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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
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 Aug 15
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 Sep 15
Application of the ethoxyresorufin-O-deethylase (EROD) assay to mixtures of halogenated aromatic compounds.
2001
Brominated dioxin-like compounds: in vitro assessment in comparison to classical dioxin-like compounds and other polyaromatic compounds.
2003 Sep
Interaction between halogenated aromatic compounds in the Ah receptor signal transduction pathway.
2004 Oct
Inhibition of human and rat CYP1A2 by TCDD and dioxin-like chemicals.
2005 Apr
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 Dec
Cytochrome P450 1A4 and 1A5 in common cormorant (Phalacrocorax carbo): evolutionary relationships and functional implications associated with dioxin and related compounds.
2006 Aug
Selected polychlorobiphenyls congeners bind to estrogen receptor alpha in human umbilical vascular endothelial (HUVE) cells modulating angiogenesis.
2006 Jan 20
Mechanistic study of polychlorinated biphenyl 126-induced CYP11B1 and CYP11B2 up-regulation.
2006 Mar
Determination of in vitro relative potency (REP) values for mono-ortho polychlorinated biphenyls after purification with active charcoal.
2006 Sep 10
The flame retardants, polybrominated diphenyl ethers, are pregnane X receptor activators.
2007 May
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008 Apr
Pharmacologic profiling of human and rat cytochrome P450 1A1 and 1A2 induction and competition.
2008 Dec
Relative potency based on hepatic enzyme induction predicts immunosuppressive effects of a mixture of PCDDS/PCDFS and PCBS.
2008 Mar 15
Association of organochlorine pesticides with peripheral neuropathy in patients with diabetes or impaired fasting glucose.
2008 Nov
Transactivation potencies of Baikal seal constitutive active/androstane receptor by persistent organic pollutants and brominated flame retardants.
2009 Aug 15
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 Feb 25
WITHDRAWN: Neurodevelopmental toxicity of prenatal polychlorinated biphenyls (PCBs) by chemical structure and activity in a birth cohort.
2009 Jul 30
Polychlorinated biphenyls, lead, and mercury are associated with liver disease in American adults: NHANES 2003-2004.
2010 Dec
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 Nov 1
Comparison of intake and systemic relative effect potencies of dioxin-like compounds in female mice after a single oral dose.
2013 Jul
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 Apr 20
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:37:20 GMT 2023
Edited
by admin
on Sat Dec 16 08:37:20 GMT 2023
Record UNII
4D6049M2OC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3,3',4,4',5-HEXACHLOROBIPHENYL
Systematic Name English
PCB 156
Common Name English
Code System Code Type Description
PUBCHEM
38019
Created by admin on Sat Dec 16 08:37:20 GMT 2023 , Edited by admin on Sat Dec 16 08:37:20 GMT 2023
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FDA UNII
4D6049M2OC
Created by admin on Sat Dec 16 08:37:20 GMT 2023 , Edited by admin on Sat Dec 16 08:37:20 GMT 2023
PRIMARY
CAS
38380-08-4
Created by admin on Sat Dec 16 08:37:20 GMT 2023 , Edited by admin on Sat Dec 16 08:37:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID0052706
Created by admin on Sat Dec 16 08:37:20 GMT 2023 , Edited by admin on Sat Dec 16 08:37:20 GMT 2023
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