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
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
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
Title | Date | PubMed |
---|---|---|
Differential effects of xenoestrogens on coactivator recruitment by estrogen receptor (ER) alpha and ERbeta. | 2000 Nov 17 |
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Hydroxylated polychlorinated biphenyls selectively bind transthyretin in blood and inhibit amyloidogenesis: rationalizing rodent PCB toxicity. | 2004 Dec |
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Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
|
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 Feb |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:21:24 GMT 2023
by
admin
on
Sat Dec 16 01:21:24 GMT 2023
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Record UNII |
LH750S39FX
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Record Status |
Validated (UNII)
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Record Version |
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105101
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67651-34-7
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DTXSID5022350
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admin on Sat Dec 16 01:21:24 GMT 2023 , Edited by admin on Sat Dec 16 01:21:24 GMT 2023
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LH750S39FX
Created by
admin on Sat Dec 16 01:21:24 GMT 2023 , Edited by admin on Sat Dec 16 01:21:24 GMT 2023
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C427824
Created by
admin on Sat Dec 16 01:21:24 GMT 2023 , Edited by admin on Sat Dec 16 01:21:24 GMT 2023
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