CC=C35

InChI

InChIKey=RAASUWZPTOJQAY-UHFFFAOYSA-N
InChI=1S/C22H14/c1-2-8-16-14-22-20-12-6-4-10-18(20)17-9-3-5-11-19(17)21(22)13-15(16)7-1/h1-14H

HIDE SMILES / InChI

Molecular Formula C22H14
Molecular Weight 278.3466
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The aryl hydrocarbon receptor-mediated and genotoxic effects of fractionated extract of standard reference diesel exhaust particle material in pulmonary, liver and prostate cells.
2015-04
Toxicity assessment of polycyclic aromatic hydrocarbons in sediments from European high mountain lakes.
2010-05
A flexible whole-genome microarray for transcriptomics in three-spine stickleback (Gasterosteus aculeatus).
2009-09-11
Hepatic transcriptomic and metabolomic responses in the stickleback (Gasterosteus aculeatus) exposed to environmentally relevant concentrations of dibenzanthracene.
2009-08-15
Circulating antibodies directed against "polycyclic aromatic hydrocarbon-like" structures in the sera of cancer patients.
2009-07
Cytogenotoxicity biomarkers in fat snook Centropomus parallelus from Cananéia and São Vicente estuaries, SP, Brazil.
2009-01
Development and validation of a gene expression oligo microarray for the gilthead sea bream (Sparus aurata).
2008-12-03
A comparison of the concentration-effect relationships of PAHs on CYP1A induction in HepG2 and Mcf7 cells.
2007-03
Metabolic enzyme induction by HepG2 cells exposed to oxygenated and nonoxygenated polycyclic aromatic hydrocarbons.
2007-02
Pt and Pd 1,4-shifts at the edge of dibenz[a,c]anthracene.
2006-05-10
Distribution of pesticides, PAHs and heavy metals in prawn ponds near Kolleru lake wetland, India.
2006-04
Inhibition of human cytochrome P450 1A1-, 1A2-, and 1B1-mediated activation of procarcinogens to genotoxic metabolites by polycyclic aromatic hydrocarbons.
2006-02
Further evaluation of the skin micronucleus test: results obtained using 10 polycyclic aromatic hydrocarbons.
2005-12-07
Spectral image adaptation and visual experience of DBA/PMMA.
2005-12
Assessing susceptibility from early-life exposure to carcinogens.
2005-09
Highly sensitive detection of discrete absorption and B-type delayed fluorescence of dibenzanthracene in PMMA.
2004-11
Dose-response studies on the induction of liver cytochromes P4501A1 and 1B1 by polycyclic aromatic hydrocarbons in arylhydrocarbon-responsive C57BL/6J mice.
2003-09
Deviation from additivity in mixture toxicity: relevance of nonlinear dose-response relationships and cell line differences in genotoxicity assays with combinations of chemical mutagens and gamma-radiation.
2002-12
Homogeneous liquid-liquid extraction and micellar electrokinetic chromatography using sweeping effect concentration system for determination of trace amounts of several polycyclic aromatic hydrocarbons.
2002-05
Structure-activity relationships of several anisidine and dibenzanthracene isomers in the w/w+ somatic assay of Drosophila melanogaster.
2002-02-15
First examples of stable arenium ions from large methylene-bridged polycyclic aromatic hydrocarbons (PAHs). Directive effects and charge delocalization mode.
2001-06-01
Differential induction of Cyp1a1, Cyp1b1, Ahd4, and Nmo1 in murine skin tumors and adjacent normal epidermis by ligands of the aryl hydrocarbon receptor.
1998-02
Short and long term effects of cytoskeleton-disrupting drugs on cytochrome P450 Cyp1a-1 induction in murine hepatoma 1c1c7 cells: suppression by the microtubule inhibitor nocodazole.
1994-05
Phorbol ester-mediated suppression of cytochrome P450 Cyp1a-1 induction in murine skin: involvement of protein kinase C.
1992-07-31
Arteriosclerotic plaque development is 'promoted' by polynuclear aromatic hydrocarbons.
1988-12
The cytosolic receptor binding affinities and AHH induction potencies of 29 polynuclear aromatic hydrocarbons.
1986-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:09:57 GMT 2025
Edited
by admin
on Mon Mar 31 19:09:57 GMT 2025
Record UNII
6OC62KCV5A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2:3,4-DIBENZANTHRACENE
Preferred Name English
2,3-BENZOTRIPHENYLENE
Common Name English
BENZO(B)TRIPHENYLENE
Systematic Name English
1,2:3,4-DIBENZOANTHRACENE
Common Name English
DIBENZO(A,C)ANTHRACENE
Systematic Name English
DIBENZ(A,C)ANTHRACENE
Systematic Name English
DIBENZ(A,C)ANTHRACENE [IARC]
Common Name English
Code System Code Type Description
CAS
215-58-7
Created by admin on Mon Mar 31 19:09:57 GMT 2025 , Edited by admin on Mon Mar 31 19:09:57 GMT 2025
PRIMARY
EPA CompTox
DTXSID9049245
Created by admin on Mon Mar 31 19:09:57 GMT 2025 , Edited by admin on Mon Mar 31 19:09:57 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-920-8
Created by admin on Mon Mar 31 19:09:57 GMT 2025 , Edited by admin on Mon Mar 31 19:09:57 GMT 2025
PRIMARY
PUBCHEM
9164
Created by admin on Mon Mar 31 19:09:57 GMT 2025 , Edited by admin on Mon Mar 31 19:09:57 GMT 2025
PRIMARY
FDA UNII
6OC62KCV5A
Created by admin on Mon Mar 31 19:09:57 GMT 2025 , Edited by admin on Mon Mar 31 19:09:57 GMT 2025
PRIMARY