Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H12Cl4 |
| Molecular Weight | 334.068 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(Cl)(Cl)C(C1=CC=C(Cl)C=C1)C2=CC=CC=C2Cl
InChI
InChIKey=MOTIYCLHZZLHHQ-UHFFFAOYSA-N
InChI=1S/C15H12Cl4/c1-15(18,19)14(10-6-8-11(16)9-7-10)12-4-2-3-5-13(12)17/h2-9,14H,1H3
| Molecular Formula | C15H12Cl4 |
| Molecular Weight | 334.068 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/8453685
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8453685
Mitometh, a methylated homolog of mitotane possesses an adrenalytic activity and has been studied for the treatment of adrenal cancer. Experiments on animals and on human cell lines have shown that mitometh was not effective in the therapy of adrenal cancer.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:46:28 GMT 2025
by
admin
on
Mon Mar 31 21:46:28 GMT 2025
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| Record UNII |
H8MTN7XVC2
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| Record Status |
Validated (UNII)
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| Record Version |
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