-
4
-
-
0030005037
-
-
Abrams, S.I., Hand, P.H., Tsang, K.Y., Schlom, J. Mutant ras epitopes as targets for cancer vaccines. Semin Oncol 1996, 23: 118-34.
-
(1996)
Mutant Ras Epitopes as Targets for Cancer Vaccines. Semin Oncol
, vol.23
, pp. 118-134
-
-
Abrams, S.I.1
Hand, P.H.2
Tsang, K.Y.3
Schlom, J.4
-
5
-
-
0029562231
-
-
Rak, J., Mitsuhashi, Y., Erdos, V., Huang, S.N., Filmus, J., Kerbel, R.S. Massive programmed cell death in intestinal epithelial cells induced by three-dimensional growth conditions: Suppression by mutant c-H-ras oncogene expression. J Cell Biol 1995, 131: 1587-98.
-
(1995)
Massive Programmed Cell Death in Intestinal Epithelial Cells Induced by Three-dimensional Growth Conditions: Suppression by Mutant C-H-ras Oncogene Expression. J Cell Biol
, vol.131
, pp. 1587-1598
-
-
Rak, J.1
Mitsuhashi, Y.2
Erdos, V.3
Huang, S.N.4
Filmus, J.5
Kerbel, R.S.6
-
6
-
-
0029860753
-
-
Perrin, D., Halazy, S., Hill, B.T. Inhibitors of the ras signal transduction pathway as potential antitumor agents. J Enzyme Inhib 1996,11:77-95.
-
(1996)
Inhibitors of the Ras Signal Transduction Pathway as Potential Antitumor Agents. J Enzyme Inhib
, vol.11
, pp. 77-95
-
-
Perrin, D.1
Halazy, S.2
Hill, B.T.3
-
9
-
-
0030909336
-
-
Boyartchuk, V.L., Ashby, M.N., Rine, J. Modulation of ras and a-factor function by carboxyl-terminalproteolysis. Science 1997, 275:1796-800.
-
(1997)
Modulation of Ras and A-factor Function by Carboxyl-terminalproteolysis. Science
, vol.275
, pp. 1796-1800
-
-
Boyartchuk, V.L.1
Ashby, M.N.2
Rine, J.3
-
10
-
-
0029789954
-
-
Liu, L, Dudler, T., Gelb, M.H. Purification ofa protein palmitoyltransferase that acts on H-ras protein and on a C-terminal N-ras peptide. J Biol Chem 1996, 271: 23269-76.
-
(1996)
Purification Ofa Protein Palmitoyltransferase that Acts on H-ras Protein and on a C-terminal N-ras Peptide. J Biol Chem
, vol.271
, pp. 23269-23276
-
-
Liu, L.1
Dudler, T.2
Gelb, M.H.3
-
12
-
-
0028892646
-
-
Lebowitz, P.F., Davide, J.P., Prendergast, G.C. Evidence that farnesyltransferase inhibitors suppress Pas transformation by interfering with Rho activity. Mol Cell Biol 1995,15: 6613-22.
-
(1995)
Evidence that Farnesyltransferase Inhibitors Suppress Pas Transformation by Interfering with Rho Activity. Mol Cell Biol
, vol.15
, pp. 6613-6622
-
-
Lebowitz, P.F.1
Davide, J.P.2
Prendergast, G.C.3
-
13
-
-
0028835253
-
-
Sepp-Lorenzino, L, Ma, 2.P., Rands, E. etal. Peptidomimetic inhibitor of farnesyl protein transi'erase blocks the anchorage-dependent and-independent growth of human tumor cell lines. Cancer Res 1995, 55: 5302-9.
-
(1995)
Peptidomimetic Inhibitor of Farnesyl Protein Transi'erase Blocks the Anchorage-dependent And-independent Growth of Human Tumor Cell Lines. Cancer Res
, vol.55
, pp. 5302-5309
-
-
Sepp-Lorenzino, L.1
Rands, E.2
-
14
-
-
0030596111
-
-
Cales, C.A., Michael, R.L, Stayrook, K.R. et al. Prenylation of oncogenic human PTPcaax protein tyrosine phosphatases. Cancer Lett 1996,110:49-55.
-
(1996)
Prenylation of Oncogenic Human PTPcaax Protein Tyrosine Phosphatases. Cancer Lett
, vol.110
, pp. 49-55
-
-
Cales, C.A.1
Michael, R.L.2
Stayrook, K.R.3
-
22
-
-
9044237262
-
-
Gibbs, J.B., Kohl, N.E., Koblan, K.S. et al. Farnesyltransferase inhibitors and anti-Ras therapy. Breast Cancer Res Treat 1996,38: 75-83.
-
(1996)
Farnesyltransferase Inhibitors and Anti-Ras Therapy. Breast Cancer Res Treat
, vol.38
, pp. 75-83
-
-
Gibbs, J.B.1
Kohl, N.E.2
Koblan, K.S.3
-
23
-
-
0029817090
-
-
Koblan, K.S., Kohl, N.E., Orner, C.A. et al. Farnesyltransferase inhibitors: a new class of cancer chemotherapeutics. Biochem Soc Trans 1996, 24:688-92.
-
(1996)
Farnesyltransferase Inhibitors: a New Class of Cancer Chemotherapeutics. Biochem Soc Trans
, vol.24
, pp. 688-692
-
-
Koblan, K.S.1
Kohl, N.E.2
Orner, C.A.3
-
24
-
-
0000649394
-
-
Der, C.J., Cox, A.D., Sebti, S.M., Hamilton, A.D. Farnesyltransferase inhibitors: Anti-Ras drugs for cancer'treatment?'Anti-Cancer Drugs 1996, 7:165-72.
-
(1996)
Farnesyltransferase Inhibitors: Anti-Ras Drugs for Cancer'treatment?'Anti-Cancer Drugs
, vol.7
, pp. 165-172
-
-
Der, C.J.1
Cox, A.D.2
Sebti, S.M.3
Hamilton, A.D.4
-
25
-
-
0030020333
-
Has inhibitors
-
Hiwasa, T. Has inhibitors. Oncol Rep 1996,3:7-14.
-
(1996)
Oncol Rep
, vol.3
, pp. 7-14
-
-
Hiwasa, T.1
-
27
-
-
0031007684
-
-
Lerner, E.C., Hamilton, A.D., Sebti, S.M. Inhibition of ras prenylation: A signaling target for novel anti-cancer drug design. AntiCancer Drug Des 1997,12: 229-38.
-
(1997)
Inhibition of Ras Prenylation: a Signaling Target for Novel Anti-cancer Drug Design. AntiCancer Drug Des
, vol.12
, pp. 229-238
-
-
Lerner, E.C.1
Hamilton, A.D.2
Sebti, S.M.3
-
28
-
-
0031017064
-
-
Huang, C.C., Casey, P.J., Fierke, C.A. Evidence fora catalytic role of zinc in protein farnesyltransferase: Spectroscopy of Co2+-farnesyltransferase indicates metal coordination of the substrate thiolate. J Biol Chem 1997, 272: 20-3.
-
(1997)
Evidence Fora Catalytic Role of Zinc in Protein Farnesyltransferase: Spectroscopy of Co2+-farnesyltransferase Indicates M
, vol.272
, pp. 20-23
-
-
Huang, C.C.1
Casey, P.J.2
Fierke, C.A.3
-
29
-
-
0030909826
-
-
Park, H.W., Boduluri, S.R., Moomaw, J.F., Casey, P.J., Beese, L.S. Crystal structure of protein farnesyltransferase at 2.25 angstrom resolution. Science 1997, 275:1800-4.
-
(1997)
Crystal Structure of Protein Farnesyltransferase at 2.25 Angstrom Resolution. Science
, vol.275
, pp. 1800-1804
-
-
Park, H.W.1
Boduluri, S.R.2
Moomaw, J.F.3
Casey, P.J.4
Beese, L.S.5
-
30
-
-
0029905595
-
-
Fu, H.W., Moomaw, J.F., Moomaw, C.R., Casey, P.J. Identification of a cysteine residue essential for activity of protein farnesyltransferase: Cys-299 is exposed only upon removal of zinc from the enzyme. J Biol Chem 1997, 271: 28541-8.
-
(1997)
Identification of a Cysteine Residue Essential for Activity of Protein Farnesyltransferase: Cys-299 Is Exposed only upon Removal of Zinc from the Enzyme. J Biol Chem
, vol.271
, pp. 28541-28548
-
-
Fu, H.W.1
Moomaw, J.F.2
Moomaw, C.R.3
Casey, P.J.4
-
31
-
-
0027137932
-
-
Stradley, S.J., Rizo J., Gierasch, L.M. Conformation of a heptapeptide substrate bound to protein farnesyltransferase. Biochemistry 1993, 32: 12586-90.
-
(1993)
Conformation of a Heptapeptide Substrate Bound to Protein Farnesyltransferase. Biochemistry
, vol.32
, pp. 12586-12590
-
-
Stradley, S.J.1
Rizo, J.2
Gierasch, L.M.3
-
32
-
-
0028936976
-
-
Koblan, K.S., Culberson, J.C., Desolms, S.J. et al. NMRstudies of novel inhibitors bound to farnesyl-protein transferase. Protein Sei 1995, 4: 681-8.
-
(1995)
NMRstudies of Novel Inhibitors Bound to Farnesyl-protein Transferase. Protein Sei
, vol.4
, pp. 681-688
-
-
Koblan, K.S.1
Culberson, J.C.2
Desolms, S.J.3
-
33
-
-
0026729445
-
-
Pompliano, D.L, Rands, E., Schaber, M.D., Mosser, S.D., Anthony, N.J., Gibbs, J.B. Steady state kinetic mechanism of Pas farnesyl: Protein transferase. Biochemistry 1992,31:3800-7.
-
(1992)
Steady State Kinetic Mechanism of Pas Farnesyl: Protein Transferase. Biochemistry
, vol.31
, pp. 3800-3807
-
-
Pompliano, D.L.1
Rands, E.2
Schaber, M.D.3
Mosser, S.D.4
Anthony, N.J.5
Gibbs, J.B.6
-
34
-
-
0029007105
-
-
Furfine, E.S., Leban, J.J., Landavazo, A., Moomaw, J.F., Casey, P.J. Protein farnesyltransferase: Kinetics of farnesyl pyrophosphate binding and product release. Biochemistry 1995, 34: 6857-62.
-
(1995)
Protein Farnesyltransferase: Kinetics of Farnesyl Pyrophosphate Binding and Product Release. Biochemistry
, vol.34
, pp. 6857-6862
-
-
Furfine, E.S.1
Leban, J.J.2
Landavazo, A.3
Moomaw, J.F.4
Casey, P.J.5
-
35
-
-
0029609580
-
-
Dolence, J.M., Cassidy, P.B., Mathis, J.R., Poulter, C.D. Yeast protein farnesyltransferase: Steady-state kinetic studies of substrate binding. Biochemistry 1995, 34:16687-94.
-
(1995)
Yeast Protein Farnesyltransferase: Steady-state Kinetic Studies of Substrate Binding. Biochemistry
, vol.34
, pp. 16687-16694
-
-
Dolence, J.M.1
Cassidy, P.B.2
Mathis, J.R.3
Poulter, C.D.4
-
36
-
-
0027301696
-
-
Pompliano, D.L., Schaber, M.D., Mosser, S.D., Orner, C.A., Shafer, J.A., Gibbs, J.B. Isoprenoid diphosphate utilization by recombinant human farnesyl:protein transferase: Interactive binding between substrates and a preferred kinetic pathway. Biochemistry 1993, 32: 8341-7.
-
(1993)
Isoprenoid Diphosphate Utilization by Recombinant Human Farnesyl:protein Transferase: Interactive Binding between Substrates and a Preferred Kinetic Pathway. Biochemistry
, vol.32
, pp. 8341-8347
-
-
Pompliano, D.L.1
Schaber, M.D.2
Mosser, S.D.3
Orner, C.A.4
Shafer, J.A.5
Gibbs, J.B.6
-
38
-
-
0030999833
-
-
Tschantz, W.R., Furfine, E.S., Casey, P.J. Substrate binding is required for release of product from mammalian protein farnesyltransferase. J Biol Chem 1997, 272: 9989-93.
-
(1997)
Substrate Binding Is Required for Release of Product from Mammalian Protein Farnesyltransferase. J Biol Chem
, vol.272
, pp. 9989-9993
-
-
Tschantz, W.R.1
Furfine, E.S.2
Casey, P.J.3
-
40
-
-
0029983874
-
-
Mu, Y.Q., Orner, C.A., Gibbs, R.A. On the stereochemical course of human protein-farnesyl transferase. J Am Chem Soc 1996, 118:1817-23.
-
(1996)
On the Stereochemical Course of Human Protein-farnesyl Transferase. J Am Chem Soc
, vol.118
, pp. 1817-1823
-
-
Mu, Y.Q.1
Orner, C.A.2
Gibbs, R.A.3
-
41
-
-
0030585321
-
-
Kumar, A., Beresini, M.H., Dhawan, P., Mehta, K.D. a-Subunit of farnesyltransferase is phosphorylated in vivo: Effect of protein phosphatase-1 on enzymatic activity. Biochem Biophys Res Commun 1996,222:445-52.
-
(1996)
Biochem Biophys Res Commun
, vol.222
, pp. 445-452
-
-
Kumar, A.1
Beresini, M.H.2
Dhawan, P.3
-
42
-
-
0029670049
-
-
Wang, T.W., Danielson, P.D., Li, B.Y., Shah, P.C., Kim, S.D., Donahoe, P.K. The p21ras farnesyltransferase alpha subunit in TGF-beta andactivin signaling. Science 1996,271:1120-2.
-
(1996)
The P21ras Farnesyltransferase Alpha Subunit in TGF-beta Andactivin Signaling. Science
, vol.271
, pp. 1120-1122
-
-
Wang, T.W.1
Danielson, P.D.2
Li, B.Y.3
Shah, P.C.4
Kim, S.D.5
Donahoe, P.K.6
-
43
-
-
0029941824
-
-
Ventura, F., Liu, F., Doody, J., Massagué, J. Interaction of transforming growth factor-beta receptor I with farnesyl-protein transfer-ase-alpha in yeast and mammalian cells. J Biol Chem 1996, 271: 13931-4.
-
(1996)
Interaction of Transforming Growth Factor-beta Receptor I with Farnesyl-protein Transfer-ase-alpha in Yeast and Mammalian Cells. J Biol Chem
, vol.271
, pp. 13931-13934
-
-
Ventura, F.1
Liu, F.2
Doody, J.3
Massagué, J.4
-
44
-
-
0039948032
-
-
Del Villar, K., Mitsuzawa, H., Yang, W., Sattler, I., Tamanoi, F. Am/no acid substitutions that convert the protein substrate specificity of farnesyltransferase to that of geranylgeranyltransferase type I. J Biol Chem 1997, 272: 680-7.
-
(1997)
Am/no Acid Substitutions that Convert the Protein Substrate Specificity of Farnesyltransferase to that of Geranylgeranyltransferase Type I. J Biol Chem
, vol.272
, pp. 680-687
-
-
Del Villar, K.1
Mitsuzawa, H.2
Yang, W.3
Sattler, I.4
Tamanoi, F.5
-
45
-
-
0030039165
-
-
Zhang, F.L., Fu, H.W., Casey, P.J., Bishop, W.R. Substitution of cadmium for zinc in farnesyl:protein transferase alters its substrate specificity. Biochemistry 1996, 35: 8166-71.
-
(1996)
Substitution of Cadmium for Zinc in Farnesyl:protein Transferase Alters Its Substrate Specificity. Biochemistry
, vol.35
, pp. 8166-8171
-
-
Zhang, F.L.1
Fu, H.W.2
Casey, P.J.3
Bishop, W.R.4
-
46
-
-
0028810275
-
-
Lerner, E.G., Qian, Y., Hamilton, A.D., Sebti, S.M. Disruption of oncogenic K-Ras4B processing and signaling by a potent geranylgeranyltransferase I inhibitor. J Biol Chem 1995, 270: 26770-3.
-
(1995)
Disruption of Oncogenic K-Ras4B Processing and Signaling by a Potent Geranylgeranyltransferase I Inhibitor. J Biol Chem
, vol.270
, pp. 26770-26773
-
-
Lerner, E.G.1
Qian, Y.2
Hamilton, A.D.3
Sebti, S.M.4
-
47
-
-
0031055466
-
-
Yokoyama, K., Zimmerman, K., Scholten, J., Gelb, M.H. Differentialprenylpyrophosphate binding to mammalian protein geranylgeranyltransferase-l and protein farnesyltransferase and its consequence on the specificity of protein prenylation. JBiolChem1997, 272: 3944-52.
-
(1997)
Differentialprenylpyrophosphate Binding to Mammalian Protein Geranylgeranyltransferase-l and Protein Farnesyltransferase and Its Consequence on the Specificity of Protein Prenylation. JBiolChem
, vol.272
, pp. 3944-3952
-
-
Yokoyama, K.1
Zimmerman, K.2
Scholten, J.3
Gelb, M.H.4
-
48
-
-
0031584823
-
-
Osman, H., Mazet, J.L., Maume, G., Maume, B.F. Geranylgeranyl as well as farnesyl moiety is transferred to ras p21 overproduced in adrenocortical cells transformed by c-ha-ras-ejoncogene. Biochem Biophys Res Commun 1997, 231:789-92.
-
(1997)
Geranylgeranyl as Well as Farnesyl Moiety Is Transferred to Ras P21 Overproduced in Adrenocortical Cells Transformed by C-ha-ras-ejoncogene. Biochem Biophys Res Commun
, vol.231
, pp. 789-792
-
-
Osman, H.1
Mazet, J.L.2
Maume, G.3
Maume, B.F.4
-
49
-
-
0030943198
-
-
Zhang, F.L., Kirschmeier, P., Carr, D. et al. Characterization of Ha-Ras, N-Ras, Ki-Ras4A, and Ki-Ras4B as in vitro substrates for farnesyl protein transferase and geranylgeranyl protein transferase type 1. J Biol Chem 1997, 272:10232-9.
-
(1997)
Characterization of Ha-Ras, N-Ras, Ki-Ras4A, and Ki-Ras4B as in Vitro Substrates for Farnesyl Protein Transferase and Geranylgeranyl Protein Transferase Type 1. J Biol Chem
, vol.272
, pp. 10232-10239
-
-
Zhang, F.L.1
Kirschmeier, P.2
Carr, D.3
-
50
-
-
0025194466
-
-
Reiss, Y., Goldstein, J.L., Seabra, M.C., Casey, P.J., Brown, M.S. Inhibition of purified p2Iras farnesyl:protein transferase by Cys-AAX tetrapeptides. Cell 1990, 62: 81-8.
-
(1990)
Inhibition of Purified P2Iras Farnesyl:protein Transferase by Cys-AAX Tetrapeptides. Cell
, vol.62
, pp. 81-88
-
-
Reiss, Y.1
Goldstein, J.L.2
Seabra, M.C.3
Casey, P.J.4
Brown, M.S.5
-
51
-
-
0026040193
-
-
Goldstein, J.L., Brown M.S., Stradley, S.J., Reiss, Y, Gierasch, L.M. Nonfarnesylated tetrapeptide inhibitors of protein farnesyltransferase. J Biol Chem 1991, 266:15575-8.
-
(1991)
Nonfarnesylated Tetrapeptide Inhibitors of Protein Farnesyltransferase. J Biol Chem
, vol.266
, pp. 15575-15578
-
-
Goldstein, J.L.1
Brown, M.S.2
Stradley, S.J.3
Reiss, Y.4
Gierasch, L.M.5
-
52
-
-
0026667497
-
-
Brown, M.S.,GoIdstein, J.L, Paris, K.J., Burnier, J.P., Marsters, U.C. Jr. Tetrapeptide inhibitors of protein farnesyltransferase: Amino-termihal substitution in phenylalanine-containing tetrapeptides restores farnesylation. Proc Natl Acad Sei USA 1992,89:8313-6.
-
(1992)
Jr. Tetrapeptide Inhibitors of Protein Farnesyltransferase: Amino-termihal Substitution in Phenylalanine-containing Tetrapeptides Restores Farnesylation. Proc Natl Acad Sei USA
, vol.89
, pp. 8313-8316
-
-
Brown, M.S.1
Goidstein, J.L.2
Paris, K.J.3
Burnier, J.P.4
Marsters, U.C.5
-
53
-
-
0027248872
-
-
Kohl, N.E., Mosser, S.D., DeSolms, S.J. et al. Selective inhibition of ras-dependent transformation by a farnesyltransferase inhibitor. Science 1993, 260:1934-7.
-
(1993)
Selective Inhibition of Ras-dependent Transformation by a Farnesyltransferase Inhibitor. Science
, vol.260
, pp. 1934-1937
-
-
Kohl, N.E.1
Mosser, S.D.2
Desolms, S.J.3
-
54
-
-
0028211246
-
-
Graham, S.L., Gibbs, J.B., Pompliano, D.L. Pseudopeptide inhibitors of ras farnesyl-proteine transferase. J Med Chem 1994, 37:725-32.
-
(1994)
Pseudopeptide Inhibitors of Ras Farnesyl-proteine Transferase. J Med Chem
, vol.37
, pp. 725-732
-
-
Graham, S.L.1
Gibbs, J.B.2
Pompliano, D.L.3
-
55
-
-
0028603395
-
-
Kohl, N.E., Wilson, F.R., Mosser, S.D. et al. Protein farnesyltransferase inhibitors block the growth of ras-dependent tumors in nude mice. Proc Natl Acad Sei USA 1994, 91: 9141-5.
-
(1994)
Protein Farnesyltransferase Inhibitors Block the Growth of Ras-dependent Tumors in Nude Mice. Proc Natl Acad Sei USA
, vol.91
, pp. 9141-9145
-
-
Kohl, N.E.1
Wilson, F.R.2
Mosser, S.D.3
-
56
-
-
0029150669
-
-
Kohl, N.E., Orner, C.A., Conner, M.W. et al. Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic mice. Nat Med 1995,1:792-7.
-
(1995)
Inhibition of Farnesyltransferase Induces Regression of Mammary and Salivary Carcinomas in Ras Transgenic Mice. Nat Med
, vol.1
, pp. 792-797
-
-
Kohl, N.E.1
Orner, C.A.2
Conner, M.W.3
-
57
-
-
0027320616
-
-
Garcia, A.M., Rowell, C., Ackermann, K., Kowalczyk, J.J., Lewis, M.D. Peptidomimetic inhibitors of ras farnesylation and function in whole cells. J Biol Chem 1993, 268:18415-8.
-
(1993)
Peptidomimetic Inhibitors of Ras Farnesylation and Function in Whole Cells. J Biol Chem
, vol.268
, pp. 18415-18418
-
-
Garcia, A.M.1
Rowell, C.2
Ackermann, K.3
Kowalczyk, J.J.4
Lewis, M.D.5
-
58
-
-
0027998986
-
-
Cox, A.D., Garcia, A.M., Westwick, J.K. et al. The CAAXpeptidomimetic compound B581 specifically blocks farnesylated, but not geranylgeranylated or myristylated, oncogenic Ras signaling and transformation. J Biol Chem 1994, 269:19203-6.
-
(1994)
The CAAXpeptidomimetic Compound B581 Specifically Blocks Farnesylated, but not Geranylgeranylated or Myristylated, Oncogenic Ras Signaling and Transformation. J Biol Chem
, vol.269
, pp. 19203-19206
-
-
Cox, A.D.1
Garcia, A.M.2
Westwick, J.K.3
-
59
-
-
0028869067
-
-
Nagasu, T., Yoshimatsu, K., Rowell, C., Lewis, M.D., Garcîa, A.M. Inhibition of human tumor xenograft growth by treatment with the farnesyl transferase inhibitor B956. Cancer Res 1995, 55: 5310-4.
-
(1995)
Inhibition of Human Tumor Xenograft Growth by Treatment with the Farnesyl Transferase Inhibitor B956. Cancer Res
, vol.55
, pp. 5310-5314
-
-
Nagasu, T.1
Yoshimatsu, K.2
Rowell, C.3
Lewis, M.D.4
Garcîa, A.M.5
-
60
-
-
0027323459
-
-
James, G.L., Goldstein, J.L., Brown, M.S. etal. Benzodiazepine peptidomimetics: Potent inhibitors of Ras farnesylation in animal cells. Science 1993, 260:1937-42.
-
(1993)
Benzodiazepine Peptidomimetics: Potent Inhibitors of Ras Farnesylation in Animal Cells. Science
, vol.260
, pp. 1937-1942
-
-
James, G.L.1
Goldstein, J.L.2
Brown, M.S.3
-
61
-
-
0027522046
-
-
61. Nigam, M., Seong, C.-M., Qian, Y, Hamilton, A.D., Sebti, S.M. Potent inhibition of human tumor p21ras farnesyltransferase by l A1A2-lackmgp21ras CA1A2Xpeptidomimetics. J Biol Chem 1993, 268:20695-8.
-
(1993)
Potent Inhibition of Human Tumor P21ras Farnesyltransferase by L A1A2-lackmgp21ras CA1A2Xpeptidomimetics. J Biol Chem
, vol.268
, pp. 20695-20698
-
-
Nigam, M.1
Seong, C.-M.2
Qian, Y.3
Hamilton, A.D.4
Sebti, S.M.5
-
62
-
-
0028352281
-
-
Qian, Y., Blaskovich, M.A., Saleem, M. et al. Design and structural requirements of potent peptidomimetic inhibitors of p21 ras farnesyltransferase. J Biol Chem 1994, 269:12410-3.
-
(1994)
Design and Structural Requirements of Potent Peptidomimetic Inhibitors of P21 Ras Farnesyltransferase. J Biol Chem
, vol.269
, pp. 12410-12413
-
-
Qian, Y.1
Blaskovich, M.A.2
Saleem, M.3
-
63
-
-
0028132044
-
-
Qian, Y, Blaskovich, M.A., Seong, C.-M., Vogt, A., Hamilton, A.D. ,Sebti,S.M. Peptidomimetic inhibitors ofp21 ras farnesyltransferase: Hydrophobie functionalization leads to disruption ofp21ras membrane association in whole cells. Bioorg Med Chem Lett 1994, 4: 2579-84.
-
(1994)
Peptidomimetic Inhibitors Ofp21 Ras Farnesyltransferase: Hydrophobie Functionalization Leads to Disruption Ofp21ras Membrane Association in Whole Cells. Bioorg Med Chem Lett
, vol.4
, pp. 2579-2584
-
-
Qian, Y.1
Blaskovich, M.A.2
Seong, C.-M.3
Vogt, A.4
Hamilton, A.D.5
Sebti, S.M.6
-
64
-
-
0028912593
-
-
Vogt, A., Qian, Y, Blaskovich, M.A., Possum, R.D., Hamilton, A.D., Sebti, S.M. A non-peptide mimetic of Ras-CAAX: Selective inhibition of famesyltransferase and Ras processing. J Biol Chem 1995,270:660-4.
-
(1995)
A Non-peptide Mimetic of Ras-CAAX: Selective Inhibition of Famesyltransferase and Ras Processing. J Biol Chem
, vol.270
, pp. 660-664
-
-
Vogt, A.1
Qian, Y.2
Blaskovich, M.A.3
Possum, R.D.4
Hamilton, A.D.5
Sebti, S.M.6
-
65
-
-
0029023145
-
-
Sun, J., Qian, Y, Hamilton, A.D., Sebti, S.M. Ras CAAXpeptidomimetic FT/ 276 selectively blocks tumor growth in nude mice of a human lung carcinoma with K-Ras mutation and p53 deletion. Cancer Res 1995, 55: 4243-7.
-
(1995)
Ras CAAXpeptidomimetic FT/ 276 Selectively Blocks Tumor Growth in Nude Mice of a Human Lung Carcinoma with K-Ras Mutation and P53 Deletion. Cancer Res
, vol.55
, pp. 4243-4247
-
-
Sun, J.1
Qian, Y.2
Hamilton, A.D.3
Sebti, S.M.4
-
66
-
-
0030046735
-
-
Qian, Y, Vogt, A., Sebti, S.M., Hamilton, A.D. Design and synthesis of non-peptide Ras CAAX mimetics as potent famesyltransferase inhibitors. J Med Chem 1996, 39: 217-23.
-
(1996)
Design and Synthesis of Non-peptide Ras CAAX Mimetics as Potent Famesyltransferase Inhibitors. J Med Chem
, vol.39
, pp. 217-223
-
-
Qian, Y.1
Vogt, A.2
Sebti, S.M.3
Hamilton, A.D.4
-
67
-
-
0031579949
-
-
Dinsmore, C.J., Williams, T.M., Hamilton, K. et al. Diarylether inhibitors of farnesyl-protein transferase. Bioorg Med Chem Lett 1997,7:1345-8.
-
(1997)
Diarylether Inhibitors of Farnesyl-protein Transferase. Bioorg Med Chem Lett
, vol.7
, pp. 1345-1348
-
-
Dinsmore, C.J.1
Williams, T.M.2
Hamilton, K.3
-
68
-
-
0030914577
-
-
Burns, C.J., Guitton, J.-D., Baudoin, B. et al. Novelconformationally extended naphthalene-based inhibitors of famesyltransferase. J Med Chem 1997, 40:1763-7.
-
(1997)
Novelconformationally Extended Naphthalene-based Inhibitors of Famesyltransferase. J Med Chem
, vol.40
, pp. 1763-1767
-
-
Burns, C.J.1
Guitton, J.-D.2
Baudoin, B.3
-
69
-
-
13344276587
-
-
Leftheris, K., Kline, T., Vite, G.D. et al. Development of highly potent inhibitors of Ras famesyltransferase possessing cellular and m vivo activity. J Med Chem 1996, 39: 224-36.
-
(1996)
Development of Highly Potent Inhibitors of Ras Famesyltransferase Possessing Cellular and M Vivo Activity. J Med Chem
, vol.39
, pp. 224-236
-
-
Leftheris, K.1
Kline, T.2
Vite, G.D.3
-
70
-
-
33847445792
-
-
Leftheris, K., Cho, Y.H., Vite, G.D. et al. Highly potent thiolbased inhibitors of ras famesyltransferase. 25th Natl Med Chem Symp (June 18-12, Ann Harbor, Ml) 1996, Abst.11.
-
(1996)
Highly Potent Thiolbased Inhibitors of Ras Famesyltransferase. 25th Natl Med Chem Symp (June 18-12, Ann Harbor, Ml)
, pp. 11
-
-
Leftheris, K.1
Cho, Y.H.2
Vite, G.D.3
-
71
-
-
0029095460
-
-
Clerc, F.F., Guitton, J.-D., Fromage, N. et al. Constrained analogs ofKCVFM with improved inhibitory properties against farnesyl transferase. Bioorg Med Chem Lett 1995, 5:1779-84.
-
(1995)
Constrained Analogs OfKCVFM with Improved Inhibitory Properties against Farnesyl Transferase. Bioorg Med Chem Lett
, vol.5
, pp. 1779-1784
-
-
Clerc, F.F.1
Guitton, J.-D.2
Fromage, N.3
-
72
-
-
0028152440
-
-
Harrington, E.M., Kowalczyk, J.J., Pinnow, S.L., Ackermann, K., Garcia, A.M., Lewis, M.D. Cysteine and methionine linked by carbon pseudopeptides inhibit farnesyl transferase. Bioorg Med Chem Lett 1994,4: 2775-80.
-
(1994)
Cysteine and Methionine Linked by Carbon Pseudopeptides Inhibit Farnesyl Transferase. Bioorg Med Chem Lett
, vol.4
, pp. 2775-2780
-
-
Harrington, E.M.1
Kowalczyk, J.J.2
Pinnow, S.L.3
Ackermann, K.4
Garcia, A.M.5
Lewis, M.D.6
-
73
-
-
0029986149
-
2-Substituted piperazines as constrained amino acids
-
Williams, T.M.,Ciccarone, T.M.,MacTough, S.C. et al.2-Substituted piperazines as constrained amino acids. Application to the synthesis of potent, non carboxylic acid inhibitors of famesyltransferase. J Med Chem 1996, 39:1345-8.
-
(1996)
Application to the Synthesis of Potent, Non Carboxylic Acid Inhibitors of Famesyltransferase. J Med Chem
, vol.39
, pp. 1345-1348
-
-
Williams, T.M.1
Ciccarone, T.M.2
MacTough, S.C.3
-
74
-
-
0028807672
-
-
Kowalczyk, J.J., Ackermann, K., Garcfa, A.M., Lewis, M.D. Phenolic replacements for cysteine in farnesyl transferase inhibitors based on CVFM. Bioorg Med Chem Lett 1995, 5: 3073-8.
-
(1995)
Phenolic Replacements for Cysteine in Farnesyl Transferase Inhibitors Based on CVFM. Bioorg Med Chem Lett
, vol.5
, pp. 3073-3078
-
-
Kowalczyk, J.J.1
Ackermann, K.2
Garcfa, A.M.3
Lewis, M.D.4
-
75
-
-
0028108888
-
-
Patel, D., Patel, M.M., Robinson, S.S., Gordon, E.M. Phenol based tripeptide inhibitors of ras farnesyl protein transferase. Bioorg Med Chem Lett 1994, 4:1883-8.
-
(1994)
Phenol Based Tripeptide Inhibitors of Ras Farnesyl Protein Transferase. Bioorg Med Chem Lett
, vol.4
, pp. 1883-1888
-
-
Patel, D.1
Patel, M.M.2
Robinson, S.S.3
Gordon, E.M.4
-
76
-
-
0030034763
-
-
Hunt, J.T., Lee, V.G., Leftheris, K. et al. Potent, cell active, nonthiol tetrapeptide inhibitors of farnesyltransferase. J Med Chem 1996,39:353-8.
-
(1996)
Potent, Cell Active, Nonthiol Tetrapeptide Inhibitors of Farnesyltransferase. J Med Chem
, vol.39
, pp. 353-358
-
-
Hunt, J.T.1
Lee, V.G.2
Leftheris, K.3
-
77
-
-
0000231277
-
-
McClard, R.W., Fujita, T.S., Stremler, K.E., Poulter, C.D. Novel phosphonylphosphinyl (P-C-P-C-) analogues of biochemically interesting diphosphates. Syntheses and properties of P-C-P-Canalogues of isopentenyl diphosphate and dimethylallyl diphosphate. J Am Chem Soc 1987,109: 5544-5.
-
(1987)
Novel Phosphonylphosphinyl (P-C-P-C-) Analogues of Biochemically Interesting Diphosphates. Syntheses and Properties of P-C-P-Canalogues of Isopentenyl Diphosphate and Dimethylallyl Diphosphate. J Am Chem Soc
, vol.109
, pp. 5544-5545
-
-
McClard, R.W.1
Fujita, T.S.2
Stremler, K.E.3
Poulter, C.D.4
-
78
-
-
0023749462
-
-
Biller, S.A., Forster, C., Gordon, E.M., Harrity, T., Scott, W.A., Ciosek, C.P., Jr. Isoprenoid (phosphinylmethyl)phosphonates as inhibitors ofsqualene synthetase. J Med Chem 1988,31:1869-71.
-
(1988)
Isoprenoid (Phosphinylmethyl)phosphonates as Inhibitors Ofsqualene Synthetase. J Med Chem
, vol.31
, pp. 1869-1871
-
-
Biller, S.A.1
Forster, C.2
Gordon, E.M.3
Harrity, T.4
Scott, W.A.5
Ciosek Jr., C.P.6
-
79
-
-
0027413551
-
-
Gibbs, J.B., Pompliano, D.L., Mosser, S.D. et al. Selective inhibition of farnesyl-protein transferase blocks Ras processing in vivo. J Biol Chem 1993, 268: 7617-20.
-
(1993)
Selective Inhibition of Farnesyl-protein Transferase Blocks Ras Processing in Vivo. J Biol Chem
, vol.268
, pp. 7617-7620
-
-
Gibbs, J.B.1
Pompliano, D.L.2
Mosser, S.D.3
-
80
-
-
0029587277
-
-
Kang, M.S., Stemerick, D.M., Zwolshen, J.H., Harry, B.S., Sunkara, P.S., Harrison, B.L. Farnesyl-derived inhibitors of ras farnesyl transferase. Biochem Biophys Res Commun 1995,217: 245-9.
-
(1995)
Farnesyl-derived Inhibitors of Ras Farnesyl Transferase. Biochem Biophys Res Commun
, vol.217
, pp. 245-249
-
-
Kang, M.S.1
Stemerick, D.M.2
Zwolshen, J.H.3
Harry, B.S.4
Sunkara, P.S.5
Harrison, B.L.6
-
81
-
-
0029823720
-
-
Mu, Y.Q., Gibbs, R.A., Eubanks L.M., Poulter, C.D. Cupratemediated synthesis and biological evaluation of cyclopropyl- and tert-butylfarnesyl diphosphate analogs. J Org Chem 1996, 61: 8010-5.
-
(1996)
Cupratemediated Synthesis and Biological Evaluation of Cyclopropyl- and Tert-butylfarnesyl Diphosphate Analogs. J Org Chem
, vol.61
, pp. 8010-8015
-
-
Mu, Y.Q.1
Gibbs, R.A.2
Eubanks, L.M.3
Poulter, C.D.4
-
82
-
-
0028941868
-
-
Cohen, LH.,Valentijn,A.R.P.M.,Roodenburg,Letal. Different analogues of farnesyl pyrophosphate inhibit squalene synthase and protein: farnesyltransferase to different extents. Biochem Pharmacol 1995, 49:839-45.
-
(1995)
Different Analogues of Farnesyl Pyrophosphate Inhibit Squalene Synthase and Protein: Farnesyltransferase to Different Extents. Biochem Pharmacol
, vol.49
, pp. 839-845
-
-
Cohen, L.H.1
Valentijn, A.R.P.M.2
Roodenburg, L.3
-
83
-
-
84987180651
-
-
Valentijn, A.R.P.M., Van der Marel, G.A., Cohen, L.H., Van Boom, J.H. An expeditious synthesis of pyrophosphate analogues of farnesyl pyrophosphate using the phosphonylating agent methyl methylphosphonomorpholidate. Synlett 1991, 663-4.
-
(1991)
An Expeditious Synthesis of Pyrophosphate Analogues of Farnesyl Pyrophosphate Using the Phosphonylating Agent Methyl Methylphosphonomorpholidate. Synlett
, pp. 663-664
-
-
Valentijn, A.R.P.M.1
Van Der Marel, G.A.2
Cohen, L.H.3
Van Boom, J.H.4
-
84
-
-
0000461896
-
-
Biller, S.A., Sofia, M.J., De Lange, B. et al. The first potent inhibitor of squalene synthase: A profound contribution of an ether oxygen to inhibitor-enzyme interaction. J Am Chem Soc 1991, 133: 8522-4.
-
(1991)
The First Potent Inhibitor of Squalene Synthase: a Profound Contribution of an Ether Oxygen to Inhibitor-enzyme Interaction. J Am Chem Soc
, vol.133
, pp. 8522-8524
-
-
Biller, S.A.1
Sofia, M.J.2
De Lange, B.3
-
85
-
-
0028967646
-
-
Manne, V., Ricca, C.S., Brown, J.G. et al. Ras farnesylation as a target for novel antitumor agents: Potent and selective farnesyl diphosphate analog inhibitors of farnesyltransferase. Drug Dev Res 1995, 34: 121-37.
-
(1995)
Ras Farnesylation as a Target for Novel Antitumor Agents: Potent and Selective Farnesyl Diphosphate Analog Inhibitors of Farnesyltransferase. Drug Dev Res
, vol.34
, pp. 121-137
-
-
Manne, V.1
Ricca, C.S.2
Brown, J.G.3
-
86
-
-
0029099129
-
-
Patel, D.V., Schmidt, R.J., Biller, S.A., Gordon, E.M., Robinson, S.S., Manne, V. Farnesyl diphosphate-based inhibitors of ras farnesyl protein transferase. J Med Chem 1995, 38: 2906-21.
-
(1995)
Farnesyl Diphosphate-based Inhibitors of Ras Farnesyl Protein Transferase. J Med Chem
, vol.38
, pp. 2906-2921
-
-
Patel, D.V.1
Schmidt, R.J.2
Biller, S.A.3
Gordon, E.M.4
Robinson, S.S.5
Manne, V.6
-
87
-
-
0030011713
-
-
Lamothe, M., Perrin, D., Blotières, D. et al. Inhibition of farnesyl protein transferase by new farnesyl phosphonate derivatives of phenylalanine. Bioorg Med Chem Lett 1996, 6:1291-6.
-
(1996)
Inhibition of Farnesyl Protein Transferase by New Farnesyl Phosphonate Derivatives of Phenylalanine. Bioorg Med Chem Lett
, vol.6
, pp. 1291-1296
-
-
Lamothe, M.1
Perrin, D.2
Blotières, D.3
|