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=CC(Cl)=C(Cl)C(Cl)=C2Cl
InChI
InChIKey=CGAILIYIKMFHPA-UHFFFAOYSA-N
InChI=1S/C12H5Cl5O/c13-7-3-5(1-2-9(7)18)6-4-8(14)11(16)12(17)10(6)15/h1-4,18H
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Hydroxylated polychlorinated biphenyls selectively bind transthyretin in blood and inhibit amyloidogenesis: rationalizing rodent PCB toxicity. | 2004 Dec |
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UDP-glucuronosyltransferase isoforms catalyzing glucuronidation of hydroxy-polychlorinated biphenyls in rat. | 2005 Oct |
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Sulfonation of 17beta-estradiol and inhibition of sulfotransferase activity by polychlorobiphenylols and celecoxib in channel catfish, Ictalurus punctatus. | 2007 Mar 10 |
Patents
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Code System | Code | Type | Description | ||
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6GW073T1WI
Created by
admin on Sat Dec 16 01:02:04 GMT 2023 , Edited by admin on Sat Dec 16 01:02:04 GMT 2023
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192190-09-3
Created by
admin on Sat Dec 16 01:02:04 GMT 2023 , Edited by admin on Sat Dec 16 01:02:04 GMT 2023
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DTXSID60172792
Created by
admin on Sat Dec 16 01:02:04 GMT 2023 , Edited by admin on Sat Dec 16 01:02:04 GMT 2023
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644180
Created by
admin on Sat Dec 16 01:02:04 GMT 2023 , Edited by admin on Sat Dec 16 01:02:04 GMT 2023
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PRIMARY |
SUBSTANCE RECORD