General Information
Drug ID
DR01193
Drug Name
Prasterone
Synonyms
17-Chetovis; 17-Hormoforin; 3beta-hydroxyandrost-5-en-17-one; 5,6-Dehydroisoandrosterone; 5,6-Dehydroisoandrostorone; 5,6-Didehydroisoandrosterone; 5-Dehydroepiandrosterone; 53-43-0; Andrestenol; Androstenolone; Caswell No 051F; DHEA; Dehydro-epi-androsterone; Dehydroepiandrosterone; Dehydroisoandrosterone; Diandron; Diandrone; Epiandrosterone, 5-dehydro-; Intrarosa; PRASTERONE; Prasterona; Prasteronum; Prestara; Psicosterone; Siscelar plus; trans-Dehydroandrosterone
Drug Type
Small molecular drug
Indication Hypercalcemia [ICD11:5B91.0] Approved [1]
Structure
3D MOL 2D MOL
Formula
C19H28O2
Canonical SMILES
CC12CCC3C(C1CCC2=O)CC=C4C3(CCC(C4)O)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
InChIKey
FMGSKLZLMKYGDP-USOAJAOKSA-N
CAS Number
CAS 53-43-0
Pharmaceutical Properties Molecular Weight 288.4 Topological Polar Surface Area 37.3
Heavy Atom Count 21 Rotatable Bond Count 0
Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2
XLogP
3.2
PubChem CID
5881
PubChem SID
103302695 ,104095449 ,11446567 ,12014907 ,12146065 ,14751238 ,14775640 ,17404931 ,1983 ,24278369 ,24702275 ,26703947 ,29224908 ,3135651 ,4449 ,46387028 ,46508824 ,47193749 ,47959958 ,48413520 ,48415849 ,49681751 ,49747225 ,49857278 ,50172721 ,53777474 ,53788218 ,56312069 ,56312916 ,56313484 ,56313819 ,56320669 ,56320670 ,57323014 ,596018 ,75250 ,7885884 ,8145544 ,8153636 ,837865 ,841442 ,87566797 ,91692812 ,92297484 ,92303742 ,92308678 ,92309040 ,92709895 ,93167098 ,96025095
ChEBI ID
ChEBI:28689
TTD Drug ID
D0K0EK
DT(s) Transporting This Drug BCRP Transporter Info Breast cancer resistance protein Substrate [2]
MRP4 Transporter Info Multidrug resistance-associated protein 4 Substrate [3]
MRP8 Transporter Info Multidrug resistance-associated protein 8 Substrate [4]
OAT3 Transporter Info Organic anion transporter 3 Substrate [5]
References
1 Prasterone was approved by FDA. The official website of the U.S. Food and Drug Administration. (2019)
2 Human intestinal transporter database: QSAR modeling and virtual profiling of drug uptake, efflux and interactions. Pharm Res. 2013 Apr;30(4):996-1007.
3 Steroid and bile acid conjugates are substrates of human multidrug-resistance protein (MRP) 4 (ATP-binding cassette C4). Biochem J. 2003 Apr 15;371(Pt 2):361-7.
4 Human multidrug resistance protein 8 (MRP8/ABCC11), an apical efflux pump for steroid sulfates, is an axonal protein of the CNS and peripheral nervous system. Neuroscience. 2006;137(4):1247-57.
5 Identification and characterization of human organic anion transporter 3 expressing predominantly in the kidney. Mol Pharmacol. 2001 May;59(5):1277-86.

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