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Details

Stereochemistry ACHIRAL
Molecular Formula C12H4Cl6
Molecular Weight 360.878
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3,3',4,4',5-HEXACHLOROBIPHENYL

SMILES

ClC1=CC(C2=CC(Cl)=C(Cl)C=C2)=C(Cl)C(Cl)=C1Cl

InChI

InChIKey=LCXMEXLGMKFLQO-UHFFFAOYSA-N
InChI=1S/C12H4Cl6/c13-7-2-1-5(3-8(7)14)6-4-9(15)11(17)12(18)10(6)16/h1-4H

HIDE SMILES / InChI

Molecular Formula C12H4Cl6
Molecular Weight 360.878
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Consensus toxicity factors for polychlorinated dibenzo-p-dioxins, dibenzofurans, and biphenyls combining in silico models and extensive in vitro screening of AhR-mediated effects in human and rodent cells.
2015-04-20
Comparison of intake and systemic relative effect potencies of dioxin-like compounds in female mice after a single oral dose.
2013-07
Polychlorinated biphenyls, lead, and mercury are associated with liver disease in American adults: NHANES 2003-2004.
2010-12
Developing tools for risk assessment in protected species: Relative potencies inferred from competitive binding of halogenated aromatic hydrocarbons to aryl hydrocarbon receptors from beluga (Delphinapterus leucas) and mouse.
2010-11-01
Transactivation potencies of Baikal seal constitutive active/androstane receptor by persistent organic pollutants and brominated flame retardants.
2009-08-15
WITHDRAWN: Neurodevelopmental toxicity of prenatal polychlorinated biphenyls (PCBs) by chemical structure and activity in a birth cohort.
2009-07-30
Cutaneous symptoms such as acneform eruption and pigmentation are closely associated with blood levels of 2,3,4,7,8-penta-chlorodibenzofurans in Yusho patients, using data mining analysis.
2009-02-25
Pharmacologic profiling of human and rat cytochrome P450 1A1 and 1A2 induction and competition.
2008-12
Association of organochlorine pesticides with peripheral neuropathy in patients with diabetes or impaired fasting glucose.
2008-11
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Relative potency based on hepatic enzyme induction predicts immunosuppressive effects of a mixture of PCDDS/PCDFS and PCBS.
2008-03-15
The flame retardants, polybrominated diphenyl ethers, are pregnane X receptor activators.
2007-05
Determination of in vitro relative potency (REP) values for mono-ortho polychlorinated biphenyls after purification with active charcoal.
2006-09-10
Cytochrome P450 1A4 and 1A5 in common cormorant (Phalacrocorax carbo): evolutionary relationships and functional implications associated with dioxin and related compounds.
2006-08
Mechanistic study of polychlorinated biphenyl 126-induced CYP11B1 and CYP11B2 up-regulation.
2006-03
Selected polychlorobiphenyls congeners bind to estrogen receptor alpha in human umbilical vascular endothelial (HUVE) cells modulating angiogenesis.
2006-01-20
Induction of cytochrome P450 1A5 mRNA, protein and enzymatic activities by dioxin-like compounds, and congener-specific metabolism and sequestration in the liver of wild jungle crow (Corvus macrorhynchos) from Tokyo, Japan.
2005-12
Inhibition of human and rat CYP1A2 by TCDD and dioxin-like chemicals.
2005-04
Interaction between halogenated aromatic compounds in the Ah receptor signal transduction pathway.
2004-10
Brominated dioxin-like compounds: in vitro assessment in comparison to classical dioxin-like compounds and other polyaromatic compounds.
2003-09
Application of the ethoxyresorufin-O-deethylase (EROD) assay to mixtures of halogenated aromatic compounds.
2001
Dose-response relationships for induction of CYP1A1 and CYP1A2 enzyme activity in liver, lung, and skin in female mice following subchronic exposure to polychlorinated biphenyls.
2000-09-15
Transactivation activity of human, zebrafish, and rainbow trout aryl hydrocarbon receptors expressed in COS-7 cells: greater insight into species differences in toxic potency of polychlorinated dibenzo-p-dioxin, dibenzofuran, and biphenyl congeners.
1999-08-15
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:12:44 GMT 2025
Edited
by admin
on Mon Mar 31 22:12:44 GMT 2025
Record UNII
4D6049M2OC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PCB 156
Preferred Name English
2,3,3',4,4',5-HEXACHLOROBIPHENYL
Systematic Name English
Code System Code Type Description
PUBCHEM
38019
Created by admin on Mon Mar 31 22:12:44 GMT 2025 , Edited by admin on Mon Mar 31 22:12:44 GMT 2025
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FDA UNII
4D6049M2OC
Created by admin on Mon Mar 31 22:12:44 GMT 2025 , Edited by admin on Mon Mar 31 22:12:44 GMT 2025
PRIMARY
CAS
38380-08-4
Created by admin on Mon Mar 31 22:12:44 GMT 2025 , Edited by admin on Mon Mar 31 22:12:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID0052706
Created by admin on Mon Mar 31 22:12:44 GMT 2025 , Edited by admin on Mon Mar 31 22:12:44 GMT 2025
PRIMARY