Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H31ClO2 |
| Molecular Weight | 362.933 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1C[C@H]2[C@@H]3C[C@H](Cl)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]2(C)[C@H]1C(C)=O
InChI
InChIKey=UMRURYMAPMZKQO-NDKKBYRMSA-N
InChI=1S/C22H31ClO2/c1-12-9-17-15-11-19(23)18-10-14(25)5-7-21(18,3)16(15)6-8-22(17,4)20(12)13(2)24/h10,12,15-17,19-20H,5-9,11H2,1-4H3/t12-,15-,16+,17+,19+,20-,21-,22+/m1/s1
Clometherone is an investigational derivative of progesterone, possessing antiestrogen and antiandrogen activities. It was developed by Eli Lilly in the 1960s and was found to significantly suppress the estrone induced uterine hypertrophy in mice at an oral or subcutaneous dose of 10ug. In a clinical trial, administration of clometherone to adult males lead to a slight increase in sebum production.
Approval Year
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C481
Created by
admin on Wed Apr 02 09:57:05 GMT 2025 , Edited by admin on Wed Apr 02 09:57:05 GMT 2025
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1857
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14515731
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01L3E93T4C
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DTXSID20204508
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SUB06719MIG
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C74147
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100000084524
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CHEMBL2105974
Created by
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5591-27-5
Created by
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Clometerone
Created by
admin on Wed Apr 02 09:57:05 GMT 2025 , Edited by admin on Wed Apr 02 09:57:05 GMT 2025
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PRIMARY |
ACTIVE MOIETY
