-
1
-
-
0022378694
-
Norhalichondrin A: An antitumor polyether macrolide from a marine sponge
-
Uemura D, Takahashi K, Yamamoto T, Katayama C, Tanaka J, Okumura Y, et al. Norhalichondrin A: an antitumor polyether macrolide from a marine sponge. J Am Chem Soc 1985;107:4796-8.
-
(1985)
J Am Chem Soc
, vol.107
, pp. 4796-4798
-
-
Uemura, D.1
Takahashi, K.2
Yamamoto, T.3
Katayama, C.4
Tanaka, J.5
Okumura, Y.6
-
2
-
-
0022709534
-
Halichondrins: Antitumor polyether macrolides from a marine sponge
-
Hirata Y, Uemura D. Halichondrins: antitumor polyether macrolides from a marine sponge. Pure Appl Chem 1986;58:701-10.
-
(1986)
Pure Appl Chem
, vol.58
, pp. 701-710
-
-
Hirata, Y.1
Uemura, D.2
-
3
-
-
78751560506
-
-
Annual meeting of the American Association for Cancer Research, Toronto, Ontario, March 18-22. Abstract 2342
-
Towle MJ, Aalfs KK, Budrow JA, Kishi Y, Littlefield BA. In vitro and in vivo anticancer properties and cell cycle effects of synthetic halichondrin B. Annual meeting of the American Association for Cancer Research, Toronto, Ontario, March 18-22, 1995. Abstract 2342.
-
(1995)
In Vitro and in Vivo Anticancer Properties and Cell Cycle Effects of Synthetic Halichondrin B
-
-
Towle, M.J.1
Aalfs, K.K.2
Budrow, J.A.3
Kishi, Y.4
Littlefield, B.A.5
-
4
-
-
17344374835
-
Comparative antitumor activities of halichondrins and vinblastine against human tumor xenografts
-
Fodstad Ø, Breistl K, Pettit GR, Shoemaker RH, Boyd MR. Comparative antitumor activities of halichondrins and vinblastine against human tumor xenografts. J Exp Ther Oncol 1996;1:119-25.
-
(1996)
J Exp Ther Oncol
, vol.1
, pp. 119-125
-
-
Fodstad Ø1
Breistl, K.2
Pettit, G.R.3
Shoemaker, R.H.4
Boyd, M.R.5
-
5
-
-
84975897156
-
Discovery of E7389, a fully synthetic macrocyclic ketone analogue of halichondrin B
-
Cragg GM, Kingston DGI, Newman DJ, editors. Boca Raton, FL: Taylor & Francis Group (CRC Press)
-
Yu MJ, Kishi Y, Littlefield BA. Discovery of E7389, a fully synthetic macrocyclic ketone analogue of halichondrin B. In: Cragg GM, Kingston DGI, Newman DJ, editors. Anticancer agents from natural products. Boca Raton, FL: Taylor & Francis Group (CRC Press) ; 2005. pp.241-65.
-
(2005)
Anticancer Agents from Natural Products
, pp. 241-265
-
-
Yu, M.J.1
Kishi, Y.2
Littlefield, B.A.3
-
6
-
-
0026774529
-
Total synthesis of halichondrin B and norhalichondrin B
-
Aicher TD, Buszek KR, Fang FG, Forsyth CJ, Jung SH, Kishi Y, et al. Total synthesis of halichondrin B and norhalichondrin B. J Am Chem Soc 1992;114:3162-3.
-
(1992)
J Am Chem Soc
, vol.114
, pp. 3162-3163
-
-
Aicher, T.D.1
Buszek, K.R.2
Fang, F.G.3
Forsyth, C.J.4
Jung, S.H.5
Kishi, Y.6
-
7
-
-
78751532290
-
Halichondrins and related compounds
-
US Patent and Trademark Office, Alexandria, VA. US Patent 5,436,238
-
Kishi Y, Fang FG, Forsyth CJ, Scola PM, Yoon SK. Halichondrins and related compounds. US Patent and Trademark Office, Alexandria, VA. US Patent 5,436,238:1995.
-
(1995)
-
-
Kishi, Y.1
Fang, F.G.2
Forsyth, C.J.3
Scola, P.M.4
Yoon, S.K.5
-
8
-
-
0001635334
-
New synthetic route to the C.14-C.38 segment of halichondrins
-
Stamos DP, Sean SC, Kishi Y. New synthetic route to the C.14-C.38 segment of halichondrins. J Org Chem 1997;62:7552-3.
-
(1997)
J Org Chem
, vol.62
, pp. 7552-7553
-
-
Stamos, D.P.1
Sean, S.C.2
Kishi, Y.3
-
9
-
-
0034658589
-
Structure-activity relationships of halichondrin B analogues: Modifications at C.30-C.38
-
Wang Y, Habgood GJ, Christ WJ, Kishi Y, Littlefield BA, Yu MJ. Structure-activity relationships of halichondrin B analogues: modifications at C.30-C.38. Bioorg Med Chem Lett 2000;10: 1029-32.
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 1029-1032
-
-
Wang, Y.1
Habgood, G.J.2
Christ, W.J.3
Kishi, Y.4
Littlefield, B.A.5
Yu, M.J.6
-
10
-
-
0035110756
-
In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B
-
Towle MJ, Salvato KA, Budrow J, Wels BF, Kuznetsov G, Aalfs KK, et al. In vitro and in vivo anticancer activities of synthetic macrocyclic ketone analogues of halichondrin B. Cancer Res 2001; 61:1013-21.
-
(2001)
Cancer Res
, vol.61
, pp. 1013-1021
-
-
Towle, M.J.1
Salvato, K.A.2
Budrow, J.3
Wels, B.F.4
Kuznetsov, G.5
Aalfs, K.K.6
-
11
-
-
84887252084
-
In vivo efficacy of E7389, a synthetic analog of the marine sponge antitubulin agent halichondrin B, against human tumor xenografts under monotherapy and combination therapy conditions
-
Washington, DC, July 11-14. Abstract 2749
-
Towle MJ, Agoulnik S, Kuznetsov G, TenDyke K, Reardon C, Cheng H, et al. In vivo efficacy of E7389, a synthetic analog of the marine sponge antitubulin agent halichondrin B, against human tumor xenografts under monotherapy and combination therapy conditions. Annual meeting of the American Association for Cancer Research, Washington, DC, July 11-14, 2003. Abstract 2749.
-
(2003)
Annual Meeting of the American Association for Cancer Research
-
-
Towle, M.J.1
Agoulnik, S.2
Kuznetsov, G.3
Tendyke, K.4
Reardon, C.5
Cheng, H.6
-
12
-
-
4143052665
-
Induction of morphological and biochemical apoptosis following prolonged mitotic blockage by halichondrin B macrocyclic ketone analog E7389
-
Kuznetsov G, Towle MJ, Cheng H, Kawamura T, TenDyke K, Liu D, et al. Induction of morphological and biochemical apoptosis following prolonged mitotic blockage by halichondrin B macrocyclic ketone analog E7389. Cancer Res 2004;64:5760-6.
-
(2004)
Cancer Res
, vol.64
, pp. 5760-5766
-
-
Kuznetsov, G.1
Towle, M.J.2
Cheng, H.3
Kawamura, T.4
Tendyke, K.5
Liu, D.6
-
13
-
-
23144433687
-
The primary antimitotic mechanism of action of the synthetic halichondrin E7389 is suppression of microtubule growth
-
Jordan MA, Kamath K, Manna T, Okouneva T, Miller HP, Davis C, et al. The primary antimitotic mechanism of action of the synthetic halichondrin E7389 is suppression of microtubule growth. Mol Cancer Ther 2005;4:1086-95.
-
(2005)
Mol Cancer Ther
, vol.4
, pp. 1086-1095
-
-
Ma, J.1
Kamath, K.2
Manna, T.3
Okouneva, T.4
Miller, H.P.5
Davis, C.6
-
14
-
-
51049119664
-
Inhibition of centromere dynamics by eribulin (E7389) during mitotic metaphase
-
Okouneva T, Azarenko O, Wilson L, Littlefield BA, Jordan MA. Inhibition of centromere dynamics by eribulin (E7389) during mitotic metaphase. Mol Cancer Ther 2008;7:2003-11.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 2003-2011
-
-
Okouneva, T.1
Azarenko, O.2
Wilson, L.3
Littlefield, B.A.4
Ma, J.5
-
15
-
-
76749127634
-
Eribulin binds at microtubule ends to a single site on tubulin to suppress dynamic instability
-
Smith J, Azarenko O, Wilson L, Zhu X, Lewis BM, Littlefield BA, et al. Eribulin binds at microtubule ends to a single site on tubulin to suppress dynamic instability. Biochemistry 2010;49:1331-37.
-
(2010)
Biochemistry
, vol.49
, pp. 1331-1337
-
-
Smith, J.1
Azarenko, O.2
Wilson, L.3
Zhu, X.4
Lewis, B.M.5
Littlefield, B.A.6
-
16
-
-
0026069885
-
Halichondrin B and homohalichondrin B, marine natural products binding in the vinca domain of tubulin. Discovery of tubulin-based mechanism of action by analysis of differential cytotoxicity data
-
Bai RL, Paull KD, Herald CL, Malspeis L, Pettit GR, Hamel E. Halichondrin B and homohalichondrin B, marine natural products binding in the vinca domain of tubulin. Discovery of tubulin-based mechanism of action by analysis of differential cytotoxicity data. J Biol Chem 1991;266:15882-9.
-
(1991)
J Biol Chem
, vol.266
, pp. 15882-15889
-
-
Bai, R.L.1
Paull, K.D.2
Herald, C.L.3
Malspeis, L.4
Pettit, G.R.5
Hamel, E.6
-
17
-
-
84896700059
-
In vivo anticancer activity of synthetic halichondrin B macrocyclic ketone analogs ER-076349 and ER-086526 correlates with ability to induce irreversible mitotic blocks
-
New Orleans, LA, March 24-28. Abstract 1976
-
Towle MJ, Salvato KA, Budrow J, Wels B, Aalfs KK, Zheng W, et al. In vivo anticancer activity of synthetic halichondrin B macrocyclic ketone analogs ER-076349 and ER-086526 correlates with ability to induce irreversible mitotic blocks. Annual meeting of the American Association for Cancer Research, New Orleans, LA, March 24-28, 2001. Abstract 1976.
-
(2001)
Annual Meeting of the American Association for Cancer Research
-
-
Towle, M.J.1
Salvato, K.A.2
Budrow, J.3
Wels, B.4
Aalfs, K.K.5
Zheng, W.6
-
18
-
-
33751097189
-
Macrocyclic analogs and methods of their use and preparation
-
US Patent and Trademark Office, Alexandria, VA. US Patent 6,214,865 B1
-
Littlefield BA, Palme MH, Seletsky BM, Towle MJ, Yu MJ, Zheng W. Macrocyclic analogs and methods of their use and preparation. US Patent and Trademark Office, Alexandria, VA. US Patent 6,214,865 B1; 2001.
-
(2001)
-
-
Littlefield, B.A.1
Palme, M.H.2
Seletsky, B.M.3
Towle, M.J.4
Yu, M.J.5
Zheng, W.6
-
19
-
-
78751530318
-
Reagents and methods for labeling terminal olefins
-
United States Patent Application, US 2006/0045846 A1
-
Horstmann TE, Lewis BM. Reagents and methods for labeling terminal olefins. United States Patent Application, 25 pp. US 2006/0045846 A1; 2006.
-
(2006)
, pp. 25
-
-
Horstmann, T.E.1
Lewis, B.M.2
-
20
-
-
5144226671
-
Macrocyclic ketone analogues of halichondrin B
-
Zheng W, Seletsky BM, Palme MH, Lydon PJ, Singer LA, Chase CE, et al. Macrocyclic ketone analogues of halichondrin B. Bioorg Med Chem Lett 2004;14:5551-54.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 5551-5554
-
-
Zheng, W.1
Seletsky, B.M.2
Palme, M.H.3
Lydon, P.J.4
Singer, L.A.5
Chase, C.E.6
-
21
-
-
0031036307
-
Raf-1/bcl-2 phosphorylation: A step from microtubule damage to cell death
-
Blagosklonny M, Giannakakou P, El-Deiry W, Kingston DG, Higgs PI, Neckers L, et al. Raf-1/bcl-2 phosphorylation: a step from microtubule damage to cell death. Cancer Res 1997;57:130-5.
-
(1997)
Cancer Res
, vol.57
, pp. 130-135
-
-
Blagosklonny, M.1
Giannakakou, P.2
El-Deiry, W.3
Kingston, D.G.4
Higgs, P.I.5
Neckers, L.6
-
23
-
-
0032880829
-
The effect of antimicrotubule agents on signal transduction pathways of apoptosis: A review
-
Wang L, Liu XM, Kreis W, Budman D. The effect of antimicrotubule agents on signal transduction pathways of apoptosis: a review. Cancer Chemother Pharmacol 1999;44:355-61.
-
(1999)
Cancer Chemother Pharmacol
, vol.44
, pp. 355-361
-
-
Wang, L.1
Liu, X.M.2
Kreis, W.3
Budman, D.4
-
24
-
-
75149132946
-
L/Bcl-2 phosphorylation acts as a functional link coupling mitotic arrest and apoptosis
-
L/Bcl-2 phosphorylation acts as a functional link coupling mitotic arrest and apoptosis. Mol Cell Biol 2010;30:640-56.
-
(2010)
Mol Cell Biol
, vol.30
, pp. 640-656
-
-
Terrano, D.T.1
Upreti, M.2
Chambers, T.C.3
-
25
-
-
0023234519
-
Certain calcium channel blockers bind specifically to multidrug-resistant human KB carcinoma membrane vesicles and inhibit drug binding to P-glycoprotein
-
Cornwell MM, Pastan I, Gottesman MM. Certain calcium channel blockers bind specifically to multidrug-resistant human KB carcinoma membrane vesicles and inhibit drug binding to P-glycoprotein. J Biol Chem 1987;262:2166-70.
-
(1987)
J Biol Chem
, vol.262
, pp. 2166-2170
-
-
Cornwell, M.M.1
Pastan, I.2
Gottesman, M.M.3
-
26
-
-
69049106647
-
Macromolecular interaction of halichondrin B analogues eribulin (E7389) and ER-076349 with tubulin by analytical ultracentrifugation
-
Alday PH, Correia JJ. Macromolecular interaction of halichondrin B analogues eribulin (E7389) and ER-076349 with tubulin by analytical ultracentrifugation. Biochemistry 2009;48:7927-38.
-
(2009)
Biochemistry
, vol.48
, pp. 7927-7938
-
-
Alday, P.H.1
Correia, J.J.2
-
27
-
-
0030008570
-
Interaction of vinca alkaloids with tubulin: A comparison of vinblastine, vincristine, and vinorelbine
-
Lobert S, Vulevic B, Correia JJ. Interaction of vinca alkaloids with tubulin: a comparison of vinblastine, vincristine, and vinorelbine. Biochemistry 1996;35:6806-14.
-
(1996)
Biochemistry
, vol.35
, pp. 6806-6814
-
-
Lobert, S.1
Vulevic, B.2
Correia, J.J.3
-
28
-
-
0021933613
-
Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro
-
Jordan MA, Himes RH, Wilson L. Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro. Cancer Res 1985;45:2741-7.
-
(1985)
Cancer Res
, vol.45
, pp. 2741-2747
-
-
Ma, J.1
Himes, R.H.2
Wilson, L.3
|