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Volumn 19, Issue 7, 2012, Pages 1021-1035

The development of MetAP-2 inhibitors in cancer treatment

Author keywords

Angiogenesis inhibitor; Antiangiogenesis; Cancer; Endothelial cells; Fumagillin; MetAP 2; MetAP 2 inhibitors; Metastasis; Methionine; Migration; Structure activity relationship; Vascular endothelial growth factor

Indexed keywords

2 HYDROXY 3 AMINOAMIDE DERIVATIVE; 5 NOROVALICIN; A 357300; ANGIOGENESIS INHIBITOR; ANTHRANILIC ACID DERIVATIVE; ANTINEOPLASTIC AGENT; BENGAMIDE A; BENGAMIDE B; CAPECITABINE; CKD 731; CKD 732; FUMAGALONE; FUMAGILLIN; FUMAGILLIN DERIVATIVE; FUMAGILLOL CHLOROACETYLCARBAMATE; FUMARRANOL; IDR 803; IDR 804; IDR 805; METHIONYL AMINOPEPTIDASE 2; METHIONYL AMINOPEPTIDASE 2 INHIBITOR; OVALICIN; OXALIPLATIN; PEPTIDE HYDROLASE INHIBITOR; PPI 2458; RK 805; RK 95113; SULFONAMIDE; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84863248391     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/092986712799320709     Document Type: Review
Times cited : (52)

References (78)
  • 1
    • 0034329475 scopus 로고    scopus 로고
    • Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms
    • Giglione, C.; Serero, A.; Pierre, M.; Boisson, B.; Meinnel, T. Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms. EMBO J., 2000, 19, 5916-5929.
    • (2000) EMBO J. , vol.19 , pp. 5916-5929
    • Giglione, C.1    Serero, A.2    Pierre, M.3    Boisson, B.4    Meinnel, T.5
  • 4
    • 0036882401 scopus 로고    scopus 로고
    • Metalloaminopeptidases: Common functional themes in disparate structural surroundings
    • Lowther, W.T.; Matthews, B.W. Metalloaminopeptidases: common functional themes in disparate structural surroundings. Chem. Rev., 2002, 102, 4581-4608.
    • (2002) Chem. Rev. , vol.102 , pp. 4581-4608
    • Lowther, W.T.1    Matthews, B.W.2
  • 5
    • 70349290496 scopus 로고    scopus 로고
    • Roles of P67/MetAP2 as a tumor suppressor
    • Datta, B. Roles of P67/MetAP2 as a tumor suppressor. Biochim. Biophys. Acta, 2009, 1796, 281-292.
    • (2009) Biochim. Biophys. Acta , vol.1796 , pp. 281-292
    • Datta, B.1
  • 7
    • 0035807015 scopus 로고    scopus 로고
    • Steady-state kinetic characterization of substrates and metal-ion specificities of the full-length and N-terminally truncated recombinant human methionine aminopeptidases (Type 2)
    • DOI 10.1021/bi010806r
    • Yang, G.; Kirkpatrick, R.B.; Ho, T.; Zhang, G.F.; Liang, P.H.; Johanson, K.O.; Casper, D.J.; Doyle, M.L.; Marino, J.P., Jr.; Thompson, S.K.; Chen, W.; Tew, D.G.; Meek, T.D. Steady-state kinetic characterization of substrates and metal-ion specificities of the full-length and N-terminally truncated recombinant human methionine aminopeptidases (type 2). Biochemistry, 2001, 40, 10645-10654. (Pubitemid 32816677)
    • (2001) Biochemistry , vol.40 , Issue.35 , pp. 10645-10654
    • Yang, G.1    Kirkpatrick, R.B.2    Ho, T.3    Zhang, G.-F.4    Liang, P.-H.5    Johanson, K.O.6    Casper, D.J.7    Doyle, M.L.8    Marino Jr., J.P.9    Thompson, S.K.10    Chen, W.11    Tew, D.G.12    Meek, T.D.13
  • 10
    • 33745056525 scopus 로고    scopus 로고
    • MAP1D, a novel methionine aminopeptidase family member is overexpressed in colon cancer
    • DOI 10.1038/sj.onc.1209383, PII 1209383
    • Leszczyniecka, M.; Bhatia, U.; Cueto, M.; Nirmala, N.R.; Towbin, H.; Vattay, A.; Wang, B.; Zabludoff, S.; Phillips, P.E. MAP1D, a novel methionine aminopeptidase family member is overexpressed in colon cancer. Oncogene, 2006, 25, 3471-3478. (Pubitemid 43877050)
    • (2006) Oncogene , vol.25 , Issue.24 , pp. 3471-3478
    • Leszczyniecka, M.1    Bhatia, U.2    Cueto, M.3    Nirmala, N.R.4    Towbin, H.5    Vattay, A.6    Wang, B.7    Zabludoff, S.8    Phillips, P.E.9
  • 11
    • 41149173642 scopus 로고    scopus 로고
    • Ectopic expression of methionine aminopeptidase-2 causes cell transformation and stimulates proliferation
    • DOI 10.1038/onc.2008.14, PII ONC200814
    • Tucker, L.A.; Zhang, Q.; Sheppard, G.S.; Lou, P.; Jiang, F.; McKeegan, E.; Lesniewski, R.; Davidsen, S.K.; Bell, R.L.; Wang, J. Ectopic expression of methionine aminopeptidase-2 causes cell transformation and stimulates proliferation. Oncogene, 2008, 27, 3967-3976. (Pubitemid 351913632)
    • (2008) Oncogene , vol.27 , Issue.28 , pp. 3967-3976
    • Tucker, L.A.1    Zhang, Q.2    Sheppard, G.S.3    Lou, P.4    Jiang, F.5    McKeegan, E.6    Lesniewski, R.7    Davidsen, S.K.8    Bell, R.L.9    Wang, J.10
  • 12
    • 0037135553 scopus 로고    scopus 로고
    • Methionine aminopeptidase 2 is a new target for the metastasis-associated protein, S100A4
    • DOI 10.1074/jbc.M202244200
    • Endo, H.; Takenaga, K.; Kanno, T.; Satoh, H.; Mori, S. Methionine aminopeptidase 2 is a new target for the metastasis-associated protein, S100A4. J. Biol. Chem., 2002, 277, 26396-26402. (Pubitemid 34967133)
    • (2002) Journal of Biological Chemistry , vol.277 , Issue.29 , pp. 26396-26402
    • Endo, H.1    Takenaga, K.2    Kanno, T.3    Satoh, H.4    Mori, S.5
  • 13
    • 79955047006 scopus 로고    scopus 로고
    • Methionine aminopeptidases as potential targets for treatment of gastrointestinal cancers and other tumours
    • Mauriz, J.L.; Martin-Renedo, J.; Garcia-Palomo, A.; Tunon, M.J.; Gonzalez- Gallego, J. Methionine aminopeptidases as potential targets for treatment of gastrointestinal cancers and other tumours. Curr. Drug Targets, 2010, 11, 1439-1457.
    • (2010) Curr. Drug Targets , vol.11 , pp. 1439-1457
    • Mauriz, J.L.1    Martin-Renedo, J.2    Garcia-Palomo, A.3    Tunon, M.J.4    Gonzalez-Gallego, J.5
  • 14
    • 22244484427 scopus 로고    scopus 로고
    • Fumagillin class inhibitors of methionine aminopeptidase-2
    • DOI 10.1358/dof.2005.030.05.895807
    • Bernier, S.G.; Westlin, W.F.; Hannig, G. Fumagillin class inhibitors of methionine aminopeptidase-2. Drugs Fut., 2005, 30, 497-508. (Pubitemid 40991871)
    • (2005) Drugs of the Future , vol.30 , Issue.5 , pp. 497-508
    • Bernier, S.G.1    Westlin, W.F.2    Hannig, G.3
  • 16
    • 34547877981 scopus 로고    scopus 로고
    • Fumagillin: An anti-infective as a parent molecule for novel angiogenesis inhibitors
    • DOI 10.1586/14737140.5.4.573
    • Lefkove, B.; Govindarajan, B.; Arbiser, J.L. Fumagillin: an anti-infective as a parent molecule for novel angiogenesis inhibitors. Expert Rev. Anti-infect. Ther., 2007, 5, 573-579. (Pubitemid 47250132)
    • (2007) Expert Review of Anti-Infective Therapy , vol.5 , Issue.4 , pp. 573-579
    • Lefkove, B.1    Govindarajan, B.2    Arbiser, J.L.3
  • 17
    • 0025204095 scopus 로고
    • Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth
    • Ingber, D.; Fujita, T.; Kishimoto, S.; Sudo, K.; Kanamaru, T.; Brem, H.; Folkman, J. Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature, 1990, 348, 555-557. (Pubitemid 120015110)
    • (1990) Nature , vol.348 , Issue.6301 , pp. 555-557
    • Ingber, D.1    Fujita, T.2    Kishimoto, S.3    Sudo, K.4    Kanamaru, T.5    Brem, H.6    Folkman, J.7
  • 19
    • 34547807609 scopus 로고    scopus 로고
    • FGFR1/PI3K/AKT signaling pathway is a novel target for antiangiogenic effects of the cancer drug fumagillin (TNP-470)
    • DOI 10.1002/jcb.21265
    • Chen, G.J.; Weylie, B.; Hu, C.; Zhu, J.; Forough, R. FGFR1/PI3K/AKT signaling pathway is a novel target for antiangiogenic effects of the cancer drug fumagillin (TNP-470). J. Cell. Biochem., 2007, 101, 1492-1504. (Pubitemid 47242778)
    • (2007) Journal of Cellular Biochemistry , vol.101 , Issue.6 , pp. 1492-1504
    • Chen, G.J.1    Weylie, B.2    Hu, C.3    Zhu, J.4    Forough, R.5
  • 22
    • 67650799640 scopus 로고    scopus 로고
    • Fumagillin inhibits colorectal cancer growth and metastasis in mice: In vivo and in vitro study of anti-angiogenesis
    • Hou, L.; Mori, D.; Takase, Y.; Meihua, P.; Kai, K.; Tokunaga, O. Fumagillin inhibits colorectal cancer growth and metastasis in mice: in vivo and in vitro study of anti-angiogenesis. Pathol. Int., 2009, 59, 448-461.
    • (2009) Pathol. Int. , vol.59 , pp. 448-461
    • Hou, L.1    Mori, D.2    Takase, Y.3    Meihua, P.4    Kai, K.5    Tokunaga, O.6
  • 24
    • 0033749398 scopus 로고    scopus 로고
    • The antiangiogenic agent TNP-470 requires p53 and p21CIP/WAF for endothelial cell growth arrest
    • Yeh, J.R.; Mohan, R.; Crews, C.M. The antiangiogenic agent TNP-470 requires p53 and p21CIP/WAF for endothelial cell growth arrest. Proc. Natl. Acad. Sci. USA, 2000, 97, 12782-12787.
    • (2000) Proc. Natl. Acad. Sci. USA , vol.97 , pp. 12782-12787
    • Yeh, J.R.1    Mohan, R.2    Crews, C.M.3
  • 26
    • 0034120430 scopus 로고    scopus 로고
    • TNP-470: An angiogenesis inhibitor in clinical development for cancer
    • Kruger, E.A.; Figg, W.D. TNP-470: an angiogenesis inhibitor in clinical development for cancer. Expert Opin. Investig. Drugs, 2000, 9, 1383-1396. (Pubitemid 30342622)
    • (2000) Expert Opinion on Investigational Drugs , vol.9 , Issue.6 , pp. 1383-1396
    • Kruger, E.A.1    Figg, W.D.2
  • 28
    • 0034901968 scopus 로고    scopus 로고
    • Phase I trial of the angiogenesis inhibitor TNP-470 for progressive androgen-independent prostate cancer
    • Logothetis, C.J.; Wu, K.K.; Finn, L.D.; Daliani, D.; Figg, W.; Ghaddar, H.; Gutterman, J.U. Phase I trial of the angiogenesis inhibitor TNP-470 for progressive androgen-independent prostate cancer. Clin. Cancer Res., 2001, 7, 1198-1203. (Pubitemid 32708670)
    • (2001) Clinical Cancer Research , vol.7 , Issue.5 , pp. 1198-1203
    • Logothetis, C.J.1    Wu, K.K.2    Finn, L.D.3    Daliani, D.4    Figg, W.5    Ghaddar, H.6    Gutterman, J.U.7
  • 30
    • 79955130099 scopus 로고    scopus 로고
    • Enhanced anti-tumor activity and safety profile of targeted nano-scaled HPMA copolymer-alendronate-TNP-470 conjugate in the treatment of bone malignances
    • Segal, E.; Pan, H.; Benayoun, L.; Kopeckova, P.; Shaked, Y.; Kopecek, J.; Satchi-Fainaro, R. Enhanced anti-tumor activity and safety profile of targeted nano-scaled HPMA copolymer-alendronate-TNP-470 conjugate in the treatment of bone malignances. Biomaterials, 2011, 32, 4450-4463.
    • (2011) Biomaterials , vol.32 , pp. 4450-4463
    • Segal, E.1    Pan, H.2    Benayoun, L.3    Kopeckova, P.4    Shaked, Y.5    Kopecek, J.6    Satchi-Fainaro, R.7
  • 31
    • 3242680935 scopus 로고    scopus 로고
    • RK-805, an endothelial-cell-growth inhibitor produced by Neosartorya sp., and a docking model with methionine aminopeptidase-2
    • DOI 10.1016/j.tet.2003.09.104, PII S0040402004008087
    • Asami, Y.; Kakeya, H.; Onose, R.; Chang, Y.H.; Toi, M.; Osada, H. RK-805, an endothelial-cell-growth inhibitor produced by Neosartorya sp., and a docking model with methionine aminopeptidase-2. Tetrahedron, 2004, 60, 7085-7091. (Pubitemid 38942935)
    • (2004) Tetrahedron , vol.60 , Issue.33 , pp. 7085-7091
    • Asami, Y.1    Kakeya, H.2    Onose, R.3    Chang, Y.-H.4    Toi, M.5    Osada, H.6
  • 32
    • 33748850356 scopus 로고    scopus 로고
    • Fumarranol, a rearranged fumagillin analogue that inhibits angiogenesis in vivo
    • DOI 10.1021/jm060559v
    • Lu, J.; Chong, C.R.; Hu, X.; Liu, J.O. Fumarranol, a rearranged fumagillin analogue that inhibits angiogenesis in vivo. J. Med. Chem., 2006, 49, 5645-5648. (Pubitemid 44423702)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.19 , pp. 5645-5648
    • Lu, J.1    Chong, C.R.2    Hu, X.3    Liu, J.O.4
  • 33
    • 0042343842 scopus 로고    scopus 로고
    • Fumagalone, a reversible inhibitor of type 2 methionine aminopeptidase and angiogenesis
    • DOI 10.1021/jm0341103
    • Zhou, G.; Tsai, C.W.; Liu, J.O. Fumagalone, a reversible inhibitor of type 2 methionine aminopeptidase and angiogenesis. J. Med. Chem., 2003, 46, 3452-3454. (Pubitemid 36909820)
    • (2003) Journal of Medicinal Chemistry , vol.46 , Issue.16 , pp. 3452-3454
    • Zhou, G.1    Tsai, C.W.2    Liu, J.O.3
  • 35
    • 33846104447 scopus 로고    scopus 로고
    • RK-95113, a new angiogenesis inhibitor produced by Aspergillus fumigatus
    • Asami, Y.; Kakeya, H.; Okada, G.; Toi, M.; Osada, H. RK-95113, a new angiogenesis inhibitor produced by Aspergillus fumigatus. J. Antibiot., 2006, 59, 724-728. (Pubitemid 46065468)
    • (2006) Journal of Antibiotics , vol.59 , Issue.11 , pp. 724-728
    • Asami, Y.1    Kakeya, H.2    Okada, G.3    Toi, M.4    Osada, H.5
  • 37
    • 13244265583 scopus 로고    scopus 로고
    • Novel inhibitors targeted to methionine aminopeptidase 2 (MetAP2) strongly inhibit the growth of cancers in xenografted nude model
    • Chun, E.; Han, C.K.; Yoon, J.H.; Sim, T.B.; Kim, Y.K.; Lee, K.Y. Novel inhibitors targeted to methionine aminopeptidase 2 (MetAP2) strongly inhibit the growth of cancers in xenografted nude model. Int. J. Cancer, 2005, 114, 124-130.
    • (2005) Int. J. Cancer , vol.114 , pp. 124-130
    • Chun, E.1    Han, C.K.2    Yoon, J.H.3    Sim, T.B.4    Kim, Y.K.5    Lee, K.Y.6
  • 38
    • 19444379385 scopus 로고    scopus 로고
    • General pharmacology of CKD-732, a new anticancer agent: Effects on central nervous, cardiovascular, and respiratory system
    • Kim, E.J.; Shin, W.H. General pharmacology of CKD-732, a new anticancer agent: effects on central nervous, cardiovascular, and respiratory system. Biol. Pharm. Bull., 2005, 28, 217-223.
    • (2005) Biol. Pharm. Bull. , vol.28 , pp. 217-223
    • Kim, E.J.1    Shin, W.H.2
  • 39
    • 77956058589 scopus 로고    scopus 로고
    • A phase I pharmacokinetic and pharmacodynamic study of CKD-732, an antiangiogenic agent, in patients with refractory solid cancer
    • Shin, S.J.; Jeung, H.C.; Ahn, J.B.; Rha, S.Y.; Roh, J.K.; Park, K.S.; Kim, D.H.; Kim, C.; Chung, H.C. A phase I pharmacokinetic and pharmacodynamic study of CKD-732, an antiangiogenic agent, in patients with refractory solid cancer. Invest. New Drugs, 2010, 28, 650-658.
    • (2010) Invest. New Drugs , vol.28 , pp. 650-658
    • Shin, S.J.1    Jeung, H.C.2    Ahn, J.B.3    Rha, S.Y.4    Roh, J.K.5    Park, K.S.6    Kim, D.H.7    Kim, C.8    Chung, H.C.9
  • 40
    • 84862256989 scopus 로고    scopus 로고
    • A Phase Ib pharmacokinetic study of the anti-angiogenic agent CKD-732 used in combination with capecitabine and oxaliplatin (XELOX) in metastatic colorectal cancer patients who progressed on irinotecan-based chemotherapy
    • 10.1007/s10637-010-9625-x
    • Shin, S.J.; Ahn, J.B.; Park, K.S.; Lee, Y.J.; Hong, Y.S.; Kim, T.W.; Kim, H.R.; Rha, S.Y.; Roh, J.K.; Kim, D.H.; Kim, C.; Chung, H.C. A Phase Ib pharmacokinetic study of the anti-angiogenic agent CKD-732 used in combination with capecitabine and oxaliplatin (XELOX) in metastatic colorectal cancer patients who progressed on irinotecan-based chemotherapy. Invest. New Drugs: doi 10.1007/s10637-010-9625-x
    • Invest. New Drugs: Doi
    • Shin, S.J.1    Ahn, J.B.2    Park, K.S.3    Lee, Y.J.4    Hong, Y.S.5    Kim, T.W.6    Kim, H.R.7    Rha, S.Y.8    Roh, J.K.9    Kim, D.H.10    Kim, C.11    Chung, H.C.12
  • 42
    • 22244488279 scopus 로고    scopus 로고
    • Methionine aminopeptidases type I and type II are essential to control cell proliferation
    • DOI 10.1002/jcb.20493
    • Bernier, S.G.; Taghizadeh, N.; Thompson, C.D.; Westlin, W.F.; Hannig, G. Methionine aminopeptidases type I and type II are essential to control cell proliferation. J. Cell. Biochem., 2005, 95, 1191-1203. (Pubitemid 41420126)
    • (2005) Journal of Cellular Biochemistry , vol.95 , Issue.6 , pp. 1191-1203
    • Bernier, S.G.1    Taghizadeh, N.2    Thompson, C.D.3    Westlin, W.F.4    Hannig, G.5
  • 47
    • 0032515029 scopus 로고    scopus 로고
    • Structure of human methionine aminopeptidase-2 complexed with fumagillin
    • Liu, S.; Widom, J.; Kemp, C.W.; Crews, C.M.; Clardy, J. Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science, 1998, 282, 1324-1327. (Pubitemid 28524496)
    • (1998) Science , vol.282 , Issue.5392 , pp. 1324-1327
    • Liu, S.1    Widom, J.2    Kemp, C.W.3    Crews, C.M.4    Clardy, J.5
  • 48
    • 0347763342 scopus 로고    scopus 로고
    • MetAP-2 Inhibitors Based on the Fumagillin Structure. Side-Chain Modification and Ring-Substituted Analogues
    • DOI 10.1021/jo035065+
    • Rodeschini, V.; Boiteau, J.G.; Van de Weghe, P.; Tarnus, C.; Eustache, J. MetAP-2 inhibitors based on the fumagillin structure. Side-chain modification and ring-substituted analogues. J. Org. Chem., 2004, 69, 357-373. (Pubitemid 38101717)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.2 , pp. 357-373
    • Rodeschini, V.1    Boiteau, J.-G.2    Van De, W.P.3    Tarnus, C.4    Eustache, J.5
  • 49
    • 21744442399 scopus 로고    scopus 로고
    • Total synthesis and antiangiogenic activity of cyclopentane analogues of fumagillol
    • DOI 10.1016/j.bmcl.2005.05.065, PII S0960894X05006633
    • Jeong, B.S.; Choi, N.S.; Ahn, S.K.; Bae, H.; Kim, H.S.; Kim, D. Total synthesis and antiangiogenic activity of cyclopentane analogues of fumagillol. Bioorg. Med. Chem. Lett., 2005, 15, 3580-3583. (Pubitemid 40942060)
    • (2005) Bioorganic and Medicinal Chemistry Letters , vol.15 , Issue.15 , pp. 3580-3583
    • Jeong, B.-S.1    Nam, S.C.2    Soon, K.A.3    Bae, H.4    Hak, S.K.5    Kim, D.6
  • 50
    • 34447095334 scopus 로고    scopus 로고
    • Design, synthesis, and antiangiogenic effects of a series of potent novel fumagillin analogues
    • DOI 10.1248/cpb.55.1024
    • Lee, H.W.; Cho, C.S.; Kang, S.K.; Yoo, Y.S.; Shin, J.S.; Ahn, S.K. Design, synthesis, and antiangiogenic effects of a series of potent novel fumagillin analogues. Chem. Pharm. Bull., 2007, 55, 1024-1029. (Pubitemid 47028524)
    • (2007) Chemical and Pharmaceutical Bulletin , vol.55 , Issue.7 , pp. 1024-1029
    • Lee, H.W.1    Cho, C.S.2    Kang, S.K.3    Yoo, Y.S.4    Shin, J.S.5    Ahn, S.K.6
  • 51
    • 0017131813 scopus 로고
    • Inhibition of aminopeptidase B and leucine aminopeptidase by bestatin and its stereoisomer
    • Suda, H.; Aoyagi, T.; Takeuchi, T.; Umezawa, H. Inhibition of aminopeptidase B and leucine aminopeptidase by bestatin and its stereoisomer. Arch. Biochem. Biophys., 1976, 177, 196-200.
    • (1976) Arch. Biochem. Biophys. , vol.177 , pp. 196-200
    • Suda, H.1    Aoyagi, T.2    Takeuchi, T.3    Umezawa, H.4
  • 56
    • 23944470359 scopus 로고    scopus 로고
    • Prospects for therapeutic inhibition of neuroblastoma angiogenesis
    • DOI 10.1016/j.canlet.2005.01.049, PII S0304383505003484
    • Shusterman, S.; Maris, J.M. Prospects for therapeutic inhibition of neuroblastoma angiogenesis. Cancer Lett., 2005, 228, 171-179. (Pubitemid 41188439)
    • (2005) Cancer Letters , vol.228 , Issue.1-2 , pp. 171-179
    • Shusterman, S.1    Maris, J.M.2
  • 58
    • 0242522298 scopus 로고    scopus 로고
    • Binding of α-hydroxy-β-amino acid inhibitors to methionine aminopeptidase. The performance of two types of scoring functions
    • DOI 10.1023/A:1026149810619
    • Jorgensen, A.T.; Sorensen, M.D.; Bjorkling, F.; Liljefors, T. Binding of α-hydroxy-β-amino acid inhibitors to methionine aminopeptidase. The performance of two types of scoring functions. J. Comput. Aided Mol. Des., 2003, 17, 383-397. (Pubitemid 37407549)
    • (2003) Journal of Computer-Aided Molecular Design , vol.17 , Issue.5-6 , pp. 383-397
    • Jorgensen, A.T.1    Sorensen, M.D.2    Bjorkling, F.3    Liljefors, T.4
  • 60
    • 34447547502 scopus 로고    scopus 로고
    • Regulation of c-Src Nonreceptor Tyrosine Kinase Activity by Bengamide A through Inhibition of Methionine Aminopeptidases
    • DOI 10.1016/j.chembiol.2007.05.010, PII S1074552107001792
    • Hu, X.; Dang, Y.; Tenney, K.; Crews, P.; Tsai, C.W.; Sixt, K.M.; Cole, P.A.; Liu, J.O. Regulation of c-Src nonreceptor tyrosine kinase activity by bengamide A through inhibition of methionine aminopeptidases. Chem. Biol., 2007, 14, 764-774. (Pubitemid 47081418)
    • (2007) Chemistry and Biology , vol.14 , Issue.7 , pp. 764-774
    • Hu, X.1    Dang, Y.2    Tenney, K.3    Crews, P.4    Tsai, C.W.5    Sixt, K.M.6    Cole, P.A.7    Liu, J.O.8
  • 63
    • 33845715488 scopus 로고    scopus 로고
    • A phase I and pharmacokinetic study of LAF389 administered to patients with advanced cancer
    • DOI 10.1097/CAD.0b013e328010ef5b, PII 0000181320070200000013
    • Dumez, H.; Gall, H.; Capdeville, R.; Dutreix, C.; van Oosterom, A.T.; Giaccone, G. A phase I and pharmacokinetic study of LAF389 administered to patients with advanced cancer. Anticancer Drugs, 2007, 18, 219-225. (Pubitemid 44967432)
    • (2007) Anti-Cancer Drugs , vol.18 , Issue.2 , pp. 219-225
    • Dumez, H.1    Gall, H.2    Capdeville, R.3    Dutreix, C.4    Van Oosterom, A.T.5    Giaccone, G.6
  • 64
    • 2342640861 scopus 로고    scopus 로고
    • Depletion of Methionine Aminopeptidase 2 Does Not Alter Cell Response to Fumagillin or Bengamides
    • DOI 10.1158/0008-5472.CAN-04-0019
    • Kim, S.; LaMontagne, K.; Sabio, M.; Sharma, S.; Versace, R.W.; Yusuff, N.; Phillips, P.E. Depletion of methionine aminopeptidase 2 does not alter cell response to fumagillin or bengamides. Cancer Res., 2004, 64, 2984-2987. (Pubitemid 38581392)
    • (2004) Cancer Research , vol.64 , Issue.9 , pp. 2984-2987
    • Kim, S.1    LaMontagne, K.2    Sabio, M.3    Sharma, S.4    Versace, R.W.5    Yusuff, N.6    Phillips, P.E.7
  • 69
    • 0023792919 scopus 로고
    • Evaluation of a soluble tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines
    • Scudiero, D.A.; Shoemaker, R.H.; Paull, K.D.; Monks, A.; Tierney, S.; Nofziger, T.H.; Currens, M.J.; Seniff, D.; Boyd, M.R. Evaluation of a soluble tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines. Cancer Res., 1988, 48, 4827-4833.
    • (1988) Cancer Res. , vol.48 , pp. 4827-4833
    • Scudiero, D.A.1    Shoemaker, R.H.2    Paull, K.D.3    Monks, A.4    Tierney, S.5    Nofziger, T.H.6    Currens, M.J.7    Seniff, D.8    Boyd, M.R.9
  • 72
    • 8544232793 scopus 로고    scopus 로고
    • Small molecule inhibitors of methionine aminopeptidase type 2 (MetAP-2) fail to inhibit endothelial cell proliferation or formation of microvessels from rat aortic rings in vitro
    • Garrabrant, T.; Tuman, R.W.; Ludovici, D.; Tominovich, R.; Simoneaux, R.L.; Galemmo, R.A., Jr.; Johnson, D.L. Small molecule inhibitors of methionine aminopeptidase type 2 (MetAP-2) fail to inhibit endothelial cell proliferation or formation of microvessels from rat aortic rings in vitro. Angiogenesis, 2004, 7, 91-96.
    • (2004) Angiogenesis , vol.7 , pp. 91-96
    • Garrabrant, T.1    Tuman, R.W.2    Ludovici, D.3    Tominovich, R.4    Simoneaux, R.L.5    Galemmo Jr., R.A.6    Johnson, D.L.7
  • 73
    • 44649174395 scopus 로고    scopus 로고
    • Hybrids of 1-deoxynojirimycin and aryl-1,2,3-triazoles and biological studies related to angiogenesis
    • DOI 10.1016/j.bmc.2008.05.012, PII S0968089608004318
    • Zhao, Y.; Zhou, Y.; O'Boyle, K.M.; Murphy, P.V. Hybrids of 1- deoxynojirimycin and aryl-1,2,3-triazoles and biological studies related to angiogenesis. Bioorg. Med. Chem., 2008, 16, 6333-6337. (Pubitemid 351783422)
    • (2008) Bioorganic and Medicinal Chemistry , vol.16 , Issue.12 , pp. 6333-6337
    • Zhao, Y.1    Zhou, Y.2    O'Boyle, K.M.3    Murphy, P.V.4
  • 74
    • 77951971475 scopus 로고    scopus 로고
    • Biological study of the angiogenesis inhibitor N-8-(3-ethynylphenoxy) octyl-1-deoxynojirimycin
    • Zhao, Y.; Zhou, Y.; O'Boyle, K.M.; Murphy, P.V. Biological study of the angiogenesis inhibitor N-(8-(3-ethynylphenoxy)octyl-1-deoxynojirimycin. Chem. Biol. Drug Des., 2010, 75, 570-577.
    • (2010) Chem. Biol. Drug Des. , vol.75 , pp. 570-577
    • Zhao, Y.1    Zhou, Y.2    O'Boyle, K.M.3    Murphy, P.V.4
  • 75
    • 38149093408 scopus 로고    scopus 로고
    • Cytotoxic 3,5-bis(benzylidene)piperidin-4-ones and N-acyl analogs displaying selective toxicity for malignant cells
    • Pati, H.N.; Das, U.; Quail, J.W.; Kawase, M.; Sakagami, H.; Dimmock, J.R. Cytotoxic 3,5-bis(benzylidene)piperidin-4-ones and N-acyl analogs displaying selective toxicity for malignant cells. Eur. J. Med. Chem., 2008, 43, 1-7.
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 1-7
    • Pati, H.N.1    Das, U.2    Quail, J.W.3    Kawase, M.4    Sakagami, H.5    Dimmock, J.R.6
  • 77
    • 33746265863 scopus 로고    scopus 로고
    • Identification of pyridinylpyrimidines as inhibitors of human methionine aminopeptidases
    • DOI 10.1002/anie.200600757
    • Hu, X.; Addlagatta, A.; Matthews, B.W.; Liu, J.O. Identification of pyridinylpyrimidines as inhibitors of human methionine aminopeptidases. Angew. Chem. Int. Ed. Engl., 2006, 45, 3772-3775. (Pubitemid 44098920)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.23 , pp. 3772-3775
    • Hu, X.1    Addlagatta, A.2    Matthews, B.W.3    Liu, J.O.4


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