rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
14
|
pubmed:dateCreated |
1999-9-24
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pubmed:abstractText |
The synthesis of a novel antithrombotic consisting of a heparin pentasaccharide conjugated to the active site inhibitor N-(2-naphtalenesulfonyl)-glycyl-(D)-4-aminophenyl-alanyl-piperidin e (NAPAP) (i.e. compound I) is reported. This conjugate shows a unique pharmacological profile both in vitro and in vivo having direct anti-thrombin and ATIII-mediated anti-Xa activity. Furthermore, conjugate I has a prolonged in vivo half-life compared to NAPAP (1.5 h vs 9 min.).
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
0960-894X
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
19
|
pubmed:volume |
9
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2013-8
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10450972-Animals,
pubmed-meshheading:10450972-Antithrombins,
pubmed-meshheading:10450972-Carbohydrate Sequence,
pubmed-meshheading:10450972-Dipeptides,
pubmed-meshheading:10450972-Drug Design,
pubmed-meshheading:10450972-Factor Xa,
pubmed-meshheading:10450972-Half-Life,
pubmed-meshheading:10450972-Heparin,
pubmed-meshheading:10450972-Inhibitory Concentration 50,
pubmed-meshheading:10450972-Magnetic Resonance Spectroscopy,
pubmed-meshheading:10450972-Mass Spectrometry,
pubmed-meshheading:10450972-Molecular Sequence Data,
pubmed-meshheading:10450972-Oligosaccharides,
pubmed-meshheading:10450972-Piperidines,
pubmed-meshheading:10450972-Rats,
pubmed-meshheading:10450972-Solubility,
pubmed-meshheading:10450972-Thrombin
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pubmed:year |
1999
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pubmed:articleTitle |
Design and synthesis of a novel synthetic NAPAP-penta-saccharide conjugate displaying a dual antithrombotic action.
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pubmed:affiliation |
Leiden Institute of Chemistry, Gorlaeus Laboratories, The Netherlands.
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pubmed:publicationType |
Journal Article
|