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Pyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III)
We have previously described a series of 4,5-dihydro-1 H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1 H-pyrazole and 1-alkyl-3-benzoyl-1 H-pyrazole as poten...
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Published in: | European journal of medicinal chemistry 2008-11, Vol.43 (11), p.2579-2591 |
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container_title | European journal of medicinal chemistry |
container_volume | 43 |
creator | Carrión, M. Dora López Cara, Luisa C. Camacho, M. Encarnación Tapias, Víctor Escames, Germaine Acuña-Castroviejo, Darío Espinosa, Antonio Gallo, Miguel A. Entrena, Antonio |
description | We have previously described a series of 4,5-dihydro-1
H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS). None of the reported compounds exhibited significant iNOS or nNOS inhibition, although the 1-benzyl-3-(2-amino-5-chlorobenzoyl)-1
H-pyrazole-5-carboxylic acid ethyl ester derivative (
10l), which shows an inhibition of 50% versus iNOS at a 1
mM final concentration and no activity against nNOS, is potentially amenable of further optimization. The reasons for the inactivity of the reported series are discussed on the basis of docking studies.
[Display omitted] The synthesis and preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS) are described. |
doi_str_mv | 10.1016/j.ejmech.2008.01.014 |
format | article |
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H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS). None of the reported compounds exhibited significant iNOS or nNOS inhibition, although the 1-benzyl-3-(2-amino-5-chlorobenzoyl)-1
H-pyrazole-5-carboxylic acid ethyl ester derivative (
10l), which shows an inhibition of 50% versus iNOS at a 1
mM final concentration and no activity against nNOS, is potentially amenable of further optimization. The reasons for the inactivity of the reported series are discussed on the basis of docking studies.
[Display omitted] The synthesis and preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS) are described.</description><identifier>ISSN: 0223-5234</identifier><identifier>EISSN: 1768-3254</identifier><identifier>DOI: 10.1016/j.ejmech.2008.01.014</identifier><identifier>PMID: 18325637</identifier><identifier>CODEN: EJMCA5</identifier><language>eng</language><publisher>Kidlington: Elsevier Masson SAS</publisher><subject>Alkylation ; Analytical, structural and metabolic biochemistry ; Animals ; Benzoyl-pyrazole ; Benzoyl-pyrazoline ; Biological and medical sciences ; Enzyme Inhibitors - chemical synthesis ; Enzyme Inhibitors - chemistry ; Enzyme Inhibitors - pharmacology ; Enzymes and enzyme inhibitors ; Fundamental and applied biological sciences. Psychology ; Inducible nitric oxide synthase ; Inhibition ; Male ; Medical sciences ; Miscellaneous ; Models, Molecular ; Molecular Structure ; Neural nitric oxide synthase ; Nitric Oxide Synthase Type I - antagonists & inhibitors ; Nitric Oxide Synthase Type I - metabolism ; Nitric Oxide Synthase Type II - antagonists & inhibitors ; Nitric Oxide Synthase Type II - metabolism ; Oxidoreductases ; Pharmacology. Drug treatments ; Protein Binding ; Pyrazoles - chemical synthesis ; Pyrazoles - chemistry ; Pyrazoles - pharmacology ; Rats ; Rats, Wistar ; Structure-Activity Relationship</subject><ispartof>European journal of medicinal chemistry, 2008-11, Vol.43 (11), p.2579-2591</ispartof><rights>2008 Elsevier Masson SAS</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-a634a8316f59d06c0c8b1564270301e9174289483feb2209f7aaaa29cca35df83</citedby><cites>FETCH-LOGICAL-c456t-a634a8316f59d06c0c8b1564270301e9174289483feb2209f7aaaa29cca35df83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20875887$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18325637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carrión, M. Dora</creatorcontrib><creatorcontrib>López Cara, Luisa C.</creatorcontrib><creatorcontrib>Camacho, M. Encarnación</creatorcontrib><creatorcontrib>Tapias, Víctor</creatorcontrib><creatorcontrib>Escames, Germaine</creatorcontrib><creatorcontrib>Acuña-Castroviejo, Darío</creatorcontrib><creatorcontrib>Espinosa, Antonio</creatorcontrib><creatorcontrib>Gallo, Miguel A.</creatorcontrib><creatorcontrib>Entrena, Antonio</creatorcontrib><title>Pyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III)</title><title>European journal of medicinal chemistry</title><addtitle>Eur J Med Chem</addtitle><description>We have previously described a series of 4,5-dihydro-1
H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS). None of the reported compounds exhibited significant iNOS or nNOS inhibition, although the 1-benzyl-3-(2-amino-5-chlorobenzoyl)-1
H-pyrazole-5-carboxylic acid ethyl ester derivative (
10l), which shows an inhibition of 50% versus iNOS at a 1
mM final concentration and no activity against nNOS, is potentially amenable of further optimization. The reasons for the inactivity of the reported series are discussed on the basis of docking studies.
[Display omitted] The synthesis and preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS) are described.</description><subject>Alkylation</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Benzoyl-pyrazole</subject><subject>Benzoyl-pyrazoline</subject><subject>Biological and medical sciences</subject><subject>Enzyme Inhibitors - chemical synthesis</subject><subject>Enzyme Inhibitors - chemistry</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Enzymes and enzyme inhibitors</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Inducible nitric oxide synthase</subject><subject>Inhibition</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Models, Molecular</subject><subject>Molecular Structure</subject><subject>Neural nitric oxide synthase</subject><subject>Nitric Oxide Synthase Type I - antagonists & inhibitors</subject><subject>Nitric Oxide Synthase Type I - metabolism</subject><subject>Nitric Oxide Synthase Type II - antagonists & inhibitors</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Oxidoreductases</subject><subject>Pharmacology. Drug treatments</subject><subject>Protein Binding</subject><subject>Pyrazoles - chemical synthesis</subject><subject>Pyrazoles - chemistry</subject><subject>Pyrazoles - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Structure-Activity Relationship</subject><issn>0223-5234</issn><issn>1768-3254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kE1r3DAQhkVpaTZp_0EpujQkB29HH5blS6GEfiyEptD2LGR5zGrxylvJDtn8-sr10twqBjSDnncQDyFvGKwZMPV-t8bdHt12zQH0Glgu-YysWKV0IXgpn5MVcC6Kkgt5Rs5T2gFAqQBekjOmM6FEtSLx-zHax6HHRG1o6WGZfJjnRANO0fZ_X3xoJ-ebHmnwY_SODg--RZqOYdzahPQqfLv7sZC5uaaHYcQw-pz2YesbPw4x0avNZnP9irzobJ_w9em-IL8-f_p587W4vfuyufl4WzhZqrGwSkirBVNdWbegHDjdsFJJXoEAhjWrJNe11KLDhnOou8rmw2vnrCjbTosLcrnsPcTh94RpNHufHPa9DThMyai64oJLmUG5gC4OKUXszCH6vY1Hw8DMrs3OLK7N7NoAyzXH3p72T80e26fQSW4G3p0Am5ztu2iD8-kfx0FXpdYz92HhMNu49xhNch6Dw9ZHdKNpB___n_wBdwyeMA</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Carrión, M. 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Encarnación ; Tapias, Víctor ; Escames, Germaine ; Acuña-Castroviejo, Darío ; Espinosa, Antonio ; Gallo, Miguel A. ; Entrena, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-a634a8316f59d06c0c8b1564270301e9174289483feb2209f7aaaa29cca35df83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Alkylation</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Benzoyl-pyrazole</topic><topic>Benzoyl-pyrazoline</topic><topic>Biological and medical sciences</topic><topic>Enzyme Inhibitors - chemical synthesis</topic><topic>Enzyme Inhibitors - chemistry</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Inducible nitric oxide synthase</topic><topic>Inhibition</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Models, Molecular</topic><topic>Molecular Structure</topic><topic>Neural nitric oxide synthase</topic><topic>Nitric Oxide Synthase Type I - antagonists & inhibitors</topic><topic>Nitric Oxide Synthase Type I - metabolism</topic><topic>Nitric Oxide Synthase Type II - antagonists & inhibitors</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Oxidoreductases</topic><topic>Pharmacology. Drug treatments</topic><topic>Protein Binding</topic><topic>Pyrazoles - chemical synthesis</topic><topic>Pyrazoles - chemistry</topic><topic>Pyrazoles - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carrión, M. Dora</creatorcontrib><creatorcontrib>López Cara, Luisa C.</creatorcontrib><creatorcontrib>Camacho, M. Encarnación</creatorcontrib><creatorcontrib>Tapias, Víctor</creatorcontrib><creatorcontrib>Escames, Germaine</creatorcontrib><creatorcontrib>Acuña-Castroviejo, Darío</creatorcontrib><creatorcontrib>Espinosa, Antonio</creatorcontrib><creatorcontrib>Gallo, Miguel A.</creatorcontrib><creatorcontrib>Entrena, Antonio</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carrión, M. Dora</au><au>López Cara, Luisa C.</au><au>Camacho, M. Encarnación</au><au>Tapias, Víctor</au><au>Escames, Germaine</au><au>Acuña-Castroviejo, Darío</au><au>Espinosa, Antonio</au><au>Gallo, Miguel A.</au><au>Entrena, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III)</atitle><jtitle>European journal of medicinal chemistry</jtitle><addtitle>Eur J Med Chem</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>43</volume><issue>11</issue><spage>2579</spage><epage>2591</epage><pages>2579-2591</pages><issn>0223-5234</issn><eissn>1768-3254</eissn><coden>EJMCA5</coden><abstract>We have previously described a series of 4,5-dihydro-1
H-pyrazole as moderately potent nNOS inhibitors. As a follow up of these studies, we report here the preparation and the preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS). None of the reported compounds exhibited significant iNOS or nNOS inhibition, although the 1-benzyl-3-(2-amino-5-chlorobenzoyl)-1
H-pyrazole-5-carboxylic acid ethyl ester derivative (
10l), which shows an inhibition of 50% versus iNOS at a 1
mM final concentration and no activity against nNOS, is potentially amenable of further optimization. The reasons for the inactivity of the reported series are discussed on the basis of docking studies.
[Display omitted] The synthesis and preliminary evaluation of a series of 1-alkyl-3-benzoyl-4,5-dihydro-1
H-pyrazole and 1-alkyl-3-benzoyl-1
H-pyrazole as potential inhibitors of both neuronal and inducible nitric oxide synthases (nNOS and iNOS) are described.</abstract><cop>Kidlington</cop><pub>Elsevier Masson SAS</pub><pmid>18325637</pmid><doi>10.1016/j.ejmech.2008.01.014</doi><tpages>13</tpages></addata></record> |
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source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Alkylation Analytical, structural and metabolic biochemistry Animals Benzoyl-pyrazole Benzoyl-pyrazoline Biological and medical sciences Enzyme Inhibitors - chemical synthesis Enzyme Inhibitors - chemistry Enzyme Inhibitors - pharmacology Enzymes and enzyme inhibitors Fundamental and applied biological sciences. Psychology Inducible nitric oxide synthase Inhibition Male Medical sciences Miscellaneous Models, Molecular Molecular Structure Neural nitric oxide synthase Nitric Oxide Synthase Type I - antagonists & inhibitors Nitric Oxide Synthase Type I - metabolism Nitric Oxide Synthase Type II - antagonists & inhibitors Nitric Oxide Synthase Type II - metabolism Oxidoreductases Pharmacology. Drug treatments Protein Binding Pyrazoles - chemical synthesis Pyrazoles - chemistry Pyrazoles - pharmacology Rats Rats, Wistar Structure-Activity Relationship |
title | Pyrazoles and pyrazolines as neural and inducible nitric oxide synthase (nNOS and iNOS) potential inhibitors (III) |
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