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Volumn 24, Issue 4, 2016, Pages 545-553
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Active site-directed plasmin inhibitors: Extension on the P2 residue
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Author keywords
Active site directed inhibitor; Plasmin inhibitor; Selectivity; Urokinase
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Indexed keywords
N (4 AMINOMETHYLCYCLOHEXANECARBONYL) LEVO TYR[O (QUINOLIN 2 YL)METHYL] NH OCTYL;
PLASMIN;
PLASMIN INHIBITOR;
TRIFLUOROACETIC ACID;
UNCLASSIFIED DRUG;
UROKINASE;
ANTIFIBRINOLYTIC AGENT;
TYROSINE;
ARTICLE;
CHEMICAL STRUCTURE;
COMPLEX FORMATION;
ENANTIOSELECTIVITY;
ENZYME ACTIVE SITE;
ENZYME INHIBITION;
ENZYME SUBSTRATE COMPLEX;
HYDROPHOBICITY;
MOLECULAR DOCKING;
MOLECULAR INTERACTION;
ANTAGONISTS AND INHIBITORS;
CHEMISTRY;
DOSE RESPONSE;
DRUG EFFECTS;
HUMAN;
METABOLISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
ANTIFIBRINOLYTIC AGENTS;
CATALYTIC DOMAIN;
DOSE-RESPONSE RELATIONSHIP, DRUG;
FIBRINOLYSIN;
HUMANS;
MOLECULAR DOCKING SIMULATION;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
TYROSINE;
UROKINASE-TYPE PLASMINOGEN ACTIVATOR;
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EID: 84956738192
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2015.12.009 Document Type: Article |
Times cited : (9)
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References (24)
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