Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H2Cl8 |
| Molecular Weight | 429.768 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(Cl)C(=C1Cl)C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C2Cl
InChI
InChIKey=HHXNVASVVVNNDG-UHFFFAOYSA-N
InChI=1S/C12H2Cl8/c13-3-1-2-4(14)7(15)5(3)6-8(16)10(18)12(20)11(19)9(6)17/h1-2H
| Molecular Formula | C12H2Cl8 |
| Molecular Weight | 429.768 |
| 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 |
|---|---|---|
| In silico prediction of pregnane X receptor activators by machine learning approaches. | 2007-01 |
|
| Environmental xenobiotics and the antihormones cyproterone acetate and spironolactone use the nuclear hormone pregnenolone X receptor to activate the CYP3A23 hormone response element. | 1998-12 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:52:28 GMT 2025
by
admin
on
Mon Mar 31 21:52:28 GMT 2025
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| Record UNII |
7Y7AX4L8DT
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| Record Status |
Validated (UNII)
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| Record Version |
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