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

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H32N2O
Molecular Weight 328.4916
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STANOZOLOL

SMILES

[H][C@@]12CC[C@](C)(O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC[C@@]4([H])CC5=C(C[C@]34C)C=NN5

InChI

InChIKey=LKAJKIOFIWVMDJ-IYRCEVNGSA-N
InChI=1S/C21H32N2O/c1-19-11-13-12-22-23-18(13)10-14(19)4-5-15-16(19)6-8-20(2)17(15)7-9-21(20,3)24/h12,14-17,24H,4-11H2,1-3H3,(H,22,23)/t14-,15+,16-,17-,19-,20-,21-/m0/s1

HIDE SMILES / InChI
Molecular Formula C21H32N2O
Molecular Weight 328.4916
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:27:01 UTC 2023
Edited
by admin
on Fri Dec 15 16:27:01 UTC 2023
Record UNII
4R1VB9P8V3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STANOZOLOL
EP   GREEN BOOK   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   VANDF   WHO-DD  
INN   USAN  
Official Name English
WIN 14833
Code English
17-METHYL-5.ALPHA.-ANDROSTANO(3,2-C)PYRAZOL-17.BETA.-OL
Common Name English
STANOZOLOL [GREEN BOOK]
Common Name English
17.BETA.-HYDROXY-17.ALPHA.-METHYL-5.ALPHA.-ANDROSTANO(3,2-C)PYRAZOLE
Common Name English
17-METHYL-2'H-5.ALPHA.-ANDROST-2-ENO(3,2-C)PYRAZOL-17.BETA.-OL
Common Name English
stanozolol [INN]
Common Name English
STANOZOLOL [MI]
Common Name English
CYCLOPENTA(7,8)PHENANTHRO(2,3-C)PYRAZOL-1-OL, 1,2,3,3A,3B,4,5,5A,6,8,10,10A,10B,11,12,12A-HEXADECAHYDRO-1,10A,12A-TRIMETHYL-
Common Name English
STANOZOLOL [JAN]
Common Name English
STANOZOLOL [USP MONOGRAPH]
Common Name English
STANOZOLOL [ORANGE BOOK]
Common Name English
STANOZOLOL [MART.]
Common Name English
ANDROSTANAZOLE
Common Name English
STANOZOLOL [EP MONOGRAPH]
Common Name English
ANDROSTANAZOL
Common Name English
STANOZOLOL [HSDB]
Common Name English
STANOZOLOL [USAN]
Common Name English
STANOZOLOL CIII [USP-RS]
Common Name English
WINSTROL
Brand Name English
STANOZOLOL [VANDF]
Common Name English
2'H-ANDROST-2-ENO(3,2-C)PYRAZOL-17-OL, 17-METHYL-, (5.ALPHA.,17.BETA.)
Common Name English
NSC-233046
Code English
NSC-43193
Code English
WIN-14833
Code English
1'H-ANDROSTANO(3,2-C)PYRAZOL-17-OL, 17-METHYL-, (5.ALPHA.,17.BETA.)-
Common Name English
STANOZOLOL CIII
USP-RS  
Common Name English
Stanozolol [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C243
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
WHO-VATC QA14AA02
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
WIKIPEDIA Designer-drugs-Stanozolol
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
CFR 21 CFR 520.2150
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
CFR 21 CFR 522.2150
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
LIVERTOX 898
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
WHO-ATC A14AA02
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
DEA NO. 4000
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
NCI_THESAURUS C2360
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
Code System Code Type Description
DRUG CENTRAL
2477
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
EPA CompTox
DTXSID3044128
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
CAS
302-96-5
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
ALTERNATIVE
CAS
875293-72-4
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
SUPERSEDED
MESH
D013197
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
INN
958
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
PUBCHEM
25249
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
HSDB
3185
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
CAS
69353-49-7
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
SUPERSEDED
EVMPD
SUB10641MIG
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
NCI_THESAURUS
C842
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
CHEBI
9249
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
CAS
10418-03-8
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
ECHA (EC/EINECS)
233-894-8
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
CAS
17966-55-1
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
SUPERSEDED
FDA UNII
4R1VB9P8V3
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
ChEMBL
CHEMBL2079587
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
WIKIPEDIA
STANOZOLOL
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
SMS_ID
100000083853
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
RXCUI
10032
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY RxNorm
NSC
233046
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
RS_ITEM_NUM
1620005
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
MERCK INDEX
m10191
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB06718
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
NSC
43193
Created by admin on Fri Dec 15 16:27:01 UTC 2023 , Edited by admin on Fri Dec 15 16:27:01 UTC 2023
PRIMARY
Related Record Type Details
Structure of 3'-HYDROXYSTANOZOLOL
METABOLITE -> PARENT
Structure of 16.BETA.-HYDROXYSTANOZOLOL
METABOLITE -> PARENT
URINE
Structure of 16.ALPHA.-HYDROXYSTANOZOLOL
METABOLITE -> PARENT
URINE
Structure of 3-HYDROXYSTANOZOLOL GLUCURONIDE
METABOLITE INACTIVE -> PARENT
Related Record Type Details
Structure of OXYMETHOLONE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (TLC)
EP
Structure of MESTANOLONE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (TLC)
EP
Related Record Type Details
Structure of STANOZOLOL
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966