메뉴 건너뛰기




Volumn 12, Issue 2, 2012, Pages 98-119

Indolinones as promising scaffold as kinase inhibitors: A review

Author keywords

Anticancer; Growth factor; Indole; Inhibitor; Isatin; Kinase

Indexed keywords

2,3 DIHYDRO 2 OXO 3 (4,5,6,7 TETRAHYDRO 1H INDOL 2 YLMETHYLENE) 1H INDOLE 5 SULFONIC ACID DIMETHYLAMIDE; 3 [1 (3H IMIDAZOL 4 YL)METHYLIDENE] 5 METHOXY 1,3 DIHYDRO INDOL 2 ONE; 3 [4 METHYL 2 (2 OXO 3 INDOLINYLMETHYLIDENYL) 3 PYRROLYL]PROPIONIC ACID; 4 (3 BROMOANILINO) 6,7 DIMETHOXYQUINAZOLINE; 5 (2,6 DICHLOROBENZYLSULFONYL) 3 [3,5 DIMETHYL 4 [2 (1 PYRROLIDINYLMETHYL) 1 PYRROLIDINYLCARBONYL] 1H PYRROL 2 YLMETHYLENE] 1,3 DIHYDRO 2H INDOL 2 ONE; 5 [(5 CHLORO 2 OXO 1,2 DIHYDRO 3H INDOL 3YLIDENE)METHYL] N [2 (DIETHYL AMINO)ETHYL] 2,4 DIMETHYL 1H PYRROLE 3 CARBOXAMIDE; 5 [(5 FLUORO 1,2 DIHYDRO 2 OXO 3H INDOL 3 YLIDENE)METHYL] N (2 HYDROXY 3 MORPHOLINOPROPYL) 2,4 DIMETHYL 1H PYRROLE 3 CARBOXAMIDE; 5 [6 [3 (4 METHOXYPHENYL)UREIDO] 2 OXO 1,2 DIHYDROINDOL 3 YLIDENE METHYL] 4 METHYL 1H PYRROLE 3 CARBOXYLIC ACID; 5,7 DIMETHOXY PHENYL INDOLIN 2 ONE; ANTINEOPLASTIC AGENT; B 5; BIBF 1000; ETHYL 3,5 DIMETHYL 4 [(INDOLIN 2 ONE 3 YLIDENE)METHYL] 1H PYRROLE 2 CARBOXYLATE; HESPERADIN; INDIRUBIN; INDOLINONE DERIVATIVE; LAPATINIB; N (3 CHLOROPHENYL) 3 [3,5 DIMETHYL 4 (4 METHYL 1 PIPERAZINYLCARBONYL) 1H PYRROL 2 YLMETHYLENE] 2,3 DIHYDRO N METHYL 2 OXO 1H INDOLE 5 SULFONAMIDE; N DEETHYLSUNITINIB; NINTEDANIB; NP 506; ORANTINIB; PHOSPHOTRANSFERASE INHIBITOR; SEMAXANIB; SU 10944; SU 4984; SU 5614; SU 9516; SUNITINIB; TOCERANIB; UNCLASSIFIED DRUG; UNINDEXED DRUG; VARGATE;

EID: 84856480124     PISSN: 13895575     EISSN: 18755607     Source Type: Journal    
DOI: 10.2174/138955712798995039     Document Type: Review
Times cited : (81)

References (115)
  • 1
    • 67649993396 scopus 로고    scopus 로고
    • Future of cancer incidence in the United States: Burdens upon an aging, changing nation
    • Smith, B.D.; Smith, G.L.; Hurria, A.; Hortobagyi, G.N.; Buchholz, T.A. Future of cancer incidence in the United States: burdens upon an aging, changing nation. J. Clin. Oncol., 2009, 27, 2758-2765.
    • (2009) J. Clin. Oncol. , vol.27 , pp. 2758-2765
    • Smith, B.D.1    Smith, G.L.2    Hurria, A.3    Hortobagyi, G.N.4    Buchholz, T.A.5
  • 2
    • 0034797512 scopus 로고    scopus 로고
    • The role of reversible protein phosphorylation in health and disease
    • Cohen, P. The role of reversible protein phosphorylation in health and disease. Eur. J. Biochem., 2001, 268, 5001-5010.
    • (2001) Eur. J. Biochem. , vol.268 , pp. 5001-5010
    • Cohen, P.1
  • 3
    • 63849310246 scopus 로고    scopus 로고
    • Crosstalk of VEGF and Notch pathways in tumour angiogenesis: Therapeutic implications
    • Li, J.L.; Harris, A.L. Crosstalk of VEGF and Notch pathways in tumour angiogenesis: therapeutic implications. Front. Biosci., 2009, 14, 3094-3110.
    • (2009) Front. Biosci. , vol.14 , pp. 3094-3110
    • Li, J.L.1    Harris, A.L.2
  • 4
    • 67650249220 scopus 로고    scopus 로고
    • Hedgehog signalling as a target in cancer stem cells
    • Medina, V.; Calvo, M.B.; Diaz-Prado, S. Hedgehog signalling as a target in cancer stem cells. Clin. Transl. Oncol., 2009, 11, 199-207.
    • (2009) Clin. Transl. Oncol. , vol.11 , pp. 199-207
    • Medina, V.1    Calvo, M.B.2    Diaz-Prado, S.3
  • 5
    • 62749196220 scopus 로고    scopus 로고
    • Recent developments in anticancer agents targeting the RAS/RAF/MEK/ ERK pathway
    • Wong, K.K. Recent developments in anticancer agents targeting the RAS/RAF/MEK/ ERK pathway. Recent. Pat. Anticancer. Drug. Discov., 2009, 4(1), 28-35.
    • (2009) Recent. Pat. Anticancer. Drug. Discov. , vol.4 , Issue.1 , pp. 28-35
    • Wong, K.K.1
  • 6
    • 67649109026 scopus 로고    scopus 로고
    • Signaling Wnt/Fz Potential roles in tumorigenesis
    • Lai, S.L.; Chien, A.J.; Moon, R.T. Wnt/Fz signaling and the cytoskeleton: Potential roles in tumorigenesis. Cell. Res., 2009, 19(5), 532-545.
    • (2009) Cell. Res. , vol.19 , Issue.5 , pp. 532-545
    • Lai, S.L.1    Chien, A.J.2    Moon, R.T.3
  • 7
    • 67650594771 scopus 로고    scopus 로고
    • The opposing roles of Wnt-5a in cancer
    • McDonald, S.L.; Silver, A. The opposing roles of Wnt-5a in cancer. Br. J. cancer., 2009, 101, 209-214.
    • (2009) Br. J. Cancer , vol.101 , pp. 209-214
    • McDonald, S.L.1    Silver, A.2
  • 8
    • 58149216052 scopus 로고    scopus 로고
    • Signaling cross-talk between TGF-beta/BMP and other pathways
    • Guo, X.; Wang, X.F. Signaling cross-talk between TGF-beta/BMP and other pathways. Cell. Res., 2009, 19, 71-88.
    • (2009) Cell. Res. , vol.19 , pp. 71-88
    • Guo, X.1    Wang, X.F.2
  • 9
    • 66349135076 scopus 로고    scopus 로고
    • The TGF-β paradox in human cancer: An update
    • Tian, M.; Schiemann, W.P. The TGF-β paradox in human cancer: an update. Future. Oncol., 2009, 5(2), 259-271.
    • (2009) Future. Oncol. , vol.5 , Issue.2 , pp. 259-271
    • Tian, M.1    Schiemann, W.P.2
  • 11
    • 63749129788 scopus 로고    scopus 로고
    • P13K and mTOR inhibitors- a new generation of targeted anticancer agents
    • Brachmann, S.; Fritsch, C.; Maira, S.M.; Echeverria, C.G. P13K and mTOR inhibitors- a new generation of targeted anticancer agents. Curr. Opin. Cell. Biol., 2009, 21(2), 194-198.
    • (2009) Curr. Opin. Cell. Biol. , vol.21 , Issue.2 , pp. 194-198
    • Brachmann, S.1    Fritsch, C.2    Maira, S.M.3    Echeverria, C.G.4
  • 12
    • 61649084727 scopus 로고    scopus 로고
    • Protein kinase C epsilon: An oncogene and emerging tumor bio marker
    • Gorin, M.A.; Pan, Q. Protein kinase C epsilon: an oncogene and emerging tumor bio marker. Mol. Cancer., 2009, 8, 1-8.
    • (2009) Mol. Cancer , vol.8 , pp. 1-8
    • Gorin, M.A.1    Pan, Q.2
  • 13
    • 63849136153 scopus 로고    scopus 로고
    • Protein kinase C isoforms: Multi-functional regulators of cell life and death
    • Reyland, M.E. Protein kinase C isoforms: multi-functional regulators of cell life and death. Front. Biosci., 2009, 14, 2386-2399.
    • (2009) Front. Biosci. , vol.14 , pp. 2386-2399
    • Reyland, M.E.1
  • 14
    • 70350772288 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors-A Review on Pharmacology, Metabolism and Side Effects
    • Hartmann, J.T.; Haap, M.; Kopp, H.G.; Lipp, H.P. Tyrosine Kinase Inhibitors-A Review on Pharmacology, Metabolism and Side Effects. Curr. Drug. Metabolism., 2009, 10, 470-481.
    • (2009) Curr. Drug. Metabolism , vol.10 , pp. 470-481
    • Hartmann, J.T.1    Haap, M.2    Kopp, H.G.3    Lipp, H.P.4
  • 15
    • 35848960151 scopus 로고    scopus 로고
    • DNA sequence selective adenine alkylation, mechanism of adduct repair, and in vivo antitumor activity of the novel achiral secoamino-cyclopropylbenz indolone analogue of duocarmycin ASI-145
    • Kiakos, K.; Sato, A.; Asao, T.; McHugh, P.J.; Lee, M.; Hartley, J.A. DNA sequence selective adenine alkylation, mechanism of adduct repair, and in vivo antitumor activity of the novel achiral secoamino-cyclopropylbenz indolone analogue of duocarmycin ASI-145. Mol. Cancer. Ther., 2007, 6, 2708-2718.
    • (2007) Mol. Cancer. Ther. , vol.6 , pp. 2708-2718
    • Kiakos, K.1    Sato, A.2    Asao, T.3    McHugh, P.J.4    Lee, M.5    Hartley, J.A.6
  • 16
    • 58149380196 scopus 로고    scopus 로고
    • Recent advances in the development of multi-kinase inhibitors
    • Krug, M.; Hilgeroth A. Recent advances in the development of multi-kinase inhibitors. Mini. Rev. Med. Chem., 2008, 8, 1312-1327.
    • (2008) Mini. Rev. Med. Chem. , vol.8 , pp. 1312-1327
    • Krug, M.1    Hilgeroth, A.2
  • 17
    • 33947504730 scopus 로고    scopus 로고
    • Sunitinib: From rational design to clinical efficacy
    • Chow, L.Q.; Eckhardt, S.G. Sunitinib: From rational design to clinical efficacy. J. Clin. Oncol., 2007, 25, 884-896.
    • (2007) J. Clin. Oncol. , vol.25 , pp. 884-896
    • Chow, L.Q.1    Eckhardt, S.G.2
  • 18
    • 34548316976 scopus 로고    scopus 로고
    • Molecular basis for Sunitinib efficacy and future clinical development
    • Sandrine, F.; George, D.; William, S.; Eric, R. Molecular basis for Sunitinib efficacy and future clinical development. Nat. Rev. Drug. Discovery., 2007, 6, 734-745.
    • (2007) Nat. Rev. Drug. Discovery , vol.6 , pp. 734-745
    • Sandrine, F.1    George, D.2    William, S.3    Eric, R.4
  • 19
    • 66649106646 scopus 로고    scopus 로고
    • Multi-center, placebo-controlled, double-blind, randomized study of oral toceranib phosphate (SU11654), a receptor tyrosine kinase inhibitor, for the treatment of dogs with recurrent (either local or distant) mast cell tumor following surgical excision
    • Cheryl, A.L.; Phyllis, B.M.; Stacey, L.W.F.; Joseph, F.B.; Anthony, W.R.; Mona P.R.; Carolyn, J.H.; Kathy, L.M.; Mary, K.K.; John, G.H.; Philip, J.B.; Guillermo, C.C.; Guy, N.M.; Gina, M.M. Multi-center, placebo-controlled, double-blind, randomized study of oral toceranib phosphate (SU11654), a receptor tyrosine kinase inhibitor, for the treatment of dogs with recurrent (either local or distant) mast cell tumor following surgical excision. Clin. Cancer. Res., 2009, 15, 3856-3865.
    • (2009) Clin. Cancer. Res. , vol.15 , pp. 3856-3865
    • Cheryl, A.L.1    Phyllis, B.M.2    Stacey, L.W.F.3    Joseph, F.B.4    Anthony, W.R.5    Mona, P.R.6    Carolyn, J.H.7    Kathy, L.M.8    Mary, K.K.9    John, G.H.10    Philip, J.B.11    Guillermo, C.C.12    Guy, N.M.13    Gina, M.M.14
  • 22
    • 84873074134 scopus 로고    scopus 로고
    • http://www.ncbi.nlm.nih.gov/pubmed/15965852.
  • 23
    • 0036325621 scopus 로고    scopus 로고
    • The protein tyrosine kinase inhibitor SU5614 inhibits VEGF-induced endothelial cell sprouting and induces growth arrest and apoptosis by inhibition of c-kit in AML cells
    • Karsten, S.; Florian, F.; Robert, V.; Wolfgang H. The protein tyrosine kinase inhibitor SU5614 inhibits VEGF-induced endothelial cell sprouting and induces growth arrest and apoptosis by inhibition of c-kit in AML cells. Experi. Hematology., 2002, 30, 767-773.
    • (2002) Experi. Hematology , vol.30 , pp. 767-773
    • Karsten, S.1    Florian, F.2    Robert, V.3    Wolfgang, H.4
  • 28
    • 33748293111 scopus 로고    scopus 로고
    • SU14813: A novel multiple receptor tyrosine kinase inhibitor with potent antiangiogenic and antitumor activity
    • Shem, P.; Laird, A.D.; Mendel, D.B. SU14813: a novel multiple receptor tyrosine kinase inhibitor with potent antiangiogenic and antitumor activity. Mol. Cancer. Ther., 2006, 5, 1774-1782.
    • (2006) Mol. Cancer. Ther. , vol.5 , pp. 1774-1782
    • Shem, P.1    Laird, A.D.2    Mendel, D.B.3
  • 29
    • 17144462419 scopus 로고    scopus 로고
    • Potent and selective inhibitors of the Met [hepatocyte growth factor/scatter factor (HGF/SF) receptor] tyrosine kinase block HGF/ SF-induced tumor cell growth and invasion
    • Xueyan, W.; Phuong, L.; Congxin, L. Potent and selective inhibitors of the Met [hepatocyte growth factor/scatter factor (HGF/SF) receptor] tyrosine kinase block HGF/ SF-induced tumor cell growth and invasion. Mol. Cancer. Ther., 2003, 2, 1085-1092.
    • (2003) Mol. Cancer. Ther. , vol.2 , pp. 1085-1092
    • Xueyan, W.1    Phuong, L.2    Congxin, L.3
  • 30
    • 65249087328 scopus 로고    scopus 로고
    • A population pharmacokinetic meta-analysis of Sunitinib malate (SU11248) and its primary metabolite (SU12662) in healthy volunteers and oncology patients
    • Brett, E.H.; Carlo, L.B.; Dongwoo, K. A population pharmacokinetic meta-analysis of Sunitinib malate (SU11248) and its primary metabolite (SU12662) in healthy volunteers and oncology patients. Clin. Cancer. Res., 2009, 15, 2497-2506.
    • (2009) Clin. Cancer. Res. , vol.15 , pp. 2497-2506
    • Brett, E.H.1    Carlo, L.B.2    Dongwoo, K.3
  • 31
    • 2342566403 scopus 로고    scopus 로고
    • Targeting FGFR3 in multiple myeloma: Inhibition of t (4;14)- positive cells by SU5402 and PD173074
    • Grand, E.K.; Chase, A.J.; Heath, C.; Rahemtulla, A.; Cross, N.C.P. Targeting FGFR3 in multiple myeloma: inhibition of t (4;14)- positive cells by SU5402 and PD173074. Leukemia., 2004, 18, 962-966.
    • (2004) Leukemia , vol.18 , pp. 962-966
    • Grand, E.K.1    Chase, A.J.2    Heath, C.3    Rahemtulla, A.4    Cross, N.C.P.5
  • 33
    • 33947416658 scopus 로고    scopus 로고
    • Sunitinib: A VEGF and PDGF receptor protein kinase and angiogenesis inhibitor
    • Robert, R.J. Sunitinib: A VEGF and PDGF receptor protein kinase and angiogenesis inhibitor. Biochem. Biophy. Res. Comm., 2007, 356, 323-328.
    • (2007) Biochem. Biophy. Res. Comm. , vol.356 , pp. 323-328
    • Robert, R.J.1
  • 34
    • 34248517506 scopus 로고    scopus 로고
    • Human B lymphocytes and non-Hodgkin's lymphoma cells become polyploid in response to the protein kinase inhibitor SU6656
    • Nathalie, D.; Carl, S.; Sonia, N.; Serge, C. Human B lymphocytes and non-Hodgkin's lymphoma cells become polyploid in response to the protein kinase inhibitor SU6656. Blood. Cells. Molecules. And. Diseases., 2007, 39, 130-134.
    • (2007) Blood. Cells. Molecules. And. Diseases , vol.39 , pp. 130-134
    • Nathalie, D.1    Carl, S.2    Sonia, N.3    Serge, C.4
  • 37
  • 38
    • 49649123154 scopus 로고    scopus 로고
    • BIBF 1120: Triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy
    • Frank, H.; Roth, G.J.; Martin, K.; et al. BIBF 1120: triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy. Cancer. Res., 2008, 68, 4774-4782.
    • (2008) Cancer. Res. , vol.68 , pp. 4774-4782
    • Frank, H.1    Roth, G.J.2    Martin, K.3
  • 39
    • 33845743957 scopus 로고    scopus 로고
    • Aurora Kinases: New Targets for Cancer Therapy
    • Richard, D.C.; Archie, T.; Schwartz, G.K. Aurora Kinases: New Targets for Cancer Therapy. Clin. Cancer. Res., 2006, 12, 6869-6875.
    • (2006) Clin. Cancer. Res. , vol.12 , pp. 6869-6875
    • Richard, D.C.1    Archie, T.2    Schwartz, G.K.3
  • 40
    • 71949119399 scopus 로고    scopus 로고
    • PHA665752, a small-molecule inhibitor of c-Met, inhibits hepatocyte growth factor-stimulated migration and proliferation of c-Met-positive neuroblastoma cells
    • Crosswell, H.E.; Dasgupta, A.; Alvarado, C.S.; Watt, T.; Christensen, J.G.; Pradip, D.; Durden, D.L.; Findley, H.W. PHA665752, a small-molecule inhibitor of c-Met, inhibits hepatocyte growth factor-stimulated migration and proliferation of c-Met-positive neuroblastoma cells. BMC. Cancer., 2009, 9, 411.
    • (2009) BMC. Cancer , vol.9 , pp. 411
    • Crosswell, H.E.1    Dasgupta, A.2    Alvarado, C.S.3    Watt, T.4    Christensen, J.G.5    Pradip, D.6    Durden, D.L.7    Findley, H.W.8
  • 44
    • 0034648765 scopus 로고    scopus 로고
    • Angiogenesis in cancer and other diseases
    • Carmeliet, P.; Jain, H.K. Angiogenesis in cancer and other diseases. Nature., 2000, 407, 249-257.
    • (2000) Nature , vol.407 , pp. 249-257
    • Carmeliet, P.1    Jain, H.K.2
  • 45
    • 72249119811 scopus 로고    scopus 로고
    • VEGF-A: A critical regulator of blood vessel growth
    • Ferrara, N. VEGF-A: a critical regulator of blood vessel growth. Eur. Cytokine. Netw., 2009, 20, 158-163.
    • (2009) Eur. Cytokine. Netw. , vol.20 , pp. 158-163
    • Ferrara, N.1
  • 47
    • 65549161379 scopus 로고    scopus 로고
    • Synthesis of potential prodrug systems for reductive activation. Prodrugs for anti-angiogenic isoflavones and VEGF receptor tyrosine kinase inhibitory oxindoles
    • Blanche, E.A.; Lesley, M.; Marie, A.C.; Jacqueline, L.W.; Christopher, J.M. Synthesis of potential prodrug systems for reductive activation. Prodrugs for anti-angiogenic isoflavones and VEGF receptor tyrosine kinase inhibitory oxindoles. Tetrahedron., 2009, 65, 4894-4903.
    • (2009) Tetrahedron , vol.65 , pp. 4894-4903
    • Blanche, E.A.1    Lesley, M.2    Marie, A.C.3    Jacqueline, L.W.4    Christopher, J.M.5
  • 48
    • 0037100281 scopus 로고    scopus 로고
    • Inhibition of constitutively active forms of mutant kit by multitargeted indolinone tyrosine kinase inhibitors
    • Liao, A.T.; Chien, M.B.; Shenoy, N.; Mendel, D.B.; McMahon, G.; Cherrington, J.M.; London, C.A. Inhibition of constitutively active forms of mutant kit by multitargeted indolinone tyrosine kinase inhibitors. Blood., 2002, 100(2), 585-593.
    • (2002) Blood , vol.100 , Issue.2 , pp. 585-593
    • Liao, A.T.1    Chien, M.B.2    Shenoy, N.3    Mendel, D.B.4    McMahon, G.5    Cherrington, J.M.6    London, C.A.7
  • 49
    • 77954215388 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of 6-arylureido-3-pyrrol-2-ylmethylideneindolin-2-one derivatives as potent receptor tyrosine kinase inhibitors
    • Khanwelkar, R.R.; Chen, G.S.; Wang, H.C.; Yu, C.W.; Huang, C.H.; Lee, O.; Chen, C.H et al. Synthesis and structure-activity relationship of 6-arylureido-3-pyrrol-2-ylmethylideneindolin-2-one derivatives as potent receptor tyrosine kinase inhibitors. Bioorg. Med. Chem., 2010, 18, 4674-4686.
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 4674-4686
    • Khanwelkar, R.R.1    Chen, G.S.2    Wang, H.C.3    Yu, C.W.4    Huang, C.H.5    Lee, O.6    Chen, C.H.7
  • 53
    • 67650714103 scopus 로고
    • Design synthesis, and evaluation of indolinones as triple angiokinase inhibitors and the discovery of a highly specific 6-methoxycarbonyl-substituted indolinone (BIBF
    • Roth, G.J.; Armin, H.; Florian, C.; Sandra, H.; Jorg, K.; Thorsten, L.; Ralf, L.; Ulrike, TG.; Rainer, W.; Frank, H. Design, synthesis, and evaluation of indolinones as triple angiokinase inhibitors and the discovery of a highly specific 6-methoxycarbonyl-substituted indolinone (BIBF 1120). J. Med. Chem., 2009, 52, 4466-4480.
    • (1120) J. Med. Chem. , vol.2009 , Issue.52 , pp. 4466-4480
    • Roth, G.J.1    Armin, H.2    Florian, C.3    Sandra, H.4    Jorg, K.5    Thorsten, L.6    Ralf, L.7    Ulrike, T.G.8    Rainer, W.9    Frank, H.10
  • 54
    • 37549024347 scopus 로고    scopus 로고
    • A double-blind phase II study of BIBF 1120 in patients suffering from relapsed advanced non-small cell lung cancer (NSCLC)
    • Von, P.; Kaiser, J.; Eschbach, C.; Stefanic, M.; Love, J.; Gatzemeier, U.; Reck, M. A double-blind phase II study of BIBF 1120 in patients suffering from relapsed advanced non-small cell lung cancer (NSCLC). J. Clin. Oncol., 2007, 25, 7635.
    • (2007) J. Clin. Oncol. , vol.25 , pp. 7635
    • Von, P.1    Kaiser, J.2    Eschbach, C.3    Stefanic, M.4    Love, J.5    Gatzemeier, U.6    Reck, M.7
  • 56
    • 17844372539 scopus 로고    scopus 로고
    • Critical update and emerging trends in epidermal growth factor receptor targeting in cancer
    • Baselga, J.; Arteaga, C.L. Critical update and emerging trends in epidermal growth factor receptor targeting in cancer. J. Clin. Oncol., 2005, 23, 2445-2459.
    • (2005) J. Clin. Oncol. , vol.23 , pp. 2445-2459
    • Baselga, J.1    Arteaga, C.L.2
  • 58
    • 0032474915 scopus 로고    scopus 로고
    • Synthesis and biological evaluations of 3-substituted indolin-2- ones: A novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases
    • Sun, L.; Ngoc, T.; Flora, T.; Harald, A.; Peter, H.; Gerald, M.; Cho, T. Synthesis and biological evaluations of 3-substituted indolin-2- ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases. J. Med. Chem., 1998, 41, 2588-2603.
    • (1998) J. Med. Chem. , vol.41 , pp. 2588-2603
    • Sun, L.1    Ngoc, T.2    Flora, T.3    Harald, A.4    Peter, H.5    Gerald, M.6    Cho, T.7
  • 59
    • 35548949853 scopus 로고    scopus 로고
    • CDK9/cyclin T1: A host cell target for antiretroviral therapy
    • Klebl, B.M.; Choidas, A. CDK9/cyclin T1: a host cell target for antiretroviral therapy. Fut. Virol., 2006, 1, 317-330.
    • (2006) Fut. Virol. , vol.1 , pp. 317-330
    • Klebl, B.M.1    Choidas, A.2
  • 60
    • 33645802169 scopus 로고    scopus 로고
    • Cyclin-dependent kinase pathways as targets for cancer treatment
    • Shapiro, G.I. Cyclin-dependent kinase pathways as targets for cancer treatment. J. Clin. Oncol., 2006, 24, 1770-1783.
    • (2006) J. Clin. Oncol. , vol.24 , pp. 1770-1783
    • Shapiro, G.I.1
  • 61
    • 0038394493 scopus 로고    scopus 로고
    • Novel pyrrolyllactone and pyrrolyllactam indolinones as potent cyclindependent kinase 2 inhibitors
    • Xiaoyuan, L.; Ping, H.; Jingrong, J.C.; Jennifer, Z.; Cho, T. Novel pyrrolyllactone and pyrrolyllactam indolinones as potent cyclindependent kinase 2 inhibitors. Bioorg. Med. Chem. Lett., 2003, 13, 1939-1942.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 1939-1942
    • Xiaoyuan, L.1    Ping, H.2    Jingrong, J.C.3    Jennifer, Z.4    Cho, T.5
  • 63
    • 0025286104 scopus 로고
    • Molecular cloning and expression of glycogen synthase kinase-3/factorA
    • Woodgett, J.R. Molecular cloning and expression of glycogen synthase kinase-3/factorA. EMBO. J., 1990, 9(8), 2431-2438.
    • (1990) EMBO. J. , vol.9 , Issue.8 , pp. 2431-2438
    • Woodgett, J.R.1
  • 64
    • 0037383322 scopus 로고    scopus 로고
    • GSK-3: Tricks of the trade for a multitasking kinase
    • Doble, B.W.; Woodgett, J.R. GSK-3: tricks of the trade for a multitasking kinase. J. Cell. Sci. 2003, 116, 1175-1186.
    • (2003) J. Cell. Sci. , vol.116 , pp. 1175-1186
    • Doble, B.W.1    Woodgett, J.R.2
  • 65
    • 33947597084 scopus 로고    scopus 로고
    • Glycogen synthase kinase-3 (GSK3): Inflammation, diseases, and therapeutics
    • Jope, R.S.; Yuskaitis, C.J.; Beurel, E. Glycogen synthase kinase-3 (GSK3): inflammation, diseases, and therapeutics. Neuro. Chem. Res., 2007, 32, 577-595.
    • (2007) Neuro. Chem. Res. , vol.32 , pp. 577-595
    • Jope, R.S.1    Yuskaitis, C.J.2    Beurel, E.3
  • 66
    • 0035477020 scopus 로고    scopus 로고
    • GSK-3 takes center stage more than 20 years after its discovery
    • Frame, S.; Cohen, P. GSK-3 takes center stage more than 20 years after its discovery. Biochem. J., 2001, 359, 1-16.
    • (2001) Biochem. J. , vol.359 , pp. 1-16
    • Frame, S.1    Cohen, P.2
  • 67
    • 0036090823 scopus 로고    scopus 로고
    • Glycogen synthase kinase-3: An emerging therapeutic target
    • Finkelman, H.E. Glycogen synthase kinase-3: an emerging therapeutic target. Trends. Mol. Med., 2002, 8, 126-132.
    • (2002) Trends. Mol. Med. , vol.8 , pp. 126-132
    • Finkelman, H.E.1
  • 68
    • 33645981950 scopus 로고    scopus 로고
    • Synthesis of 3-substituted-2-xoindole analogues and their evaluation as kinase inhibitors, anticancer and antiangiogenic agents
    • Abadi, A.H.; Abou-Seri, S.M.; Abdel-Rahman, D.E.; Christian, K.; Olivier, L.; Laurent, M. Synthesis of 3-substituted-2-xoindole analogues and their evaluation as kinase inhibitors, anticancer and antiangiogenic agents. Eur. J. Med. Chem., 2006, 41, 296-305.
    • (2006) Eur. J. Med. Chem. , vol.4 , Issue.1 , pp. 296-305
    • Abadi, A.H.1    Abou-Seri, S.M.2    Abdel-Rahman, D.E.3    Christian, K.4    Olivier, L.5    Laurent, M.6
  • 72
    • 0035147448 scopus 로고    scopus 로고
    • Inhibition of cyclin-dependent kinase 1(CDK1) by indirubin derivatives in human tumour cells
    • Marko, D.; Schatzle, S.; Friedel, A.; Genzlinger, A.; Zankl, H.; Meijer, L.; Eisenbrand, G. Inhibition of cyclin-dependent kinase 1(CDK1) by indirubin derivatives in human tumour cells. Br. J. Cancer., 2001, 84(2), 283-289.
    • (2001) Br. J. Cancer. , vol.84 , Issue.2 , pp. 283-289
    • Marko, D.1    Schatzle, S.2    Friedel, A.3    Genzlinger, A.4    Zankl, H.5    Meijer, L.6    Eisenbrand, G.7
  • 73
    • 36049006209 scopus 로고    scopus 로고
    • Diversity of the intracellular mechanisms underlying the antitumor properties of indirubins
    • Meijer, L.; Shearer, J.; Bettayeb, K.; Ferandin, Y. Diversity of the intracellular mechanisms underlying the antitumor properties of indirubins. Int. Congres. Ser., 2007, 1304, 60-74.
    • (2007) Int. Congres. Ser. , vol.1304 , pp. 60-74
    • Meijer, L.1    Shearer, J.2    Bettayeb, K.3    Ferandin, Y.4
  • 74
    • 0035808457 scopus 로고    scopus 로고
    • Indirubins inhibit glycogen synthase kinase- 3 beta and CDK5/P25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease - A property common to most cycline-dependent kinase inhibitors?
    • Leclerc, S.; Garnier, M.; Hoessel, R.; Marko, D.; Bibb, J.A.; Snyder, G.L.; Greengard, P.; Biernat, J.; Wu, Y.Z.; Mandelkow, E.M.; Eisenbrand, G.; Meijer, L. Indirubins inhibit glycogen synthase kinase- 3 beta and CDK5/P25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease - A property common to most cycline-dependent kinase inhibitors? J. Biol. Chem., 2001, 276(1), 251-260.
    • (2001) J. Biol. Chem. , vol.276 , Issue.1 , pp. 251-260
    • Leclerc, S.1    Garnier, M.2    Hoessel, R.3    Marko, D.4    Bibb, J.A.5    Snyder, G.L.6    Greengard, P.7    Biernat, J.8    Wu, Y.Z.9    Mandelkow, E.M.10    Eisenbrand, G.11    Meijer, L.12
  • 75
    • 8644224855 scopus 로고    scopus 로고
    • Molecular mechanisms of indirubin and its derivatives: Novel anticancer molecules with their origin in traditional Chinese phytomedicine
    • Eisenbrand, G.; Hippe, F.; Jakobs, S.; Muehlbeyer, S. Molecular mechanisms of indirubin and its derivatives: novel anticancer molecules with their origin in traditional Chinese phytomedicine. J. Cancer. Res. Clin. Oncol., 2004, 130(11), 627-635.
    • (2004) J. Cancer. Res. Clin. Oncol. , vol.130 , Issue.11 , pp. 627-635
    • Eisenbrand, G.1    Hippe, F.2    Jakobs, S.3    Muehlbeyer, S.4
  • 76
    • 33747698455 scopus 로고    scopus 로고
    • Indirubin enhances tumor necrosis factor-induced apoptosis through modulation of nuclear factor-kappa B signaling pathway
    • Sethi, G.; Ahn, K.S.; Sandur, S.K.; Lin, X.; Chaturvedi, M.M.; Aggarwal, B.B. Indirubin enhances tumor necrosis factor-induced apoptosis through modulation of nuclear factor-kappa B signaling pathway. J. Biol. Chem., 2006, 281(33), 23425-23435.
    • (2006) J. Biol. Chem. , vol.281 , Issue.33 , pp. 23425-23435
    • Sethi, G.1    Ahn, K.S.2    Sandur, S.K.3    Lin, X.4    Chaturvedi, M.M.5    Aggarwal, B.B.6
  • 78
    • 0345448068 scopus 로고    scopus 로고
    • Transient induction of cytochromes P450 1A1 and 1B1 in MCF-7 human breast cancer cells by indirubin
    • Spink, B.C.; Hussain, M.M.; Katz, B.H.; Eisele, L.; Spink, D.C. Transient induction of cytochromes P450 1A1 and 1B1 in MCF-7 human breast cancer cells by indirubin. Biochem. Pharmacol., 2003, 66(12), 2313-2321.
    • (2003) Biochem. Pharmacol. , vol.66 , Issue.12 , pp. 2313-2321
    • Spink, B.C.1    Hussain, M.M.2    Katz, B.H.3    Eisele, L.4    Spink, D.C.5
  • 80
    • 27744489247 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of novel indirubin derivatives as potent anti-proliferative agents with CDK2 inhibitory activities
    • Myoung, J.M.; Sang, K.L.; Lee, J.W.; Song, W.K.; Kim, S.K.; Kim, J.I.; Chunghee, C.; Choia, S.J.; Yong-Chul, K. Synthesis and structure-activity relationships of novel indirubin derivatives as potent anti-proliferative agents with CDK2 inhibitory activities. Bioorg. Med. Chem., 2006, 14, 237-246.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 237-246
    • Myoung, J.M.1    Sang, K.L.2    Lee, J.W.3    Song, W.K.4    Kim, S.K.5    Kim, J.I.6    Chunghee, C.7    Choia, S.J.8    Yong-Chul, K.9
  • 83
    • 2442589341 scopus 로고    scopus 로고
    • Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases
    • Panagiotis, P.; Prokopios, M.; Alexios-Leandros, S.; Vassilios, M. Emmanuel, M.; Aldo, T.; Andrea, M.; et al. Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases. J. Med. Chem. 2004, 47, 935-946.
    • (2004) J. Med. Chem. , vol.47 , pp. 935-946
    • Panagiotis, P.1    Prokopios, M.2    Alexios-Leandros, S.3    Vassilios, M.4    Emmanuel, M.5    Aldo, T.6    Andrea, M.7
  • 85
    • 27844461512 scopus 로고    scopus 로고
    • Epithelial-mesenchymal transition in development and cancer: Role of phosphatidylinositol 3' kinase/Akt pathways
    • Larue, L.; Bellacosa, A. Epithelial-mesenchymal transition in development and cancer: role of phosphatidylinositol 3' kinase/Akt pathways. Oncogene., 2005, 24, 7443-7454.
    • (2005) Oncogene , vol.24 , pp. 7443-7454
    • Larue, L.1    Bellacosa, A.2
  • 90
    • 33749544080 scopus 로고    scopus 로고
    • An orally administered multitarget tyrosine kinase inhibitor, SU11248, is a novel potent inhibitor of thyroid oncogenic RET/papillary thyroid cancer kinases
    • Kim, D.W.; Jo, Y.S.; Jung, H.S et al. An orally administered multitarget tyrosine kinase inhibitor, SU11248, is a novel potent inhibitor of thyroid oncogenic RET/papillary thyroid cancer kinases. J. Clin. Endocrinol. Metab., 2006, 91, 4070-4076.
    • (2006) J. Clin. Endocrinol. Metab. , vol.91 , pp. 4070-4076
    • Kim, D.W.1    Jo, Y.S.2    Jung, H.S.3
  • 93
    • 34347358646 scopus 로고    scopus 로고
    • JNK signalling: A possible target to prevent neurodegeneration
    • Borsello, T.; Forloni, G. JNK signalling: a possible target to prevent neurodegeneration. Curr. Pharma. Des., 2007, 13, 1875-1886.
    • (2007) Curr. Pharma. Des. , vol.13 , pp. 1875-1886
    • Borsello, T.1    Forloni, G.2
  • 95
    • 0037230304 scopus 로고    scopus 로고
    • Activation of the JNK signaling pathway: Breaking the brake on apoptosis
    • Lin, A. Activation of the JNK signaling pathway: breaking the brake on apoptosis. Bio. Essays., 2003, 25(1), 17-24.
    • (2003) Bio. Essays. , vol.25 , Issue.1 , pp. 17-24
    • Lin, A.1
  • 97
    • 6344270057 scopus 로고    scopus 로고
    • Aurora kinases in spindle assembly and chromosome segregation
    • Ducat, D.; Zheng, Y. Aurora kinases in spindle assembly and chromosome segregation. Exp. Cell. Res., 2004, 301, 60-67.
    • (2004) Exp. Cell. Res. , vol.301 , pp. 60-67
    • Ducat, D.1    Zheng, Y.2
  • 98
    • 18044391525 scopus 로고    scopus 로고
    • Aurora kinases, aneuploidy and cancer, a coincidence or a real link?
    • Giet, R.; Petretti, C.; Pringent, C. Aurora kinases, aneuploidy and cancer, a coincidence or a real link? Trends. Cell. Biol., 2005, 15(5), 241-50.
    • (2005) Trends. Cell. Biol. , vol.15 , Issue.5 , pp. 241-250
    • Giet, R.1    Petretti, C.2    Pringent, C.3
  • 99
    • 33751085368 scopus 로고    scopus 로고
    • Overexpression of aurora kinase A in mouse mammary epithelium induces genetic instability preceding mammary tumor formation
    • Wang, X.; Zhou, Y.X.; Qiao, W.; Tominaga, Y.; Ouchi, M.; Ouchi, T.; Deng, C.X. Overexpression of aurora kinase A in mouse mammary epithelium induces genetic instability preceding mammary tumor formation. Oncogene., 2006, 25, 7148-7158.
    • (2006) Oncogene , vol.25 , pp. 7148-7158
    • Wang, X.1    Zhou, Y.X.2    Qiao, W.3    Tominaga, Y.4    Ouchi, M.5    Ouchi, T.6    Deng, C.X.7
  • 101
    • 0031795119 scopus 로고    scopus 로고
    • Protein tyrosine kinases: Structure, substrate specificity, and drug discovery
    • Obeidi, F.A.; Wu, J.J.; Lam, K.S. Protein tyrosine kinases: structure, substrate specificity, and drug discovery. Biopolymers., 1998, 47, 197-223.
    • (1998) Biopolymers , vol.47 , pp. 197-223
    • Obeidi, F.A.1    Wu, J.J.2    Lam, K.S.3
  • 102
    • 0346887165 scopus 로고    scopus 로고
    • Design and synthesis of aminopropyl tetrahydroindole-based indolin-2- ones as selective and potent inhibitors of Src and Yes tyrosine kinase
    • Guan, H.; Laird, A.D.; Blake, R.A.; Tanga, C.; Liang, C. Design and synthesis of aminopropyl tetrahydroindole-based indolin-2- ones as selective and potent inhibitors of Src and Yes tyrosine kinase. Bioorg. Med. Chem. Lett., 2004, 14, 187-190.
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 187-190
    • Guan, H.1    Laird, A.D.2    Blake, R.A.3    Tanga, C.4    Liang, C.5
  • 103
    • 34147094335 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3-(Substituted-benzylidene)-1,3-dihydro-indolin derivatives as human protein kinase ck2 and p60c-src tyrosine kinase inhibitors
    • Olgen, S.; Gotz, C.; Jose, J. Synthesis and biological evaluation of 3-(Substituted-benzylidene)-1,3-dihydro-indolin derivatives as human protein kinase ck2 and p60c-src tyrosine kinase inhibitors. Biol. Pharm. Bull., 2007, 30(4), 715-718.
    • (2007) Biol. Pharm. Bull. , vol.30 , Issue.4 , pp. 715-718
    • Olgen, S.1    Gotz, C.2    Jose, J.3
  • 104
    • 21744448193 scopus 로고    scopus 로고
    • Synthesis and anti-tyrosine kinase activity of 3-(substituted-benzylidene)-1, 3-dihydro-indolin derivatives: Investigation of their role against p60c-Src receptor tyrosine kinase with the application of receptor docking studies
    • Olgen, S.; Akaho, E.; Nebioglu, D. Synthesis and anti-tyrosine kinase activity of 3-(substituted-benzylidene)-1, 3-dihydro-indolin derivatives: investigation of their role against p60c-Src receptor tyrosine kinase with the application of receptor docking studies. IL. Farmaco., 2005, 60, 497-506.
    • (2005) IL. Farmaco. , vol.60 , pp. 497-506
    • Olgen, S.1    Akaho, E.2    Nebioglu, D.3
  • 105
  • 108
    • 9244251125 scopus 로고    scopus 로고
    • Cell-cycle checkpoints and cancer
    • Kastan, M.B.; Bartek, J. Cell-cycle checkpoints and cancer. Nature., 2004, 432, 316-323.
    • (2004) Nature , vol.432 , pp. 316-323
    • Kastan, M.B.1    Bartek, J.2
  • 109
    • 0034707047 scopus 로고    scopus 로고
    • The DNA damage response: Putting checkpoints in perspective
    • Zhou, B.B.; Elledge, S.J. The DNA damage response: putting checkpoints in perspective. Nature., 2000, 408, 433-439.
    • (2000) Nature , vol.408 , pp. 433-439
    • Zhou, B.B.1    Elledge, S.J.2
  • 110
    • 33745856631 scopus 로고    scopus 로고
    • Chk1 inhibitors for novel cancer treatment
    • Tao, ZF.; Lin, N.H. Chk1 inhibitors for novel cancer treatment. Anticancer. Agents. Med. Chem., 2006, 6, 377-378.
    • (2006) Anticancer. Agents. Med. Chem. , vol.6 , pp. 377-378
    • Tao, Z.F.1    Lin, N.H.2
  • 112
    • 27944448722 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3-ethylidene-1.;3-dihydro-indol-2-ones as novel checkpoint 1 inhibitors
    • Lin, N.H.; Xia, P.; Kovar, P.; Park, C.; Chen, Z.; Zhang, H.; Rosenberg, S.H.; Sham, H.L. Synthesis and biological evaluation of 3-ethylidene-1.;3-dihydro-indol-2-ones as novel checkpoint 1 inhibitors. Bioorg. Med. Chem. Lett., 2006, 16, 421-426.
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 421-426
    • Lin, N.H.1    Xia, P.2    Kovar, P.3    Park, C.4    Chen, Z.5    Zhang, H.6    Rosenberg, S.H.7    Sham, H.L.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.