Discovery and Structure−Activity Relationship of N-(Ureidoalkyl)-Benzyl-Piperidines As Potent Small Molecule CC Chemokine Receptor-3 (CCR3) Antagonists-Reference-Cited by-同舟云学术

Discovery and Structure−Activity Relationship of N-(Ureidoalkyl)-Benzyl-Piperidines As Potent Small Molecule CC Chemokine Receptor-3 (CCR3) Antagonists

Published:2002-07-11 Issue:17 Volume:45 Page:3794-3804
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

De Lucca George V.¹,Kim Ui T.¹,Johnson Curt¹,Vargo Brian J.¹,Welch Patricia K.¹,Covington Maryanne¹,Davies Paul¹,Solomon Kimberly A.¹,Newton Robert C.¹,Trainor George L.¹,Decicco Carl P.¹,Ko Soo S.¹

Affiliation:

1. Bristol-Myers Squibb Company, Experimental Station, Wilmington, Delaware 19880-0336

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0201767

Reference40 articles.

1. Molecular Cloning of Human Eotaxin, an Eosinophil-selective CC Chemokine, and Identification of a Specific Eosinophil Eotaxin Receptor, CC Chemokine Receptor 3

2. Eotaxin-2, a Novel CC Chemokine that Is Selective for the Chemokine Receptor CCR3, and Acts Like Eotaxin on Human Eosinophil and Basophil Leukocytes

3. Molecular Cloning of a Novel Human CC Chemokine (Eotaxin-3) That Is a Functional Ligand of CC Chemokine Receptor 3

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