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Volumn 44, Issue 11, 2015, Pages 5004-5016

New AMD3100 derivatives for CXCR4 chemokine receptor targeted molecular imaging studies: Synthesis, anti-HIV-1 evaluation and binding affinities

(10) Poty, Sophie a Désogère, Pauline a Goze, Christine a Boschetti, Frédéric b D'huys, Thomas c Schols, Dominique c Cawthorne, Christopher d Archibald, Stephen J d Maëcke, Helmut R e Denat, Franck a

a UNIVERSITÉ DE BOURGOGNE (France)

b CheMatech (France)

c REGA INSTITUTE FOR MEDICAL RESEARCH (Belgium)

d UNIVERSITY OF HULL (United Kingdom)

e UNIVERSITY OF FREIBURG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODIES; BINDING ENERGY; ISOTOPES; MONOCLONAL ANTIBODIES; REACTION INTERMEDIATES; STEM CELLS;

BINDING AFFINITIES; CHEMOKINE RECEPTOR ANTAGONISTS; CHEMOKINE RECEPTORS; FLUORESCENT PROBES; HAEMATOPOIETIC STEM CELLS; POSITRON-EMITTING ISOTOPES; STRUCTURAL MODIFICATIONS; THERAPEUTIC DRUGS;

MOLECULAR IMAGING;

4,4-DIFLUORO-4-BORA-3A,4A-DIAZA-S-INDACENE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; BORON DERIVATIVE; CHEMOKINE RECEPTOR CXCR4; HETEROCYCLIC COMPOUND; PLERIXAFOR;

CALCIUM SIGNALING; CHEMISTRY; DRUG DESIGN; DRUG EFFECTS; HALOGENATION; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS 1; JURKAT CELL LINE; METABOLISM; POSITRON EMISSION TOMOGRAPHY; SYNTHESIS;

ANTI-HIV AGENTS; BORON COMPOUNDS; CALCIUM SIGNALING; CHEMISTRY TECHNIQUES, SYNTHETIC; DRUG DESIGN; HALOGENATION; HETEROCYCLIC COMPOUNDS; HIV-1; HUMANS; JURKAT CELLS; POSITRON-EMISSION TOMOGRAPHY; RECEPTORS, CXCR4;

EID: 84924308992 PISSN: 14779226 EISSN: 14779234 Source Type: Journal
DOI: 10.1039/c4dt02972k Document Type: Article

Times cited : (32)

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