Page last updated: 2024-12-07

benz(j)aceanthrylene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Benz(j)aceanthrylene is a polycyclic aromatic hydrocarbon (PAH) that has been identified as a potent environmental mutagen and carcinogen. It is found in coal tar, diesel exhaust, and other combustion products. Benz(j)aceanthrylene is particularly carcinogenic in the skin and lungs. It has been shown to induce tumors in animals and is considered to be a significant human health risk. Benz(j)aceanthrylene is studied to understand its carcinogenic properties and to develop strategies for reducing human exposure to this compound. Synthesis of benz(j)aceanthrylene involves complex organic chemical reactions and is not commonly performed due to its carcinogenic nature.'

Cross-References

ID SourceID
PubMed CID104987
CHEMBL ID153437
CHEBI ID82290
MeSH IDM0113259

Synonyms (18)

Synonym
ccris 2269
naphth(2,1-d)acenaphthylene
benzo(7,8)aceanthrylene
benz(j)aceanthrylene
cholanthrylene
brn 4247917
CHEMBL153437
benzo[j]aceanthrylene
chebi:82290 ,
202-33-5
benz[j]aceanthrylene
C19195
unii-844qxh8pk1
844qxh8pk1 ,
benz(j)aceanthrylene [iarc]
AKOS025296229
DTXSID30174041
Q27155860

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The spectrum of activity of benz[j]aceanthrylene over the 5 Ames tester strains is similar to that of benzo[a]pyrene, and the dose-response curves for strain TA98 are comparable."( Benz[j]aceanthrylene: a novel polycyclic aromatic hydrocarbon with bacterial mutagenic activity.
Claxton, L; Easterling, R; Gold, A; Nesnow, S; Sangaiah, R; Toney, GE; Toney, SH, 1983
)
0.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
phenanthrenesAny benzenoid aromatic compound that consists of a phenanthrene skeleton and its substituted derivatives thereof.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (12)

Assay IDTitleYearJournalArticle
AID201033Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, with metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 5 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201030Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, with metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 1.0 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201035Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, without metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 1.0 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201034Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, without metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 0.5 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201037Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, without metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 20 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201036Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, without metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 10 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201031Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, with metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 10 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201038Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, without metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 5 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID200703Specific mutagenicity in the presence of protein S9, was expressed as His+ revertants/nmol, calculated by least-square linear regression.1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201032Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, with metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 20 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID200702Specific mutagenicity in the absence of protein S9, was expressed as His+ revertants/nmol, calculated by least-square linear regression.1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
AID201029Mutagenicity determined by Ames assay in Salmonella Typhimurium strain TA98, with metabolic activation by Aroclor 1254 induced rat liver S9 at a dose of 0.5 ug/plate1991Journal of medicinal chemistry, Feb, Volume: 34, Issue:2
Synthesis and biological activity of bay-region metabolites of a cyclopenta-fused polycyclic aromatic hydrocarbon: benz[j]aceanthrylene.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (27.78)18.7374
1990's13 (72.22)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 16.94

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index16.94 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index4.70 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (16.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.56%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other17 (94.44%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]