Prasterone
Overview
Prasterone is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL90593).
API suppliers (8)
Suppliers of Prasterone evidenced by a US FDA Type II Drug Master File or an EU Certificate of Suitability (CEP). Sources: FDA DMF list, EDQM certification database.
Country recorded for 6 of 8 suppliers.
2 of 8 hold a GMP certificate on record in the EU or UK registers
- JIANGSU JIAERKE PHARMACEUTICALS GROUP CORP LTDChina2 active DMF
- FIS FABBRICA ITALIANA SINTETICI SPAItaly1 active DMF GMP on record
- ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO LTD1 active DMF
- Pfizer Inc.United States1 active DMF
- HUBEI GOTO BIOPHARM CO LTDChina1 active DMF
- HUBEI GOTO BIOTECHNOLOGY CO LTDChina1 active DMF
- Organon & Co.United States GMP on record
- DIOSYNTH BV
Patent & exclusivity (US)
Per the FDA Orange Book (1 approved US product), the latest listed US patent on Prasterone expires 19 Mar 2031. Generic API sourcing typically opens up once these lapse.
Chemical identity
- IUPAC name
- (3S,8R,9S,10R,13S,14S)-3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one
- Canonical SMILES
- C[C@]12CC[C@H]3[C@H]([C@@H]1CCC2=O)CC=C4[C@@]3(CC[C@@H](C4)O)C
- InChIKey
- FMGSKLZLMKYGDP-USOAJAOKSA-N
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