Pregled bibliografske jedinice broj: 25643
Biotransformations of Anabolic Steroids Using Recombinant Human CYP3A4
Biotransformations of Anabolic Steroids Using Recombinant Human CYP3A4 // ISSX Proceedings, vol. 13
Bethesda (MD): International Society for the Study of Xenobiotics, 1999. str. 81-81 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 25643 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Biotransformations of Anabolic Steroids Using Recombinant Human CYP3A4
Autori
Rendić, Slobodan ; Nolteernsting, Eckhardt ; Schänzer Wilhelm
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
ISSX Proceedings, vol. 13
/ - Bethesda (MD) : International Society for the Study of Xenobiotics, 1999, 81-81
Skup
5th International ISSX Meeting
Mjesto i datum
Cairns, Australija, 25.10.1998. - 29.10.1998
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
Anabolic steroids; human CYP Enzymes; recombinant enzymes
(Biotransformations of Anabolic Steroids Using Recombinant Human CYP3A4)
Sažetak
Two formats of human recombinant CYP3A4 have been used for in vitro study of metabolism of anabolic steroids i.e. microsomes prepared from insect cells expressing human enzyme and purified recombinant human CYP3A4 (PANVERA, USA). Structures of metabolites as trimethylsilyl-ether derivatives were determined by the GC/MS method. The reference 6beta-hydroxylated metabolites were synthesized as reported by Schanzer et al., Steroids, 60:353, 1995. After incubation of anabolic steroids with CYP3A4 enzyme systems formation of the following metabolites is suggested:
STEROID METABOLITE
Testosterone, 6beta-hydroxy-
17alpha-Methyltestosterone 6beta-hydroxy-
Methandienone 6beta-hydroxy-
4-Chloro-1,2-dehydro-17alpha-methyltestosterone 6beta-hydroxy-
Boldenone monohydroxy-
(most probably 6beta-hydroxy-)
5beta-Androstane-3alpha, 17beta-diol 5alpha-dihydrotestosterone (DHT) and monohydroxy-
5beta-Androstane-3alpha, 17beta-iol no metabolites identified
5alpha-Dihydrotestosterone (DHT) monohydroxy-
Androst-4-ene-3,17-dion mono- and bishydroxy-
Androst-4-ene-3beta,17beta-diol testosterone and monohydroxy-
Androst-5-ene-3beta,17beta-diol no metabolites identified
The results indicate that 6beta-hydroxylation is a common and preferential metabolic pathway for 3-one-, 4-ene-steroids when incubated with human CYP3A4 enzyme in vitro.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija
POVEZANOST RADA
Projekti:
006241
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Profili:
Slobodan Rendić
(autor)