Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C16H24O2 |
Molecular Weight | 248.3606 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](O)[C@@]1(C)CCC3=C(CC)C(=O)CC[C@@]23[H]
InChI
InChIKey=DOTDLCMVUVGSDP-VRKREXBASA-N
InChI=1S/C16H24O2/c1-3-10-11-8-9-16(2)13(5-7-15(16)18)12(11)4-6-14(10)17/h12-13,15,18H,3-9H2,1-2H3/t12-,13+,15+,16+/m1/s1
Molecular Formula | C16H24O2 |
Molecular Weight | 248.3606 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Inocoterone acetate (USAN) (also known as RU-38882, RU-882) is the acetate ester of inocoterone a steroid-like nonsteroidal antiandrogen (NSAA) that was developed for topical administration to treat acne but was never marketed. Inocoterone acetate is actually not a silent antagonist of the androgen receptor but rather a weak partial agonist, similarly to steroidal antiandrogens like cyproterone acetate. In this double-blind study of 126 male subjects with acne, a topical solution of the antiandrogen inocoterone produced a modest but statistically significant reduction in the number of inflammatory acne lesions.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1387778
topical solution containing 10% inocoterone
Route of Administration:
Topical
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:16:44 GMT 2023
by
admin
on
Fri Dec 15 15:16:44 GMT 2023
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Record UNII |
Q35F31B844
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Record Status |
Validated (UNII)
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Record Version |
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SUB08189MIG
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Inocoterone
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100000083398
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11776794
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83646-97-3
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DTXSID10232491
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C174865
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5845
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CHEMBL2107564
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Q35F31B844
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admin on Fri Dec 15 15:16:44 GMT 2023 , Edited by admin on Fri Dec 15 15:16:44 GMT 2023
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Related Record | Type | Details | ||
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ACTIVE MOIETY |