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Volumn 53, Issue 3, 2010, Pages 1128-1137

Pyridinylquinoxalines and pyridinylpyridopyrazines as lead compounds for novel p38α mitogen-activated protein kinase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DICARBONYL DERIVATIVE; 2(3) (4 FLUOROPHENYL) 3 (2) (PYRIDIN 4 YL)QUINOXALINE; 2(3) (4 FLUOROPHENYL) 3(2) (PYRIDIN 4 YL)PYRIDOPYRAZINE; AMINOPYRIDINE DERIVATIVE; LEAD; MITOGEN ACTIVATED PROTEIN KINASE 14; MITOGEN ACTIVATED PROTEIN KINASE P38 INHIBITOR; PHENYLENEDIAMINE DERIVATIVE; PYRAZINE DERIVATIVE; QUINOXALINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77249141072     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm901392x     Document Type: Article
Times cited : (35)

References (22)
  • 1
    • 0035413618 scopus 로고    scopus 로고
    • Chen, Z.; Gibson, T. B.; Robinson, F.; Silvestro, L.; Pearson, G.; Xu, B.; Wright, A.; Vanderbilt, C.; Cobb, M. H. MAP kinases. Chem. Rev. 2001, 101, 2449-2476.
    • Chen, Z.; Gibson, T. B.; Robinson, F.; Silvestro, L.; Pearson, G.; Xu, B.; Wright, A.; Vanderbilt, C.; Cobb, M. H. MAP kinases. Chem. Rev. 2001, 101, 2449-2476.
  • 2
    • 0142026209 scopus 로고    scopus 로고
    • p38 MAP kinases: Key signalling molecules as therapeutic targets for inflammatory diseases
    • Kumar, S.; Boehm, J.; Lee, J. C. p38 MAP kinases: Key signalling molecules as therapeutic targets for inflammatory diseases. Nat. Rev. Drug Discovery 2003, 2, 717-726.
    • (2003) Nat. Rev. Drug Discovery , vol.2 , pp. 717-726
    • Kumar, S.1    Boehm, J.2    Lee, J.C.3
  • 3
    • 29144511607 scopus 로고    scopus 로고
    • MAPK signalling pathways as molecular targets for anti-inflammatory therapy: From molecular mechanisms to therapeutic benefits
    • Kaminska, B. MAPK signalling pathways as molecular targets for anti-inflammatory therapy: From molecular mechanisms to therapeutic benefits. Biochim. Biophys. Acta 2005, 1754, 253-262.
    • (2005) Biochim. Biophys. Acta , vol.1754 , pp. 253-262
    • Kaminska, B.1
  • 4
    • 52449118840 scopus 로고    scopus 로고
    • Targeting the ribose and phosphate binding site of p38 mitogen-activated protein (MAP) kinase: Synthesis and biological testing of 2-alkylsulfanyl-, 4(5)-aryl-, 5(4)-heteroaryl- substituted imidazoles
    • Koch, P.; Baeuerlein, C.; Jank, H.; Laufer, S. Targeting the ribose and phosphate binding site of p38 mitogen-activated protein (MAP) kinase: Synthesis and biological testing of 2-alkylsulfanyl-, 4(5)-aryl-, 5(4)-heteroaryl- substituted imidazoles. J. Med. Chem. 2008, 51, 5630-5640.
    • (2008) J. Med. Chem , vol.51 , pp. 5630-5640
    • Koch, P.1    Baeuerlein, C.2    Jank, H.3    Laufer, S.4
  • 5
    • 38549166647 scopus 로고    scopus 로고
    • Towards the improvement of the synthesis of novel 4(5)-aryl-5(4)-heteroaryl-2-thio-substituted imidazoles and their p38MAPkinase inhibitory activity
    • Laufer, S.; Koch, P. Towards the improvement of the synthesis of novel 4(5)-aryl-5(4)-heteroaryl-2-thio-substituted imidazoles and their p38MAPkinase inhibitory activity. Org. Biomol. Chem. 2008, 6, 437-439.
    • (2008) Org. Biomol. Chem , vol.6 , pp. 437-439
    • Laufer, S.1    Koch, P.2
  • 6
    • 33644873660 scopus 로고    scopus 로고
    • Small molecular anti-cykotine agents
    • Wagner, G.; Laufer, S. Small molecular anti-cykotine agents. Med. Res. Rev. 2006, 26, 1-62.
    • (2006) Med. Res. Rev , vol.26 , pp. 1-62
    • Wagner, G.1    Laufer, S.2
  • 7
    • 33947626488 scopus 로고    scopus 로고
    • From five- to six-membered rings: 3,4-Diarylquinolinone as lead for novelp38MAPkinase inhibitors
    • Peifer, C.; Kinkel, K.; Abadleh, M.; Schollmeyer, D.; Laufer, S. From five- to six-membered rings: 3,4-Diarylquinolinone as lead for novelp38MAPkinase inhibitors. J. Med. Chem. 2007, 50, 1213-1221.
    • (2007) J. Med. Chem , vol.50 , pp. 1213-1221
    • Peifer, C.1    Kinkel, K.2    Abadleh, M.3    Schollmeyer, D.4    Laufer, S.5
  • 8
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click chemistry: Diverse chemical function from a few good reactions. Angew. Chem., Int. Ed. 2001, 40, 2004-2021.
    • (2001) Angew. Chem., Int. Ed , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 9
    • 38949106966 scopus 로고    scopus 로고
    • Room temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid
    • Li, Z.; Li, W.; Sun, Y.; Huang, H.; Ouyang, P. Room temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid. J. Heterocycl. Chem. 2008, 45, 285-288.
    • (2008) J. Heterocycl. Chem , vol.45 , pp. 285-288
    • Li, Z.1    Li, W.2    Sun, Y.3    Huang, H.4    Ouyang, P.5
  • 10
    • 23744463590 scopus 로고    scopus 로고
    • Molecular iodine. A powerful catalyst for the easy and efficient synthesis of quinoxalines
    • More, S. V.; Sastry, M. N. V.; Wang, C. C.; Yao, C. F. Molecular iodine. A powerful catalyst for the easy and efficient synthesis of quinoxalines. Tetrahedron Lett. 2005, 46, 6345-6348.
    • (2005) Tetrahedron Lett , vol.46 , pp. 6345-6348
    • More, S.V.1    Sastry, M.N.V.2    Wang, C.C.3    Yao, C.F.4
  • 11
    • 33645404779 scopus 로고    scopus 로고
    • Cerium(IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, efficient and green approach to the synthesis of quinoxalines
    • More, S. V.; Sastry, M. N. V.; Yao, C. F. Cerium(IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, efficient and green approach to the synthesis of quinoxalines. Green Chem. 2006, 8, 91-95.
    • (2006) Green Chem , vol.8 , pp. 91-95
    • More, S.V.1    Sastry, M.N.V.2    Yao, C.F.3
  • 12
    • 2942519827 scopus 로고    scopus 로고
    • General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines
    • Zhao, Z.; Wisnoski, D. D.; Wolkenberg, S. E.; Leister, W. H.; Wang, Y.; Lindsley, C. W. General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines. Tetrahedron Lett. 2004, 45, 4873-4876.
    • (2004) Tetrahedron Lett , vol.45 , pp. 4873-4876
    • Zhao, Z.1    Wisnoski, D.D.2    Wolkenberg, S.E.3    Leister, W.H.4    Wang, Y.5    Lindsley, C.W.6
  • 14
    • 0001038733 scopus 로고    scopus 로고
    • Rational development of practical catalysts for aromatic carbon-nitrogen bond formation
    • Wolfe, J. P.; Wagaw, S.; Marcoux, J. F.; Buchwald, S. L. Rational development of practical catalysts for aromatic carbon-nitrogen bond formation. Acc. Chem. Res. 1998, 31, 805-818.
    • (1998) Acc. Chem. Res , vol.31 , pp. 805-818
    • Wolfe, J.P.1    Wagaw, S.2    Marcoux, J.F.3    Buchwald, S.L.4
  • 15
    • 70349758388 scopus 로고    scopus 로고
    • 3-(4-Fluorophenyl)-2-(4-pyridyl) pyrido[2,3-b]pyrazine
    • Koch, P.; Schollmeyer, D.; Laufer, S. 3-(4-Fluorophenyl)-2-(4-pyridyl) pyrido[2,3-b]pyrazine. Acta Crystallogr. 2009, E65, o2546.
    • (2009) Acta Crystallogr , vol.E65
    • Koch, P.1    Schollmeyer, D.2    Laufer, S.3
  • 16
    • 70349778753 scopus 로고    scopus 로고
    • 2-(4-Fluorophenyl)-3-(4-pyridyl) pyrido[2,3-b]pyrazine
    • Koch, P.; Schollmeyer, D.; Laufer, S. 2-(4-Fluorophenyl)-3-(4-pyridyl) pyrido[2,3-b]pyrazine. Acta Crystallogr. 2009, E65, o2512.
    • (2009) Acta Crystallogr , vol.E65
    • Koch, P.1    Schollmeyer, D.2    Laufer, S.3
  • 17
    • 67649836759 scopus 로고    scopus 로고
    • 4-[3-(4-Fluorophenyl)quinoxalin-2- yl]-N-isopropylpyridin-2-amine
    • Koch, P.; Schollmeyer, D.; Laufer, S. 4-[3-(4-Fluorophenyl)quinoxalin-2- yl]-N-isopropylpyridin-2-amine. Acta Crystallogr. 2009, E65, o1344.
    • (2009) Acta Crystallogr , vol.E65
    • Koch, P.1    Schollmeyer, D.2    Laufer, S.3
  • 18
    • 27644589566 scopus 로고    scopus 로고
    • An immunosorbent, nonradioactive p38 MAP kinase assay comparable to standard radioactive liquid-phase assays
    • Laufer, S.; Thuma, S.; Peifer, C.; Greim, C.; Herweh, Y.; Albrecht, A.; Dehner, F. An immunosorbent, nonradioactive p38 MAP kinase assay comparable to standard radioactive liquid-phase assays. Anal. Biochem. 2005, 344, 135-137.
    • (2005) Anal. Biochem , vol.344 , pp. 135-137
    • Laufer, S.1    Thuma, S.2    Peifer, C.3    Greim, C.4    Herweh, Y.5    Albrecht, A.6    Dehner, F.7
  • 20
    • 77249154091 scopus 로고    scopus 로고
    • Jaguar, version 7.5; Schroedinger, LLC: New York, 2008
    • Jaguar, version 7.5; Schroedinger, LLC: New York, 2008.
  • 21
    • 77249086649 scopus 로고    scopus 로고
    • Schroedinger Suite 2008, Induced Fit Docking Protocol. Glide, version 5.0; Schroedinger, LLC: New York, 2005
    • Schroedinger Suite 2008, Induced Fit Docking Protocol. Glide, version 5.0; Schroedinger, LLC: New York, 2005.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.