| Literature DB >> 3386266 |
D Giudici1, G Ornati, G Briatico, F Buzzetti, P Lombardi, E di Salle.
Abstract
FCE 24304 (6-methylenandrosta-1,4-diene-3,17-dione), a new irreversible aromatase inhibitor, has been identified and characterized in vitro and in vivo. The compound caused time-dependent inactivation of human placental aromatase with a t1/2 of 13.9 min and ki of 26 nM. When tested in PMSG-treated rats, ovarian aromatase activity was reduced 24 h after dosing by both the s.c. (ED50 1.8 mg/kg) and the oral (ED50 3.7 mg/kg) routes. No interference with 5 alpha-reductase activity nor any significant binding affinity for estrogen receptor was found. Slight binding affinity for the androgen receptor (RBA 0.2% of DHT) was observed.Entities:
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Year: 1988 PMID: 3386266 DOI: 10.1016/0022-4731(88)90129-x
Source DB: PubMed Journal: J Steroid Biochem ISSN: 0022-4731 Impact factor: 4.292