Structure function differences in nonpeptide CCR1 antagonists for human and mouse CCR1

Journal of Immunology

Volumn 170, Issue 4, 2003, Pages 1910-1916

  Onuffer, James ^a   McCarrick, Margaret A ^b,c   Dunning, Laura ^b   Liang, Meina ^b,d   Rosser, Mary ^a   Wei, Guo Ping ^b   Ng, Howard ^b,e   Horuk, Richard ^a  

^a BAYER AG   (Germany)

^b Discovery Research Group   (United States)

^c CELGENE CORPORATION   (United States)

^d Abgenix Inc   (United States)

^e GLAXOSMITHKLINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXYPIPERIDINE DERIVATIVE; BX 510; BX 511; BX 513; BX 514; BX 515; BX 516; BX 519; BX 520; BX 521; BX 522; BX 523; CARBENOID; CHEMOKINE RECEPTOR CCR1; DIBENZOTHIEPIN DERIVATIVE; G PROTEIN COUPLED RECEPTOR; PIPERIDINE; PIPERIDINE DERIVATIVE; RECEPTOR BLOCKING AGENT; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG POTENCY; DRUG RECEPTOR BINDING; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; SPECIES DIFFERENCE; STRUCTURE ACTIVITY RELATION;

EID: 0037442002     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.170.4.1910     Document Type: Article

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