메뉴 건너뛰기




Volumn 58, Issue 4, 2015, Pages 1929-1939

Overcoming mutagenicity and ion channel activity: Optimization of selective spleen tyrosine kinase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; HETEROCYCLIC COMPOUND; POTASSIUM CHANNEL HERG; PROTEIN KINASE SYK INHIBITOR; PROTEIN KINASE INHIBITOR; PROTEIN TYROSINE KINASE;

EID: 84923878590     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm5018169     Document Type: Article
Times cited : (24)

References (35)
  • 2
    • 80051948193 scopus 로고    scopus 로고
    • New drugs beyond biologics in rheumatoid arthritis: The kinase inhibitors
    • Bonilla-Hernán, M. G.; Miranda-Carús, M. E.; Martin-Mola, E. New drugs beyond biologics in rheumatoid arthritis: The kinase inhibitors Rheumatology 2011, 50, 1542-1550
    • (2011) Rheumatology , vol.50 , pp. 1542-1550
    • Bonilla-Hernán, M.G.1    Miranda-Carús, M.E.2    Martin-Mola, E.3
  • 3
    • 33749023888 scopus 로고    scopus 로고
    • Mechanisms of disease: The molecular and cellular basis of joint destruction in rheumatoid arthritis
    • Müller-Ladner, U.; Pap, T.; Gay, R. E.; Neidhart, M.; Gay, S. Mechanisms of disease: The molecular and cellular basis of joint destruction in rheumatoid arthritis J. Clin. Pract. Rheumatol. 2005, 1, 102-110
    • (2005) J. Clin. Pract. Rheumatol. , vol.1 , pp. 102-110
    • Müller-Ladner, U.1    Pap, T.2    Gay, R.E.3    Neidhart, M.4    Gay, S.5
  • 4
    • 33745912510 scopus 로고    scopus 로고
    • Differential survival of leukocyte subsets mediated by synovial, bone marrow, and skin fibroblasts: Site-specific versus activation-dependent survival of T cells and neutrophils
    • Filer, A.; Parsonage, G.; Smith, E.; Osborne, C.; Thomas, A. M.; Curnow, S. J.; Rainger, G. E.; Raza, K.; Nash, G. B.; Lord, J.; Salmon, M.; Buckley, C. D. Differential survival of leukocyte subsets mediated by synovial, bone marrow, and skin fibroblasts: Site-specific versus activation-dependent survival of T cells and neutrophils Arthritis Rheum. 2006, 54, 2096-2108
    • (2006) Arthritis Rheum. , vol.54 , pp. 2096-2108
    • Filer, A.1    Parsonage, G.2    Smith, E.3    Osborne, C.4    Thomas, A.M.5    Curnow, S.J.6    Rainger, G.E.7    Raza, K.8    Nash, G.B.9    Lord, J.10    Salmon, M.11    Buckley, C.D.12
  • 5
    • 37549036732 scopus 로고    scopus 로고
    • Fcγ receptors as regulators of immune responses
    • Nimmerjahn, F.; Ravetch, J. V. Fcγ receptors as regulators of immune responses Nat. Rev. Immunol. 2008, 8, 34-47
    • (2008) Nat. Rev. Immunol. , vol.8 , pp. 34-47
    • Nimmerjahn, F.1    Ravetch, J.V.2
  • 7
    • 84905459655 scopus 로고    scopus 로고
    • Getting Syk: Spleen tyrosine kinase as a therapeutic target
    • Geahlen, R. L. Getting Syk: Spleen tyrosine kinase as a therapeutic target Trends Pharmacol. Sci. 2014, 35, 414-422
    • (2014) Trends Pharmacol. Sci. , vol.35 , pp. 414-422
    • Geahlen, R.L.1
  • 8
    • 77952887713 scopus 로고    scopus 로고
    • The Syk tyrosine kinase: A crucial player in diverse biological functions
    • Mocsai, A.; Ruland, J.; Tybulewicz, V. L. J. The Syk tyrosine kinase: A crucial player in diverse biological functions Nat. Rev. Immunol. 2010, 10, 387-402
    • (2010) Nat. Rev. Immunol. , vol.10 , pp. 387-402
    • Mocsai, A.1    Ruland, J.2    Tybulewicz, V.L.J.3
  • 13
    • 84875845688 scopus 로고    scopus 로고
    • Effects of fostamatinib (R788), an oral spleen tyrosine kinase inhibitor, on health-related quality of life in patients with active rheumatoid arthritis: Analyses of patient-reported outcomes from a randomized, double-blind, placebo-controlled trial
    • Weinblatt, M. E.; Kavanaugh, A.; Genovese, M. C.; Jones, D. A.; Musser, T. K.; Grossbard, E. B.; Magilavy, D. B. Effects of fostamatinib (R788), an oral spleen tyrosine kinase inhibitor, on health-related quality of life in patients with active rheumatoid arthritis: analyses of patient-reported outcomes from a randomized, double-blind, placebo-controlled trial J. Rheumatol. 2013, 40, 369-378
    • (2013) J. Rheumatol. , vol.40 , pp. 369-378
    • Weinblatt, M.E.1    Kavanaugh, A.2    Genovese, M.C.3    Jones, D.A.4    Musser, T.K.5    Grossbard, E.B.6    Magilavy, D.B.7
  • 15
    • 35348984015 scopus 로고    scopus 로고
    • Hypertension secondary to anti-angiogenic therapy: Experience with bevacizumab
    • For the role of VEGF inhibition in hypertension see
    • For the role of VEGF inhibition in hypertension see: Pande, A.; Lombardo, J.; Spangethal, E.; Javle, M. Hypertension secondary to anti-angiogenic therapy: Experience with bevacizumab Anticancer Res. 2007, 27, 3465-3470
    • (2007) Anticancer Res. , vol.27 , pp. 3465-3470
    • Pande, A.1    Lombardo, J.2    Spangethal, E.3    Javle, M.4
  • 16
    • 78649759107 scopus 로고    scopus 로고
    • The Syk inhibitor fostamatinib disodium (R788) inhibits tumor growth in the E-TCL1 transgenic mouse model of CLL by blocking antigen-dependent B-cell receptor signaling
    • Suljagic, M.; Longo, P. G.; Bennardo, S.; Perlas, E.; Leone, G.; Laurenti, L.; Efremov, D. G. The Syk inhibitor fostamatinib disodium (R788) inhibits tumor growth in the E-TCL1 transgenic mouse model of CLL by blocking antigen-dependent B-cell receptor signaling Blood 2010, 116, 4894-4905
    • (2010) Blood , vol.116 , pp. 4894-4905
    • Suljagic, M.1    Longo, P.G.2    Bennardo, S.3    Perlas, E.4    Leone, G.5    Laurenti, L.6    Efremov, D.G.7
  • 20
    • 79251600617 scopus 로고    scopus 로고
    • Dialkylbiaryl phosphines in Pd-catalyzed amination: A users guide
    • Surry, D. S.; Buchwald, S. L. Dialkylbiaryl phosphines in Pd-catalyzed amination: A users guide Chem. Sci. 2011, 2, 27-50
    • (2011) Chem. Sci. , vol.2 , pp. 27-50
    • Surry, D.S.1    Buchwald, S.L.2
  • 21
    • 49249152617 scopus 로고
    • A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
    • Miyaura, N.; Yamada, K.; Suzuki, A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides Tetrahedron Lett. 1979, 36, 3437-3440
    • (1979) Tetrahedron Lett. , vol.36 , pp. 3437-3440
    • Miyaura, N.1    Yamada, K.2    Suzuki, A.3
  • 23
    • 61849088556 scopus 로고    scopus 로고
    • Structural insights for design of potent spleen tyrosine kinase inhibitors from crystallographic analysis of three inhibitor complexes
    • Villasenor, A. G.; Kendra, R.; Ho, H.; Wang, S.; Papp, E.; Shaw, D.; Barnett, J. W.; Browner, M. F.; Kuglstatter, A. Structural insights for design of potent spleen tyrosine kinase inhibitors from crystallographic analysis of three inhibitor complexes Chem. Biol. Drug Des. 2009, 73, 466-470
    • (2009) Chem. Biol. Drug Des. , vol.73 , pp. 466-470
    • Villasenor, A.G.1    Kendra, R.2    Ho, H.3    Wang, S.4    Papp, E.5    Shaw, D.6    Barnett, J.W.7    Browner, M.F.8    Kuglstatter, A.9
  • 24
    • 80053004364 scopus 로고    scopus 로고
    • Structural alert/reactive metabolite concept as applied in medicinal chemistry to mitigate the risk of idiosyncratic drug toxicity: A perspective based on the critical examination of trends in the top 200 drugs marketed in the United States
    • Stepan, A. F.; Walker, D. P.; Bauman, J.; Price, D. A.; Baillie, T. A.; Kalgutkar, A. S.; Aleo, M. D. Structural alert/reactive metabolite concept as applied in medicinal chemistry to mitigate the risk of idiosyncratic drug toxicity: A perspective based on the critical examination of trends in the top 200 drugs marketed in the United States Chem. Res. Toxicol. 2011, 24, 1345-1410
    • (2011) Chem. Res. Toxicol. , vol.24 , pp. 1345-1410
    • Stepan, A.F.1    Walker, D.P.2    Bauman, J.3    Price, D.A.4    Baillie, T.A.5    Kalgutkar, A.S.6    Aleo, M.D.7
  • 26
    • 0034461768 scopus 로고    scopus 로고
    • Drug-like properties and the causes of poor solubility and poor permeability
    • Lipinski, C. A. Drug-like properties and the causes of poor solubility and poor permeability J. Pharmacol. Toxicol. 2000, 44, 235-249
    • (2000) J. Pharmacol. Toxicol. , vol.44 , pp. 235-249
    • Lipinski, C.A.1
  • 27
    • 33747505446 scopus 로고    scopus 로고
    • Medicinal chemistry of hERG optimizations: Highlights and hang-ups
    • Jamieson, C.; Moir, E. M.; Rankovic, Z.; Wishart, G. Medicinal chemistry of hERG optimizations: Highlights and hang-ups J. Med. Chem. 2006, 49, 5029-5046
    • (2006) J. Med. Chem. , vol.49 , pp. 5029-5046
    • Jamieson, C.1    Moir, E.M.2    Rankovic, Z.3    Wishart, G.4
  • 29
    • 70049093343 scopus 로고    scopus 로고
    • Role of hERG potassium channel assays in drug development
    • Higher throughput binding assay measures displacement of MK-499, a strong binder to the hERG ion channel
    • Higher throughput binding assay measures displacement of MK-499, a strong binder to the hERG ion channel. Priest, B. T.; Bell, I. M.; Garcia, M. L. Role of hERG potassium channel assays in drug development Channels 2008, 2, 87-93
    • (2008) Channels , vol.2 , pp. 87-93
    • Priest, B.T.1    Bell, I.M.2    Garcia, M.L.3
  • 30
    • 80052282205 scopus 로고    scopus 로고
    • A risk assessment of human ether-A-Go-Go-related gene potassium channel inhibition by using lipophilicity and basicity for drug discovery
    • Kawai, Y.; Tsukamoto, S.; Ito, J.; Akimoto, K.; Takahashi, M. A risk assessment of human ether-a-go-go-related gene potassium channel inhibition by using lipophilicity and basicity for drug discovery Chem. Pharm. Bull. (Tokyo) 2011, 59, 1110-1116
    • (2011) Chem. Pharm. Bull. (Tokyo) , vol.59 , pp. 1110-1116
    • Kawai, Y.1    Tsukamoto, S.2    Ito, J.3    Akimoto, K.4    Takahashi, M.5
  • 32
    • 84923869199 scopus 로고    scopus 로고
    • http://www.ich.org/fileadmin/Public-Web-Site/ICH-Products/Guidelines/Safety/S2-R1/Step4/S2R1-Step4.pdf.
  • 33
    • 0036464507 scopus 로고    scopus 로고
    • Crystal structure of 9-amino-N-[2-(4-morpholinyl)ethyl]-4-acridinecarboxamide bound to d(CGTACG)2: Implications for structure-activity relationships of acridinecarboxamide topoisomerase poisons
    • Adams, A.; Guss, J. M.; Denny, W. A.; Wakelin, L. P. Crystal structure of 9-amino-N-[2-(4-morpholinyl)ethyl]-4-acridinecarboxamide bound to d(CGTACG)2: implications for structure-activity relationships of acridinecarboxamide topoisomerase poisons Nucleic Acids Res. 2002, 30, 719-725
    • (2002) Nucleic Acids Res. , vol.30 , pp. 719-725
    • Adams, A.1    Guss, J.M.2    Denny, W.A.3    Wakelin, L.P.4
  • 34
    • 0034610346 scopus 로고    scopus 로고
    • DNA binding and alkylation by the "left half" of azinomycin B
    • Zang, H.; Gates, K. S. DNA binding and alkylation by the "left half" of azinomycin B Biochemistry 2000, 39, 14968-14975
    • (2000) Biochemistry , vol.39 , pp. 14968-14975
    • Zang, H.1    Gates, K.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.