000 01407 a2200385 4500
005 20250516074303.0
264 0 _c20120423
008 201204s 0 0 eng d
022 _a1520-4804
024 7 _a10.1021/jm2011996
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSaupe, Sebastian M
245 0 0 _aA new strategy for the development of highly potent and selective plasmin inhibitors.
_h[electronic resource]
260 _bJournal of medicinal chemistry
_cFeb 2012
300 _a1171-80 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAmino Acid Sequence
650 0 4 _aAntifibrinolytic Agents
_xchemical synthesis
650 0 4 _aCyclization
650 0 4 _aDipeptides
_xchemical synthesis
650 0 4 _aEnzyme Assays
650 0 4 _aFibrinolysin
_xmetabolism
650 0 4 _aKinetics
650 0 4 _aModels, Molecular
650 0 4 _aMolecular Sequence Data
650 0 4 _aPeptides, Cyclic
_xchemical synthesis
650 0 4 _aPeptidomimetics
_xchemical synthesis
650 0 4 _aProtein Conformation
650 0 4 _aStereoisomerism
650 0 4 _aStructure-Activity Relationship
650 0 4 _aTriazoles
_xchemical synthesis
700 1 _aSteinmetzer, Torsten
773 0 _tJournal of medicinal chemistry
_gvol. 55
_gno. 3
_gp. 1171-80
856 4 0 _uhttps://doi.org/10.1021/jm2011996
_zAvailable from publisher's website
999 _c21490915
_d21490915