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Angewandte Chemie - International Edition

Volumn 53, Issue 47, 2014, Pages 12827-12831

Combining topology and sequence design for the discovery of potent antimicrobial peptide dendrimers against multidrug-resistant pseudomonas aeruginosa

(6) Stach, Michaela a Siriwardena, Thissa N a Köhler, Thilo b Van Delden, Christian b Darbre, Tamis a Reymond, Jean Louis a

a UNIVERSITY OF BERN (Switzerland)

b UNIVERSITY OF GENEVA (Switzerland)

Author keywords

antibiotics; antimicrobial peptides; dendrimers; peptides; Pseudomonas aeruginosa

Indexed keywords

ANTIBIOTICS; BACTERIA; DENDRIMERS; HEALTH RISKS; MICROORGANISMS; PEPTIDES; POLYPEPTIDES; PUBLIC HEALTH; TOPOLOGY;

AMINO ACID SEQUENCE; ANTIMICROBIAL PEPTIDE; BACTERIAL PATHOGENS; CLINICAL ISOLATES; MULTIDRUG RESISTANTS; PEPTIDE DENDRIMERS; PEPTIDE SEQUENCES; PSEUDOMONAS AERUGINOSA;

ANTIMICROBIAL AGENTS;

ANTIMICROBIAL CATIONIC PEPTIDE; DENDRIMER;

CHEMISTRY; CONFORMATION; DRUG DEVELOPMENT; DRUG EFFECTS; MICROBIAL SENSITIVITY TEST; MULTIDRUG RESISTANCE; PSEUDOMONAS AERUGINOSA; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

ANTIMICROBIAL CATIONIC PEPTIDES; DENDRIMERS; DRUG DISCOVERY; DRUG RESISTANCE, MULTIPLE, BACTERIAL; MICROBIAL SENSITIVITY TESTS; MOLECULAR CONFORMATION; PSEUDOMONAS AERUGINOSA; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84911378146 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201409270 Document Type: Article

Times cited : (95)

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