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Details

Stereochemistry RACEMIC
Molecular Formula C15H23N3O3
Molecular Weight 293.3614
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of S-40503

SMILES

CN(C)[C@H]1C[C@H](NC2=CC=C(C=C12)[N+]([O-])=O)C(C)(C)CO

InChI

InChIKey=YNYAUBNZRZVNLX-KBPBESRZSA-N
InChI=1S/C15H23N3O3/c1-15(2,9-19)14-8-13(17(3)4)11-7-10(18(20)21)5-6-12(11)16-14/h5-7,13-14,16,19H,8-9H2,1-4H3/t13-,14-/m0/s1

HIDE SMILES / InChI

Molecular Formula C15H23N3O3
Molecular Weight 293.3614
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Tue Apr 01 16:41:18 GMT 2025
Edited
by admin
on Tue Apr 01 16:41:18 GMT 2025
Record UNII
TBF49WHM83
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
S-40503
Common Name English
2-(4-(DIMETHYLAMINO)-6-NITRO-1,2,3,4-TETRAHYDROQUINOLIN-2-YL)-2-METHYLPROPAN-1-OL
Preferred Name English
2-QUINOLINEETHANOL, 4-(DIMETHYLAMINO)-1,2,3,4-TETRAHYDRO-.BETA.,.BETA.-DIMETHYL-6-NITRO-
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-S-40503
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
Code System Code Type Description
FDA UNII
TBF49WHM83
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID801027128
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
PRIMARY
CAS
404920-28-1
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
PRIMARY
CAS
1345011-36-0
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
ALTERNATIVE
WIKIPEDIA
S-40503
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
PRIMARY S-40503 is an investigational selective androgen receptor modulator (SARM) developed by the Japanese company Kaken Pharmaceuticals, which was developed for the treatment of osteoporosis. SARMs are a new class of drugs which produce tissue-specific anabolic effects in some tissues such as muscle and bone, but without stimulating androgen receptors in other tissues such as in the prostate gland, thus avoiding side effects such as benign prostatic hypertrophy which can occur following treatment with unselective androgens like testosterone or anabolic steroids.
DRUG BANK
DB13938
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
PRIMARY
PUBCHEM
57398987
Created by admin on Tue Apr 01 16:41:18 GMT 2025 , Edited by admin on Tue Apr 01 16:41:18 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY