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J Nat Prod ; 60(10): 997-1002, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9358642

ABSTRACT

The isolation and structure elucidation of five novel natural Diels--Alder-type adducts, named palodesangrens A-E (1-5), from the Peruvian folk medicine known as "palo de sangre" (Brosimum rubescens) is described. The structures of the Diels--Alder adducts, consisting of chalcone derivatives and a prenylcoumarin, were elucidated by analysis of spectroscopic data including 2D NMR. Some of these compounds showed potent inhibitory activity towards 5 alpha-dihydrotestosterone (DHT) binding with an androgen receptor to form a DHT-receptor complex that causes androgen-dependent diseases.


Subject(s)
Androgen Antagonists/isolation & purification , Chalcone/isolation & purification , Coumarins/isolation & purification , Plants, Medicinal/chemistry , 5-alpha Reductase Inhibitors , Androgen Antagonists/chemistry , Androgen Antagonists/pharmacology , Androgen Receptor Antagonists , Animals , Chalcone/analogs & derivatives , Chalcone/chemistry , Chalcone/pharmacology , Chromatography, High Pressure Liquid , Coumarins/chemistry , Coumarins/pharmacology , In Vitro Techniques , Magnetic Resonance Spectroscopy , Male , Peru , Plant Epidermis/chemistry , Rats , Rats, Wistar , Spectrometry, Mass, Fast Atom Bombardment
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