Abstract:
:A series of dialkyl, dicycloalkyl, and diaryl ester analogues of nifedipine, in which the ortho-nitro phenyl group at position 4 is replaced by the 4-(5)-chloro-2-ethyl-5-(4)-imidazolyl substituent, were synthesized and evaluated as calcium channel antagonists using the high K+ contraction of guinea pig ileal longitudinal smooth muscle. The results for the symmetrical ester series showed that increasing the length of the chain in C3- and C5-ester substituents increased the activity and the most active compound was the diphenylethyl ester derivative, so it was more active than the reference drug nifedipine. In unsymmetrical diester series, when R1 is methyl or ethyl, increasing lipophilic properties in the R substituent, increased the activity. The most active compounds were methyl/phenethyl and ethyl/phenethyl ester derivatives, being slightly more active than nifedipine.
journal_name
Arch Pharm (Weinheim)journal_title
Archiv der Pharmazieauthors
Davood A,Mansouri N,Rerza Dehpour A,Shafaroudi H,Alipour E,Shafiee Adoi
10.1002/ardp.200600013subject
Has Abstractpub_date
2006-06-01 00:00:00pages
299-304issue
6eissn
0365-6233issn
1521-4184journal_volume
339pub_type
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