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Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties.

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Title: Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties.
Authors: Kawai M; Cancer Research, Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, IL 60064, USA. megumi.kawai@abbott.com, BaMaung NY, Fidanze SD, Erickson SA, Tedrow JS, Sanders WJ, Vasudevan A, Park C, Hutchins C, Comess KM, Kalvin D, Wang J, Zhang Q, Lou P, Tucker-Garcia L, Bouska J, Bell RL, Lesniewski R, Henkin J, Sheppard GS
Source: Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2006 Jul 01; Vol. 16 (13), pp. 3574-7. Date of Electronic Publication: 2006 May 02.
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Science Ltd Country of Publication: England NLM ID: 9107377 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0960-894X (Print) Linking ISSN: 0960894X NLM ISO Abbreviation: Bioorg Med Chem Lett Subsets: MEDLINE
Database: MEDLINE Ultimate
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DbLabel: MEDLINE Ultimate
An: 16632353
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PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties.
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  Data: <searchLink fieldCode="AU" term="%22Kawai+M%22">Kawai M</searchLink>; Cancer Research, Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, IL 60064, USA. megumi.kawai@abbott.com<br /><searchLink fieldCode="AU" term="%22BaMaung+NY%22">BaMaung NY</searchLink><br /><searchLink fieldCode="AU" term="%22Fidanze+SD%22">Fidanze SD</searchLink><br /><searchLink fieldCode="AU" term="%22Erickson+SA%22">Erickson SA</searchLink><br /><searchLink fieldCode="AU" term="%22Tedrow+JS%22">Tedrow JS</searchLink><br /><searchLink fieldCode="AU" term="%22Sanders+WJ%22">Sanders WJ</searchLink><br /><searchLink fieldCode="AU" term="%22Vasudevan+A%22">Vasudevan A</searchLink><br /><searchLink fieldCode="AU" term="%22Park+C%22">Park C</searchLink><br /><searchLink fieldCode="AU" term="%22Hutchins+C%22">Hutchins C</searchLink><br /><searchLink fieldCode="AU" term="%22Comess+KM%22">Comess KM</searchLink><br /><searchLink fieldCode="AU" term="%22Kalvin+D%22">Kalvin D</searchLink><br /><searchLink fieldCode="AU" term="%22Wang+J%22">Wang J</searchLink><br /><searchLink fieldCode="AU" term="%22Zhang+Q%22">Zhang Q</searchLink><br /><searchLink fieldCode="AU" term="%22Lou+P%22">Lou P</searchLink><br /><searchLink fieldCode="AU" term="%22Tucker-Garcia+L%22">Tucker-Garcia L</searchLink><br /><searchLink fieldCode="AU" term="%22Bouska+J%22">Bouska J</searchLink><br /><searchLink fieldCode="AU" term="%22Bell+RL%22">Bell RL</searchLink><br /><searchLink fieldCode="AU" term="%22Lesniewski+R%22">Lesniewski R</searchLink><br /><searchLink fieldCode="AU" term="%22Henkin+J%22">Henkin J</searchLink><br /><searchLink fieldCode="AU" term="%22Sheppard+GS%22">Sheppard GS</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229107377%22">Bioorganic & medicinal chemistry letters</searchLink> [Bioorg Med Chem Lett] 2006 Jul 01; Vol. 16 (13), pp. 3574-7. <i>Date of Electronic Publication: </i>2006 May 02.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Science+Ltd%22">Elsevier Science Ltd </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9107377 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0960-894X (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220960894X%22">0960894X </searchLink><i>NLM ISO Abbreviation: </i>Bioorg Med Chem Lett <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=16632353
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        Value: 10.1016/j.bmcl.2006.03.085
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        Text: English
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              Text: 2006 Jul 01
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              Y: 2006
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