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Details

Stereochemistry ACHIRAL
Molecular Formula C12H6Cl4O
Molecular Weight 307.987
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

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

SMILES

OC1=CC=C(C=C1)C2=CC(Cl)=C(Cl)C(Cl)=C2Cl

InChI

InChIKey=RESKVBRHSNTJNG-UHFFFAOYSA-N
InChI=1S/C12H6Cl4O/c13-9-5-8(10(14)12(16)11(9)15)6-1-3-7(17)4-2-6/h1-5,17H

HIDE SMILES / InChI

Molecular Formula C12H6Cl4O
Molecular Weight 307.987
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Detection and measurement of the agonistic activities of PCBs and mono-hydroxylated PCBs to the constitutive androstane receptor using a recombinant yeast assay.
2015-10
Human sex hormone-binding globulin binding affinities of 125 structurally diverse chemicals and comparison with their binding to androgen receptor, estrogen receptor, and α-fetoprotein.
2015-02
Rat α-Fetoprotein binding affinities of a large set of structurally diverse chemicals elucidated the relationships between structures and binding affinities.
2012-11-19
Estrogen receptor independent neurotoxic mechanism of bisphenol A, an environmental estrogen.
2007-03
Differential activation of wild-type estrogen receptor alpha and C-terminal deletion mutants by estrogens, antiestrogens and xenoestrogens in breast cancer cells.
2007-01
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Activation of kinase pathways in MCF-7 cells by 17beta-estradiol and structurally diverse estrogenic compounds.
2006-02
Long-term effects of neonatal exposure to hydroxylated polychlorinated biphenyls in the BALB/cCrgl mouse.
2005-08
Hydroxylated polychlorinated biphenyls selectively bind transthyretin in blood and inhibit amyloidogenesis: rationalizing rodent PCB toxicity.
2004-12
Free energies of binding of polychlorinated biphenyls to the estrogen receptor from a single simulation.
2004-02-01
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003-10
Differential activation of wild-type and variant forms of estrogen receptor alpha by synthetic and natural estrogenic compounds using a promoter containing three estrogen-responsive elements.
2001-07
4-hydroxy-2',4',6'-trichlorobiphenyl and 4-hydroxy-2',3',4',5'-tetrachlorobiphenyl are estrogenic in rainbow trout.
2001-02
Toxicology of environmental estrogens.
2001
Differential effects of xenoestrogens on coactivator recruitment by estrogen receptor (ER) alpha and ERbeta.
2000-11-17
Several synthetic chemicals inhibit progesterone receptor-mediated transactivation in yeast.
1997-04-07
Antiestrogenic activity of hydroxylated polychlorinated biphenyl congeners identified in human serum.
1997-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:48:22 GMT 2025
Edited
by admin
on Mon Mar 31 20:48:22 GMT 2025
Record UNII
LH750S39FX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(1,1'-BIPHENYL)-4-OL, 2',3',4',5'-TETRACHLORO-
Preferred Name English
4'-HYDROXY-2,3,4,5-TETRACHLOROBIPHENYL
Systematic Name English
2,3,4,5-TETRACHLORO-4'-BIPHENYLOL
Systematic Name English
2',3',4',5'-TETRACHLORO-(1,1'-BIPHENYL)-4-OL
Systematic Name English
2',3',4',5'-TETRACHLOROBIPHENYL-4-OL
Systematic Name English
Code System Code Type Description
PUBCHEM
105101
Created by admin on Mon Mar 31 20:48:22 GMT 2025 , Edited by admin on Mon Mar 31 20:48:22 GMT 2025
PRIMARY
CAS
67651-34-7
Created by admin on Mon Mar 31 20:48:22 GMT 2025 , Edited by admin on Mon Mar 31 20:48:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID5022350
Created by admin on Mon Mar 31 20:48:22 GMT 2025 , Edited by admin on Mon Mar 31 20:48:22 GMT 2025
PRIMARY
FDA UNII
LH750S39FX
Created by admin on Mon Mar 31 20:48:22 GMT 2025 , Edited by admin on Mon Mar 31 20:48:22 GMT 2025
PRIMARY
MESH
C427824
Created by admin on Mon Mar 31 20:48:22 GMT 2025 , Edited by admin on Mon Mar 31 20:48:22 GMT 2025
PRIMARY