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Volumn 19, Issue 3, 2009, Pages 295-303

Recent developments in CCR2 antagonists

Author keywords

Asthma; CCR2 antagonist; MCP 1; Multiple sclerosis; Rheumatoid arthritis

Indexed keywords

1H INDOLE 2 CARBOXYLIC ACID N (PIPERIDIN 4 YL)AMIDE; [3 ISOPROPYL 3 [[3 (TRIFLUOROMETHYL) 7,8 DIHYDRO 1,6 NAPHTHYRIDIN 6(5H) YL]CARBONYL]CYCLOPENTYL][3 METHOXYTETRAHYDRO 2H PYRAN 4 YL]AMINE SALT; AMINOPYRROLIDINE DERIVATIVE; BENZOTHIADIAZINE DERIVATIVE; BINDARIT; BMS 741672; CCX 140; CHEMOKINE RECEPTOR ANTAGONIST; CHEMOKINE RECEPTOR CCR2 ANTAGONIST; DEXAMETHASONE; DIAMINOPROPIONAMIDE GLYCINE DIPEPTIDE; DIPIPERIDINE DERIVATIVE; GSK 1344386B; INCB 3284; INCB 3344; INCB 8696; INDAZOLE DERIVATIVE; MERCAPTOIMIDAZOLE; MK 0812; N [3,5 BIS(TRIFLUOROMETHYL)BENZYL] 1 METHYL 3 METHYL 11H SPIRO[INDENE 1,44 PIPERIDIN] 11 YL]CYCLOPENTANECARBOXAMIDE; N PIPERIDINYLETHYLCYCLOHEXYL INDOLECARBOXAMIDE DERIVATIVE; NIBR 1282; NIBR 177; PIPERAZINE DERIVATIVE; PIPERIDINYLCARBOXAMIDE DERIVATIVE; PLACEBO; PYRROLIDIN 2 ONE DERIVATIVE; PYRROLIDINE DERIVATIVE; PYRROLIDINYLCARBOXAMIDE DERIVATIVE; QUATERNARY AMMONIUM DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 67649400529     PISSN: 13543776     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543770902755129     Document Type: Review
Times cited : (161)

References (42)
  • 2
    • 33846849095 scopus 로고    scopus 로고
    • Leishmania-derived murine monocyte chemoattractant protein 1 enhances the recruitment of a restrictive population of CC chemokine receptor 2-positive macrophages
    • DOI 10.1128/IAI.01314-06
    • Conrad SM, Strauss-Ayali D, Field AE, et al. Leishmania-derived murine monocyte chemoattractant protein 1 enhances the recruitment of a restrictive population of CC chemokine receptor 2-positive macrophages. Infect Immun 2007;75:653-665 (Pubitemid 46203427)
    • (2007) Infection and Immunity , vol.75 , Issue.2 , pp. 653-665
    • Conrad, S.M.1    Strauss-Ayali, D.2    Field, A.E.3    Mack, M.4    Mosser, D.M.5
  • 3
    • 0032572719 scopus 로고    scopus 로고
    • Decreased lesion formation in CCR2(-/-) mice reveals a role for chemokines in the initiation of atherosclerosis
    • DOI 10.1038/29788
    • Boring L, Gosling J, Cleary M, et al. Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis. Nature 1998;394:894-897 (Pubitemid 28410911)
    • (1998) Nature , vol.394 , Issue.6696 , pp. 894-897
    • Boring, L.1    Gosling, J.2    Cleary, M.3    Charo, I.F.4
  • 4
    • 29144443977 scopus 로고    scopus 로고
    • Chemokine receptor CCR2 expression by systemic sclerosis fibroblasts: Evidence for autocrine regulation of myofibroblast differentiation
    • DOI 10.1002/art.21396
    • Carulli MT, Ong VH, Ponticos M, et al. Chemokine receptor CCR2 expression by systemic sclerosis fibroblasts: evidence for autocrine regulation of myofibroblast differentiation. Arthritis Rheum 2005;52:3772-3782 (Pubitemid 41798215)
    • (2005) Arthritis and Rheumatism , vol.52 , Issue.12 , pp. 3772-3782
    • Carulli, M.T.1    Ong, V.H.2    Ponticos, M.3    Shiwen, X.4    Abraham, D.J.5    Black, C.M.6    Denton, C.P.7
  • 6
    • 7244242357 scopus 로고    scopus 로고
    • Chemokines in the pathogenesis of vascular disease
    • DOI 10.1161/01.RES.0000146672.10582.17
    • Charo IF, Taubman MB. Chemokines in the pathogenesis of Vascular Disease. Circ Res 2004;95:858-866 (Pubitemid 39435000)
    • (2004) Circulation Research , vol.95 , Issue.9 , pp. 858-866
    • Charo, I.F.1    Taubman, M.B.2
  • 9
    • 0030140458 scopus 로고    scopus 로고
    • Monocyte chemoattractant protein 1: A potential regulator of monocyte recruitment in inflammatory disease
    • DOI 10.1016/1357-4310(96)88772-7
    • Rollins BJ. Monocyte chemoattractant protein 1: a potential regulator of monocyte recruitment in inflammatory disease. Mol Med Today 1996;2:198-204 (Pubitemid 126401890)
    • (1996) Molecular Medicine Today , vol.2 , Issue.5 , pp. 198-204
    • Rollins, B.J.1
  • 11
    • 4344562943 scopus 로고    scopus 로고
    • New anti-inflammatory therapies and targets for asthma and chronic obstructive pulmonary disease
    • DOI 10.1517/14728222.8.4.265
    • Belvisi MG, Hele DJ, Birrell MA. New anti-inflammatory therapies and targets for asthma and chronic obstructive pulmonary disease. Expert Opin Ther Target 2004;8:265-285 (Pubitemid 39117693)
    • (2004) Expert Opinion on Therapeutic Targets , vol.8 , Issue.4 , pp. 265-285
    • Belvisi, M.G.1    Hele, D.J.2    Birrell, M.A.3
  • 12
    • 67649409926 scopus 로고    scopus 로고
    • Preparation of [(1R,3S)-3-isopropyl-3-[[3-(trifluoromethyl)-7,8-dihydro- 1,6-naphthyridin-6(5H)-yl]carbonyl] cyclopentyl][(3S,4S)-3-methoxytetrahydro-2H- pyran-4-yl]amine salt as chemokine receptor CCR-2 antagonist
    • Merck. WO2005044795
    • Merck.Preparation of [(1R,3S)-3-isopropyl-3-[[3-(trifluoromethyl)-7,8- dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl] cyclopentyl][(3S,4S)-3- methoxytetrahydro-2H-pyran-4-yl]amine salt as chemokine receptor CCR-2 antagonist. WO2005044795; 2005
    • (2005)
  • 15
    • 67649390530 scopus 로고    scopus 로고
    • Preparation of mercaptoimidazoles as CCR2 receptor antagonists
    • Janssen. WO2005118578
    • Janssen. Preparation of mercaptoimidazoles as CCR2 receptor antagonists. WO2005118578; 2005
    • (2005)
  • 16
    • 67649408492 scopus 로고    scopus 로고
    • Substituted dipiperidines as CCR2 antagonists, their preparation, pharmaceutical compositions, and use in therapy
    • Janssen. US2006069123
    • Janssen. Substituted dipiperidines as CCR2 antagonists, their preparation, pharmaceutical compositions, and use in therapy. US2006069123; 2006
    • (2006)
  • 17
    • 67649387736 scopus 로고    scopus 로고
    • Preparation of quaternary ammonium salts as chemoattractant cytokine receptor 2 antagonists
    • Janssen. WO2006012135
    • Janssen. Preparation of quaternary ammonium salts as chemoattractant cytokine receptor 2 antagonists. WO2006012135; 2006
    • (2006)
  • 18
    • 67649413966 scopus 로고    scopus 로고
    • Substituted cyclopentyl piperidine CCR2 antagonists for treatment of CCR2 -mediated inflammatory syndromes and disorders
    • Janssen. WO2008109238
    • Janssen. Substituted cyclopentyl piperidine CCR2 antagonists for treatment of CCR2 -mediated inflammatory syndromes and disorders. WO2008109238; 2008
    • (2008)
  • 20
    • 52649182235 scopus 로고    scopus 로고
    • Pharmacological profile of JNJ-27141491 [(S)-3-[(3,4-difluorophenyl) propyl]-5-isoxazol-5-yl-2-thioxo-2,3-dihydro-1Himidazole- 4-carboxyl acid methyl ester], as a noncompetitive and orally active antagonist of the human chemokine receptor CCR2
    • Buntinx M, Hermans B, Goossens J, et al. Pharmacological profile of JNJ-27141491 [(S)-3-[(3,4-difluorophenyl)propyl]-5-isoxazol-5-yl-2-thioxo-2,3- dihydro-1Himidazole- 4-carboxyl acid methyl ester], as a noncompetitive and orally active antagonist of the human chemokine receptor CCR2. J Pharmacol Exp Ther 2008;327:1-9
    • (2008) J Pharmacol Exp Ther , vol.327 , pp. 1-9
    • Buntinx, M.1    Hermans, B.2    Goossens, J.3
  • 21
    • 67649408490 scopus 로고    scopus 로고
    • Preparation of 3-cycloalkylaminopyrrolidine chemokine receptor antagonists as antiinflammatory and immunomodulatory bioactive compounds
    • Incyte. WO2005060665
    • Incyte. Preparation of 3-cycloalkylaminopyrrolidine chemokine receptor antagonists as antiinflammatory and immunomodulatory bioactive compounds. WO2005060665; 2005
    • (2005)
  • 22
    • 67649407044 scopus 로고    scopus 로고
    • Preparation of piperidinyl and piperazinyl 3- aminocyclopentanecarboxamides as modulators of chemokine receptors
    • Pfizer. US2006004018
    • Pfizer. Preparation of piperidinyl and piperazinyl 3- aminocyclopentanecarboxamides as modulators of chemokine receptors. US2006004018; 2006
    • (2006)
  • 26
    • 76149100531 scopus 로고    scopus 로고
    • Preparation of pyrrolidin-2-one derivatives as chemokine receptor modulators
    • Bristol-Myers Squibb. WO2008014360
    • Bristol-Myers Squibb. Preparation of pyrrolidin-2-one derivatives as chemokine receptor modulators. WO2008014360; 2008
    • (2008)
  • 27
    • 67649392018 scopus 로고    scopus 로고
    • Preparation of 1H-indole-2- Carboxylic acid N-(piperidin-4-yl)amides and related derivatives as chemokine receptor, particularly CCR2 and CCR5 antagonists
    • Novartis. WO2005077932
    • Novartis. Preparation of 1H-indole-2- carboxylic acid N-(piperidin-4-yl)amides and related derivatives as chemokine receptor, particularly CCR2 and CCR5 antagonists. WO2005077932; 2005
    • (2005)
  • 28
    • 67649412823 scopus 로고    scopus 로고
    • Preparation of N-piperidinylethylcyclohexyl indolecarboxamide derivatives as inhibitors of chemokine receptors or macrophage protein
    • Novartis. WO2008101905
    • Novartis. Preparation of N-piperidinylethylcyclohexyl indolecarboxamide derivatives as inhibitors of chemokine receptors or macrophage protein. WO2008101905; 2008
    • (2008)
  • 29
    • 67649405756 scopus 로고    scopus 로고
    • Preparation of aryl and heteroaryl sulfonamides as CCR2 antagonists
    • ChemoCentryx. WO2006076644
    • ChemoCentryx. Preparation of aryl and heteroaryl sulfonamides as CCR2 antagonists. WO2006076644; 2006
    • (2006)
  • 30
    • 67649400100 scopus 로고    scopus 로고
    • Preparation of N-phenylbenzenesulfonamide derivatives as CCR2 inhibitors
    • ChemoCentryx. WO2008008374
    • ChemoCentryx. Preparation of N-phenylbenzenesulfonamide derivatives as CCR2 inhibitors. WO2008008374; 2008
    • (2008)
  • 31
    • 67649405754 scopus 로고    scopus 로고
    • N-(Triazolylpyridinyl)-benzenesulfonamides as chemokine receptor antagonists, their preparation, pharmaceutical compositions, and use in therapy
    • ChemoCentryx. WO2008008375
    • ChemoCentryx. N-(Triazolylpyridinyl)-benzenesulfonamides as chemokine receptor antagonists, their preparation, pharmaceutical compositions, and use in therapy. WO2008008375; 2008
    • (2008)
  • 32
    • 67649407042 scopus 로고    scopus 로고
    • Preparation of pyridinyl sulfonamide modulators of chemokine receptors
    • Glaxo. WO 2007067875
    • Glaxo. Preparation of pyridinyl sulfonamide modulators of chemokine receptors. WO 2007067875; 2007
    • (2007)
  • 33
    • 67649398545 scopus 로고    scopus 로고
    • Preparation of benzenesulfonamide inhibitors of CCR2 chemokine receptor
    • Glaxo. WO 2007014008
    • Glaxo. Preparation of benzenesulfonamide inhibitors of CCR2 chemokine receptor. WO 2007014008; 2007
    • (2007)
  • 34
    • 67649405757 scopus 로고    scopus 로고
    • Preparation of azolylmethylbenzenesulfonamides as CCR2 chemokine receptor antagonists
    • Glaxo. WO2007014054
    • Glaxo. Preparation of azolylmethylbenzenesulfonamides as CCR2 chemokine receptor antagonists. WO2007014054; 2007
    • (2007)
  • 35
    • 67649389136 scopus 로고    scopus 로고
    • Use of an indazolemethoxyalkanoic acid to prepare a pharmaceutical composition
    • Angelini. WO2008061671
    • Angelini. Use of an indazolemethoxyalkanoic acid to prepare a pharmaceutical composition. WO2008061671; 2008
    • (2008)
  • 36
    • 67649390529 scopus 로고    scopus 로고
    • Preparation of pyrrolidinylazepans and pyrrolidinyloxepanes as antagonists of CCR2 chemokine receptors
    • Millennium. WO2007053495
    • Millennium. Preparation of pyrrolidinylazepans and pyrrolidinyloxepanes as antagonists of CCR2 chemokine receptors. WO2007053495; 2007
    • (2007)
  • 37
    • 67649401448 scopus 로고    scopus 로고
    • Preparation of bipyrrolidine and thienylpyrrolidine derivatives as antagonists of CCR2
    • Millennium. WO2007053499
    • Millennium. Preparation of bipyrrolidine and thienylpyrrolidine derivatives as antagonists of CCR2. WO2007053499; 2007
    • (2007)
  • 38
    • 67649392020 scopus 로고    scopus 로고
    • Preparation of pyrrolidinylpiperidines and related compounds as antagonists of chemokine CCR2 inhibitors
    • Millennium. WO2007053498
    • Millennium. Preparation of pyrrolidinylpiperidines and related compounds as antagonists of chemokine CCR2 inhibitors. WO2007053498; 2007
    • (2007)
  • 39
    • 67649400099 scopus 로고    scopus 로고
    • Aminopyrrolidine derivatives as chemokine receptor antagonists and their preparation, pharmaceutical compositions and use in the treatment of autoimmune diseases
    • Abbott. WO2008060621
    • Abbott. Aminopyrrolidine derivatives as chemokine receptor antagonists and their preparation, pharmaceutical compositions and use in the treatment of autoimmune diseases. WO2008060621; 2008
    • (2008)
  • 40
    • 67649404361 scopus 로고    scopus 로고
    • Piperazine derivatives, processes for preparing them, pharmaceutical compositions containing them, and their use as antagonists of CC chemokines (CCR2b and CCR5) for the treatment of inflammatory diseases
    • Astrazeneca AB. WO2007071952
    • Astrazeneca AB. Piperazine derivatives, processes for preparing them, pharmaceutical compositions containing them, and their use as antagonists of CC chemokines (CCR2b and CCR5) for the treatment of inflammatory diseases. WO2007071952; 2007
    • (2007)
  • 41
    • 67649409924 scopus 로고    scopus 로고
    • Preparation of benzothiadiazine compounds and their use as chemokine receptor antagonists
    • Epix. WO2008045558
    • Epix. Preparation of benzothiadiazine compounds and their use as chemokine receptor antagonists. WO2008045558; 2008
    • (2008)
  • 42
    • 67649387735 scopus 로고    scopus 로고
    • Preparation of piperidinyl and pyrrolidinyl carboxamide compounds as chemokine receptor antagonists for treating diseases associated with monocyte, leukocyte, and lymphocyte accumulation
    • Epix. WO2008045564
    • Epix. Preparation of piperidinyl and pyrrolidinyl carboxamide compounds as chemokine receptor antagonists for treating diseases associated with monocyte, leukocyte, and lymphocyte accumulation. WO2008045564; 2008
    • (2008)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.