Source:http://linkedlifedata.com/resource/pubmed/id/15261268
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
|
pubmed:dateCreated |
2004-7-20
|
pubmed:abstractText |
A series of novel, highly potent 2-carboxyindole-based factor Xa inhibitors is described. Structural requirements for neutral ligands, which bind in the S1 pocket of factor Xa were investigated with the 2-carboxyindole scaffold. This privileged fragment assembly approach yielded a set of equipotent, selective inhibitors with structurally diverse neutral P1 substituents.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0960-894X
|
pubmed:author |
pubmed-author:BauerArminA,
pubmed-author:CzechJörgJ,
pubmed-author:DuddaAngelaA,
pubmed-author:EssrichMelanieM,
pubmed-author:LauxVolkerV,
pubmed-author:LorenzMartinM,
pubmed-author:MatterHansH,
pubmed-author:NazaréMarcM,
pubmed-author:RitterKurtK,
pubmed-author:SchreuderHermanH,
pubmed-author:UrmannMatthiasM,
pubmed-author:WehnerVolkmarV,
pubmed-author:WillDavid WDW
|
pubmed:issnType |
Print
|
pubmed:day |
16
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4191-5
|
pubmed:meshHeading | |
pubmed:year |
2004
|
pubmed:articleTitle |
Factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of neutral P1 substituents.
|
pubmed:affiliation |
Aventis Pharma Deutschland GmbH, D-65926 Frankfurt am Main, Germany. marc.nazare@aventis.com
|
pubmed:publicationType |
Journal Article
|