U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H26O2
Molecular Weight 286.4085
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7.ALPHA.-METHYLESTRADIOL

SMILES

C[C@@H]1CC2=CC(O)=CC=C2[C@H]3CC[C@]4(C)[C@@H](O)CC[C@H]4[C@H]13

InChI

InChIKey=DXWWYJWUFULMAP-JZHXJEGVSA-N
InChI=1S/C19H26O2/c1-11-9-12-10-13(20)3-4-14(12)15-7-8-19(2)16(18(11)15)5-6-17(19)21/h3-4,10-11,15-18,20-21H,5-9H2,1-2H3/t11-,15-,16+,17+,18-,19+/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H24O2
Molecular Weight 284.3927
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 12:58:55 GMT 2025
Edited
by admin
on Wed Apr 02 12:58:55 GMT 2025
Record UNII
VD3UG279PS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7.ALPHA.-METHYL-E2
Preferred Name English
7.ALPHA.-METHYLESTRADIOL
Common Name English
7.ALPHA.-METHYLESTRA-1,3,5(10)-TRIENE-3,17.BETA.-DIOL
Systematic Name English
ESTRA-1,3,5(10)-TRIENE-3,17.BETA.-DIOL, 7.ALPHA.-METHYL-
Systematic Name English
ESTRA-1,3,5(10)-TRIENE-3,17-DIOL, 7-METHYL-, (7.ALPHA.,17.BETA.)-
Systematic Name English
Code System Code Type Description
CAS
10448-97-2
Created by admin on Wed Apr 02 12:58:55 GMT 2025 , Edited by admin on Wed Apr 02 12:58:55 GMT 2025
PRIMARY
FDA UNII
VD3UG279PS
Created by admin on Wed Apr 02 12:58:55 GMT 2025 , Edited by admin on Wed Apr 02 12:58:55 GMT 2025
PRIMARY
WIKIPEDIA
7.alpha.-Methylestradiol
Created by admin on Wed Apr 02 12:58:55 GMT 2025 , Edited by admin on Wed Apr 02 12:58:55 GMT 2025
PRIMARY
PUBCHEM
10424124
Created by admin on Wed Apr 02 12:58:55 GMT 2025 , Edited by admin on Wed Apr 02 12:58:55 GMT 2025
PRIMARY
EPA CompTox
DTXSID801336309
Created by admin on Wed Apr 02 12:58:55 GMT 2025 , Edited by admin on Wed Apr 02 12:58:55 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
PARENT -> METABOLITE ACTIVE
Considered to be responsible for the estrogenic activity of trestolone.
Related Record Type Details
ACTIVE MOIETY