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Bioorganic and Medicinal Chemistry Letters

Volumn 23, Issue 12, 2013, Pages 3551-3555

Development of a triclosan scaffold which allows for adaptations on both the A- and B-ring for transport peptides

(12) Muench, Stephen P a Stec, Jozef b Zhou, Ying c Afanador, Gustavo A d McPhillie, Martin J e Hickman, Mark R f Lee, Patty J f Leed, Susan E f Auschwitz, Jennifer M g Prigge, Sean T d Rice, David W e McLeod, Rima c

a UNIVERSITY OF LEEDS (United Kingdom)

b UNIVERSITY OF ILLINOIS AT CHICAGO (United States)

c UNIVERSITY OF CHICAGO (United States)

d JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH (United States)

e UNIVERSITY OF SHEFFIELD (United Kingdom)

f Institute of Behavioral Research (United States)

g CHICAGO STATE UNIVERSITY (United States)

Author keywords

Enoyl reductase Triclosan Toxoplasma Plasmodium

Indexed keywords

PEPTIDE; SOLVENT; TRICLOSAN;

ANTIMALARIAL ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG DELIVERY SYSTEM; DRUG DESIGN; DRUG POTENCY; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IC 50; MINIMUM INHIBITORY CONCENTRATION; MOLECULAR DYNAMICS; PLASMODIUM FALCIPARUM; PROTEIN TRANSPORT; RING OPENING; SKIN FIBROBLAST;

BINDING SITES; CARRIER PROTEINS; ENOYL-(ACYL-CARRIER-PROTEIN) REDUCTASE (NADH); MODELS, MOLECULAR; PLASMODIUM FALCIPARUM; TOXOPLASMA; TRICLOSAN;

TOXOPLASMA;

EID: 84878106964 PISSN: 0960894X EISSN: 14643405 Source Type: Journal
DOI: 10.1016/j.bmcl.2013.04.035 Document Type: Article

Times cited : (12)

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