prasterone

prasterone

Clinical data
Trade names	Intrarosa, others
Other names	EL-10; GL-701; KYH-3102; Androst-5-en-3β-ol-17-one; 3β-Hydroxyandrost-5-en-17-one; 5,6-Didehydroepiandrosterone;
AHFS/Drugs.com	Monograph
MedlinePlus	a617012
License data	US DailyMed: Prasterone
Pregnancy category	AU: D
Routes of administration	By mouth, vaginal (rectal), intramuscular (as prasterone enanthate), injection (as prasterone sodium sulfate)
Drug class	Androgen; Anabolic steroid; Estrogen; Neurosteroid
ATC code	G03XX01 (WHO) G03EA03 (WHO) (combination with estrogen) QA14AA07 (WHO)
Legal status
Legal status	AU: S4 (Prescription only) BR: Class C5 (Anabolic steroids) CA: Schedule IV US: ℞-only EU: Rx-only
Pharmacokinetic data
Bioavailability	50%
Metabolism	Liver
Metabolites	• Androsterone
Elimination half-life	DHEA: 25 minutes
Excretion	Urine
Identifiers
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
CAS Number	53-43-0 Y
PubChem CID	5881
IUPHAR/BPS	2370
DrugBank	DB01708 Y
ChemSpider	5670 Y
UNII	459AG36T1B
KEGG	D08409
ChEBI	CHEBI:28689 Y
ChEMBL	ChEMBL90593 Y
Chemical and physical data
Formula	C19H28O2
Molar mass	288.431 g·mol−1
3D model (JSmol)	Interactive image
Melting point	148.5 °C (299.3 °F)
SMILES O=C3[C@]2(CC[C@@H]1[C@@]4(C(=C/C[C@H]1[C@@H]2CC3)\C[C@@H](O)CC4)C)C
InChI InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3/t13-,14-,15-,16-,18-,19-/m0/s1 Y Key:FMGSKLZLMKYGDP-USOAJAOKSA-N Y
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Angol

Főnév

prasterone (tsz. prasterones)

1. (gyógyszertan) praszteron

További információk

• prasterone - Szótár.net (en-hu)
• prasterone - Sztaki (en-hu)
• prasterone - Merriam–Webster
• prasterone - Cambridge
• prasterone - WordNet
• prasterone - Яндекс (en-ru)
• prasterone - Google (en-hu)
• prasterone - Wikidata
• prasterone - Wikipédia (angol)