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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
Structure of INOCOTERONE

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

HIDE SMILES / InChI

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.

Originator

Sources: Ukrainskii Khimicheskii Zhurnal (Russian Edition) (1964), 30, (8), 862-7

Approval Year

PubMed

PubMed

TitleDatePubMed
A stable prostatic bioluminescent cell line to investigate androgen and antiandrogen effects.
2000 Feb 25
Patents

Patents

Sample Use Guides

topical solution containing 10% inocoterone
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:16:44 GMT 2023
Edited
by admin
on Fri Dec 15 15:16:44 GMT 2023
Record UNII
Q35F31B844
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
INOCOTERONE
INN  
INN  
Official Name English
inocoterone [INN]
Common Name English
17.BETA.-HYDROXY-2,5-SECO-A-DINORESTR-9-EN-5-ONE
Common Name English
Code System Code Type Description
EVMPD
SUB08189MIG
Created by 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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WIKIPEDIA
Inocoterone
Created by 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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SMS_ID
100000083398
Created by 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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PUBCHEM
11776794
Created by 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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CAS
83646-97-3
Created by 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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EPA CompTox
DTXSID10232491
Created by 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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NCI_THESAURUS
C174865
Created by 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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INN
5845
Created by 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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ChEMBL
CHEMBL2107564
Created by admin on Fri Dec 15 15:16:44 GMT 2023 , Edited by admin on Fri Dec 15 15:16:44 GMT 2023
PRIMARY
FDA UNII
Q35F31B844
Created by admin on Fri Dec 15 15:16:44 GMT 2023 , Edited by admin on Fri Dec 15 15:16:44 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY