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Bioorg Med Chem Lett ; 10(3): 277-9, 2000 Feb 07.
Article in English | MEDLINE | ID: mdl-10698453

ABSTRACT

A series of 2,3-disubstituted-4-phenylquinolines were prepared and were found to inhibit the apical sodium co-dependent bile acid transporter (ASBT). Alkyl and ester substitution at the 3-position showed comparable activities while substitution at the 2-position was much more sensitive to the nature of the substituent. The synthesis and in vitro potency data are presented for this novel class of compounds.


Subject(s)
Carrier Proteins/antagonists & inhibitors , Hydroxysteroid Dehydrogenases , Membrane Glycoproteins , Quinolines/pharmacology , Sodium/pharmacology , Molecular Structure , Quinolines/chemistry
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