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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H28O2
Molecular Weight 288.4244
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Methyl-19-nortestosterone, 6?-

SMILES

C[C@H]1C[C@H]2[C@@H]3CC[C@H](O)[C@@]3(C)CC[C@@H]2[C@H]4CCC(=O)C=C14

InChI

InChIKey=IADMIEQJGFYVBM-ZKLJSNIQSA-N
InChI=1S/C19H28O2/c1-11-9-16-14(13-4-3-12(20)10-15(11)13)7-8-19(2)17(16)5-6-18(19)21/h10-11,13-14,16-18,21H,3-9H2,1-2H3/t11-,13+,14+,16+,17-,18-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H28O2
Molecular Weight 288.4244
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:44:41 GMT 2025
Edited
by admin
on Mon Mar 31 21:44:41 GMT 2025
Record UNII
P4E5ESL9MY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(6?,17?)-17-Hydroxy-6-methylestr-4-en-3-one
Preferred Name English
Methyl-19-nortestosterone, 6?-
Common Name English
6?-Methyl-19-nortestosterone
Common Name English
(6S,8R,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
Systematic Name English
(17S)-17-Hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
Systematic Name English
Estr-4-en-3-one, 17-hydroxy-6-methyl-, (6?,17?)-
Common Name English
Estr-4-en-3-one, 17?-hydroxy-6?-methyl-
Common Name English
Code System Code Type Description
CAS
72205-40-4
Created by admin on Mon Mar 31 21:44:41 GMT 2025 , Edited by admin on Mon Mar 31 21:44:41 GMT 2025
PRIMARY
PUBCHEM
23622606
Created by admin on Mon Mar 31 21:44:41 GMT 2025 , Edited by admin on Mon Mar 31 21:44:41 GMT 2025
PRIMARY
FDA UNII
P4E5ESL9MY
Created by admin on Mon Mar 31 21:44:41 GMT 2025 , Edited by admin on Mon Mar 31 21:44:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID60992932
Created by admin on Mon Mar 31 21:44:41 GMT 2025 , Edited by admin on Mon Mar 31 21:44:41 GMT 2025
PRIMARY