메뉴 건너뛰기




Volumn 967, Issue , 2013, Pages 99-113

The use of JAK-specific inhibitors as chemical biology tools

Author keywords

Chemical probe; JAK inhibitor; JAK1; JAK2; JAK3; Kinase inhibitor; TYK2

Indexed keywords

JANUS KINASE; JANUS KINASE INHIBITOR; PROTEIN KINASE INHIBITOR;

EID: 84878760390     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-62703-242-1_7     Document Type: Chapter
Times cited : (2)

References (60)
  • 6
    • 33750497611 scopus 로고    scopus 로고
    • Chronic idiopathic myelofibrosis (CIMF) resulting from a unique 3;9 translocation disrupting the Janus kinase 2 (JAK2) gene
    • Mark HF, Sotomayor EA, Nelson M, Chaves F, Sanger WG, Kaleem Z, Caughron SK (2006) Chronic idiopathic myelofibrosis (CIMF) resulting from a unique 3;9 translocation disrupting the Janus kinase 2 (JAK2) gene. Exp Mol Pathol 81:217–223.
    • (2006) Exp Mol Pathol , vol.81 , pp. 217-223
    • Mark, H.F.1    Sotomayor, E.A.2    Nelson, M.3    Chaves, F.4    Sanger, W.G.5    Kaleem, Z.6    Caughron, S.K.7
  • 8
    • 77249142404 scopus 로고    scopus 로고
    • The art of the chemical probe
    • Frye SV (2010) The art of the chemical probe. Nat Chem Biol 6:159–161.
    • (2010) Nat Chem Biol , vol.6 , pp. 159-161
    • Frye, S.V.1
  • 9
    • 72449192809 scopus 로고    scopus 로고
    • Guidelines for the effective use of chemical inhibitors of protein function to understand their roles in cell regulation
    • Cohen P (2009) Guidelines for the effective use of chemical inhibitors of protein function to understand their roles in cell regulation. Biochem J 425:53–54.
    • (2009) Biochem J , vol.425 , pp. 53-54
    • Cohen, P.1
  • 12
    • 0032526999 scopus 로고    scopus 로고
    • Inhibition of Cdk2 activation by selected tyrphostins causes cell cycle arrest at late G1 and S phase
    • Kleinberger-Doron N, Shelah N, Capone R, Gazit A, Levitzki A (1998) Inhibition of Cdk2 activation by selected tyrphostins causes cell cycle arrest at late G1 and S phase. Exp Cell Res 241:340–351.
    • (1998) Exp Cell Res , vol.241 , pp. 340-351
    • Kleinberger-Doron, N.1    Shelah, N.2    Capone, R.3    Gazit, A.4    Levitzki, A.5
  • 14
    • 0027198702 scopus 로고
    • Selective inhibition of the epidermal growth factor and HER2/neu receptors by tyrphostins
    • Osherov N, Gazit A, Gilon C, Levitzki A (1993) Selective inhibition of the epidermal growth factor and HER2/neu receptors by tyrphostins. J Biol Chem 268:11134–11142.
    • (1993) J Biol Chem , vol.268 , pp. 11134-11142
    • Osherov, N.1    Gazit, A.2    Gilon, C.3    Levitzki, A.4
  • 17
    • 35548976764 scopus 로고    scopus 로고
    • 8-benzyl-4-oxo-8-azabicyclo(3.2.1)oct-2-ene-6,7-dicarboxylic acid (SD-1008), a novel Janus kinase 2 inhibitor, increases chemotherapy sensitivity in human ovarian cancer cells
    • Duan Z, Bradner J, Greenberg E, Mazitschek R, Foster R, Mahoney J, Seiden MV (2007) 8-benzyl-4-oxo-8-azabicyclo(3.2.1)oct-2-ene-6,7-dicarboxylic acid (SD-1008), a novel Janus kinase 2 inhibitor, increases chemotherapy sensitivity in human ovarian cancer cells. Mol Pharmacol 72:1137–1145.
    • (2007) Mol Pharmacol , vol.72 , pp. 1137-1145
    • Duan, Z.1    Bradner, J.2    Greenberg, E.3    Mazitschek, R.4    Foster, R.5    Mahoney, J.6    Seiden, M.V.7
  • 18
    • 53349108950 scopus 로고    scopus 로고
    • Z3, a novel Jak2 tyrosine kinase small-molecule inhibitor that suppresses Jak2-mediated pathologic cell growth
    • Sayyah J, Magis A, Ostrov DA, Allan RW, Braylan RC, Sayeski PP (2008) Z3, a novel Jak2 tyrosine kinase small-molecule inhibitor that suppresses Jak2-mediated pathologic cell growth. Mol Cancer Ther 7:2308–2318.
    • (2008) Mol Cancer Ther , vol.7 , pp. 2308-2318
    • Sayyah, J.1    Magis, A.2    Ostrov, D.A.3    Allan, R.W.4    Braylan, R.C.5    Sayeski, P.P.6
  • 19
    • 17144369135 scopus 로고    scopus 로고
    • Identification of 1,2,3,4,5,6-hexabromocyclohexane as a small molecule inhibitor of jak2 tyrosine kinase autophosphorylation (Correction of autophophorylation)
    • Sandberg EM, Ma X, He K, Frank SJ, Ostrov DA, Sayeski PP (2005) Identification of 1,2,3,4,5,6-hexabromocyclohexane as a small molecule inhibitor of jak2 tyrosine kinase autophosphorylation (correction of autophophorylation). J Med Chem 48:2526–2533.
    • (2005) J Med Chem , vol.48 , pp. 2526-2533
    • Sandberg, E.M.1    Ma, X.2    He, K.3    Frank, S.J.4    Ostrov, D.A.5    Sayeski, P.P.6
  • 20
    • 0033053383 scopus 로고    scopus 로고
    • Structure-based design of specific inhibitors of Janus kinase 3 as apoptosis-inducing antileukemic agents
    • Sudbeck EA, Liu X-P, Narla RK, Mahajan S, Ghosh S, Mao C, Uckun FM (1999) Structure-based design of specific inhibitors of Janus kinase 3 as apoptosis-inducing antileukemic agents. Clin Cancer Res 5:1569–1582.
    • (1999) Clin Cancer Res , vol.5 , pp. 1569-1582
    • Sudbeck, E.A.1    Liu, X.-P.2    Narla, R.K.3    Mahajan, S.4    Ghosh, S.5    Mao, C.6    Uckun, F.M.7
  • 22
    • 0034689408 scopus 로고    scopus 로고
    • Naphthyl ketones: A new class of Janus kinase 3 inhibitors
    • Torr V, Culbert EJ (2000) Naphthyl ketones: a new class of Janus kinase 3 inhibitors. Bioorg Med Chem Lett 10:575–579.
    • (2000) Bioorg Med Chem Lett , vol.10 , pp. 575-579
    • Torr, V.1    Culbert, E.J.2
  • 24
    • 0037079735 scopus 로고    scopus 로고
    • Selective inhibitor of Janus tyrosine kinase 3, PNU156804, prolongs allograft survival and acts synergistically with cyclosporine but additively with rapamycin
    • Stepkowski SM, Erwin-Cohen RA, Behbod F, Wang ME, Qu X, Tejpal N, Nagy ZS, Kahan BD, Kirken RA (2002) Selective inhibitor of Janus tyrosine kinase 3, PNU156804, prolongs allograft survival and acts synergistically with cyclosporine but additively with rapamycin. Blood 99:680–689.
    • (2002) Blood , vol.99 , pp. 680-689
    • Stepkowski, S.M.1    Erwin-Cohen, R.A.2    Behbod, F.3    Wang, M.E.4    Qu, X.5    Tejpal, N.6    Nagy, Z.S.7    Kahan, B.D.8    Kirken, R.A.9
  • 26
    • 77649145949 scopus 로고    scopus 로고
    • NSC114792, a novel small molecule identified through structure-based computational database screening, selectively inhibits JAK3
    • Kim BH, Jee JG, Yin CH, Sandoval C, Jayabose S, Kitamura D, Bach EA, Baeg GH (2010) NSC114792, a novel small molecule identified through structure-based computational database screening, selectively inhibits JAK3. Mol Cancer 9:36.
    • (2010) Mol Cancer , vol.9 , pp. 36
    • Kim, B.H.1    Jee, J.G.2    Yin, C.H.3    Sandoval, C.4    Jayabose, S.5    Kitamura, D.6    Bach, E.A.7    Baeg, G.H.8
  • 28
    • 57549101230 scopus 로고    scopus 로고
    • Small-molecule inhibitors of PDK1
    • Peifer C, Alessi DR (2008) Small-molecule inhibitors of PDK1. ChemMedChem 3:1810–1838.
    • (2008) Chemmedchem , vol.3 , pp. 1810-1838
    • Peifer, C.1    Alessi, D.R.2
  • 29
    • 77956535304 scopus 로고    scopus 로고
    • Multi-pathway cellular analysis of compound selectivity
    • Hancock MK, Lebakken CS, Wang J, Bi K (2010) Multi-pathway cellular analysis of compound selectivity. Mol Biosyst 6:1834–1843.
    • (2010) Mol Biosyst , vol.6 , pp. 1834-1843
    • Hancock, M.K.1    Lebakken, C.S.2    Wang, J.3    Bi, K.4
  • 38
    • 77949468470 scopus 로고    scopus 로고
    • Therapeutic potential of JAK2 inhibitors. Hematology
    • Verstovsek S (2009) Therapeutic potential of JAK2 inhibitors. Hematology Am Soc Hematol Educ Program 636–642. Volume: 2009.
    • (2009) Am Soc Hematol Educ Program , vol.2009 , pp. 636-642
    • Verstovsek, S.1
  • 47
    • 0037061628 scopus 로고    scopus 로고
    • A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening
    • McGovern SL, Caselli E, GrigorieffN, Shoichet BK (2002) A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening. J Med Chem 45:1712–1722.
    • (2002) J Med Chem , vol.45 , pp. 1712-1722
    • McGovern, S.L.1    Caselli, E.2    Grigorieff, N.3    Shoichet, B.K.4
  • 52
    • 47049098437 scopus 로고    scopus 로고
    • Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and the proliferation of primary erythroid cells from patients with myeloproliferative disorders
    • Hexner EO, SerdikoffC, Jan M, Swider CR, Robinson C, Yang S, Angeles T, Emerson SG, Carroll M, Ruggeri B, Dobrzanski P (2008) Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and the proliferation of primary erythroid cells from patients with myeloproliferative disorders. Blood 111:5663–5671.
    • (2008) Blood , vol.111 , pp. 5663-5671
    • Hexner, E.O.1    Serdikoff, C.2    Jan, M.3    Swider, C.R.4    Robinson, C.5    Yang, S.6    Angeles, T.7    Emerson, S.G.8    Carroll, M.9    Ruggeri, B.10    Dobrzanski, P.11
  • 53
    • 68749084623 scopus 로고    scopus 로고
    • CYT387, a selective JAK1/JAK2 inhibitor: In vitro assessment of kinase selectivity and preclinical studies using cell lines and primary cells from polycythemia vera patients
    • Pardanani A, Lasho T, Smith G, Burns CJ, Fantino E, Tefferi A (2009) CYT387, a selective JAK1/JAK2 inhibitor: in vitro assessment of kinase selectivity and preclinical studies using cell lines and primary cells from polycythemia vera patients. Leukemia 23:1441–1445.
    • (2009) Leukemia , vol.23 , pp. 1441-1445
    • Pardanani, A.1    Lasho, T.2    Smith, G.3    Burns, C.J.4    Fantino, E.5    Tefferi, A.6
  • 58
    • 79960178510 scopus 로고    scopus 로고
    • Discovery of the macrocycle 11-(2-pyrrolidin-1-yl-ethoxy)-14,19-dioxa-5,7,26-triaza-tetracyclo[19.3.1. 1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8,10,12(27),16,21,23-decaene (SB1518), a potent Janus kinase 2/fms-like tyrosine kinase-3 (JAK2/FLT3) inhibitor for the treatment of myelofibrosis and lymphoma
    • William AD, Lee AC, Blanchard S, Poulsen A, Teo EL, Nagaraj H, Tan E, Chen D, Williams M, Sun ET, Goh KC, Ong WC, Goh SK, Hart S, Jayaraman R, Pasha MK, Ethirajulu K, Wood JM, Dymock BW (2011) Discovery of the macrocycle 11-(2-pyrrolidin-1-yl-ethoxy)-14,19-dioxa-5,7,26-triaza-tetracyclo[19.3.1. 1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8,10,12(27),16,21,23-decaene (SB1518), a potent Janus kinase 2/fms-like tyrosine kinase-3 (JAK2/FLT3) inhibitor for the treatment of myelofibrosis and lymphoma. J Med Chem 54:4638–4658.
    • (2011) J Med Chem , vol.54 , pp. 4638-4658
    • William, A.D.1    Lee, A.C.2    Blanchard, S.3    Poulsen, A.4    Teo, E.L.5    Nagaraj, H.6    Tan, E.7    Chen, D.8    Williams, M.9    Sun, E.T.10    Goh, K.C.11    Ong, W.C.12    Goh, S.K.13    Hart, S.14    Jayaraman, R.15    Pasha, M.K.16    Ethirajulu, K.17    Wood, J.M.18    Dymock, B.W.19


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.