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Volumn 9, Issue 11, 2017, Pages 1193-1211

Oxindole-based SYK and JAK3 dual inhibitors for rheumatoid arthritis: Designing, synthesis and biological evaluation

Author keywords

autoimmune disorders; B cell signaling; Janus kinase 3 (JAK3); molecular dynamics; oxindole; spleen tyrosine kinase (SYK)

Indexed keywords

3 (FURAN 2YL METHYLENE) N METHYL 2 OXOINDOLINE 5 SULFONAMIDE; 3 BENZYLIDENE N METHYL 2 OXOINDOLINE 5 SULFONAMIDE; 3(4 HYDROXYBENZYLIDENE) N METHYL 2 OXOINDOLINE 5 SULFONAMIDE; 3[(1 H INDOL 3 YL) METHYLENE] N METHYL 2 OXOINDOLINE 5 SULFONAMIDE; JANUS KINASE 3 INHIBITOR; N METHYL 2 OXO 3[(PYRIDIN 2YL) METHYLENE]INDOLINE 5 SULFONAMIDE; OXINDOLE; PROTEIN KINASE SYK INHIBITOR; UNCLASSIFIED DRUG; 2-OXINDOLE; ANTIRHEUMATIC AGENT; INDOLE DERIVATIVE; JANUS KINASE 3; PROTEIN KINASE SYK;

EID: 85025655646     PISSN: 17568919     EISSN: 17568927     Source Type: Journal    
DOI: 10.4155/fmc-2017-0037     Document Type: Article
Times cited : (21)

References (58)
  • 1
    • 80054928002 scopus 로고    scopus 로고
    • Genomics and the multifactorial nature of human autoimmune disease
    • Cho JH, Gregersen PK. Genomics and the multifactorial nature of human autoimmune disease. N. Engl. J. Med. 365, 1612-1623 (2011
    • (2011) N. Engl. J. Med , vol.365 , pp. 1612-1623
    • Cho, J.H.1    Gregersen, P.K.2
  • 2
    • 84862286715 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors as potential drugs for B-cell lymphoid malignancies and autoimmune disorders
    • Robak T, Robak E. Tyrosine kinase inhibitors as potential drugs for B-cell lymphoid malignancies and autoimmune disorders. Expert Opin. Investig. Drugs 21, 921-947 (2012
    • (2012) Expert Opin. Investig. Drugs , vol.21 , pp. 921-947
    • Robak, T.1    Robak, E.2
  • 3
    • 60449117455 scopus 로고    scopus 로고
    • Kinase inhibitors for the treatment of inflammatory and autoimmune disorders
    • Bhagwat SS. Kinase inhibitors for the treatment of inflammatory and autoimmune disorders. Purinergic Signal. 5, 107-115 (2009
    • (2009) Purinergic Signal , vol.5 , pp. 107-115
    • Bhagwat, S.S.1
  • 4
    • 84939181015 scopus 로고    scopus 로고
    • Protein-kinase inhibitors: A new treatment pathway for autoimmune and inflammatory diseases?
    • Hernández-Flórez D, Valor L. Protein-kinase inhibitors: a new treatment pathway for autoimmune and inflammatory diseases? Reumatol. Clin. 12, 91-99 (2016
    • (2016) Reumatol. Clin , vol.12 , pp. 91-99
    • Hernández-Flórez, D.1    Valor, L.2
  • 5
    • 0030660418 scopus 로고    scopus 로고
    • Inhibitors of tyrosine kinases involved in inflammation and autoimmune
    • Myers MR, He W, Hulme C. Inhibitors of tyrosine kinases involved in inflammation and autoimmune. Curr. Pharm. Des. 3, 473-502 (1997
    • (1997) Curr. Pharm. des , vol.3 , pp. 473-502
    • Myers, M.R.1    He, W.2    Hulme, C.3
  • 6
    • 33745155113 scopus 로고    scopus 로고
    • Multiple targeted tyrosine kinase inhibition in the clinic: All for one or one for all?
    • de Jonge MJ, Verweij J. Multiple targeted tyrosine kinase inhibition in the clinic: all for one or one for all? J. Eur. J. Cancer 42, 1351-1356 (2006
    • (2006) J. Eur. J. Cancer , vol.42 , pp. 1351-1356
    • De Jonge, M.J.1    Verweij, J.2
  • 7
    • 41549108420 scopus 로고    scopus 로고
    • From single-to multi-target drugs in cancer therapy: When aspecificity becomes an advantage
    • Petrelli A, Giordano S. From single-to multi-target drugs in cancer therapy: when aspecificity becomes an advantage. Curr. Med. Chem. 15, 422-432 (2008
    • (2008) Curr. Med. Chem , vol.15 , pp. 422-432
    • Petrelli, A.1    Giordano, S.2
  • 8
    • 33947423448 scopus 로고    scopus 로고
    • Approval summary: Sunitinib for the treatment of imatinib refractory or intolerant gastrointestinal stromal tumors and advanced renal cell carcinoma
    • Goodman VL, Rock EP, Dagher R, et al. Approval summary: sunitinib for the treatment of imatinib refractory or intolerant gastrointestinal stromal tumors and advanced renal cell carcinoma. Clin. Cancer Res. 13, 1367-1373 (2007
    • (2007) Clin. Cancer Res , vol.13 , pp. 1367-1373
    • Goodman, V.L.1    Rock, E.P.2    Dagher, R.3
  • 9
    • 84857828099 scopus 로고    scopus 로고
    • Kinase inhibitors in the treatment of immune-mediated disease
    • Kontzias A, Laurence A, Gadina M, O?Shea JJ. Kinase inhibitors in the treatment of immune-mediated disease. F1000 Med Rep. 4, 1-8 (2012
    • (2012) F1000 Med Rep , vol.4 , pp. 1-8
    • Kontzias, A.1    Laurence, A.2    Gadina, M.3    O'Shea, J.J.4
  • 10
    • 84881000237 scopus 로고    scopus 로고
    • Inhibitors of switch kinase ?spleen tyrosine kinase? in inflammation and immunemediated disorders: A review
    • Kaur M, Singh M, Silakari O. Inhibitors of switch kinase ?spleen tyrosine kinase? in inflammation and immunemediated disorders: a review. Eur. J. Med. Chem. 67, 434-446 (2013
    • (2013) Eur. J. Med. Chem , vol.67 , pp. 434-446
    • Kaur, M.1    Singh, M.2    Silakari, O.3
  • 11
    • 3543143671 scopus 로고    scopus 로고
    • Targeting syk as a treatment for allergic and autoimmune disorders expert opin
    • Wong BR, Grossbard EB, Payan DH, Masuda ES. Targeting Syk as a treatment for allergic and autoimmune disorders. Expert Opin. Investig. Drugs 13, 743-762 (2004
    • (2004) Investig. Drugs , vol.13 , pp. 743-762
    • Wong, B.R.1    Grossbard, E.B.2    Payan, D.H.3    Masuda, E.S.4
  • 12
    • 34547922794 scopus 로고    scopus 로고
    • Syk kinase as a treatment target for therapy in autoimmune diseases
    • Kyttaris VC, Tsokos GC. Syk kinase as a treatment target for therapy in autoimmune diseases. Clin. Immunol. 124, 235-247 (2007
    • (2007) Clin. Immunol , vol.124 , pp. 235-247
    • Kyttaris, V.C.1    Tsokos, G.C.2
  • 14
    • 67649397492 scopus 로고    scopus 로고
    • CP-690550, a JAK3 inhibitor as an immunosuppressant for the treatment of rheumatoid arthritis, transplant rejection, psoriasis and other immune-mediated disorders
    • West K. CP-690550, a JAK3 inhibitor as an immunosuppressant for the treatment of rheumatoid arthritis, transplant rejection, psoriasis and other immune-mediated disorders. Curr. Opin. Investig. Drugs. 10, 491-504 (2009
    • (2009) Curr. Opin. Investig. Drugs , vol.10 , pp. 491-504
    • West, K.1
  • 15
    • 84872011053 scopus 로고    scopus 로고
    • Kinase inhibitors: A new class of antirheumatic drugs
    • Kyttaris VC. Kinase inhibitors: a new class of antirheumatic drugs. Drug Des. Devel. Ther. 6, 245-250 (2012
    • (2012) Drug Des. Devel. Ther , vol.6 , pp. 245-250
    • Kyttaris, V.C.1
  • 16
    • 84873348026 scopus 로고    scopus 로고
    • 2012 FDA drug approvals
    • Mullard A. 2012 FDA drug approvals. Nat. Rev. Drug Discov. 12, 87-90 (2013
    • (2013) Nat. Rev. Drug Discov , vol.12 , pp. 87-90
    • Mullard, A.1
  • 19
    • 12444324540 scopus 로고    scopus 로고
    • Potent small molecule inhibitors of spleen tyrosine kinase (Syk
    • Lai JY, Cox PJ, Patel R, et al. Potent small molecule inhibitors of spleen tyrosine kinase (Syk). Bioorg. Med. Chem. Lett. 13, 3111-3114 (2003
    • (2003) Bioorg. Med. Chem. Lett , vol.13 , pp. 3111-3114
    • Lai, J.Y.1    Cox, P.J.2    Patel, R.3
  • 21
    • 85025622335 scopus 로고    scopus 로고
    • Maestro version 9.3 LLC New York NY
    • Maestro, version 9.3, User Manual, Schrödinger, LLC, New York, NY (2012
    • (2012) User Manual Schrödinger
  • 22
    • 85025622335 scopus 로고    scopus 로고
    • Ligprep version 2.5 LLCNew York NY
    • Ligprep, version 2.5, User Manual, Schrödinger, LLC, New York, NY (2012
    • (2012) User Manual Schrödinger
  • 23
    • 51849126692 scopus 로고    scopus 로고
    • PHASE version 3.4 LLC New York NY
    • PHASE, version 3.4, Schrödinger, LLC, New York, NY (2012
    • (2012) Schrödinger
  • 24
    • 33845868822 scopus 로고    scopus 로고
    • PHASE: A new engine for pharmacophore perception, 3D QSAR model development, and 3D database screening: 1 methodology and preliminary results
    • Dixon SL, Smondyrev AM, Knoll EH, Rao SN, Shaw DE, Friesner RA. PHASE: a new engine for pharmacophore perception, 3D QSAR model development, and 3D database screening: 1. Methodology and preliminary results. J. Comput. Aided Mol. Des. 20, 647-671 (2006
    • (2006) J. Comput. Aided Mol. des , vol.20 , pp. 647-671
    • Dixon, S.L.1    Smondyrev, A.M.2    Knoll, E.H.3    Rao, S.N.4    Shaw, D.E.5    Friesner, R.A.6
  • 26
    • 84871563714 scopus 로고    scopus 로고
    • Designing of new multi-targeted inhibitors of spleen tyrosine kinase (Syk) and zeta-associated protein of 70kDa (ZAP-70) using hierarchical virtual screening protocol
    • Kaur M, Kumari A, Bahia MS, Silakari O. Designing of new multi-targeted inhibitors of spleen tyrosine kinase (Syk) and zeta-associated protein of 70kDa (ZAP-70) using hierarchical virtual screening protocol. J. Mol. Graph. Model. 39, 165-175 (2013
    • (2013) J. Mol. Graph. Model , vol.39 , pp. 165-175
    • Kaur, M.1    Kumari, A.2    Bahia, M.S.3    Silakari, O.4
  • 27
    • 42749092988 scopus 로고    scopus 로고
    • The importance of the domain of applicability in QSAR modeling
    • Weaver S, Gleeson MP. The importance of the domain of applicability in QSAR modeling. J. Mol. Graph. Model. 26, 1315-1326 (2008
    • (2008) J. Mol. Graph. Model , vol.26 , pp. 1315-1326
    • Weaver, S.1    Gleeson, M.P.2
  • 28
    • 84859172580 scopus 로고    scopus 로고
    • Molecular modeling on pyrimidine-urea inhibitors of TNF-α production: An integrated approach using a combination of molecular docking, classification techniques, and 3D-QSAR CoMSIA
    • Mouchlis VD, Melagraki G, Mavromoustakos T, Kollias G, Afantitis A. Molecular modeling on pyrimidine-urea inhibitors of TNF-α production: an integrated approach using a combination of molecular docking, classification techniques, and 3D-QSAR CoMSIA. J. Chem. Inf. Model. 52, 711-723 (2012
    • (2012) J. Chem. Inf. Model , vol.52 , pp. 711-723
    • Mouchlis, V.D.1    Melagraki, G.2    Mavromoustakos, T.3    Kollias, G.4    Afantitis, A.5
  • 29
    • 84987100711 scopus 로고
    • Crossvalidation, bootstrapping, and partial least squares compared with multiple regression in conventional QSAR studies
    • Cramer RD, Bunce JD, Patterson DE, Frank IE. Crossvalidation, bootstrapping, and partial least squares compared with multiple regression in conventional QSAR studies. Quant. Struct.-Act. Relat. 7(1), 18-25 (1988
    • (1988) Quant. Struct.-Act. Relat , vol.7 , Issue.1 , pp. 18-25
    • Cramer, R.D.1    Bunce, J.D.2    Patterson, D.E.3    Frank, I.E.4
  • 31
    • 84880529288 scopus 로고    scopus 로고
    • Protein and ligand preparation: Parameters, protocols, and influence on virtual screening enrichments
    • Sastry GM, Adzhigirey M, Day T, Annabhimoju R, Sherman W. Protein and ligand preparation: parameters, protocols, and influence on virtual screening enrichments. J. Comput. Aided Mol. Des. 27, 221-234 (2013
    • (2013) J. Comput. Aided Mol. des , vol.27 , pp. 221-234
    • Sastry, G.M.1    Adzhigirey, M.2    Day, T.3    Annabhimoju, R.4    Sherman, W.5
  • 33
    • 84871023029 scopus 로고    scopus 로고
    • Rational design of highly selective spleen tyrosine kinase inhibitors
    • Lucas MC, Goldstein DM, Hermann JC, et al. Rational design of highly selective spleen tyrosine kinase inhibitors. J. Med. Chem. 55, 10414-10423 (2012
    • (2012) J. Med. Chem , vol.55 , pp. 10414-10423
    • Lucas, M.C.1    Goldstein, D.M.2    Hermann, J.C.3
  • 34
    • 19944429284 scopus 로고    scopus 로고
    • A novel mode of Gleevec binding is revealed by the structure of spleen tyrosine kinase
    • Atwell S, Adams JM, Badger J, et al. A novel mode of Gleevec binding is revealed by the structure of spleen tyrosine kinase. J. Biol. Chem. 279, 55827-55832 (2004
    • (2004) J. Biol. Chem , vol.279 , pp. 55827-55832
    • Atwell, S.1    Adams, J.M.2    Badger, J.3
  • 35
    • 84899654993 scopus 로고    scopus 로고
    • Syk inhibitors with high potency in presence of blood
    • Thoma G, Blanz J, Bühlmayer P, et al. Syk inhibitors with high potency in presence of blood. Bioorg. Med. Chem. Lett. 24, 2278-2282 (2014
    • (2014) Bioorg. Med. Chem. Lett , vol.24 , pp. 2278-2282
    • Thoma, G.1    Blanz, J.2    Bühlmayer, P.3
  • 36
    • 84882403995 scopus 로고    scopus 로고
    • Triosephosphate isomerase is a common crystallization contaminant of soluble His-tagged proteins produced in Escherichia coli
    • Kozlov G, Vinaik R, Gehring K. Triosephosphate isomerase is a common crystallization contaminant of soluble His-tagged proteins produced in Escherichia coli. Acta Crystallogr. Sect. F. Struct. Biol. Cryst. Commun. 69, 499-502 (2013
    • (2013) Acta Crystallogr. Sect. F. Struct. Biol. Cryst. Commun , vol.69 , pp. 499-502
    • Kozlov, G.1    Vinaik, R.2    Gehring, K.3
  • 38
    • 84862786957 scopus 로고    scopus 로고
    • X-ray crystallographic structure-based design of selective thienopyrazole inhibitors for interleukin-2-inducible tyrosine kinase
    • McLean LR, Zhang Y, Zaidi N, et al. X-ray crystallographic structure-based design of selective thienopyrazole inhibitors for interleukin-2-inducible tyrosine kinase. Bioorg. Med. Chem. Lett. 22, 3296-3300 (2012
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , pp. 3296-3300
    • McLean, L.R.1    Zhang, Y.2    Zaidi, N.3
  • 39
    • 84900343387 scopus 로고    scopus 로고
    • Discovery of GS-9973, a selective and orally efficacious inhibitor of spleen tyrosine kinase
    • Currie KS, Kropf JE, Lee T, et al. Discovery of GS-9973, a selective and orally efficacious inhibitor of spleen tyrosine kinase. J. Med. Chem. 57, 3856-3873 (2014
    • (2014) J. Med. Chem , vol.57 , pp. 3856-3873
    • Currie, K.S.1    Kropf, J.E.2    Lee, T.3
  • 40
    • 77954385114 scopus 로고    scopus 로고
    • Structural and thermodynamic characterization of the TYK2 and JAK3 kinase domains in complex with CP-690550 and CMP-6
    • Chrencik JE, Patny A, Leung IK, et al. Structural and thermodynamic characterization of the TYK2 and JAK3 kinase domains in complex with CP-690550 and CMP-6. J. Mol. Biol. 400, 413-433 (2010
    • (2010) J. Mol. Biol , vol.400 , pp. 413-433
    • Chrencik, J.E.1    Patny, A.2    Leung, I.K.3
  • 41
    • 84872312946 scopus 로고    scopus 로고
    • 3-Amido pyrrolopyrazine JAK kinase inhibitors: Development of a JAK3 vs JAK1 selective inhibitor and evaluation in cellular and in vivo models
    • Soth M, Hermann JC, Yee C, et al. 3-Amido pyrrolopyrazine JAK kinase inhibitors: development of a JAK3 vs JAK1 selective inhibitor and evaluation in cellular and in vivo models. J. Med. Chem. 56, 345-356 (2013
    • (2013) J. Med. Chem , vol.56 , pp. 345-356
    • Soth, M.1    Hermann, J.C.2    Yee, C.3
  • 42
    • 78651070500 scopus 로고    scopus 로고
    • Identification of a potent Janus kinase 3 inhibitor with high selectivity within the Janus kinase family
    • Thoma G, Nuninger F, Falchetto R, et al. Identification of a potent Janus kinase 3 inhibitor with high selectivity within the Janus kinase family. J. Med. Chem. 54, 284-288 (2011
    • (2011) J. Med. Chem , vol.54 , pp. 284-288
    • Thoma, G.1    Nuninger, F.2    Falchetto, R.3
  • 43
    • 70449586603 scopus 로고    scopus 로고
    • Fragment-based discovery of BACE1 inhibitors using functional assays
    • Godemann R, Madden J, Krämer J, et al. Fragment-based discovery of BACE1 inhibitors using functional assays. Biochemistry 48, 10743-10751 (2009
    • (2009) Biochemistry , vol.48 , pp. 10743-10751
    • Godemann, R.1    Madden, J.2    Krämer, J.3
  • 44
    • 70449558129 scopus 로고    scopus 로고
    • Molecular recognition at the active site of catechol-o-methyltransferase: Energetically favorable replacement of a water molecule imported by a bisubstrate inhibitor
    • Ellermann M, Jakob-Roetne R, Lerner C, et al. Molecular recognition at the active site of catechol-o-methyltransferase: energetically favorable replacement of a water molecule imported by a bisubstrate inhibitor. Angew. Chem. Int. Ed. Engl. 48, 9092-9096 (2009
    • (2009) Angew. Chem. Int. Ed. Engl , vol.48 , pp. 9092-9096
    • Ellermann, M.1    Jakob-Roetne, R.2    Lerner, C.3
  • 45
    • 23044495944 scopus 로고    scopus 로고
    • Crystal structure of the Jak3 kinase domain in complex with a staurosporine analog
    • Boggon TJ, Li Y, Manley PW, Eck MJ. Crystal structure of the Jak3 kinase domain in complex with a staurosporine analog. Blood 106, 996-1002 (2005
    • (2005) Blood , vol.106 , pp. 996-1002
    • Boggon, T.J.1    Li, Y.2    Manley, P.W.3    Eck, M.J.4
  • 46
    • 84975074225 scopus 로고    scopus 로고
    • Prediction of proteinligand binding poses via a combination of induced fit docking and metadynamics simulations
    • Clark AJ, Tiwary P, Borrelli K, et al. Prediction of proteinligand binding poses via a combination of induced fit docking and metadynamics simulations. J. Chem. Theory Comput. 12, 2990-2998 (2016
    • (2016) J. Chem. Theory Comput , vol.12 , pp. 2990-2998
    • Clark, A.J.1    Tiwary, P.2    Borrelli, K.3
  • 47
    • 33745088619 scopus 로고    scopus 로고
    • Use of an induced fit receptor structure in virtual screening
    • Sherman W, Beard HS, Farid R. Use of an induced fit receptor structure in virtual screening. Chem. Biol. Drug Des. 67, 83-84 (2006
    • (2006) Chem. Biol. Drug des , vol.67 , pp. 83-84
    • Sherman, W.1    Beard, H.S.2    Farid, R.3
  • 48
    • 85025662403 scopus 로고    scopus 로고
    • Schrodinger, LLC, New York, NY
    • QikProp, version 3.5 Schrodinger, LLC, New York, NY (2012
    • (2012) Qik Prop Version 3.5
  • 49
    • 84876566858 scopus 로고    scopus 로고
    • Schrödinger, LLC, New York, NY
    • Prime, version 3.1. Schrödinger, LLC, New York, NY (2012
    • (2012) Prime, Version 3.1
  • 50
    • 19244370071 scopus 로고    scopus 로고
    • Design, synthesis, and evaluations of substituted 3-[(3-or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases
    • Sun L, Tran N, Liang C, et al. Design, synthesis, and evaluations of substituted 3-[(3-or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases. J. Med. Chem. 42, 5120-5130 (1999
    • (1999) J. Med. Chem , vol.42 , pp. 5120-5130
    • Sun, L.1    Tran, N.2    Liang, C.3
  • 51
    • 0012901356 scopus 로고
    • Sur un nouvel isomère de l?indigotine; Par MM
    • Wahl A, Bagard P. Sur un nouvel isomère de l?indigotine; par MM. Bull. Soc. Chim. 5, 1033-1039 (1909
    • (1909) Bull. Soc. Chim , vol.5 , pp. 1033-1039
    • Wahl, A.1    Bagard, P.2
  • 52
    • 0023664272 scopus 로고
    • Genistein, a specific inhibitor of tyrosine-specific protein kinases
    • Akiyama T, Ishida J, Nakagawa S, et al. Genistein, a specific inhibitor of tyrosine-specific protein kinases. J. Biol. Chem. 262, 5592-5595 (1987
    • (1987) J. Biol. Chem , vol.262 , pp. 5592-5595
    • Akiyama, T.1    Ishida, J.2    Nakagawa, S.3
  • 53
    • 0013223828 scopus 로고    scopus 로고
    • A FRET-based assay platform for ultra-high density drug screening of protein kinases and phosphatases
    • Rodems SM, Hamman BD, Lin C, et al. A FRET-based assay platform for ultra-high density drug screening of protein kinases and phosphatases. Assay Drug Dev. Technol. 1, 9-19 (2002
    • (2002) Assay Drug Dev. Technol , vol.1 , pp. 9-19
    • Rodems, S.M.1    Hamman, B.D.2    Lin, C.3
  • 54
    • 0033003760 scopus 로고    scopus 로고
    • A simple statistical parameter for use in evaluation and validation of high throughput screening assays
    • Zhang JH, Chung TD, Oldenburg KR. A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J. Biomol. Screen. 4, 67-73 (1999
    • (1999) J. Biomol. Screen , vol.4 , pp. 67-73
    • Zhang, J.H.1    Chung, T.D.2    Oldenburg, K.R.3
  • 55
    • 77954057644 scopus 로고    scopus 로고
    • version 2.2. D E. Shaw Research, New York, NY, USA
    • Desmond Molecular Dynamics System, version 2.2. D. E. Shaw Research, New York, NY, USA (2009
    • (2009) Desmond Molecular Dynamics System
  • 56
    • 0034121690 scopus 로고    scopus 로고
    • Diseasemodifying activity of SB 242235, a selective inhibitor of p38 mitogen-activated protein kinase, in rat adjuvant-induced arthritis
    • Badger AM, Griswold DE, Kapadia R, et al. Diseasemodifying activity of SB 242235, a selective inhibitor of p38 mitogen-activated protein kinase, in rat adjuvant-induced arthritis. Arthritis Rheum. 43, 175 (2000
    • (2000) Arthritis Rheum , vol.43 , pp. 175
    • Badger, A.M.1    Griswold, D.E.2    Kapadia, R.3
  • 58
    • 84908428541 scopus 로고    scopus 로고
    • The novel kinase inhibitor PRT062070 (cerdulatinib) demonstrates efficacy in models of autoimmunity and B-cell cancer
    • Coffey G, Betz A, DeGuzman F, et al. The novel kinase inhibitor PRT062070 (cerdulatinib) demonstrates efficacy in models of autoimmunity and B-cell cancer. J. Pharm. Exp. Ther. 351, 538-548 (2014
    • (2014) J. Pharm. Exp. Ther , vol.351 , pp. 538-548
    • Coffey, G.1    Betz, A.2    DeGuzman, F.3


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