Mrv0541 01131417192D          

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    7.9901   -4.8153    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  3  1  1  0  0  0  0
  7  1  1  0  0  0  0
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 13  2  1  0  0  0  0
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  5  2  1  0  0  0  0
  6  3  1  0  0  0  0
 14  3  1  0  0  0  0
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  8  4  2  0  0  0  0
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 17  6  1  0  0  0  0
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 15  8  1  0  0  0  0
  9  8  1  0  0  0  0
 12  9  1  0  0  0  0
 15 10  1  0  0  0  0
 19 10  1  0  0  0  0
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 19 17  1  0  0  0  0
 11 28  1  0  0  0  0
M  END
> <ID>
CHEBI:9249

> <NAME>
stanozolol

> <DEFINITION>
An organic heteropentacyclic compound resulting from the formal condensation of the 3-keto-aldehyde moiety of oxymetholone with hydrazine. Like oxymetholone, it is a synthetic anabolic steroid. It has both anabolic and androgenic properties, and has been used to treat hereditary angioedema and various vascular disorders. It has also been widely abused by professional athletes.

> <STAR>
3

> <SYNONYM>
Androstanazole

> <IUPAC_NAME>
(1S,3aS,3bR,5aS,10aS,10bS,12aS)-1,10a,12a-trimethyl-1,2,3,3a,3b,4,5,5a,6,7,10,10a,10b,11,12,12a-hexadecahydrocyclopenta[5,6]naphtho[1,2-f]indazol-1-ol

> <INN>
stanozololum; stanozolol; stanozolol; estanozolol

> <BRAND_NAME>
Winstrol; Strombaject; Stromba

> <FORMULA>
C21H32N2O

> <MASS>
328.49160

> <MONOISOTOPIC_MASS>
328.25146

> <CHARGE>
0

> <SMILES>
C[C@]1(O)CC[C@H]2[C@@H]3CC[C@H]4Cc5[nH]ncc5C[C@]4(C)[C@H]3CC[C@]12C

> <INCHI>
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

> <INCHIKEY>
LKAJKIOFIWVMDJ-IYRCEVNGSA-N

> <CAS_REGISTRY_NUMBER>
10418-03-8

> <REAXYS_REGISTRY_NUMBER>
8359772

> <CHEMIDPLUS>
10418-03-8

> <DRUGBANK_ACCESSION>
DB06718

> <KEGG_COMPOUND_ACCESSION>
C07311

> <KEGG_DRUG_ACCESSION>
D00444

> <NIST_CHEMISTRY_WEBBOOK>
10418-03-8

> <WIKIPEDIA_ACCESSION>
Stanozolol

> <PUBMED_CITATION>
20020362; 20209649; 20480277; 21496393; 21769864; 22197661; 22729959; 23374366; 23873860; 23978309; 24021270; 24405322

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