-
1
-
-
0034329475
-
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
-
3
-
-
0034615568
-
Structure and function of the methionine aminopeptidases
-
DOI 10.1016/S0167-4838(99)00271-X, PII S016748389900271X
-
Lowther, W.T.; Matthews, B.W. Structure and function of the methionine aminopeptidases. Biochim. Biophys. Acta, 2000, 1477, 157-167. (Pubitemid 30119899)
-
(2000)
Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
, vol.1477
, Issue.1-2
, pp. 157-167
-
-
Lowther, W.T.1
Matthews, B.W.2
-
4
-
-
0036882401
-
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
-
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
-
6
-
-
0038333336
-
Physiologically relevant metal cofactor for methionine aminopeptidase-2 is manganese
-
DOI 10.1021/bi020670c
-
Wang, J.; Sheppard, G.S.; Lou, P.; Kawai, M.; Park, C.; Egan, D.A.; Schneider, A.; Bouska, J.; Lesniewski, R.; Henkin, J. Physiologically relevant metal cofactor for methionine aminopeptidase-2 is manganese. Biochemistry, 2003, 42, 5035-5042. (Pubitemid 36532057)
-
(2003)
Biochemistry
, vol.42
, Issue.17
, pp. 5035-5042
-
-
Wang, J.1
Sheppard, G.S.2
Lou, P.3
Kawai, M.4
Park, C.5
Egan, D.A.6
Schneider, A.7
Bouska, J.8
Lesniewski, R.9
Henkin, J.10
-
7
-
-
0035807015
-
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
-
8
-
-
33745468383
-
Structural basis of catalysis by monometalated methionine aminopeptidase
-
DOI 10.1073/pnas.0602433103
-
Ye, Q.Z.; Xie, S.X.; Ma, Z.Q.; Huang, M.; Hanzlik, R.P. Structural basis of catalysis by monometalated methionine aminopeptidase. Proc. Natl. Acad. Sci. USA, 2006, 103, 9470-9475. (Pubitemid 43955849)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.25
, pp. 9470-9475
-
-
Ye, Q.-Z.1
Xie, S.-X.2
Ma, Z.-Q.3
Huang, M.4
Hanzlik, R.P.5
-
9
-
-
33845310513
-
Elucidation of the function of type 1 human methionine aminopeptides during cell cycle progression
-
DOI 10.1073/pnas.0608389103
-
Hu, X.; Addlagatta, A.; Lu, J.; Matthews, B.W.; Liu, J.O. Elucidation of the function of type 1 human methionine aminopeptidase during cell cycle progression. Proc. Natl. Acad. Sci. USA, 2006, 103, 18148-18153. (Pubitemid 44871627)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.48
, pp. 18148-18153
-
-
Hu, X.1
Addlagatta, A.2
Lu, J.3
Matthews, B.W.4
Liu, J.O.5
-
10
-
-
33745056525
-
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
-
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
-
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
-
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
-
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
-
15
-
-
3242727454
-
A methionine aminopeptidase-2 inhibitor, PPI-2458, for the treatment of rheumatoid arthritis
-
DOI 10.1073/pnas.0404105101
-
Bernier, S.G.; Lazarus, D.D.; Clark, E.; Doyle, B.; Labenski, M.T.; Thompson, C.D.; Westlin, W.F.; Hannig, G. A methionine aminopeptidase-2 inhibitor, PPI-2458, for the treatment of rheumatoid arthritis. Proc. Natl. Acad. Sci. USA, 2004, 101, 10768-10773. (Pubitemid 38955817)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.29
, pp. 10768-10773
-
-
Bernier, S.G.1
Lazarus, D.D.2
Clark, E.3
Doyle, B.4
Labenski, M.T.5
Thompson, C.D.6
Westlin, W.F.7
Hannig, G.8
-
16
-
-
34547877981
-
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
-
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
-
18
-
-
0030924753
-
The anti-angiogenic agent fumagillin covalently binds and inhibits the methionine aminopeptidase, MetAP-2
-
DOI 10.1073/pnas.94.12.6099
-
Sin, N.; Meng, L.; Wang, M.Q.; Wen, J.J.; Bornmann, W.G.; Crews, C.M. The anti-angiogenic agent fumagillin covalently binds and inhibits the methionine aminopeptidase, MetAP-2. Proc. Natl. Acad. Sci. USA, 1997, 94, 6099-6103. (Pubitemid 27270643)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.12
, pp. 6099-6103
-
-
Sin, N.1
Meng, L.2
Wang, M.Q.W.3
Wen, J.J.4
Bornmann, W.G.5
Crews, C.M.6
-
19
-
-
34547807609
-
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
-
20
-
-
0033942066
-
Trial of oral fumagillin for the treatment of intestinal microsporidiosis in patients with HIV infection
-
Molina, J.M.; Goguel, J.; Sarfati, C.; Michiels, J.F.; Desportes-Livage, I.; Balkan, S.; Chastang, C.; Cotte, L.; Maslo, C.; Struxiano, A.; Derouin, F.; Decazes, J.M. Trial of oral fumagillin for the treatment of intestinal microsporidiosis in patients with HIV infection. AIDS, 2000, 14, 1341-1348.
-
(2000)
AIDS
, vol.14
, pp. 1341-1348
-
-
Molina, J.M.1
Goguel, J.2
Sarfati, C.3
Michiels, J.F.4
Desportes-Livage, I.5
Balkan, S.6
Chastang, C.7
Cotte, L.8
Maslo, C.9
Struxiano, A.10
Derouin, F.11
Decazes, J.M.12
-
21
-
-
20044386113
-
Fumagillin treatment of hepatocellular carcinoma in rats: An in vivo study of antiangiogenesis
-
Sheen, I.S.; Jeng, K.S.; Jeng, W.J.; Jeng, C.J.; Wang, Y.C.; Gu, S.L.; Tseng, S.Y.; Chu, C.M.; Lin, C.H.; Chang, K.M. Fumagillin treatment of hepatocellular carcinoma in rats: an in vivo study of antiangiogenesis. World J. Gastroenterol., 2005, 11, 771-777.
-
(2005)
World J. Gastroenterol.
, vol.11
, pp. 771-777
-
-
Sheen, I.S.1
Jeng, K.S.2
Jeng, W.J.3
Jeng, C.J.4
Wang, Y.C.5
Gu, S.L.6
Tseng, S.Y.7
Chu, C.M.8
Lin, C.H.9
Chang, K.M.10
-
22
-
-
67650799640
-
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
-
23
-
-
0026082066
-
Potent anti-angiogenic action of AGM-1470: Comparison to the fumagillin parent
-
Kusaka, M.; Sudo, K.; Fujita, T.; Marui, S.; Itoh, F.; Ingber, D.; Folkman, J. Potent anti-angiogenic action of AGM-1470: comparison to the fumagillin parent. Biochem. Biophys. Res. Commun., 1991, 174, 1070-1076.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.174
, pp. 1070-1076
-
-
Kusaka, M.1
Sudo, K.2
Fujita, T.3
Marui, S.4
Itoh, F.5
Ingber, D.6
Folkman, J.7
-
24
-
-
0033749398
-
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
-
25
-
-
0041848512
-
Angiogenesis inhibitor TNP-470 (AGM-1470) suppresses vascular smooth muscle cell proliferation after balloon injury in rats
-
DOI 10.1016/S0022-4804(03)00119-7
-
Ogata, T.; Kurabayashi, M.; Maeno, T.; Sekiguchi, K.; Hoshino, Y.; Ishikawa, S.; Takei, H.; Nagai, R.; Morishita, Y. Angiogenesis inhibitor TNP-470 (AGM-1470) suppresses vascular smooth muscle cell proliferation after balloon injury in rats. J. Surg. Res., 2003, 112, 117-121. (Pubitemid 36904035)
-
(2003)
Journal of Surgical Research
, vol.112
, Issue.2
, pp. 117-121
-
-
Ogata, T.1
Kurabayashi, M.2
Maeno, T.3
Sekiguchi, K.-I.4
Hoshino, Y.-I.5
Ishikawa, S.6
Takei, H.7
Nagai, R.8
Morishita, Y.9
-
26
-
-
0034120430
-
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
-
27
-
-
0037112010
-
Safety and pharmacokinetic effects of TNP-470, an angiogenesis inhibitor, combined with paclitaxel in patients with solid tumors: Evidence for activity in non-small-cell lung cancer
-
DOI 10.1200/JCO.2002.04.006
-
Herbst, R.S.; Madden, T.L.; Tran, H.T.; Blumenschein, G.R., Jr.; Meyers, C.A.; Seabrooke, L.F.; Khuri, F.R.; Puduvalli, V.K.; Allgood, V.; Fritsche, H.A., Jr.; Hinton, L.; Newman, R.A.; Crane, E.A.; Fossella, F.V.; Dordal, M.; Goodin, T.; Hong, W.K. Safety and pharmacokinetic effects of TNP- 470, an angiogenesis inhibitor, combined with paclitaxel in patients with solid tumors: evidence for activity in non-small-cell lung cancer. J. Clin. Oncol., 2002, 20, 4440-4447. (Pubitemid 35334755)
-
(2002)
Journal of Clinical Oncology
, vol.20
, Issue.22
, pp. 4440-4447
-
-
Herbst, R.S.1
Madden, T.L.2
Tran, H.T.3
Blumenschein Jr., G.R.4
Meyers, C.A.5
Seabroake, L.F.6
Khuri, F.R.7
Puduvalli, V.K.8
Allgood, V.9
Fritsche Jr., H.A.10
Hinton, L.11
Newman, R.A.12
Crane, E.A.13
Fossella, F.V.14
Dordal, M.15
Goodin, T.16
Hong, W.K.17
-
28
-
-
0034901968
-
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
-
29
-
-
2342586114
-
Targeting angiogenesis with a conjugate of HPMA copolymer and TNP-470
-
DOI 10.1038/nm1002
-
Satchi-Fainaro, R.; Puder, M.; Davies, J.W.; Tran, H.T.; Sampson, D.A.; Greene, A.K.; Corfas, G.; Folkman, J. Targeting angiogenesis with a conjugate of HPMA copolymer and TNP-470. Nat. Med., 2004, 10, 255-261. (Pubitemid 38667615)
-
(2004)
Nature Medicine
, vol.10
, Issue.3
, pp. 255-261
-
-
Satchi-Fainaro, R.1
Puder, M.2
Davies, J.W.3
Tran, H.T.4
Sampson, D.A.5
Greene, A.K.6
Corfas, G.7
Folkman, J.8
-
30
-
-
79955130099
-
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
-
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
-
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
-
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
-
34
-
-
0036131928
-
5-Demethylovalicin, as a methionine aminopeptidase-2 inhibitor produced by Chrysosporium
-
Son, K.H.; Kwon, J.Y.; Jeong, H.W.; Kim, H.K.; Kim, C.J.; Chang, Y.H.; Choi, J.D.; Kwon, B.M. 5-demethylovalicin, as a methionine aminopeptidase-2 inhibitor produced by Chrysosporium. Bioorg. Med. Chem., 2002, 10, 185-188.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 185-188
-
-
Son, K.H.1
Kwon, J.Y.2
Jeong, H.W.3
Kim, H.K.4
Kim, C.J.5
Chang, Y.H.6
Choi, J.D.7
Kwon, B.M.8
-
35
-
-
33846104447
-
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
-
36
-
-
0001462209
-
Design and synthesis of highly potent fumagillin analogues from homology modeling for a human MetAP-2
-
DOI 10.1016/S0960-894X(99)00577-6, PII S0960894X99005776
-
Han, C.K.; Ahn, S.K.; Choi, N.S.; Hong, R.K.; Moon, S.K.; Chun, H.S.; Lee, S.J.; Kim, J.W.; Hong, C.I.; Kim, D.; Yoon, J.H.; No, K.T. Design and synthesis of highly potent fumagillin analogues from homology modeling for a human MetAP-2. Bioorg. Med. Chem. Lett., 2000, 10, 39-43. (Pubitemid 30014666)
-
(2000)
Bioorganic and Medicinal Chemistry Letters
, vol.10
, Issue.1
, pp. 39-43
-
-
Han, C.K.1
Ahn, S.K.2
Choi, N.S.3
Hong, R.K.4
Moon, S.K.5
Chun, H.S.6
Lee, S.J.7
Kim, J.W.8
Hong, C.I.9
Kim, D.10
Yoon, J.H.11
No, K.T.12
-
37
-
-
13244265583
-
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
-
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
-
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
-
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
-
41
-
-
0347517817
-
Investigation of novel fumagillin analogues as angiogenesis inhibitors
-
DOI 10.1016/j.bmcl.2003.10.008
-
Pyun, H.J.; Fardis, M.; Tario, J.; Yang, C.Y.; Ruckman, J.; Henninger, D.; Jin, H.L.; Kim, C.U. Investigation of novel fumagillin analogues as angiogenesis inhibitors. Bioorg. Med. Chem. Lett., 2004, 14, 91-94. (Pubitemid 38010200)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.1
, pp. 91-94
-
-
Pyun, H.-J.1
Fardis, M.2
Tario, J.3
Yang, C.Y.4
Ruckman, J.5
Henninger, D.6
Jin, H.7
Kim, C.U.8
-
42
-
-
22244488279
-
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
-
43
-
-
33744740720
-
Inhibitionof melanoma tumor growth by a pharmacological inhibitor of MetAP-2, PPI-2458
-
Hannig, G.; Lazarus, D.D.; Bernier, S.G.; Karp, R.M.; Lorusso, J.; Qiu, D.; Labenski, M.T.; Wakefield, J.D.; Thompson, C.D.; Westlin, W.F. Inhibitionof melanoma tumor growth by a pharmacological inhibitor of MetAP-2, PPI-2458. Int. J. Oncol., 2006, 28, 955-963.
-
(2006)
Int. J. Oncol.
, vol.28
, pp. 955-963
-
-
Hannig, G.1
Lazarus, D.D.2
Bernier, S.G.3
Karp, R.M.4
Lorusso, J.5
Qiu, D.6
Labenski, M.T.7
Wakefield, J.D.8
Thompson, C.D.9
Westlin, W.F.10
-
44
-
-
33646391501
-
A novel methionine aminopeptidase-2 inhibitor, PPI-2458, inhibits non- Hodgkin's lymphoma cell proliferation in vitro and in vivo
-
Cooper, A.C.; Karp, R.M.; Clark, E.J.; Taghizadeh, N.R.; Hoyt, J.G.; Labenski, M.T.; Murray, M.J.; Hannig, G.; Westlin, W.F.; Thompson, C.D. A novel methionine aminopeptidase-2 inhibitor, PPI-2458, inhibits non- Hodgkin's lymphoma cell proliferation in vitro and in vivo. Clin. Cancer Res., 2006, 12, 2583-2590.
-
(2006)
Clin. Cancer Res.
, vol.12
, pp. 2583-2590
-
-
Cooper, A.C.1
Karp, R.M.2
Clark, E.J.3
Taghizadeh, N.R.4
Hoyt, J.G.5
Labenski, M.T.6
Murray, M.J.7
Hannig, G.8
Westlin, W.F.9
Thompson, C.D.10
-
45
-
-
73249148673
-
Carbamate analogues of fumagillin as potent, targeted inhibitors of methionine aminopeptidase-2
-
Arico-Muendel, C.C.; Benjamin, D.R.; Caiazzo, T.M.; Centrella, P.A.; Contonio, B.D.; Cook, C.M.; Doyle, E.G.; Hannig, G.; Labenski, M.T.; Searle, L.L.; Lind, K.; Morgan, B.A.; Olson, G.; Paradise, C.L.; Self, C.; Skinner, S.R.; Sluboski, B.; Svendsen, J.L.; Thompson, C.D.; Westlin, W.; White, K.F. Carbamate analogues of fumagillin as potent, targeted inhibitors of methionine aminopeptidase-2. J. Med. Chem., 2009, 52, 8047-8056.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 8047-8056
-
-
Arico-Muendel, C.C.1
Benjamin, D.R.2
Caiazzo, T.M.3
Centrella, P.A.4
Contonio, B.D.5
Cook, C.M.6
Doyle, E.G.7
Hannig, G.8
Labenski, M.T.9
Searle, L.L.10
Lind, K.11
Morgan, B.A.12
Olson, G.13
Paradise, C.L.14
Self, C.15
Skinner, S.R.16
Sluboski, B.17
Svendsen, J.L.18
Thompson, C.D.19
Westlin, W.20
White, K.F.21
more..
-
46
-
-
13044300888
-
Molecular recognition of angiogenesis inhibitors fumagillin and ovalicin by methionine aminopeptidase 2
-
DOI 10.1073/pnas.95.26.15183
-
Griffith, E.C.; Su, Z.; Niwayama, S.; Ramsay, C.A.; Chang, Y.H.; Liu, J.O. Molecular recognition of angiogenesis inhibitors fumagillin and ovalicin by methionine aminopeptidase 2. Proc. Natl. Acad. Sci. USA, 1998, 95, 15183-15188. (Pubitemid 29018673)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.26
, pp. 15183-15188
-
-
Griffith, E.C.1
Zhuang, S.U.2
Niwayama, S.3
Ramsay, C.A.4
Chang, Y.-H.5
Liu, J.O.6
-
47
-
-
0032515029
-
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
-
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
-
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
-
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
-
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
-
52
-
-
0025770253
-
Leucine aminopeptidase: Bestatin inhibition and a model for enzyme-catalyzed peptide hydrolysis
-
Burley, S.K.; David, P.R.; Lipscomb, W.N. Leucine aminopeptidase: bestatin inhibition and a model for enzyme-catalyzed peptide hydrolysis. Proc. Natl. Acad. Sci. USA, 1991, 88, 6916-6920. (Pubitemid 21915060)
-
(1991)
Proceedings of the National Academy of Sciences of the United States of America
, vol.88
, Issue.16
, pp. 6916-6920
-
-
Burley, S.K.1
David, P.R.2
Lipscomb, W.N.3
-
53
-
-
10744228072
-
3-Amino-2-hydroxyamides and related compounds as inhibitors of methionine aminopeptidase-2
-
Sheppard, G.S.; Wang, J.; Kawai, M.; BaMaung, N.Y.; Craig, R.A.; Erickson, S.A.; Lynch, L.; Patel, J.; Yang, F.; Searle, X.B.; Lou, P.; Park, C.; Kim, K.H.; Henkin, J.; Lesniewski, R. 3-Amino-2-hydroxyamides and related compounds as inhibitors of methionine aminopeptidase-2. Bioorg. Med. Chem. Lett., 2004, 14, 865-868.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 865-868
-
-
Sheppard, G.S.1
Wang, J.2
Kawai, M.3
BaMaung, N.Y.4
Craig, R.A.5
Erickson, S.A.6
Lynch, L.7
Patel, J.8
Yang, F.9
Searle, X.B.10
Lou, P.11
Park, C.12
Kim, K.H.13
Henkin, J.14
Lesniewski, R.15
-
54
-
-
10744229380
-
Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2
-
Wang, J.; Sheppard, G.S.; Lou, P.; Kawai, M.; BaMaung, N.; Erickson, S.A.; Tucker-Garcia, L.; Park, C.; Bouska, J.; Wang, Y.C.; Frost, D.; Tapang, P.; Albert, D.H.; Morgan, S.J.; Morowitz, M.; Shusterman, S.; Maris, J.M.; Lesniewski, R.; Henkin, J. Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2. Cancer Res., 2003, 63, 7861-7869.
-
(2003)
Cancer Res.
, vol.63
, pp. 7861-7869
-
-
Wang, J.1
Sheppard, G.S.2
Lou, P.3
Kawai, M.4
BaMaung, N.5
Erickson, S.A.6
Tucker-Garcia, L.7
Park, C.8
Bouska, J.9
Wang, Y.C.10
Frost, D.11
Tapang, P.12
Albert, D.H.13
Morgan, S.J.14
Morowitz, M.15
Shusterman, S.16
Maris, J.M.17
Lesniewski, R.18
Henkin, J.19
-
55
-
-
20244370722
-
Methionine aminopeptidase 2 inhibition is an effective treatment strategy for neuroblastoma in preclinical models
-
DOI 10.1158/1078-0432.CCR-04-1917
-
Morowitz, M.J.; Barr, R.; Wang, Q.; King, R.; Rhodin, N.; Pawel, B.; Zhao, H.; Erickson, S.A.; Sheppard, G.S.; Wang, J.; Maris, J.M.; Shusterman, S. Methionine aminopeptidase 2 inhibition is an effective treatment strategy for neuroblastoma in preclinical models. Clin. Cancer Res., 2005, 11, 2680-2685. (Pubitemid 40569469)
-
(2005)
Clinical Cancer Research
, vol.11
, Issue.7
, pp. 2680-2685
-
-
Morowitz, M.J.1
Barr, R.2
Wang, Q.3
King, R.4
Rhodin, N.5
Pawel, B.6
Zhao, H.7
Erickson, S.A.8
Sheppard, G.S.9
Wang, J.10
Maris, J.M.11
Shusterman, S.12
-
56
-
-
23944470359
-
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
-
57
-
-
41149086699
-
Correlation of tumor growth suppression and methionine aminopetidase-2 activity blockade using an orally active inhibitor
-
DOI 10.1073/pnas.0708766105
-
Wang, J.; Tucker, L.A.; Stavropoulos, J.; Zhang, Q.; Wang, Y.C.; Bukofzer, G.; Niquette, A.; Meulbroek, J.A.; Barnes, D.M.; Shen, J.; Bouska, J.; Donawho, C.; Sheppard, G.S.; Bell, R.L. Correlation of tumor growth suppression and methionine aminopetidase-2 activity blockade using an orally active inhibitor. Proc. Natl. Acad. Sci. USA, 2008, 105, 1838-1843. (Pubitemid 351439426)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.6
, pp. 1838-1843
-
-
Wang, J.1
Tucker, L.A.2
Stavropoulos, J.3
Zhang, Q.4
Wang, Y.-C.5
Bukofzer, G.6
Niquette, A.7
Meulbroek, J.A.8
Barnes, D.M.9
Shen, J.10
Bouska, J.11
Donawho, C.12
Sheppard, G.S.13
Bell, R.L.14
-
58
-
-
0242522298
-
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
-
59
-
-
9144222006
-
Proteomics-based target identification: Bengamides as a new class of methionine aminopeptidase inhibitors
-
DOI 10.1074/jbc.M309039200
-
Towbin, H.; Bair, K.W.; DeCaprio, J.A.; Eck, M.J.; Kim, S.; Kinder, F.R.; Morollo, A.; Mueller, D.R.; Schindler, P.; Song, H.K.; van Oostrum, J.; Versace, R.W.; Voshol, H.; Wood, J.; Zabludoff, S.; Phillips, P.E. Proteomics-based target identification: bengamides as a new class of methionine aminopeptidase inhibitors. J. Biol. Chem., 2003, 278, 52964-52971. (Pubitemid 38035898)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.52
, pp. 52964-52971
-
-
Towbin, H.1
Bair, K.W.2
DeCaprio, J.A.3
Eck, M.J.4
Kim, S.5
Kinder, F.R.6
Morollo, A.7
Mueller, D.R.8
Schindler, P.9
Song, H.K.10
Van Oostrum, J.11
Versace, R.W.12
Voshol, H.13
Wood, J.14
Zabludoff, S.15
Phillips, P.E.16
-
60
-
-
34447547502
-
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
-
61
-
-
0035831239
-
Bengamides revisited: New structures and antitumor studies
-
DOI 10.1021/jo001380+
-
Thale, Z.; Kinder, F.R.; Bair, K.W.; Bontempo, J.; Czuchta, A.M.; Versace, R.W.; Phillips, P.E.; Sanders, M.L.; Wattanasin, S.; Crews, P. Bengamides revisited: new structures and antitumor studies. J. Org. Chem., 2001, 66, 1733-1741. (Pubitemid 32205111)
-
(2001)
Journal of Organic Chemistry
, vol.66
, Issue.5
, pp. 1733-1741
-
-
Thale, Z.1
Kinder, F.R.2
Bair, K.W.3
Bontempo, J.4
Czuchta, A.M.5
Versace, R.W.6
Phillips, P.E.7
Sanders, M.L.8
Wattanasin, S.9
Crews, P.10
-
62
-
-
0035950061
-
Synthesis and antitumor activity of ester-modified analogues of bengamide B
-
DOI 10.1021/jm010188c
-
Kinder, F.R., Jr.; Versace, R.W.; Bair, K.W.; Bontempo, J.M.; Cesarz, D.; Chen, S.; Crews, P.; Czuchta, A.M.; Jagoe, C.T.; Mou, Y.; Nemzek, R.; Phillips, P.E.; Tran, L.D.; Wang, R.M.; Weltchek, S.; Zabludoff, S. Synthesis and antitumor activity of ester-modified analogues of bengamide B. J. Med. Chem., 2001, 44, 3692-3699. (Pubitemid 33026677)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.22
, pp. 3692-3699
-
-
Kinder Jr., F.R.1
Versace, R.W.2
Bair, K.W.3
Bontempo, J.M.4
Cesarz, D.5
Chen, S.6
Crews, P.7
Czuchta, A.M.8
Jagoe, C.T.9
Mou, Y.10
Nemzek, R.11
Phillips, P.E.12
Tran, L.D.13
Wang, R.14
Weltchek, S.15
Zabludoff, S.16
-
63
-
-
33845715488
-
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
-
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
-
65
-
-
33646824129
-
Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties
-
Kawai, M.; BaMaung, N.Y.; Fidanze, S.D.; Erickson, S.A.; Tedrow, J.S.; Sanders, W.J.; Vasudevan, A.; Park, C.; Hutchins, C.; Comess, K.M.; Kalvin, D.; Wang, J.; Zhang, Q.; Lou, P.; Tucker-Garcia, L.; Bouska, J.; Bell, R.L.; Lesniewski, R.; Henkin, J.; Sheppard, G.S. Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties. Bioorg. Med. Chem. Lett., 2006, 16, 3574-3577.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 3574-3577
-
-
Kawai, M.1
BaMaung, N.Y.2
Fidanze, S.D.3
Erickson, S.A.4
Tedrow, J.S.5
Sanders, W.J.6
Vasudevan, A.7
Park, C.8
Hutchins, C.9
Comess, K.M.10
Kalvin, D.11
Wang, J.12
Zhang, Q.13
Lou, P.14
Tucker-Garcia, L.15
Bouska, J.16
Bell, R.L.17
Lesniewski, R.18
Henkin, J.19
Sheppard, G.S.20
more..
-
66
-
-
33745655190
-
Discovery and optimization of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2: A structural basis for the reduction of albumin binding
-
Sheppard, G.S.; Wang, J.; Kawai, M.; Fidanze, S.D.; BaMaung, N.Y.; Erickson, S.A.; Barnes, D.M.; Tedrow, J.S.; Kolaczkowski, L.; Vasudevan, A.; Park, D.C.; Wang, G.T.; Sanders, W.J.; Mantei, R.A.; Palazzo, F.; Tucker-Garcia, L.; Lou, P.; Zhang, Q.; Park, C.H.; Kim, K.H.; Petros, A.; Olejniczak, E.; Nettesheim, D.; Hajduk, P.; Henkin, J.; Lesniewski, R.; Davidsen, S.K.; Bell, R.L. Discovery and optimization of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2: a structural basis for the reduction of albumin binding. J. Med. Chem., 2006, 49, 3832-3849.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3832-3849
-
-
Sheppard, G.S.1
Wang, J.2
Kawai, M.3
Fidanze, S.D.4
BaMaung, N.Y.5
Erickson, S.A.6
Barnes, D.M.7
Tedrow, J.S.8
Kolaczkowski, L.9
Vasudevan, A.10
Park, D.C.11
Wang, G.T.12
Sanders, W.J.13
Mantei, R.A.14
Palazzo, F.15
Tucker-Garcia, L.16
Lou, P.17
Zhang, Q.18
Park, C.H.19
Kim, K.H.20
Petros, A.21
Olejniczak, E.22
Nettesheim, D.23
Hajduk, P.24
Henkin, J.25
Lesniewski, R.26
Davidsen, S.K.27
Bell, R.L.28
more..
-
67
-
-
34247353336
-
Lead optimization of methionine aminopeptidase-2 (MetAP2) inhibitors containing sulfonamides of 5,6-disubstituted anthranilic acids
-
DOI 10.1016/j.bmcl.2007.02.062, PII S0960894X07002594
-
Wang, G.T.; Mantei, R.A.; Kawai, M.; Tedrow, J.S.; Barnes, D.M.; Wang, J.; Zhang, Q.; Lou, P.; Garcia, L.A.; Bouska, J.; Yates, M.; Park, C.; Judge, R.A.; Lesniewski, R.; Sheppard, G.S.; Bell, R.L. Lead optimization of methionine aminopeptidase-2 (MetAP2) inhibitors containing sulfonamides of 5,6-disubstituted anthranilic acids. Bioorg. Med. Chem. Lett., 2007, 17, 2817-2822. (Pubitemid 46636248)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.10
, pp. 2817-2822
-
-
Wang, G.T.1
Mantei, R.A.2
Kawai, M.3
Tedrow, J.S.4
Barnes, D.M.5
Wang, J.6
Zhang, Q.7
Lou, P.8
Garcia, L.A.9
Bouska, J.10
Yates, M.11
Park, C.12
Judge, R.A.13
Lesniewski, R.14
Sheppard, G.S.15
Bell, R.L.16
-
68
-
-
34548079335
-
Highly potent inhibitors of methionine aminopeptidase-2 based on a 1,2,4-triazole pharmacophore
-
DOI 10.1021/jm061182w
-
Marino, J.P., Jr.; Fisher, P.W.; Hofmann, G.A.; Kirkpatrick, R.B.; Janson, C.A.; Johnson, R.K.; Ma, C.; Mattern, M.; Meek, T.D.; Ryan, M.D.; Schulz, C.; Smith, W.W.; Tew, D.G.; Tomazek, T.A., Jr.; Veber, D.F.; Xiong, W.C.; Yamamoto, Y.; Yamashita, K.; Yang, G.; Thompson, S.K. Highly potent inhibitors of methionine aminopeptidase-2 based on a 1,2,4-triazole pharmacophore. J. Med. Chem., 2007, 50, 3777-3785. (Pubitemid 47292041)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.16
, pp. 3777-3785
-
-
Marino Jr., J.P.1
Fisher, P.W.2
Hofmann, G.A.3
Kirkpatrick, R.B.4
Janson, C.A.5
Johnson, R.K.6
Ma, C.7
Mattern, M.8
Meek, T.D.9
Ryan, M.D.10
Schulz, C.11
Smith, W.W.12
Tew, D.G.13
Tomazek Jr., T.A.14
Veber, D.F.15
Xiong, W.C.16
Yamamoto, Y.17
Yamashita, K.18
Yang, G.19
Thompson, S.K.20
more..
-
69
-
-
0023792919
-
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
-
70
-
-
24744461365
-
4-Aryl-1,2,3-triazole: A novel template for a reversible methionine aminopeptidase 2 inhibitor, optimized to inhibit angiogenesis in vivo
-
DOI 10.1021/jm050408c
-
Kallander, L.S.; Lu, Q.; Chen, W.; Tomaszek, T.; Yang, G.; Tew, D.; Meek, T.D.; Hofmann, G.A.; Schulz-Pritchard, C.K.; Smith, W.W.; Janson, C.A.; Ryan, M.D.; Zhang, G.F.; Johanson, K.O.; Kirkpatrick, R.B.; Ho, T.F.; Fisher, P.W.; Mattern, M.R.; Johnson, R.K.; Hansbury, M.J.; Winkler, J.D.; Ward, K.W.; Veber, D.F.; Thompson, S.K. 4-Aryl-1,2,3-triazole: a novel template for a reversible methionine aminopeptidase 2 inhibitor, optimized to inhibit angiogenesis in vivo. J. Med. Chem., 2005, 48, 5644-5647. (Pubitemid 41298336)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.18
, pp. 5644-5647
-
-
Kallander, L.S.1
Lu, Q.2
Chen, W.3
Tomaszek, T.4
Yang, G.5
Tew, D.6
Meek, T.D.7
Hofmann, G.A.8
Schulz-Pritchard, C.K.9
Smith, W.W.10
Janson, C.A.11
Ryan, M.D.12
Zhang, G.-F.13
Johanson, K.O.14
Kirkpatrick, R.B.15
Ho, T.F.16
Fisher, P.W.17
Mattern, M.R.18
Johnson, R.K.19
Hansbury, M.J.20
Winkler, J.D.21
Ward, K.W.22
Veber, D.F.23
Thompson, S.K.24
more..
-
71
-
-
0041735178
-
The 1.15 Å crystal structure of the Staphylococcus aureus methionyl-aminopeptidase and complexes with triazole based inhibitors
-
DOI 10.1016/S0022-2836(03)00862-3
-
Oefner, C.; Douangamath, A.; D'Arcy, A.; Hafeli, S.; Mareque, D.; Mac Sweeney, A.; Padilla, J.; Pierau, S.; Schulz, H.; Thormann, M.; Wadman, S.; Dale, G.E. The 1.15Å crystal structure of the Staphylococcus aureus methionyl-aminopeptidase and complexes with triazole based inhibitors. J. Mol. Biol., 2003, 332, 13-21. (Pubitemid 36999727)
-
(2003)
Journal of Molecular Biology
, vol.332
, Issue.1
, pp. 13-21
-
-
Oefner, C.1
Douangamath, A.2
D'Arcy, A.3
Hafeli, S.4
Mareque, D.5
Sweeney, A.M.6
Padilla, J.7
Pierau, S.8
Schulz, H.9
Thormann, M.10
Wadman, S.11
Dale, G.E.12
-
72
-
-
8544232793
-
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
-
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
-
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
-
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
-
76
-
-
70350099250
-
NC2213: A novel methionine aminopeptidase 2 inhibitor in human colon cancer HT29 cells
-
Selvakumar, P.; Lakshmikuttyamma, A.; Das, U.; Pati, H.N.; Dimmock, J.R.; Sharma, R.K. NC2213: a novel methionine aminopeptidase 2 inhibitor in human colon cancer HT29 cells. Mol. Cancer, 2009, 8, 65-71.
-
(2009)
Mol. Cancer
, vol.8
, pp. 65-71
-
-
Selvakumar, P.1
Lakshmikuttyamma, A.2
Das, U.3
Pati, H.N.4
Dimmock, J.R.5
Sharma, R.K.6
-
77
-
-
33746265863
-
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
-
78
-
-
78650350269
-
Effect of nitroxoline on angiogenesis and growth of human bladder cancer
-
Shim, J.S.; Matsui, Y.; Bhat, S.; Nacev, B.A.; Xu, J.; Bhang, H.E.; Dhara, S.; Han, K.C.; Chong, C.R.; Pomper, M.G.; So, A.; Liu, J.O. Effect of nitroxoline on angiogenesis and growth of human bladder cancer. J. Natl. Cancer Inst., 2010, 102, 1855-1873.
-
(2010)
J. Natl. Cancer Inst.
, vol.102
, pp. 1855-1873
-
-
Shim, J.S.1
Matsui, Y.2
Bhat, S.3
Nacev, B.A.4
Xu, J.5
Bhang, H.E.6
Dhara, S.7
Han, K.C.8
Chong, C.R.9
Pomper, M.G.10
So, A.11
Liu, J.O.12
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