Synthesis and Urease Enzyme Inhibitory Effects of Some Dicoumarols
Dicoumarols 1-10 with substituted phenyl residues at C-11 were synthesized and screened for their urease inhibition effects. All synthesized compounds showed varying degree of urease inhibitory activity ranging from IC50 = 74.30-91.35 μM.
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Veröffentlicht in: | Journal of enzyme inhibition and medicinal chemistry 2004-08, Vol.19 (4), p.367-371 |
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container_title | Journal of enzyme inhibition and medicinal chemistry |
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creator | Khan, Khalid M. Iqbal, Sajid Lodhi, Muhammad A. Maharvi, Ghulam M. Perveen, Shahnaz Choudhary, M. I. Atta-ur-Rahman Chohan, Zahid H. Supuran, Claudiu T. |
description | Dicoumarols 1-10 with substituted phenyl residues at C-11 were synthesized and screened for their urease inhibition effects. All synthesized compounds showed varying degree of urease inhibitory activity ranging from IC50 = 74.30-91.35 μM. |
doi_str_mv | 10.1080/14756360409162452 |
format | Article |
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All synthesized compounds showed varying degree of urease inhibitory activity ranging from IC50 = 74.30-91.35 μM.</description><subject>4-Hydroxycoumarin</subject><subject>Derivatives</subject><subject>Dicoumarol</subject><subject>Dicumarol - analogs & derivatives</subject><subject>Dicumarol - chemical synthesis</subject><subject>Dicumarol - pharmacology</subject><subject>Enzyme Inhibitors - chemical synthesis</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Fabaceae - enzymology</subject><subject>Molecular Structure</subject><subject>Urease - antagonists & inhibitors</subject><subject>Urease - chemistry</subject><subject>Urease Inhibitors</subject><issn>1475-6366</issn><issn>1475-6374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kFFLwzAUhYMobk5_gC_SJ9-qSdOkDfqic-pg4MPcc0jTG9rRNjNpkfrr7dhQRNjTvdx7zuHwIXRJ8A3BKb4lccI45TjGgvAoZtERGm9vIadJfPyzcz5CZ96vMY5IROJTNCKMsVQwNkaPy75pC_ClD1STBysHykMwa776GoJ5U5RZ2VrXBzNjQLc-sCZY2uH1VGrb1crZyp-jE6MqDxf7OUGr59n79DVcvL3Mpw-LUMc4asM854xQlmQmTROd0ZillAARQKI8JwJHFDMhADCNlCFCGK0JzRRNTZwzzBmdoOtd7sbZjw58K-vSa6gq1YDtvOQJFjRJ00FIdkLtrPcOjNy4cujaS4LlFpz8B27wXO3Du6yG_NexJzUI7neCsjHW1erTuiqXreor64xTjS69pIfy7_7YC1BVW2jlQK5t55oB3IF236AwjJs</recordid><startdate>20040801</startdate><enddate>20040801</enddate><creator>Khan, Khalid M.</creator><creator>Iqbal, Sajid</creator><creator>Lodhi, Muhammad A.</creator><creator>Maharvi, Ghulam M.</creator><creator>Perveen, Shahnaz</creator><creator>Choudhary, M. 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subjects | 4-Hydroxycoumarin Derivatives Dicoumarol Dicumarol - analogs & derivatives Dicumarol - chemical synthesis Dicumarol - pharmacology Enzyme Inhibitors - chemical synthesis Enzyme Inhibitors - pharmacology Fabaceae - enzymology Molecular Structure Urease - antagonists & inhibitors Urease - chemistry Urease Inhibitors |
title | Synthesis and Urease Enzyme Inhibitory Effects of Some Dicoumarols |
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