New therapeutics that modulate chemokine networks
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[1] R. Fernandez-Botran. A small-molecule antagonist of human and murine CCR1 receptors , 2001, Expert opinion on investigational drugs.
[2] H. Sarau,et al. Discovery of potent and selective phenylalanine derived CCR3 antagonists. Part 1. , 2001, Bioorganic & medicinal chemistry letters.
[3] H. Sarau,et al. Discovery of potent and selective phenylalanine derived CCR3 receptor antagonists. Part 2. , 2001, Bioorganic & medicinal chemistry letters.
[4] R. Hertzberg,et al. Identification of a Potent, Selective Non-peptide CXCR2 Antagonist That Inhibits Interleukin-8-induced Neutrophil Migration* , 1998, The Journal of Biological Chemistry.
[5] O. Nishimura,et al. Discovery of novel, potent, and selective small-molecule CCR5 antagonists as anti-HIV-1 agents: synthesis and biological evaluation of anilide derivatives with a quaternary ammonium moiety. , 2000, Journal of medicinal chemistry.
[6] M. Baes,et al. Lessons from knockout mice. I: Phenotypes of mice with peroxisome biogenesis disorders. , 2003, Advances in experimental medicine and biology.
[7] D. Hazuda,et al. 1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent anti-HIV activity. , 2001, Bioorganic & medicinal chemistry letters.
[8] R. Flinn. The challenges. , 1979, Delaware medical journal.
[9] M. Baggiolini,et al. The Ligands of CXC Chemokine Receptor 3, I-TAC, Mig, and IP10, Are Natural Antagonists for CCR3* , 2001, The Journal of Biological Chemistry.
[10] Serena Xu,et al. SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[11] M. Baggiolini,et al. Chemokines and their receptors in lymphocyte traffic and HIV infection. , 2000, Advances in immunology.
[12] A. Trkola,et al. HIV-1 escape from a small molecule, CCR5-specific entry inhibitor does not involve CXCR4 use , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[13] M. Maccoss,et al. Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 3: a proposed pharmacophore model for 1-[N-(methyl)-N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted)piperidin-1-yl]butanes. , 2001, Bioorganic & medicinal chemistry letters.
[14] M. Montjovent,et al. Extension of Recombinant Human RANTES by the Retention of the Initiating Methionine Produces a Potent Antagonist (*) , 1996, The Journal of Biological Chemistry.
[15] S. Mccombie,et al. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. I: 2(S)-methyl piperazine as a key pharmacophore element. , 2001, Bioorganic & medicinal chemistry letters.
[16] D. Taub,et al. Identification and Characterization of Small Molecule Functional Antagonists of the CCR1 Chemokine Receptor* , 1998, The Journal of Biological Chemistry.
[17] B. Rollins,et al. Chemokines and disease , 2001, Nature Immunology.
[18] M. Peck,et al. A Small Molecule Antagonist of Chemokine Receptors CCR1 and CCR3 , 2000, The Journal of Biological Chemistry.
[19] M. Maccoss,et al. 1,3,4-Trisubstituted Pyrrolidine CCR5 Receptor Antagonists. Part 1. Discovery of the Pyrrolidine Scaffold and Determination of Its Stereochemical Requirements. , 2001 .
[20] P. Murphy,et al. Cloning of complementary DNA encoding a functional human interleukin-8 receptor. , 1991, Science.
[21] J. Fujisawa,et al. Inhibitory Effects of Small-Molecule CCR5 Antagonists on Human Immunodeficiency Virus Type 1 Envelope-Mediated Membrane Fusion and Viral Replication , 2001, Antimicrobial Agents and Chemotherapy.
[22] M. Schwarz,et al. Interfering with chemokine networks--the hope for new therapeutics. , 1999, Current opinion in chemical biology.
[23] T. Schwartz,et al. A broad-spectrum chemokine antagonist encoded by Kaposi's sarcoma-associated herpesvirus. , 1997, Science.
[24] L. F. Kolakowski,et al. Functional and biochemical analysis of the cloned Duffy antigen: identity with the red blood cell chemokine receptor. , 1994, Blood.
[25] R. Horuk,et al. Species selectivity of a small molecule antagonist for the CCR1 chemokine receptor. , 2000, European journal of pharmacology.
[27] C. Power,et al. The strategy of blocking the chemokine system to combat disease , 2000, Immunological reviews.
[28] Pascal Poignard,et al. Highly Potent RANTES Analogues either Prevent CCR5-Using Human Immunodeficiency Virus Type 1 Infection In Vivo or Rapidly Select for CXCR4-Using Variants , 1999, Journal of Virology.
[29] W I Wood,et al. Structure and functional expression of a human interleukin-8 receptor. , 1991, Science.
[30] D. Hazuda,et al. Design, synthesis, and SAR of heterocycle-containing antagonists of the human CCR5 receptor for the treatment of HIV-1 infection. , 2001, Bioorganic & medicinal chemistry letters.
[31] A. Koch,et al. Selective lymphocyte chemokine receptor expression in the rheumatoid joint. , 2001, Arthritis and rheumatism.
[32] Paige Lacy,et al. A report from the International Eosinophil Society: eosinophils in a tug of war. , 2001, The Journal of allergy and clinical immunology.
[33] T. Schwartz,et al. Potent inhibition of HIV-1 infectivity in macrophages and lymphocytes by a novel CCR5 antagonist. , 1997, Science.
[34] A. Howell,et al. A randomized phase-II study of BB-10010 (macrophage inflammatory protein- 1alpha) in patients with advanced breast cancer receiving 5-fluorouracil, adriamycin, and cyclophosphamide chemotherapy. , 1998, Blood.
[35] B. Neustadt,et al. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. II. Discovery of 1-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4- methyl-4-[3(S)-methyl-4-[1(S)-[4-(trifluoromethyl)phenyl]ethyl]-1-piperazinyl]- piperidine N1-oxide (Sch-350634), an orally bioavailable, potent CCR5 antagonist. , 2001, Journal of medicinal chemistry.
[36] B. Rollins,et al. Structure/activity analysis of human monocyte chemoattractant protein-1 (MCP-1) by mutagenesis. Identification of a mutated protein that inhibits MCP-1-mediated monocyte chemotaxis. , 1994, The Journal of biological chemistry.
[37] A. Gronenborn,et al. Analysis of hydrophobicity in the α and β chemokine families and its relevance to dimerization , 1994 .
[38] T. Schwartz,et al. Is there a 'lock' for all agonist 'keys' in 7TM receptors? , 1996, Trends in pharmacological sciences.
[39] J. White,et al. Nonpeptide CXCR2 antagonist prevents neutrophil accumulation in hyperoxia-exposed newborn rats. , 2001, The Journal of pharmacology and experimental therapeutics.
[40] F. Balkwill,et al. Epithelial cancer cell migration: a role for chemokine receptors? , 2001, Cancer research.
[41] J. Moore,et al. AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor , 1998, Nature Medicine.
[42] J. Moore,et al. HIV-1 entry inhibitors: Evading the issue , 1999, Nature Medicine.
[43] M. Maze,et al. Role of Signal Transduction in Anesthetic Action , 1991 .
[44] M. Ishikawa,et al. Discovery of a novel CCR3 selective antagonist. , 2001, Bioorganic & medicinal chemistry letters.
[45] R. Solari,et al. An Interleukin 5 Mutant Distinguishes between Two Functional Responses in Human Eosinophils , 1997, The Journal of experimental medicine.
[46] M. Mack,et al. Aminooxypentane-RANTES Induces CCR5 Internalization but Inhibits Recycling: A Novel Inhibitory Mechanism of HIV Infectivity , 1998, The Journal of experimental medicine.
[47] J. Gong,et al. An Antagonist of Monocyte Chemoattractant Protein 1 (MCP-1) Inhibits Arthritis in the MRL-lpr Mouse Model , 1997, The Journal of experimental medicine.
[48] C. Cohen,et al. A chemokine receptor CCR-1 antagonist reduces renal fibrosis after unilateral ureter ligation. , 2002, The Journal of clinical investigation.
[49] Frank Diehl,et al. Identification of the Binding Site for a Novel Class of CCR2b Chemokine Receptor Antagonists , 2000, The Journal of Biological Chemistry.
[50] D. Hazuda,et al. Discovery of human CCR5 antagonists containing hydantoins for the treatment of HIV-1 infection. , 2001, Bioorganic & medicinal chemistry letters.
[51] T. Mcclanahan,et al. Involvement of chemokine receptors in breast cancer metastasis , 2001, Nature.
[52] A. Zlotnik,et al. Chemokines: a new classification system and their role in immunity. , 2000, Immunity.
[53] H. Sarau,et al. Identification of Potent, Selective Non-peptide CC Chemokine Receptor-3 Antagonist That Inhibits Eotaxin-, Eotaxin-2-, and Monocyte Chemotactic Protein-4-induced Eosinophil Migration* , 2000, The Journal of Biological Chemistry.
[54] I. Forbes,et al. Conformationally restricted indolopiperidine derivatives as potent CCR2B receptor antagonists. , 2001, Bioorganic & medicinal chemistry letters.
[55] Hiroaki Mitsuya,et al. Novel Low Molecular Weight Spirodiketopiperazine Derivatives Potently Inhibit R5 HIV-1 Infection through Their Antagonistic Effects on CCR5* , 2001, The Journal of Biological Chemistry.
[56] A. Naya,et al. Design, synthesis, and discovery of a novel CCR1 antagonist. , 2001, Journal of medicinal chemistry.
[57] Dominique Schols,et al. AMD3100, a Potent and Specific Antagonist of the Stromal Cell-Derived Factor-1 Chemokine Receptor CXCR4, Inhibits Autoimmune Joint Inflammation in IFN-γ Receptor-Deficient Mice1 , 2001, The Journal of Immunology.
[58] B. Rollins,et al. MCP-1 in Human Disease , 1999 .
[59] D. S. Garrett,et al. High-resolution solution structure of the beta chemokine hMIP-1 beta by multidimensional NMR. , 1994, Science.
[60] R. Strieter,et al. Chemokines in Disease , 1996 .
[61] M. Shiraishi. Discovery of Novel, Potent, and Selective Small‐Molecule CCR5 Antagonists as Anti‐HIV‐1 Agents: Synthesis and Biological Evaluation of Anilide Derivatives with a Quaternary Ammonium Moiety. , 2000 .
[62] E. De Clercq,et al. Synthesis and structure-activity relationships of phenylenebis(methylene)-linked bis-azamacrocycles that inhibit HIV-1 and HIV-2 replication by antagonism of the chemokine receptor CXCR4. , 1999, Journal of medicinal chemistry.
[63] J. Demartino,et al. Binding and Functional Properties of Recombinant and Endogenous CXCR3 Chemokine Receptors* , 1998, The Journal of Biological Chemistry.
[64] E. Clercq,et al. Inhibition of T-tropic HIV Strains by Selective Antagonization of the Chemokine Receptor CXCR4 , 1997, The Journal of experimental medicine.
[65] W. Sebald,et al. Conversion of human interleukin‐4 into a high affinity antagonist by a single amino acid replacement. , 1992, The EMBO journal.
[66] R. Ransohoff,et al. CCR1+/CCR5+ mononuclear phagocytes accumulate in the central nervous system of patients with multiple sclerosis. , 2001, The American journal of pathology.
[67] C. Weber,et al. A Non-peptide Functional Antagonist of the CCR1 Chemokine Receptor Is Effective in Rat Heart Transplant Rejection* , 2001, The Journal of Biological Chemistry.
[68] I. Charo,et al. Involvement of chemokine receptor 2 and its ligand, monocyte chemoattractant protein-1, in the development of atherosclerosis: lessons from knockout mice , 2001, Current opinion in lipidology.
[69] W. Greenlee,et al. Discovery of 4-[(Z)-(4-bromophenyl)- (ethoxyimino)methyl]-1'-[(2,4-dimethyl-3- pyridinyl)carbonyl]-4'-methyl-1,4'- bipiperidine N-oxide (SCH 351125): an orally bioavailable human CCR5 antagonist for the treatment of HIV infection. , 2001, Journal of medicinal chemistry.
[70] B. Dewald,et al. RANTES and MCP-3 Antagonists Bind Multiple Chemokine Receptors (*) , 1996, The Journal of Biological Chemistry.
[71] E A Emini,et al. Antagonists of the human CCR5 receptor as anti-HIV-1 agents. part 1: discovery and initial structure-activity relationships for 1 -amino-2-phenyl-4-(piperidin-1-yl)butanes. , 2001, Bioorganic & medicinal chemistry letters.
[72] A. H. Drummond,et al. BB-10010: an active variant of human macrophage inflammatory protein-1 alpha with improved pharmaceutical properties. , 1995, Blood.
[73] R. Horuk,et al. Discovery of novel non-peptide CCR1 receptor antagonists. , 1999, Journal of medicinal chemistry.
[74] D. Taub,et al. Identification and Characterization of a Potent, Selective, and Orally Active Antagonist of the CC Chemokine Receptor-1* , 2000, The Journal of Biological Chemistry.
[75] O. Nishimura,et al. A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[76] Edward J. Fuchs,et al. Pharmacokinetics and Safety of AMD-3100, a Novel Antagonist of the CXCR-4 Chemokine Receptor, in Human Volunteers , 2000, Antimicrobial Agents and Chemotherapy.
[77] R. Egan,et al. Effect of Sch 55700, a Humanized Monoclonal Antibody to Human Interleukin-5, on Eosinophilic Responses and Bronchial Hyperreactivity , 1999, Arzneimittelforschung.
[78] R. Horuk,et al. CCR1-specific non-peptide antagonist: efficacy in a rabbit allograft rejection model. , 2001, Immunology letters.
[79] M. Schwarz,et al. Recent developments in modulating chemokine networks , 1999 .
[80] I. Forbes,et al. CCR2B receptor antagonists: conversion of a weak HTS hit to a potent lead compound. , 2000, Bioorganic & Medicinal Chemistry Letters.
[81] M. Ishikawa,et al. Identification of a potent and nonpeptidyl ccr3 antagonist. , 2001, Biochemical and biophysical research communications.
[82] Berger Ea. HIV entry and tropism: the chemokine receptor connection. , 1997 .
[83] C. Mackay,et al. Chemokines and chemokine receptors in T-cell priming and Th1/Th2-mediated responses. , 1998, Immunology today.
[84] J. Hoxie,et al. CC-chemokines enhance the replication of T-tropic strains of HIV-1 in CD4(+) T cells: role of signal transduction. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[85] ANTAGONISTS OF MONOCYTE CHEMOATTRACTANT PROTEIN 1 IDENTIFIED BY MODIFICATION OF FUNCTIONALLY CRITICAL NH2-TERMINAL RESIDUES , 1995 .
[86] D. Hazuda,et al. Combinatorial synthesis of CCR5 antagonists. , 2001, Bioorganic & medicinal chemistry letters.