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Details

Stereochemistry ACHIRAL
Molecular Formula C18H18
Molecular Weight 234.3355
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RETENE

SMILES

CC(C)C1=CC=C2C(C=CC3=C2C=CC=C3C)=C1

InChI

InChIKey=NXLOLUFNDSBYTP-UHFFFAOYSA-N
InChI=1S/C18H18/c1-12(2)14-7-10-17-15(11-14)8-9-16-13(3)5-4-6-18(16)17/h4-12H,1-3H3

HIDE SMILES / InChI

Molecular Formula C18H18
Molecular Weight 234.3355
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Developmental toxicity and endocrine disrupting potency of 4-azapyrene, benzo[b]fluorene and retene in the zebrafish Danio rerio.
2012-04
Measuring the toxicity of alkyl-phenanthrenes to early life stages of medaka (Oryzias latipes) using partition-controlled delivery.
2011-02
The effects of the alkyl polycyclic aromatic hydrocarbon retene on rainbow trout (Oncorhynchus mykiss) immune response.
2010-11-01
Embryotoxicity of retene in cotreatment with 2-aminoanthracene, a cytochrome P4501A inhibitor, in rainbow trout (Oncorhynchus mykiss).
2009-06
Evidence for multiple mechanisms of toxicity in larval rainbow trout (Oncorhynchus mykiss) co-treated with retene and alpha-naphthoflavone.
2008-07-07
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Inhibition of CYP1A enzymes by alpha-naphthoflavone causes both synergism and antagonism of retene toxicity to rainbow trout (Oncorhynchus mykiss).
2007-03-10
Concentrations, sources and temporal trends in atmospheric polycyclic aromatic hydrocarbons in a major conurbation.
2005-07
Is oxidative stress the mechanism of blue sac disease in retene-exposed trout larvae?
2005-03
In vitro and in vivo comparisons of fish-specific CYP1A induction relative potency factors for selected polycyclic aromatic hydrocarbons.
2004-11
High sensitivity of northern pike larvae to UV-B but no UV-photoinduced toxicity of retene.
2004-03-10
Partiton-controlled delivery of toxicants: a novel in vivo approach for embryo toxicity testing.
2003-05-15
CYP1A induction and blue sac disease in early developmental stages of rainbow trout (Oncorhynchus Mykiss) exposed to retene.
2003-04-11
Histopathological responses of newly hatched larvae of whitefish (Coregonus lavaretus s.l.) to UV-B induced toxicity of retene.
2003-04-10
Juvenile sea bass liver biotransformation and erythrocytic genotoxic responses to pulp mill contaminants.
2002-09
Estrous cycle-regulated expression of CYP1B1 mRNA in the rat ovary.
2002-09
Altering cytochrome P4501A activity affects polycyclic aromatic hydrocarbon metabolism and toxicity in rainbow trout (Oncorhynchus mykiss).
2002-09
Bioavailability to juvenile rainbow trout (Oncorynchus mykiss) of retene and other mixed-function oxygenase-active compounds from sediments.
2002-01
Photoinduced toxicity of retene to Daphnia magna under enhanced UV-B radiation.
2001-11
Amino acid metabolism during total parenteral nutrition in healthy volunteers: evaluation of a new amino acid solution.
2001-10
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:03 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:03 GMT 2025
Record UNII
0W2D2E1P9Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RETENE
MI  
Common Name English
NSC-26317
Preferred Name English
RETENE [MI]
Common Name English
1-METHYL-7-(1-METHYLETHYL)PHENANTHRENE
Systematic Name English
Code System Code Type Description
MESH
C447880
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
PRIMARY
PUBCHEM
10222
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
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EPA CompTox
DTXSID7058701
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
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WIKIPEDIA
RETENE
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
PRIMARY
FDA UNII
0W2D2E1P9Q
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
PRIMARY
NSC
26317
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-597-9
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
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CAS
483-65-8
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
PRIMARY
MERCK INDEX
m9553
Created by admin on Mon Mar 31 19:56:03 GMT 2025 , Edited by admin on Mon Mar 31 19:56:03 GMT 2025
PRIMARY Merck Index