Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H5Cl5O |
Molecular Weight | 342.433 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(Cl)C=C(C=C1)C2=C(Cl)C(Cl)=C(Cl)C=C2Cl
InChI
InChIKey=QLPPOBFMEBKBOZ-UHFFFAOYSA-N
InChI=1S/C12H5Cl5O/c13-6-3-5(1-2-9(6)18)10-7(14)4-8(15)11(16)12(10)17/h1-4,18H
Molecular Formula | C12H5Cl5O |
Molecular Weight | 342.433 |
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 |
---|---|---|
Potent inhibition of estrogen sulfotransferase by hydroxylated PCB metabolites: a novel pathway explaining the estrogenic activity of PCBs. | 2000 May |
|
Hydroxylated polychlorinated biphenyls selectively bind transthyretin in blood and inhibit amyloidogenesis: rationalizing rodent PCB toxicity. | 2004 Dec |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 00:36:28 GMT 2023
by
admin
on
Sat Dec 16 00:36:28 GMT 2023
|
Record UNII |
5WCD5150FG
|
Record Status |
Validated (UNII)
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Record Version |
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-
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5WCD5150FG
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DTXSID20172793
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644181
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admin on Sat Dec 16 00:36:28 GMT 2023 , Edited by admin on Sat Dec 16 00:36:28 GMT 2023
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192190-10-6
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admin on Sat Dec 16 00:36:28 GMT 2023 , Edited by admin on Sat Dec 16 00:36:28 GMT 2023
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