The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27419473 |
4 |
Neolignans from the Arils of Myristica fragrans as Potent Antagonists of CC Chemokine Receptor 3. |
Kindai University |
25497216 |
99 |
Rodent selectivity of piperidine-4-yl-1H-indoles, a series of CC chemokine receptor-3 (CCR3) antagonists: insights from a receptor model. |
Boehringer Ingelheim Pharma |
23142617 |
57 |
Discovery and evolution of phenoxypiperidine hydroxyamide dual CCR3/H1 antagonists. Part I. |
Astrazeneca |
23116889 |
88 |
Discovery and evolution of phenoxypiperidine hydroxyamide dual CCR3/H1 antagonists. Part II: optimising in vivo clearance. |
Astrazeneca |
23075267 |
85 |
Discovery and lead optimization of a novel series of CC chemokine receptor 1 (CCR1)-selective piperidine antagonists via parallel synthesis. |
Bristol-Myers Squibb |
22931505 |
69 |
Chemokine receptor antagonists. |
National Heart and Lung Institute |
23031591 |
90 |
The discovery of CCR3/H1 dual antagonists with reduced hERG risk. |
Astrazeneca |
23046963 |
23 |
Pyrrolidinyl phenylurea derivatives as novel CCR3 antagonists. |
Toray Industries |
23031649 |
4 |
The therapeutic journey of benzimidazoles: a review. |
Punjabi University |
23021991 |
153 |
Scaffold-hopping with zwitterionic CCR3 antagonists: identification and optimisation of a series with good potency and pharmacokinetics leading to the discovery of AZ12436092. |
Astrazeneca |
22749826 |
28 |
Discovery and structure-activity relationships of urea derivatives as potent and novel CCR3 antagonists. |
Toray Industries |
18752960 |
48 |
Design and synthesis of 6-fluoro-2-naphthyl derivatives as novel CCR3 antagonists with reduced CYP2D6 inhibition. |
Astellas Pharma |
17951061 |
20 |
Synthesis and structure-activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists. |
Astellas Pharma |
18096386 |
131 |
From rigid cyclic templates to conformationally stabilized acyclic scaffolds. Part I: the discovery of CCR3 antagonist development candidate BMS-639623 with picomolar inhibition potency against eosinophil chemotaxis. |
Bristol-Myers Squibb |
16198561 |
99 |
Novel CCR1 antagonists with oral activity in the mouse collagen induced arthritis. |
Novartis Institutes For Biomedical Research |
14505678 |
21 |
Design and synthesis of novel CCR3 antagonists. |
Roche Palo Alto |
21940167 |
12 |
Design and synthesis of a library of chemokine antagonists. |
Novartis Institutes of Biomedical Research |
21341682 |
37 |
Discovery, optimization, and pharmacological characterization of novel heteroaroylphenylureas antagonists of C-C chemokine ligand 2 function. |
Telik |
19674898 |
31 |
Spiropiperidine CCR5 antagonists. |
Roche Palo Alto |
19620010 |
43 |
Synthesis, biological evaluation, and metabolic stability of acrylamide derivatives as novel CCR3 antagonists. |
Astellas Pharma |
19131247 |
42 |
Discovery of trisubstituted cyclohexanes as potent CC chemokine receptor 2 (CCR2) antagonists. |
Bristol-Myers Squibb |
19014885 |
32 |
Discovery of a potent, selective and orally bioavailable 3,9-diazaspiro[5.5]undeca-2-one CCR5 antagonist. |
Roche Palo Alto |
19010676 |
28 |
Urea based CCR3 antagonists employing a tetrahydro-1,3-oxazin-2-one spacer. |
Bristol-Myers Squibb |
18160284 |
46 |
From rigid cyclic templates to conformationally stabilized acyclic scaffolds. Part II: Acyclic replacements for the (3S)-3-benzylpiperidine in a series of potent CCR3 antagonists. |
Bristol-Myers Squibb |
17720492 |
107 |
Capped diaminopropionamide-glycine dipeptides are inhibitors of CC chemokine receptor 2 (CCR2). |
Bristol-Myers Squibb |
17532633 |
29 |
Pyrazolone methylamino piperidine derivatives as novel CCR3 antagonists. |
Ucb Pharma |
17418570 |
141 |
CC chemokine receptor-3 (CCR3) antagonists: improving the selectivity of DPC168 by reducing central ring lipophilicity. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
16931001 |
93 |
2,4-Disubstituted piperidines as selective CC chemokine receptor 3 (CCR3) antagonists: synthesis and selectivity. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
16698264 |
37 |
Discovery of 3,5-bis(trifluoromethyl)benzyl L-arylglycinamide based potent CCR2 antagonists. |
Merck Research Laboratories |
16539392 |
29 |
Highly potent and orally active CCR5 antagonists as anti-HIV-1 agents: synthesis and biological activities of 1-benzazocine derivatives containing a sulfoxide moiety. |
Takeda Pharmaceutical |
15908209 |
25 |
The synthesis of substituted bipiperidine amide compounds as CCR3 ligands: antagonists versus agonists. |
Schering-Plough Research Institute |
15771462 |
125 |
Discovery of CC chemokine receptor-3 (CCR3) antagonists with picomolar potency. |
Pharmaceutical Research Institute |
15743194 |
91 |
Novel ligands for the chemokine receptor-3 (CCR3): a receptor-modeling study based on 5D-QSAR. |
Biographics Laboratory 3R |
15713390 |
53 |
The synthesis of substituted bipiperidine amide compounds as CCR3 antagonists. |
Schering-Plough Research Institute |
15664858 |
36 |
N-Arylalkylpiperidine urea derivatives as CC chemokine receptor-3 (CCR3) antagonists. |
Dbristol-Myers Squibb |
15664834 |
31 |
Pyrrolidinohydroquinazolines--a novel class of CCR3 modulators. |
Boehringer Ingelheim Pharma Gmbh And |
15026042 |
50 |
Discovery of N-propylurea 3-benzylpiperidines as selective CC chemokine receptor-3 (CCR3) antagonists. |
Bristol-Myers Squibb Pharmaceutical Research Institute |
12166951 |
146 |
Discovery and structure-activity relationship of N-(ureidoalkyl)-benzyl-piperidines as potent small molecule CC chemokine receptor-3 (CCR3) antagonists. |
Bristol-Myers Squibb |
12067561 |
97 |
CCR3 antagonists: a potential new therapy for the treatment of asthma. Discovery and structure-activity relationships. |
Bristol-Myers Squibb |
11720852 |
51 |
Design, synthesis, and SAR of heterocycle-containing antagonists of the human CCR5 receptor for the treatment of HIV-1 infection. |
Merck Research Laboratories |
11720851 |
52 |
Discovery of human CCR5 antagonists containing hydantoins for the treatment of HIV-1 infection. |
Merck Research Laboratories |
11378374 |
39 |
Discovery of potent and selective phenylalanine derived CCR3 receptor antagonists. Part 2. |
Smithkline Beecham Pharmaceuticals |
11378373 |
35 |
Discovery of potent and selective phenylalanine derived CCR3 antagonists. Part 1. |
Smithkline Beecham Pharmaceuticals |
11354381 |
19 |
Discovery of a novel CCR3 selective antagonist. |
Banyu Tsukuba Research Institute |
11311066 |
76 |
Design, synthesis, and discovery of a novel CCR1 antagonist. |
Banyu Tsukuba Research Institute In Collaboration With Merck Research Laboratories |
11206474 |
51 |
Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: structure-activity relationships for substituted 2-Aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes. |
Merck Research Laboratories |
10821717 |
29 |
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. |
Takeda Chemical Industries |
29406702 |
128 |
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists. |
Gsk Pharmaceuticals R & D |