Stanozolol
Winstrol (stanozolol) is a small molecule pharmaceutical. Stanozolol was first approved as Winstrol on 1984-05-14. It is known to target androgen receptor and estrogen receptor.
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Stanozolol
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
WINSTROL | Lundbeck | N-012885 DISCN | 1984-05-14 | 1 products, RLD |
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41 clinical trials
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Indications Phases 4
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | 1 | — | — | — | 4 | 5 |
Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Obesity | D009765 | EFO_0001073 | E66.9 | — | — | — | — | 3 | 3 |
Metabolic syndrome | D024821 | EFO_0000195 | E88.81 | — | — | — | — | 2 | 2 |
Type 2 diabetes mellitus | D003924 | EFO_0001360 | E11 | — | — | — | — | 2 | 2 |
Blood pressure | D001794 | EFO_0004325 | — | — | — | — | 2 | 2 | |
Sarcopenia | D055948 | EFO_1000653 | M62.84 | — | — | — | — | 2 | 2 |
Growth | D006128 | — | — | — | — | 2 | 2 | ||
Milk hypersensitivity | D016269 | EFO_0007369 | — | — | — | — | 2 | 2 | |
Cognition | D003071 | EFO_0003925 | — | — | — | — | 1 | 1 | |
Muscle weakness | D018908 | HP_0001324 | — | — | — | — | 1 | 1 | |
Aging | D000375 | GO_0007568 | R41.81 | — | — | — | — | 1 | 1 |
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Epidemiology
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Drug
General
Drug common name | STANOZOLOL |
INN | stanozolol |
Description | Stanozolol is 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. It has a role as an androgen and an anabolic agent. It is a 17beta-hydroxy steroid, a tertiary alcohol, an anabolic androgenic steroid and an organic heteropentacyclic compound. It is functionally related to an oxymetholone. |
Classification | Small molecule |
Drug class | beta-blockers (propranolol type) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | C[C@]12Cc3c[nH]nc3C[C@@H]1CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC[C@]2(C)O |
Identifiers
PDB | — |
CAS-ID | 10418-03-8 |
RxCUI | 10032 |
ChEMBL ID | CHEMBL2079587 |
ChEBI ID | 9249 |
PubChem CID | 25249 |
DrugBank | DB06718 |
UNII ID | 4R1VB9P8V3 (ChemIDplus, GSRS) |
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9 adverse events reported
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