-
1
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
Jordan, M. A.; Wilson, L. Microtubules as a target for anticancer drugs. Nat. Rev. Cancer 2004, 4, 253-265.
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
2
-
-
0032523959
-
Inhibition of microtubule assembly in tumor cells by 3-bromo-acetylamino benzoylurea, a new cancericidal compound
-
Jiang, J. D.; Wang, Y.; Roboz, J.; Strauchen, J.; Holland, J. F.; Bekesi, J. G. Inhibition of microtubule assembly in tumor cells by 3-bromo-acetylamino benzoylurea, a new cancericidal compound. Cancer Res. 1998, 58, 2126-2133.
-
(1998)
Cancer Res.
, vol.58
, pp. 2126-2133
-
-
Jiang, J.D.1
Wang, Y.2
Roboz, J.3
Strauchen, J.4
Holland, J.F.5
Bekesi, J.G.6
-
3
-
-
0033052777
-
Mechanisms of action of and resistance to anti-tubulin agents: Microtubule dynamics, drug transport and cell death
-
Dumontet, C.; Sikic, B. I. Mechanisms of action of and resistance to anti-tubulin agents: microtubule dynamics, drug transport and cell death. J. Clin. Oncol. 1999, 17, 1061-1070.
-
(1999)
J. Clin. Oncol.
, vol.17
, pp. 1061-1070
-
-
Dumontet, C.1
Sikic, B.I.2
-
4
-
-
0035433029
-
Past and future of the mitotic spindle as an oncology target
-
Wood, K. W.; Cornwell, W. D.; Jackson, J. R. Past and future of the mitotic spindle as an oncology target. Curr. Opin. Pharmacol. 2001, 1, 370-7.
-
(2001)
Curr. Opin. Pharmacol.
, vol.1
, pp. 370-377
-
-
Wood, K.W.1
Cornwell, W.D.2
Jackson, J.R.3
-
5
-
-
33646481056
-
Inhibitors of mitotic kinesins: Next-generation antimitotics
-
(a) Sarli, V.; Giannis, A. Inhibitors of mitotic kinesins: next-generation antimitotics. ChemMedChem 2006, 1, 293-298.
-
(2006)
ChemMedChem
, vol.1
, pp. 293-298
-
-
Sarli, V.1
Giannis, A.2
-
6
-
-
22244459880
-
Induction of apoptosis by an inhibitor of the mitotic kinesin KSP requires both activation of the spindle assembly checkpoint and mitotic slippage
-
(b) Tao, W.; South, V. J.; Zhang, Y.; Davide, J. P.; Farrell, L.; Kohl, N. E.; Sepp-Lorenzino, L.; Lobell, R. B. Induction of apoptosis by an inhibitor of the mitotic kinesin KSP requires both activation of the spindle assembly checkpoint and mitotic slippage. Cancer Cell 2005, 8, 49-59.
-
(2005)
Cancer Cell
, vol.8
, pp. 49-59
-
-
Tao, W.1
South, V.J.2
Zhang, Y.3
Davide, J.P.4
Farrell, L.5
Kohl, N.E.6
Sepp-Lorenzino, L.7
Lobell, R.B.8
-
7
-
-
21444449874
-
Inhibitors of kinesin motor proteins-research and clinical progress
-
(c) Duhl, D. M.; Renhowe, P. A. Inhibitors of kinesin motor proteins-research and clinical progress. Curr. Opin. Drug Discover Dev. 2005, 8, 431-436.
-
(2005)
Curr. Opin. Drug Discover Dev.
, vol.8
, pp. 431-436
-
-
Duhl, D.M.1
Renhowe, P.A.2
-
8
-
-
0037342895
-
Mechanisms of proteasome inhibitor PS-341-induced G2-M-phase arrest and apoptosis in human non-small cell lung cancer cell lines
-
(a) Ling, Y. H.; Liebes, L.; Jiang, J. D.; Holland, J. F.; Elliott, P. J.; Adams, J.; Muggia, F. M.; Perez-Soler, R. Mechanisms of proteasome inhibitor PS-341-induced G2-M-phase arrest and apoptosis in human non-small cell lung cancer cell lines. Clin. Cancer Res. 2003, 9, 1145-1154.
-
(2003)
Clin. Cancer Res.
, vol.9
, pp. 1145-1154
-
-
Ling, Y.H.1
Liebes, L.2
Jiang, J.D.3
Holland, J.F.4
Elliott, P.J.5
Adams, J.6
Muggia, F.M.7
Perez-Soler, R.8
-
9
-
-
0036690648
-
PS-341, a novel proteasome inhibitor, induces Bcl-2 phosphorylation and cleavage in association with G2-M phase arrest and apoptosis
-
(b) Ling, Y. H.; Liebes, L.; Ng, B.; Buckley, M.; Elliott, P. J.; Adams, J.; Jiang, J. D.; Muggia, F. M.; Perez-Soler, R. PS-341, a novel proteasome inhibitor, induces Bcl-2 phosphorylation and cleavage in association with G2-M phase arrest and apoptosis. Mol. Cancer Ther. 2002, 1, 841-849.
-
(2002)
Mol. Cancer Ther.
, vol.1
, pp. 841-849
-
-
Ling, Y.H.1
Liebes, L.2
Ng, B.3
Buckley, M.4
Elliott, P.J.5
Adams, J.6
Jiang, J.D.7
Muggia, F.M.8
Perez-Soler, R.9
-
10
-
-
0023217561
-
Antineoplastic agents, 122. Constituents of Combretum caffrum
-
(a) Pettit, G. R.; Cragg, G. M.; Singh, S. B. Antineoplastic agents, 122. Constituents of Combretum caffrum. J. Nat. Prod. 1987, 50, 386-391.
-
(1987)
J. Nat. Prod.
, vol.50
, pp. 386-391
-
-
Pettit, G.R.1
Cragg, G.M.2
Singh, S.B.3
-
11
-
-
0024513175
-
Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4
-
(b) Pettit, G. R.; Singh, S. B.; Hamel, E.; Lin, C. M.; Alberts, D. S.; Garcia-Kendall, D. Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4. Experientia 1989, 45, 209-211.
-
(1989)
Experientia
, vol.45
, pp. 209-211
-
-
Pettit, G.R.1
Singh, S.B.2
Hamel, E.3
Lin, C.M.4
Alberts, D.S.5
Garcia-Kendall, D.6
-
12
-
-
4544277194
-
Combretastatin A4 phosphate: Background and current clinical status
-
Young, S. L.; Chaplin, D. J. Combretastatin A4 phosphate: background and current clinical status. Expert Opin. Invest. Drugs 2004, 13, 1171-1182.
-
(2004)
Expert Opin. Invest. Drugs
, vol.13
, pp. 1171-1182
-
-
Young, S.L.1
Chaplin, D.J.2
-
13
-
-
0029800934
-
Antitumor activity of combretastatin-A4-phosphate, a natural product tubulin inhibitor
-
Dorr, R. T.; Dvorakova, K.; Snead, K.; Alberts, D. S.; Salmon, S. E.; Pettit, G. R. Antitumor activity of combretastatin-A4-phosphate, a natural product tubulin inhibitor. Invest. New Drugs 1996, 14, 131-137.
-
(1996)
Invest. New Drugs
, vol.14
, pp. 131-137
-
-
Dorr, R.T.1
Dvorakova, K.2
Snead, K.3
Alberts, D.S.4
Salmon, S.E.5
Pettit, G.R.6
-
14
-
-
20344379950
-
Disrupting tumor blood vessels
-
Tozer, G. M.; Kanthou, C.; Baguley, B. C. Disrupting tumor blood vessels. Nat. Rev. Cancer 2005, 5, 423-435.
-
(2005)
Nat. Rev. Cancer
, vol.5
, pp. 423-435
-
-
Tozer, G.M.1
Kanthou, C.2
Baguley, B.C.3
-
15
-
-
0036282385
-
The Biology of the combretastatins as tumour targeting agents
-
(b) Tozer, G. M.; Kanthou, C.; Parkins, C. S.; Hill, S. A. The Biology of the combretastatins as tumour targeting agents. Int. J. Exp. Pathol. 2002, 83, 21-38.
-
(2002)
Int. J. Exp. Pathol.
, vol.83
, pp. 21-38
-
-
Tozer, G.M.1
Kanthou, C.2
Parkins, C.S.3
Hill, S.A.4
-
16
-
-
0026047751
-
Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization
-
Cushman, M.; Nagarathnam, D.; Gopal, D.; Chakraborti, A. K.; Lin, C. M.; Hamel, E. Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential anticancer agents that inhibit tubulin polymerization. J Med. Chem. 1991, 34, 2579-2588.
-
(1991)
J Med. Chem.
, vol.34
, pp. 2579-2588
-
-
Cushman, M.1
Nagarathnam, D.2
Gopal, D.3
Chakraborti, A.K.4
Lin, C.M.5
Hamel, E.6
-
17
-
-
0026734208
-
Synthesis and evaluation of analogues of (Z)-1-(4-methoxyphenyl)-2-(3,4, 5-trimethoxyphenyl) ethene as potential cytotoxic and antimitotic agents
-
Cushman, M.; Nagarathnam, D.; Gopal, D.; He, H.-M.; Lin, C. M.; Hamel, E. Synthesis and evaluation of analogues of (Z)-1-(4-methoxyphenyl)-2-(3,4,5- trimethoxyphenyl) ethene as potential cytotoxic and antimitotic agents. J. Med. Chem. 1992, 35, 2293-2306.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2293-2306
-
-
Cushman, M.1
Nagarathnam, D.2
Gopal, D.3
He, H.-M.4
Lin, C.M.5
Hamel, E.6
-
18
-
-
0041421003
-
Combretastatin A-4 analogues as antimitotic antitumor agents
-
(a) Nam, N. H. Combretastatin A-4 analogues as antimitotic antitumor agents. Curr. Med. Chem. 2003, 10, 1697-1722.
-
(2003)
Curr. Med. Chem.
, vol.10
, pp. 1697-1722
-
-
Nam, N.H.1
-
19
-
-
18744379774
-
Pharmaceutical design of antimitotic agents based on combretastatins
-
(b) Hsieh, H. P.; Liou, J. P.; Mahindroo, N. Pharmaceutical design of antimitotic agents based on combretastatins. Curr. Pharm. Des. 2005, 11, 1655-1677.
-
(2005)
Curr. Pharm. Des.
, vol.11
, pp. 1655-1677
-
-
Hsieh, H.P.1
Liou, J.P.2
Mahindroo, N.3
-
20
-
-
15144356733
-
Novel combretastatin analogues effective against murine solid tumors: Design and structure-activity relationships
-
(a) Ohsumi, K.; Nakagawa, R.; Fukuda, Y.; Hatanaka, T.; Morinaga, Y.; Nihei, Y.; Ohishi, K.; Suga, Y.; Akiyama, Y.; Tsuji, T. Novel combretastatin analogues effective against murine solid tumors: design and structure-activity relationships. J. Med. Chem. 1998, 41, 3022-3032.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3022-3032
-
-
Ohsumi, K.1
Nakagawa, R.2
Fukuda, Y.3
Hatanaka, T.4
Morinaga, Y.5
Nihei, Y.6
Ohishi, K.7
Suga, Y.8
Akiyama, Y.9
Tsuji, T.10
-
21
-
-
18244368487
-
Synthesis and cytotoxic evaluation of combretafurazans
-
(b) Tron, G. C.; Pagliai, F.; Grosso, E. D.; Genazzani, A. A.; Sorba, G. Synthesis and cytotoxic evaluation of combretafurazans, J. Med. Chem. 2005, 48, 3260-3268.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 3260-3268
-
-
Tron, G.C.1
Pagliai, F.2
Grosso, E.D.3
Genazzani, A.A.4
Sorba, G.5
-
22
-
-
25844473382
-
Synthesis and cytotoxicity of epoxide and pyrazole analogues of the combretastatins
-
(c) LeBlanc, R.; Dickson, J.; Brown, T.; Stewart, M.; Pati, H. N.; VanDerveer, D.; Arman, H.; Harris, J.; Pennington, W.; Holt, H. L.; Lee, M. Synthesis and cytotoxicity of epoxide and pyrazole analogues of the combretastatins. Bioorg. Med. Chem. 2005, 13, 6025-6034.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 6025-6034
-
-
LeBlanc, R.1
Dickson, J.2
Brown, T.3
Stewart, M.4
Pati, H.N.5
Vanderveer, D.6
Arman, H.7
Harris, J.8
Pennington, W.9
Holt, H.L.10
Lee, M.11
-
23
-
-
2942616949
-
A new family of quinolone and quinoxaline analogues of combretastatins
-
(d) Perez-Melero, C.; Maya, A. B. S.; Rey, B. D.; Pelaez, R.; Caballero, E.; Medarde M. A new family of quinolone and quinoxaline analogues of combretastatins. Bioorg. Med. Chem. Lett. 2004, 14, 3771-3774.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 3771-3774
-
-
Perez-Melero, C.1
Maya, A.B.S.2
Rey, B.D.3
Pelaez, R.4
Caballero, E.5
Medarde, M.6
-
24
-
-
33744785404
-
Novel combretastatin analogues endowed with antitumor activity
-
(e) Simoni, D.; Romagnoli, R.; Baruchello, R.; Rondanin, R.; Rizzi, M.; Pavani, M. G.; Alloatti, D.; Giannini, G.; Marcellini, M.; Riccioni, T.; Castorina, M.; Guglielmi, M. B.; Bucci, F.; Carminati, P.; Pisano, C. Novel combretastatin analogues endowed with antitumor activity. J. Med. Chem. 2006, 49, 3143-3152.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3143-3152
-
-
Simoni, D.1
Romagnoli, R.2
Baruchello, R.3
Rondanin, R.4
Rizzi, M.5
Pavani, M.G.6
Alloatti, D.7
Giannini, G.8
Marcellini, M.9
Riccioni, T.10
Castorina, M.11
Guglielmi, M.B.12
Bucci, F.13
Carminati, P.14
Pisano, C.15
-
25
-
-
0013209248
-
Auticancer and antiviral sulfonamides
-
(a) Scozzafava, A.; Owa, T.; Mastrolorenzo, A.; Supuran, C. T. Auticancer and antiviral sulfonamides. Curr. Med. Chem. 2003, 10, 925-953.
-
(2003)
Curr. Med. Chem.
, vol.10
, pp. 925-953
-
-
Scozzafava, A.1
Owa, T.2
Mastrolorenzo, A.3
Supuran, C.T.4
-
26
-
-
0036279815
-
Sulfonamides and sulfonylated derivatives as anticancer agents
-
(b) Casini, A.; Scozzafava, A.; Mastrolorenzo, A.; Supuran, C. T. Sulfonamides and sulfonylated derivatives as anticancer agents. Curr. Cancer Drug Targets 2002, 2, 55-75.
-
(2002)
Curr. Cancer Drug Targets
, vol.2
, pp. 55-75
-
-
Casini, A.1
Scozzafava, A.2
Mastrolorenzo, A.3
Supuran, C.T.4
-
27
-
-
0026719782
-
Novel sulfonamides as potential, systemically active antitumor agents
-
(a) Yoshino, Y.; Ueda, N.; Niijima, J.; Sugumi, H.; Kotake, Y.; Koyanagi, N.; Yoshimatsu, K.; Asada, M.; Watanabe, T.; Nagasu, T.; Tsukahara, K.; Iijima, A.; Kitoh, K. Novel sulfonamides as potential, systemically active antitumor agents. J. Med. Chem. 1992, 35, 2496-2497.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2496-2497
-
-
Yoshino, Y.1
Ueda, N.2
Niijima, J.3
Sugumi, H.4
Kotake, Y.5
Koyanagi, N.6
Yoshimatsu, K.7
Asada, M.8
Watanabe, T.9
Nagasu, T.10
Tsukahara, K.11
Iijima, A.12
Kitoh, K.13
-
28
-
-
0030756156
-
Mechanism of action of E7010: Inhibition of mitosis by binding to the colchicine site of tubulin
-
(b) Yoshimatsu, K.; Yamaguchi, A.; Yoshino, H.; Koyanagi, N.; Kitoh, K. Mechanism of action of E7010: inhibition of mitosis by binding to the colchicine site of tubulin. Cancer Res. 1997, 57, 3208-3213.
-
(1997)
Cancer Res.
, vol.57
, pp. 3208-3213
-
-
Yoshimatsu, K.1
Yamaguchi, A.2
Yoshino, H.3
Koyanagi, N.4
Kitoh, K.5
-
29
-
-
0028351192
-
In vivo tumor growth inhibition produced by a novel sulfonamide, E7010, against rodent and human tumors
-
(c) Koyanagi, N.; Nagasu, T.; Fujita, F.; Watanabe, T.; Tsukahara, K.; Funahashi, Y.; Fujita, M.; Taguchi, T.; Yoshino, H.; Kitoh, K. In vivo tumor growth inhibition produced by a novel sulfonamide, E7010, against rodent and human tumors. Cancer Res. 1994, 54, 1702-1706.
-
(1994)
Cancer Res.
, vol.54
, pp. 1702-1706
-
-
Koyanagi, N.1
Nagasu, T.2
Fujita, F.3
Watanabe, T.4
Tsukahara, K.5
Funahashi, Y.6
Fujita, M.7
Taguchi, T.8
Yoshino, H.9
Kitoh, K.10
-
30
-
-
4344647867
-
Tumor selective anti effects of the novel antimitotic compound ABT-751: An in vivo rat regional hemodynamic study
-
(d) Segretti, J. A.; Polakowski, J. S.; Koch, K. A.; Marsh, K. C.; Bauch, J. L.; Rosenber, S. H.; Sham, H. L.; Cox, B. F.; Reinhart, G. A. Tumor selective anti effects of the novel antimitotic compound ABT-751: an in vivo rat regional hemodynamic study. Cancer Chemother. Pharmacol. 2004, 54, 273-281.
-
(2004)
Cancer Chemother. Pharmacol.
, vol.54
, pp. 273-281
-
-
Segretti, J.A.1
Polakowski, J.S.2
Koch, K.A.3
Marsh, K.C.4
Bauch, J.L.5
Rosenber, S.H.6
Sham, H.L.7
Cox, B.F.8
Reinhart, G.A.9
-
31
-
-
13044294012
-
Selective, covalent modification of β-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors
-
Shan, B.; Medina, J. C.; Santha, E.; Frankmoelle, W. P.; Chou, T.-C.; Learned, R. M.; Narbut, M. R.; Stott, D.; Wu, P.; Jaen, J. C.; Rosen, T.; Timmermans, P. B. M. W. M.; Beckmann, H. Selective, covalent modification of β-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors. Proc. Natl. Acad. Sci. U.S.A. 1999, 96, 5686-5691.
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 5686-5691
-
-
Shan, B.1
Medina, J.C.2
Santha, E.3
Frankmoelle, W.P.4
Chou, T.-C.5
Learned, R.M.6
Narbut, M.R.7
Stott, D.8
Wu, P.9
Jaen, J.C.10
Rosen, T.11
Timmermans, P.B.M.W.M.12
Beckmann, H.13
-
32
-
-
33750128848
-
Preparation of benzenesulfonamides and benzamides regulating low-density lipoprotein (LDL) receptor expression and of inhibiting abnormal cell proliferation
-
WO 9936391, 1999
-
Medina, J. C. Preparation of benzenesulfonamides and benzamides regulating low-density lipoprotein (LDL) receptor expression and of inhibiting abnormal cell proliferation. WO 9936391, 1999.
-
-
-
Medina, J.C.1
-
33
-
-
33750129670
-
Preparation of sulfonamides as cell proliferation inhibitors
-
U.S. 6521658, 2003
-
(a) Li, Q.; Sham, H.; Woods, K. W.; Steiner, B. A.; Gwaltney, S. L., II; Barr, K. J.; Imade, H. M.; Rosenberg, S. Preparation of sulfonamides as cell proliferation inhibitors. U.S. 6521658, 2003.
-
-
-
Li, Q.1
Sham, H.2
Woods, K.W.3
Steiner, B.A.4
Gwaltney II, S.L.5
Barr, K.J.6
Imade, H.M.7
Rosenberg, S.8
-
34
-
-
0036902919
-
Recent advances in the field of tubulin polymerization inhibitors
-
(b) Prinz, H. Recent advances in the field of tubulin polymerization inhibitors. Expert Rev. Anticancer Ther. 2002, 2, 695-708.
-
(2002)
Expert Rev. Anticancer Ther.
, vol.2
, pp. 695-708
-
-
Prinz, H.1
-
35
-
-
33750142626
-
Substituted carbazoles as tubulin polymerization inhibitors and their use for the treatment of cancer
-
EP 1253141, 2002
-
Caulfield, T.; Cherrier, M.; Combeau, C.; Mailliet, P. Substituted carbazoles as tubulin polymerization inhibitors and their use for the treatment of cancer. EP 1253141, 2002.
-
-
-
Caulfield, T.1
Cherrier, M.2
Combeau, C.3
Mailliet, P.4
-
36
-
-
12444339842
-
2 receptor antagonists. 1. Bicyclo[2.2.1]heptane derivatives
-
2 receptor antagonists. 1. bicyclo[2.2.1]heptane derivatives. J. Med. Chem. 2003, 46, 2436-2445.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2436-2445
-
-
Mitsumori, S.1
Tsuri, T.2
Honma, T.3
Hiramatsu, Y.4
Okada, T.5
Hashizume, H.6
Inagaki, M.7
Arimura, A.8
Yasui, K.9
Asanuma, F.10
Kishino, J.11
Ohtani, M.12
-
37
-
-
0021364661
-
Selective reduction of aromatic nitro compounds with stannous chloride in nonacidic and nonaqueous medium
-
Bellamy, F. D.; Ou, K. Selective reduction of aromatic nitro compounds with stannous chloride in nonacidic and nonaqueous medium. Tetrahedron Lett. 1984, 25, 839-842.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 839-842
-
-
Bellamy, F.D.1
Ou, K.2
-
38
-
-
33744820579
-
Medicinal chemistry of combretastatin A4: Present and future directions
-
Tron, G. C.; Pirali, T.; Sorba, G.; Pagliai, F.; Busacca, S.; Genazzani, A. A. Medicinal chemistry of combretastatin A4: Present and future directions. J. Med. Chem. 2006, 49, 3033-3044.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3033-3044
-
-
Tron, G.C.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
39
-
-
0032880829
-
The effect of antimicrotubule agents on signal transduction pathways of apoptosis: A review
-
Wang, L. G.; Liu, X. M.; Kreis, W.; Budman, D. R. The effect of antimicrotubule agents on signal transduction pathways of apoptosis: a review. Cancer Chemother. Pharmacol. 1999, 44, 355-361.
-
(1999)
Cancer Chemother. Pharmacol.
, vol.44
, pp. 355-361
-
-
Wang, L.G.1
Liu, X.M.2
Kreis, W.3
Budman, D.R.4
-
40
-
-
33645787195
-
Molecular structure and conformations of benzene-sulfonamide: Gas electron diffraction and quantum chemical calculations
-
Petrov, V.; Petrova, V.; Girichev, G. V.; Oberhammer, H.; Giricheva, N. I.; Ivanov, S. Molecular structure and conformations of benzene-sulfonamide: gas electron diffraction and quantum chemical calculations. J. Org. Chem. 2006, 71, 2952-2956.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 2952-2956
-
-
Petrov, V.1
Petrova, V.2
Girichev, G.V.3
Oberhammer, H.4
Giricheva, N.I.5
Ivanov, S.6
-
41
-
-
33750110719
-
Peculiarities of composition and chemical conversion of carbazole and its derivatives. XXVIII. The synthesis of sulfamide compounds in the carbazole series
-
Proshechkina, T. I.; Shishkina, V. I.; Pushkareva, Z. V.; Radtsev, V. S.; Popova, E. N. Peculiarities of composition and chemical conversion of carbazole and its derivatives. XXVIII. The synthesis of sulfamide compounds in the carbazole series. Khim.-Farm. Zh. 1968, 2, 24-27.
-
(1968)
Khim.-Farm. Zh.
, vol.2
, pp. 24-27
-
-
Proshechkina, T.I.1
Shishkina, V.I.2
Pushkareva, Z.V.3
Radtsev, V.S.4
Popova, E.N.5
-
42
-
-
0035950186
-
Hydrophilic, prodrug analogues of T138067 are efficacious in controlling tumor growth in vivo and show a decreased ability to cross the blood brain barrier
-
Rubenstein, S. M.; Baichwal, V.; Beckmann, H.; Clark, D. L.; Frankmoelle, W.; Roche, D.; Santha, E.; Schwender, S.; Thoolen, M.; Ye, Q.; Jaen, J. C. Hydrophilic, prodrug analogues of T138067 are efficacious in controlling tumor growth in vivo and show a decreased ability to cross the blood brain barrier. J. Med. Chem. 2001, 44, 3599-3605.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3599-3605
-
-
Rubenstein, S.M.1
Baichwal, V.2
Beckmann, H.3
Clark, D.L.4
Frankmoelle, W.5
Roche, D.6
Santha, E.7
Schwender, S.8
Thoolen, M.9
Ye, Q.10
Jaen, J.C.11
-
43
-
-
0025299767
-
Evaluation of p-F-Phe-m-bis-(2-chloroethyl) amino-L-Phe-Met-ethoxy HCl against transplantable and spontaneous murine neoplasia
-
Yagi, M. J.; Bekesi, J. G. Evaluation of p-F-Phe-m-bis-(2-chloroethyl) amino-L-Phe-Met-ethoxy HCl against transplantable and spontaneous murine neoplasia. Cancer Chemother. Pharmacol. 1990, 26, 215-220.
-
(1990)
Cancer Chemother. Pharmacol.
, vol.26
, pp. 215-220
-
-
Yagi, M.J.1
Bekesi, J.G.2
|