-
1
-
-
33746555648
-
Bryostatin-1; pharmacology and therapeutic potential as a CNS drug [J]
-
Sun MK, Alkon DL. Bryostatin-1; pharmacology and therapeutic potential as a CNS drug [J]. CNS Drug Rev, 2006,12:1-8.
-
(2006)
CNS Drug Rev
, vol.12
, pp. 1-8
-
-
Sun, M.K.1
Alkon, D.L.2
-
2
-
-
16244401633
-
Dual effects of bryostatin-1 on spatial memory and depression [J]
-
Sun MK, Alkon DL. Dual effects of bryostatin-1 on spatial memory and depression [J]. Eur J Pharmacol, 2005,512:43-51.
-
(2005)
Eur J Pharmacol
, vol.512
, pp. 43-51
-
-
Sun, M.K.1
Alkon, D.L.2
-
3
-
-
0346096818
-
Bryostatin-1: A novel PKC inhibitor in clinical development [J]
-
Kortmansky J , Schwartz GK. Bryostatin-1: a novel PKC inhibitor in clinical development [J]. Cancer Invest, 2003,21:924-936.
-
(2003)
Cancer Invest
, vol.21
, pp. 924-936
-
-
Kortmansky, J.1
Schwartz, G.K.2
-
4
-
-
34250732910
-
Synergistic effect of AS101 and bryostatin-1 on myeloid leukemia cell differentiation in vitro and in an animal model [J]
-
Hayun M, Okun E, Hayun R, et al. Synergistic effect of AS101 and bryostatin-1 on myeloid leukemia cell differentiation in vitro and in an animal model [J]. Leukemia, 2007,21:1504-1513.
-
(2007)
Leukemia
, vol.21
, pp. 1504-1513
-
-
Hayun, M.1
Okun, E.2
Hayun, R.3
-
5
-
-
33746912263
-
Differential effect of bryostatin 1 and phorbol 12-myristate 13-acetate on HOP-92 cell proliferation is mediated by down-regulation of protein kinase Cdelta [J]
-
Choi SH, Hyman T, Blumberg PM. Differential effect of bryostatin 1 and phorbol 12-myristate 13-acetate on HOP-92 cell proliferation is mediated by down-regulation of protein kinase Cdelta [J]. Cancer Res, 2006, 66: 7261-7269.
-
(2006)
Cancer Res
, vol.66
, pp. 7261-7269
-
-
Choi, S.H.1
Hyman, T.2
Blumberg, P.M.3
-
6
-
-
0035702714
-
Mitogen-activated protein kinase is required for bryostatin 1-induced differentiation of the human acute lymphoblastic leukemia cell line Reh [J]
-
Wall NR, Mohammad RM, Al-Katib AM. Mitogen-activated protein kinase is required for bryostatin 1-induced differentiation of the human acute lymphoblastic leukemia cell line Reh [J]. Cell Growth Differ, 2001, 12:641 -647.
-
(2001)
Cell Growth Differ
, vol.12
, pp. 641-647
-
-
Wall, N.R.1
Mohammad, R.M.2
Al-Katib, A.M.3
-
7
-
-
85009914876
-
Primary acute myeloid leukaemia blasts resistant to cytokine-induced differentiation to dendritic-like leukaemia cells can be forced to differentiate by the addition of bryostatin-1 [J]
-
Roddie PH, Horton Y, Turner ML. Primary acute myeloid leukaemia blasts resistant to cytokine-induced differentiation to dendritic-like leukaemia cells can be forced to differentiate by the addition of bryostatin-1 [J]. Leukemia, 2002,16:84-93.
-
(2002)
Leukemia
, vol.16
, pp. 84-93
-
-
Roddie, P.H.1
Horton, Y.2
Turner, M.L.3
-
8
-
-
1242316960
-
1alpha, 25-Dihydroxyvitamin D3 and bryostatin-1 synergize to induce monocytic differentiation of NB4 acute promyelocytic leukemia cells by modulating cell cycle progression [J]
-
Clark CS, Konyer JE, Meckling KA. 1alpha, 25-Dihydroxyvitamin D3 and bryostatin-1 synergize to induce monocytic differentiation of NB4 acute promyelocytic leukemia cells by modulating cell cycle progression [J]. Exp Cell Res, 2004,294:301-311.
-
(2004)
Exp Cell Res
, vol.294
, pp. 301-311
-
-
Clark, C.S.1
Konyer, J.E.2
Meckling, K.A.3
-
9
-
-
0036225876
-
Bryostatin 1 increases 1-beta-D- arabinofuranosylcytosine-induced cytochrome c release and apoptosis in human leukemia cells ectopically expressing Bcl-x(L) [J]
-
Wang Z, Wang S, Dai Y, et al. Bryostatin 1 increases 1-beta-D- arabinofuranosylcytosine-induced cytochrome c release and apoptosis in human leukemia cells ectopically expressing Bcl-x(L) [J]. J Pharmacol Exp Ther, 2002, 301:568-577.
-
(2002)
J Pharmacol Exp Ther
, vol.301
, pp. 568-577
-
-
Wang, Z.1
Wang, S.2
Dai, Y.3
-
10
-
-
25144434873
-
Enhancement of cisplatin sensitivity of cisplatin-resistant human cervical carcinoma cells by bryostatin 1 [J]
-
Mohanty S, Huang J, Basu A. Enhancement of cisplatin sensitivity of cisplatin-resistant human cervical carcinoma cells by bryostatin 1 [J]. Clin Cancer Res, 2005, 1: 6730 - 6737.
-
(2005)
Clin Cancer Res
, vol.1
, pp. 6730-6737
-
-
Mohanty, S.1
Huang, J.2
Basu, A.3
-
11
-
-
33746901998
-
The antineoplastic agent bryostatin-1 differentially regulates IFN-gamma receptor subunits in monocytic cells; transcriptional and posttranscriptional control of IFN-gamma R2 [J]
-
Garcia CS, Curiel RE, Mwatibo JM, et al. The antineoplastic agent bryostatin-1 differentially regulates IFN-gamma receptor subunits in monocytic cells; transcriptional and posttranscriptional control of IFN-gamma R2 [J]. J Immunol, 2006,177:2707-2716
-
(2006)
J Immunol
, vol.177
, pp. 2707-2716
-
-
Garcia, C.S.1
Curiel, R.E.2
Mwatibo, J.M.3
-
12
-
-
1842582465
-
Phase II trial of the combination of bryostatin-1 and cisplatin in advanced or recurrent carcinoma of the cervix; a New York Gynecologic Oncology Group study [J]
-
Nezhat F, Wadler S, Muggia F, et al. Phase II trial of the combination of bryostatin-1 and cisplatin in advanced or recurrent carcinoma of the cervix; a New York Gynecologic Oncology Group study [J]. Gynecol Oncol, 2004,93:144-148.
-
(2004)
Gynecol Oncol
, vol.93
, pp. 144-148
-
-
Nezhat, F.1
Wadler, S.2
Muggia, F.3
-
13
-
-
20144371613
-
Bryostatin-1 in combination with calcium ionophore promotes the maturation of human umbilical cord-blood monocyte-derived dendritic cells capable of activating neonatal alloreactive T cells [J]
-
Do Y, Mainali E, Nagarkatti PS, et al. Bryostatin-1 in combination with calcium ionophore promotes the maturation of human umbilical cord-blood monocyte-derived dendritic cells capable of activating neonatal alloreactive T cells [J]. Cell Immunol, 2004, 231:8-13.
-
(2004)
Cell Immunol
, vol.231
, pp. 8-13
-
-
Do, Y.1
Mainali, E.2
Nagarkatti, P.S.3
-
14
-
-
0035992301
-
Phase I trial and correlative laboratory studies of bryostatin 1 (NSC 339555) and high-dose 1-β-D-arabinofuranosylcytosine in patients with refractory acute leukemia [J]
-
Cragg LH, Andreeff M, Feldman E, et al. Phase I trial and correlative laboratory studies of bryostatin 1 (NSC 339555) and high-dose 1-β-D-arabinofuranosylcytosine in patients with refractory acute leukemia [J]. Clin Cancer Res, 2002,8:2123-2133.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 2123-2133
-
-
Cragg, L.H.1
Andreeff, M.2
Feldman, E.3
-
15
-
-
0345459958
-
Phase I study of prolonged infusion bryostatin-1 in patients with advanced malignancies [J]
-
Marshall JL, Bangalore N, El-Ashry D, et al. Phase I study of prolonged infusion bryostatin-1 in patients with advanced malignancies [J]. Cancer Biol Ther, 2002,1: 409-416.
-
(2002)
Cancer Biol Ther
, vol.1
, pp. 409-416
-
-
Marshall, J.L.1
Bangalore, N.2
El-Ashry, D.3
-
16
-
-
0036954116
-
Phase I study of bryostatin-1 and fludarabine in patients with chronic lymphocytic leukemia and indolent non-Hodgkin's lymphoma [J]
-
Roberts JD, Smith MR, Feldman EJ, et al. Phase I study of bryostatin-1 and fludarabine in patients with chronic lymphocytic leukemia and indolent non-Hodgkin's lymphoma [J]. Clin Lymphoma, 2002,3:184-188.
-
(2002)
Clin Lymphoma
, vol.3
, pp. 184-188
-
-
Roberts, J.D.1
Smith, M.R.2
Feldman, E.J.3
-
17
-
-
33750313170
-
Phase I study of bryostatin 1 and fludarabine in patients with chronic lymphocytic leukemia and indolent (non-Hodgkin's) lymphoma [J]
-
Roberts JD, Smith MR, Feldman EJ, et al. Phase I study of bryostatin 1 and fludarabine in patients with chronic lymphocytic leukemia and indolent (non-Hodgkin's) lymphoma [J]. Clin Cancer Res, 2006,12:5809-5816.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 5809-5816
-
-
Roberts, J.D.1
Smith, M.R.2
Feldman, E.J.3
-
18
-
-
33646501280
-
A multi-center phase II study of sequential paclitaxel and bryostatin-1 ( NSC 339555) in patients with untreated, advanced gastric or gastroesophageal junction adenocarcinoma [J]
-
Ajani JA, Jiang Y, Faust J, et al. A multi-center phase II study of sequential paclitaxel and bryostatin-1 ( NSC 339555) in patients with untreated, advanced gastric or gastroesophageal junction adenocarcinoma [J]. Invest New Drugs, 2006,24:353-357.
-
(2006)
Invest New Drugs
, vol.24
, pp. 353-357
-
-
Ajani, J.A.1
Jiang, Y.2
Faust, J.3
-
19
-
-
33845777994
-
Phase I study of bryostatin 1 and gemcitabine [J]
-
El-Rayes BF, Gadgeel S, Shields AF, et al. Phase I study of bryostatin 1 and gemcitabine [J]. Clin Cancer Res, 2006,12:7059-7062.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 7059-7062
-
-
El-Rayes, B.F.1
Gadgeel, S.2
Shields, A.F.3
-
20
-
-
0035136529
-
Ecteinascidin 743 induces protein-linked DNA breaks in human colon carcinoma HCT116 cells and is cytotoxic independently of topoisomerase I expression [J]
-
Takebayashi Y, Goldwasser F, Urasaki Y, et al. Ecteinascidin 743 induces protein-linked DNA breaks in human colon carcinoma HCT116 cells and is cytotoxic independently of topoisomerase I expression [J]. Clin Cancer Res, 2001,7:185-191.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 185-191
-
-
Takebayashi, Y.1
Goldwasser, F.2
Urasaki, Y.3
-
21
-
-
33846438202
-
Extreme sensitivity to Yondelis (Trabectedin, ET-743) in low passaged sarcoma cell lines correlates with mutated p53 [J]
-
Moneo V, Serelde BG, Fominaya J, et al. Extreme sensitivity to Yondelis (Trabectedin, ET-743) in low passaged sarcoma cell lines correlates with mutated p53 [J]. J Cell Biochem, 2007,100:339-348.
-
(2007)
J Cell Biochem
, vol.100
, pp. 339-348
-
-
Moneo, V.1
Serelde, B.G.2
Fominaya, J.3
-
22
-
-
0037096739
-
Ecteinascidin-743 inhibits activated but not constitutive transcription [J]
-
Friedman D, Hu Z, Kolb EA, et al. Ecteinascidin-743 inhibits activated but not constitutive transcription [J]. Cancer Res, 2002,62:3377-3381.
-
(2002)
Cancer Res
, vol.62
, pp. 3377-3381
-
-
Friedman, D.1
Hu, Z.2
Kolb, E.A.3
-
23
-
-
0037074625
-
A3. (ET743) -DNA complex that both resembles an RNA-DNA hybrid and mimicks zinc finger-induced DNA structural distortions [J]
-
Marco E, García-Nieto R, Mendieta J, et al. A3. (ET743) -DNA complex that both resembles an RNA-DNA hybrid and mimicks zinc finger-induced DNA structural distortions [J]. J Med Chem, 2002,45:871-880.
-
(2002)
J Med Chem
, vol.45
, pp. 871-880
-
-
Marco, E.1
García-Nieto, R.2
Mendieta, J.3
-
24
-
-
0034813203
-
Sensitivity of soft tissue sarcoma cell lines to chemotherapeutic agents: Identification of ecteinascidin-743 as a potent cytotoxic agent [J]
-
Li WW, Takahashi N, Jhanwar S, et al. Sensitivity of soft tissue sarcoma cell lines to chemotherapeutic agents: identification of ecteinascidin-743 as a potent cytotoxic agent [J]. Clin Cancer Res, 2001,7:2908-2911.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 2908-2911
-
-
Li, W.W.1
Takahashi, N.2
Jhanwar, S.3
-
25
-
-
31444456167
-
ET-743: A novel agent with activity in soft tissue sarcomas [J]
-
Fayette J, Coquard IR, Alberti L, et al. ET-743: a novel agent with activity in soft tissue sarcomas [J]. Oncologist, 2005,10:827-832.
-
(2005)
Oncologist
, vol.10
, pp. 827-832
-
-
Fayette, J.1
Coquard, I.R.2
Alberti, L.3
-
26
-
-
0036895987
-
-
Scotlandi K, Perdichizzi S, Manara MC, et al. Effectiveness of ecteinascidin-743 against drug-sensitive and -resistant bone tumor cells [J]. Clin Cancer Res, 2002,8.-3893-3903.
-
Scotlandi K, Perdichizzi S, Manara MC, et al. Effectiveness of ecteinascidin-743 against drug-sensitive and -resistant bone tumor cells [J]. Clin Cancer Res, 2002,8.-3893-3903.
-
-
-
-
27
-
-
14844312905
-
Marine natural products as anticancer drugs [J]
-
Simmons TL, Andrianasolo E, McPhail K, et al. Marine natural products as anticancer drugs [J]. Mol Cancer Ther, 2005,4:333-342.
-
(2005)
Mol Cancer Ther
, vol.4
, pp. 333-342
-
-
Simmons, T.L.1
Andrianasolo, E.2
McPhail, K.3
-
28
-
-
0038380364
-
Overcoming multidrug drug resistance in P-glycoprotein/MDR1-overexpressing cell lines by ecteinascidin 743 [J]
-
Kanzaki A, Takebayashi Y, Ren XQ, et al. Overcoming multidrug drug resistance in P-glycoprotein/MDR1-overexpressing cell lines by ecteinascidin 743 [J]. Mol Cancer Ther, 2002,1:1327 - 1334.
-
(2002)
Mol Cancer Ther
, vol.1
, pp. 1327-1334
-
-
Kanzaki, A.1
Takebayashi, Y.2
Ren, X.Q.3
-
29
-
-
33748033029
-
ET-743: A novel agent with activity in soft-tissue sarcomas [J]
-
Fayette J, Coquard IR, Alberti L, et al. ET-743: a novel agent with activity in soft-tissue sarcomas [J]. Curr Opin Oncol, 2006,18:347-353.
-
(2006)
Curr Opin Oncol
, vol.18
, pp. 347-353
-
-
Fayette, J.1
Coquard, I.R.2
Alberti, L.3
-
30
-
-
33745259879
-
A phase II study of Yondelis (trabectedin, ET-743) as a 24-h continuous intravenous infusion in pretreated advanced breast cancer [J]
-
Zelek L, Yovine A, Brain E, et al. A phase II study of Yondelis (trabectedin, ET-743) as a 24-h continuous intravenous infusion in pretreated advanced breast cancer [J]. Br J Cancer, 2006,94:1610-1614.
-
(2006)
Br J Cancer
, vol.94
, pp. 1610-1614
-
-
Zelek, L.1
Yovine, A.2
Brain, E.3
-
31
-
-
0037384048
-
A phase II trial of dolastatin-10 in recurrent platinum-sensitive ovarian carcinoma: A Gynecologic Oncology Group study [J]
-
Hoffman M, Blessing J, Lentz S. A phase II trial of dolastatin-10 in recurrent platinum-sensitive ovarian carcinoma: a Gynecologic Oncology Group study [J]. Gynecol Oncol, 2003,89:95-98.
-
(2003)
Gynecol Oncol
, vol.89
, pp. 95-98
-
-
Hoffman, M.1
Blessing, J.2
Lentz, S.3
-
32
-
-
0141892724
-
Antitumor activity of TZT-1027 (soblidotin) against vascular endothelial growth factor-secreting human lung cancer in vivo [J]
-
Natsume T, Watanabe J, Koh Y, et al. Antitumor activity of TZT-1027 (soblidotin) against vascular endothelial growth factor-secreting human lung cancer in vivo [J]. Cancer Sci, 2003,94:826-833.
-
(2003)
Cancer Sci
, vol.94
, pp. 826-833
-
-
Natsume, T.1
Watanabe, J.2
Koh, Y.3
-
33
-
-
0141447346
-
Dolastatin 15 binds in the Vinca domain of tubulin as demonstrated by hummel-dreyer chromatography [J]
-
Cruz-Monserrate Z, Mullaney J, Harran P, et al. Dolastatin 15 binds in the Vinca domain of tubulin as demonstrated by hummel-dreyer chromatography [J]. Eur J Biochem, 2003,270:3822-3828.
-
(2003)
Eur J Biochem
, vol.270
, pp. 3822-3828
-
-
Cruz-Monserrate, Z.1
Mullaney, J.2
Harran, P.3
-
34
-
-
34248592567
-
Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate [J]
-
Ray A, Okouneva T, Manna T, et al. Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate [J]. Cancer Res, 2007, 67:3767-3776.
-
(2007)
Cancer Res
, vol.67
, pp. 3767-3776
-
-
Ray, A.1
Okouneva, T.2
Manna, T.3
-
35
-
-
4344650390
-
Marine natural products and related compounds in clinical and advanced preclinical trials [J]
-
Newman DJ, Cragg GM. Marine natural products and related compounds in clinical and advanced preclinical trials [J]. J Nat Prod, 2004,67:1216-1238.
-
(2004)
J Nat Prod
, vol.67
, pp. 1216-1238
-
-
Newman, D.J.1
Cragg, G.M.2
-
36
-
-
0030515609
-
Compounds produced from potential tunicate-blue-green algal symbiosis [J]
-
Sings HL, Rinehart KL. Compounds produced from potential tunicate-blue-green algal symbiosis [J]. J Ind Microbiol Biotechnol, 1996,17:385-396.
-
(1996)
J Ind Microbiol Biotechnol
, vol.17
, pp. 385-396
-
-
Sings, H.L.1
Rinehart, K.L.2
-
37
-
-
0041733458
-
Effect of aplidin in acute lymphoblastic leukaemia cells [J]
-
Erba E, Serafini M , Gaipa G, et al. Effect of aplidin in acute lymphoblastic leukaemia cells [J]. Br J Cancer, 2003,89:763-773.
-
(2003)
Br J Cancer
, vol.89
, pp. 763-773
-
-
Erba, E.1
Serafini, M.2
Gaipa, G.3
-
38
-
-
0037265805
-
Aplidine, a new anticancer agent of marine origin, inhibits vascular endothelial growth factor (VEGF) secretion and blocks VEGF-VEGFR-1 (flt-1) autocrine loop in human leukemia cells MOLT-4 [J]
-
Broggini M, Marchini SV, Galliera E, et al. Aplidine, a new anticancer agent of marine origin, inhibits vascular endothelial growth factor (VEGF) secretion and blocks VEGF-VEGFR-1 (flt-1) autocrine loop in human leukemia cells MOLT-4 [J]. Leukemia, 2003,17:52-59.
-
(2003)
Leukemia
, vol.17
, pp. 52-59
-
-
Broggini, M.1
Marchini, S.V.2
Galliera, E.3
-
39
-
-
47249141130
-
-
Jimeno J, Faircloth G, Fernandez Souse-Faro JM, et al. New marine derived anticancer therapeutics; a journey from the sea to clinical trials [J]. Marine Drugs, 2004, 2.14-29.
-
Jimeno J, Faircloth G, Fernandez Souse-Faro JM, et al. New marine derived anticancer therapeutics; a journey from the sea to clinical trials [J]. Marine Drugs, 2004, 2.14-29.
-
-
-
-
40
-
-
0344082608
-
-
Amador ML, Jimeno J, Paz-Ares L, et al. Progress in the development and acquisition of anticancer agents from marine sources [J]. Ann Oncol, 2003,14-1607-1615.
-
Amador ML, Jimeno J, Paz-Ares L, et al. Progress in the development and acquisition of anticancer agents from marine sources [J]. Ann Oncol, 2003,14-1607-1615.
-
-
-
-
41
-
-
33748745549
-
Phase I study of aplidine in a dailyx5 one-hour infusion every 3 weeks in patients with solid tumors refractory to standard therapy. A National Cancer Institute of Canada Clinical Trials Group study; NCIC CTG IND 115 [J]
-
Maroun JA, Belanger K, Seymour L, et al. Phase I study of aplidine in a dailyx5 one-hour infusion every 3 weeks in patients with solid tumors refractory to standard therapy. A National Cancer Institute of Canada Clinical Trials Group study; NCIC CTG IND 115 [J]. Ann Oncol, 2006,17:1371-1378.
-
(2006)
Ann Oncol
, vol.17
, pp. 1371-1378
-
-
Maroun, J.A.1
Belanger, K.2
Seymour, L.3
-
42
-
-
0038627550
-
Psammaplins from the sponge Pseudoceratina purpurea: Inhibition of both histone deacetylase and DNA methyltransferase [J]
-
Pifia IC, Gautschi JT, Wang GY, et al. Psammaplins from the sponge Pseudoceratina purpurea: inhibition of both histone deacetylase and DNA methyltransferase [J]. J Org Chem, 2003,68:3866-3873.
-
(2003)
J Org Chem
, vol.68
, pp. 3866-3873
-
-
Pifia, I.C.1
Gautschi, J.T.2
Wang, G.Y.3
-
43
-
-
0346094302
-
Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro [J]
-
Shim JS, Lee HS, Shin J, et al. Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro [J]. Cancer Lett, 2004, 203:163-169.
-
(2004)
Cancer Lett
, vol.203
, pp. 163-169
-
-
Shim, J.S.1
Lee, H.S.2
Shin, J.3
-
44
-
-
0141953928
-
The discovery of NVP-LAQ824; from concept to clinic [J]
-
Remiszewski SW. The discovery of NVP-LAQ824; from concept to clinic [J]. Curr Med Chem, 2003,10:2393-2402.
-
(2003)
Curr Med Chem
, vol.10
, pp. 2393-2402
-
-
Remiszewski, S.W.1
-
45
-
-
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 [J]
-
Bai RL, Paull KD, Herald CL, et al. 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]. J Biol Chem, 1991,266:15882-15889.
-
(1991)
J Biol Chem
, vol.266
, pp. 15882-15889
-
-
Bai, R.L.1
Paull, K.D.2
Herald, C.L.3
-
46
-
-
2142818569
-
A quantitative evaluation of the effects of inhibitors of tubulin assembly on polymerization induced by discodermolide, epothilone B, and paclitaxel [J]
-
Dabydeen D, Florence G, Paterson I, et al. A quantitative evaluation of the effects of inhibitors of tubulin assembly on polymerization induced by discodermolide, epothilone B, and paclitaxel [J]. Cancer Chemother Pharmacol, 2004,53:397-403.
-
(2004)
Cancer Chemother Pharmacol
, vol.53
, pp. 397-403
-
-
Dabydeen, D.1
Florence, G.2
Paterson, I.3
-
47
-
-
33751102419
-
Comparison of the activities of the truncated halichondrin B analog NSC 707389 (E7389) with those of the parent compound and a proposed binding site on tubulin [J]
-
Dabydeen DA, Burnett JC, Bai R, et al. Comparison of the activities of the truncated halichondrin B analog NSC 707389 (E7389) with those of the parent compound and a proposed binding site on tubulin [J]. Mol Pharmacol, 2006,70:1866-1875.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1866-1875
-
-
Dabydeen, D.A.1
Burnett, J.C.2
Bai, R.3
-
48
-
-
42549160421
-
Anthracenedione derivative 1403P-3 induces apoptosis in KB and KBv200 cells via reactive oxygen species-independent mitochondrial pathway and death receptor pathway [J]
-
Zhang JY, Wu HY, Xia XK, et al. Anthracenedione derivative 1403P-3 induces apoptosis in KB and KBv200 cells via reactive oxygen species-independent mitochondrial pathway and death receptor pathway [J]. Cancer Biol Ther. 2007,6:1413-1421.
-
(2007)
Cancer Biol Ther
, vol.6
, pp. 1413-1421
-
-
Zhang, J.Y.1
Wu, H.Y.2
Xia, X.K.3
-
49
-
-
35549004397
-
Structural and biological properties of vermistatin and two new vermistatin derivatives isolated from the marine-mangrove endophytic fungus guignardia sp. No 4382 [J]
-
Xia XK, Huang HR, She ZG, et al. Structural and biological properties of vermistatin and two new vermistatin derivatives isolated from the marine-mangrove endophytic fungus guignardia sp. No 4382 [J]. Helv Chim Acta, 2007,90:1925-1931.
-
(2007)
Helv Chim Acta
, vol.90
, pp. 1925-1931
-
-
Xia, X.K.1
Huang, H.R.2
She, Z.G.3
-
50
-
-
34547815196
-
Sipholenol A, a marine-derived sipholane triterpene, potently reverses P-glycoprotein (ABCB1) -mediated multidrug resistance in cancer cells [J]
-
Shi Z, Jain S, Kim IW, et al. Sipholenol A, a marine-derived sipholane triterpene, potently reverses P-glycoprotein (ABCB1) -mediated multidrug resistance in cancer cells [J]. Cancer Sci. 2007,98:1373-1380.
-
(2007)
Cancer Sci
, vol.98
, pp. 1373-1380
-
-
Shi, Z.1
Jain, S.2
Kim, I.W.3
|