-
1
-
-
33745276531
-
A boronic-chalcone derivative exhibits potent anticancer activity through inhibition of the proteasome
-
Achanta, G., A. Modzelewska, L. Feng, S. R. Khan, and P. Huang. 2006. A boronic-chalcone derivative exhibits potent anticancer activity through inhibition of the proteasome. Mol. Pharmacol. 70: 426-433.
-
(2006)
Mol. Pharmacol
, vol.70
, pp. 426-433
-
-
Achanta, G.1
Modzelewska, A.2
Feng, L.3
Khan, S.R.4
Huang, P.5
-
2
-
-
2942726181
-
Synthesis and biological evaluation of novel curcumin analogs as anti-cancer and anti-angiogenesis agents
-
Adams, B. K., E. M. Ferstl, M. C. Davis, M. Herold, S. Kurtkaya, R. F. Camalier, M. G. Hollingshead et al. 2004. Synthesis and biological evaluation of novel curcumin analogs as anti-cancer and anti-angiogenesis agents. Bioorg. Med. Chem. 12: 3871-3873.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 3871-3873
-
-
Adams, B.K.1
Ferstl, E.M.2
Davis, M.C.3
Herold, M.4
Kurtkaya, S.5
Camalier, R.F.6
Hollingshead, M.G.7
-
3
-
-
6944250259
-
Role of resveratrol in prevention and therapy of cancer: Preclinical and clinical studies
-
Aggarwal, B. B., A. Bhardwaj, R. S. Aggarwal, N. P. Seeram, S. Shishodia, and Y. Takada. 2004. Role of resveratrol in prevention and therapy of cancer: Preclinical and clinical studies. Anticancer Res. 24: 2783-2840.
-
(2004)
Anticancer Res
, vol.24
, pp. 2783-2840
-
-
Aggarwal, B.B.1
Bhardwaj, A.2
Aggarwal, R.S.3
Seeram, N.P.4
Shishodia, S.5
Takada, Y.6
-
4
-
-
33646028804
-
Molecular targets of dietary agents for prevention and therapy of cancer
-
Aggarwal, B. B. and S. Shishodia. 2006a. Molecular targets of dietary agents for prevention and therapy of cancer. Biochem. Pharmacol. 71: 1397-1421.
-
(2006)
Biochem. Pharmacol
, vol.71
, pp. 1397-1421
-
-
Aggarwal, B.B.1
Shishodia, S.2
-
5
-
-
85059381228
-
-
Resveratrol in health and disease. London, U.K.: Taylor & Francis
-
Aggarwal, B. B. and S. Shishodia. 2006b. Oxidative Stress and Disease, Vol. 20. Resveratrol in health and disease. London, U.K.: Taylor & Francis.
-
(2006)
Oxidative Stress and Disease
, vol.20
-
-
Aggarwal, B.B.1
Shishodia, S.2
-
6
-
-
33845425572
-
Design, synthesis, and antiproliferative and CDK2-cyclin A inhibitory activity of novel flavopiridol analogues
-
Ahn, Y. M., L. Vogeti, C.-J. Liu Santhapuram, K. R. Hari, J. M. White, V. Vasandani, L. A. Mitscher et al. 2007. Design, synthesis, and antiproliferative and CDK2-cyclin A inhibitory activity of novel flavopiridol analogues. Bioorg. Med. Chem. 15: 702-713.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 702-713
-
-
Ahn, Y.M.1
Vogeti, L.2
Liu Santhapuram, C.-J.3
Hari, K.R.4
White, J.M.5
Vasandani, V.6
Mitscher, L.A.7
-
7
-
-
33645814383
-
Mechanisms of the antiangiogenic activity by the hop flavonoid xanthohumol: NF-κB and Akt as targets
-
Albini, A., R. Dell’Eva, R. Vene, N. Ferrari, D. R. Buhler, D. M. Noonan, and G. Fassina. 2006. Mechanisms of the antiangiogenic activity by the hop flavonoid xanthohumol: NF-κB and Akt as targets. FASEB J. 20: 527-529.
-
(2006)
FASEB J
, vol.20
, pp. 527-529
-
-
Albini, A.1
Dell’Eva, R.2
Vene, R.3
Ferrari, N.4
Buhler, D.R.5
Noonan, D.M.6
Fassina, G.7
-
8
-
-
77954136382
-
Chemoenzymatic synthe¬sis and some biological properties of O-phosphoryl derivatives of (E)-resveratrol
-
Aleo, D., V. Cardile, R. Chillemi, G. Granata, and S. Sciuto. 2008. Chemoenzymatic synthe¬sis and some biological properties of O-phosphoryl derivatives of (E)-resveratrol. Nat. Prod. Comm. 3: 1693-1700.
-
(2008)
Nat. Prod. Comm
, vol.3
, pp. 1693-1700
-
-
Aleo, D.1
Cardile, V.2
Chillemi, R.3
Granata, G.4
Sciuto, S.5
-
9
-
-
0036240701
-
The proteasome: A novel target for cancer chemo¬therapy
-
Almond, J. B. and G. M. Cohen. 2002. The proteasome: A novel target for cancer chemo¬therapy. Leukemia 16: 433-443.
-
(2002)
Leukemia
, vol.16
, pp. 433-443
-
-
Almond, J.B.1
Cohen, G.M.2
-
10
-
-
0036098904
-
Antiangiogenic activity of synthetic dihydrobenzofuran lignans
-
Apers, S., D. Paper, J. Buergermeister, S. Baronikova, S. Van Dyck, G. Lemiere, A. Vlietinck, and L. Pieters. 2002. Antiangiogenic activity of synthetic dihydrobenzofuran lignans. J. Nat. Prod. 65: 718-720.
-
(2002)
J. Nat. Prod
, vol.65
, pp. 718-720
-
-
Apers, S.1
Paper, D.2
Buergermeister, J.3
Baronikova, S.4
Van Dyck, S.5
Lemiere, G.6
Vlietinck, A.7
Pieters, L.8
-
11
-
-
11844249453
-
Lignans and neolignans as lead compounds
-
Apers, S., A. Vlietinck, and L. Pieters. 2003. Lignans and neolignans as lead compounds. Phytochem. Rev. 2: 201-217.
-
(2003)
Phytochem. Rev
, vol.2
, pp. 201-217
-
-
Apers, S.1
Vlietinck, A.2
Pieters, L.3
-
13
-
-
75149145989
-
Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-inflammatory and antioxidant agents
-
Bandgar, B. P., S. S. Gawande, R. G. Bodade, J. V. Totre, and C. N. Khobragade. 2010. Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-inflammatory and antioxidant agents. Bioorg. Med. Chem. 18: 1364-1370.
-
(2010)
Bioorg. Med. Chem
, vol.18
, pp. 1364-1370
-
-
Bandgar, B.P.1
Gawande, S.S.2
Bodade, R.G.3
Totre, J.V.4
Khobragade, C.N.5
-
14
-
-
42249104716
-
Efficacy of selected natural products as therapeutic agents against cancer
-
Banerjee, S., Z. Wang, M. Mohammad, F. H. Sarkar, and R. M. Mohammad. 2008. Efficacy of selected natural products as therapeutic agents against cancer. J. Nat. Prod. 71: 492-496.
-
(2008)
J. Nat. Prod
, vol.71
, pp. 492-496
-
-
Banerjee, S.1
Wang, Z.2
Mohammad, M.3
Sarkar, F.H.4
Mohammad, R.M.5
-
15
-
-
70349467857
-
Curcumin derivatives: Molecular basis of their anti-cancer activity
-
Basile, V., E. Ferrari, S. Lazzari, S. Belluti, F. Pignedoli, and C. Imbriano. 2009. Curcumin derivatives: Molecular basis of their anti-cancer activity. Biochem. Pharmacol. 78: 1305-1315.
-
(2009)
Biochem. Pharmacol
, vol.78
, pp. 1305-1315
-
-
Basile, V.1
Ferrari, E.2
Lazzari, S.3
Belluti, S.4
Pignedoli, F.5
Imbriano, C.6
-
16
-
-
84856551003
-
Antiangiogenic properties of an unusual benzo[k, l]xanthene lignan derived from CAPE (Caffeic Acid Phenethyl Ester)
-
press
-
Basini, G., L. Baioni, S. Bussolanti, F. Grasselli, C. Daquino, C. Spatafora, and C. Tringali. 2010a. Antiangiogenic properties of an unusual benzo[k, l]xanthene lignan derived from CAPE (Caffeic Acid Phenethyl Ester). Invest. New Drug. In press, DOI 10.1007/s10637-010-9550-z.
-
(2010)
Invest. New Drug
-
-
Basini, G.1
Baioni, L.2
Bussolanti, S.3
Grasselli, F.4
Daquino, C.5
Spatafora, C.6
Tringali, C.7
-
17
-
-
79251511885
-
Biological effects on granulosa cells of hydroxylated and methylated resveratrol analogues
-
Basini, G., C. Tringali, L. Baioni, S. Bussolati, C. Spatafora, and F. Grasselli. 2010b. Biological effects on granulosa cells of hydroxylated and methylated resveratrol analogues. Mol. Nutr. Food Res. 54: S236-S243.
-
(2010)
Mol. Nutr. Food Res
, vol.54
, pp. S236-S243
-
-
Basini, G.1
Tringali, C.2
Baioni, L.3
Bussolati, S.4
Spatafora, C.5
Grasselli, F.6
-
18
-
-
33745962138
-
Therapeutic potential of resveratrol: The in vivo evidence
-
Baur, J. A. and D. A. Sinclair. 2006. Therapeutic potential of resveratrol: The in vivo evidence. Nat. Rev. Drug Discov. 5: 493-506.
-
(2006)
Nat. Rev. Drug Discov
, vol.5
, pp. 493-506
-
-
Baur, J.A.1
Sinclair, D.A.2
-
19
-
-
17844388310
-
Antiangiogenic and vascular-targeting activity of the microtubule-destabilizing trans-resveratrol derivative 3,5,4′-trimethoxystilbene
-
Belleri, M., D. Ribatti, S. Nicoli, F. Cotelli, L. Forti, V. Vannini, L. A. Stivala, and M. Presta. 2005. Antiangiogenic and vascular-targeting activity of the microtubule-destabilizing trans-resveratrol derivative 3,5,4′-trimethoxystilbene. Mol. Pharmacol. 67: 1451-1459.
-
(2005)
Mol. Pharmacol
, vol.67
, pp. 1451-1459
-
-
Belleri, M.1
Ribatti, D.2
Nicoli, S.3
Cotelli, F.4
Forti, L.5
Vannini, V.6
Stivala, L.A.7
Presta, M.8
-
20
-
-
45549092981
-
Evidence that the anticarcinogenic effect of caffeic acid phenethyl ester in the resistant hepatocyte model involves modifications of cytochrome P450
-
Beltran-Ramirez, O., L. Aleman-Lazarini, M. Salcido-Neyoyet, S. Hernandez-Garcia, S. Fattel-Fazenda, E. Arce-Popoca, J. Arellanes-Robledo et al. 2008. Evidence that the anticarcinogenic effect of caffeic acid phenethyl ester in the resistant hepatocyte model involves modifications of cytochrome P450. Toxicol. Sci. 104: 100-106.
-
(2008)
Toxicol. Sci
, vol.104
, pp. 100-106
-
-
Beltran-Ramirez, O.1
Aleman-Lazarini, L.2
Salcido-Neyoyet, M.3
Hernandez-Garcia, S.4
Fattel-Fazenda, S.5
Arce-Popoca, E.6
Arellanes-Robledo, J.7
-
21
-
-
33750231566
-
Clinical trials of natural products as chemo¬preventive agents for prostate cancer
-
Bemis, D. L., A. E. Katz, and R. Buttyan. 2006. Clinical trials of natural products as chemo¬preventive agents for prostate cancer. Expert Opin. Investig. Drugs 15: 1191-1200.
-
(2006)
Expert Opin. Investig. Drugs
, vol.15
, pp. 1191-1200
-
-
Bemis, D.L.1
Katz, A.E.2
Buttyan, R.3
-
22
-
-
58149316225
-
Digalloylresveratrol, a new phenolic acid derivative induces apoptosis and cell cycle arrest in human HT-29 colon cancer cells
-
Bernhaus, A., M. Fritzer-Szekeres, M. Grusch, P. Saiko, G. Krupitza, S. Venkateswarlu, G. Trimurtulu, W. Jaeger, and T. Szekeres. 2009a. Digalloylresveratrol, a new phenolic acid derivative induces apoptosis and cell cycle arrest in human HT-29 colon cancer cells. Cancer Lett. 274: 299-304.
-
(2009)
Cancer Lett
, vol.274
, pp. 299-304
-
-
Bernhaus, A.1
Fritzer-Szekeres, M.2
Grusch, M.3
Saiko, P.4
Krupitza, G.5
Venkateswarlu, S.6
Trimurtulu, G.7
Jaeger, W.8
Szekeres, T.9
-
23
-
-
70349235911
-
Antitumor effects of KITC, a new resveratrol derivative, in AsPC-1 and BxPC-3 human pancreatic carcinoma cells
-
Bernhaus, A., M. Ozsvar-Kozma, P. Saiko, M. Jaschke, A. Lackner, M. Grusch, Z. Horvath et al. 2009b. Antitumor effects of KITC, a new resveratrol derivative, in AsPC-1 and BxPC-3 human pancreatic carcinoma cells. Invest. New Drugs 27: 393-401.
-
(2009)
Invest. New Drugs
, vol.27
, pp. 393-401
-
-
Bernhaus, A.1
Ozsvar-Kozma, M.2
Saiko, P.3
Jaschke, M.4
Lackner, A.5
Grusch, M.6
Horvath, Z.7
-
24
-
-
0021130576
-
Chemical constituents of Crotalaria madurensis
-
Bhakuni, D. S. and R. Chaturvedi. 1984. Chemical constituents of Crotalaria madurensis. J. Nat. Prod. 47: 585-591.
-
(1984)
J. Nat. Prod
, vol.47
, pp. 585-591
-
-
Bhakuni, D.S.1
Chaturvedi, R.2
-
25
-
-
0001635377
-
Podophyllotoxin derivatives: Drug discovery and develop¬ment
-
Bohlin, L. and B. Rosen. 1996. Podophyllotoxin derivatives: Drug discovery and develop¬ment. Drug Discov. Today 1: 343-351.
-
(1996)
Drug Discov. Today
, vol.1
, pp. 343-351
-
-
Bohlin, L.1
Rosen, B.2
-
26
-
-
54849417391
-
Natural polyphenols as proteasome modulators and their role as anti-cancer com¬pounds
-
Bonfili, L., V. Cecarini, M. Amici, M. Cuccioloni, M. Angeletti, J. N. Keller, and A. M. Eleuteri. 2008. Natural polyphenols as proteasome modulators and their role as anti-cancer com¬pounds. FEBS J. 275: 5512-5526.
-
(2008)
FEBS J
, vol.275
, pp. 5512-5526
-
-
Bonfili, L.1
Cecarini, V.2
Amici, M.3
Cuccioloni, M.4
Angeletti, M.5
Keller, J.N.6
Eleuteri, A.M.7
-
27
-
-
66249095944
-
A dihydrobenzofuran lignan induces cell death by modulating mitochondrial pathway and G2/M cell cycle arrest
-
Bose, J. S., V. Gangan, R. Prakash, S. K. Jain, and S. K. Manna. 2009. A dihydrobenzofuran lignan induces cell death by modulating mitochondrial pathway and G2/M cell cycle arrest. J. Med. Chem. 52: 3184-3190.
-
(2009)
J. Med. Chem
, vol.52
, pp. 3184-3190
-
-
Bose, J.S.1
Gangan, V.2
Prakash, R.3
Jain, S.K.4
Manna, S.K.5
-
28
-
-
36549012724
-
Evolution and current status of research in phenolic compounds
-
Boudet, A.-M. 2007. Evolution and current status of research in phenolic compounds. Phytochemistry 68: 2722-2735.
-
(2007)
Phytochemistry
, vol.68
, pp. 2722-2735
-
-
Boudet, A.-M.1
-
29
-
-
41849087682
-
Antimitotic and antiprolifera¬tive activities of chalcones: Forward structure-activity relationship
-
Boumendjel, A., J. Boccard, P.-A. Carrupt, E. Nicolle, M. Blanc, A. Geze, L. Choisnard, D. Wouessidjewe, E.-L. Matera, and C. Dumontet. 2008. Antimitotic and antiprolifera¬tive activities of chalcones: Forward structure-activity relationship. J. Med. Chem. 51: 2307-2310.
-
(2008)
J. Med. Chem
, vol.51
, pp. 2307-2310
-
-
Boumendjel, A.1
Boccard, J.2
Carrupt, P.-A.3
Nicolle, E.4
Blanc, M.5
Geze, A.6
Choisnard, L.7
Wouessidjewe, D.8
Matera, E.-L.9
Dumontet, C.10
-
30
-
-
68349130136
-
A novel chalcone deriva¬tive which acts as a microtubule depolymerising agent and an inhibitor of P-gp and BCRP in in-vitro and in-vivo glioblastoma models
-
Boumendjel, A., A. McLeer-Florin, P. Champelovier, D. Allegro, D. Muhammad, F. Souard, M. Derouazi, V. Peyrot, B. Toussaint, and J. Boutonnat. 2009. A novel chalcone deriva¬tive which acts as a microtubule depolymerising agent and an inhibitor of P-gp and BCRP in in-vitro and in-vivo glioblastoma models. BMC Cancer 9: 242.
-
(2009)
BMC Cancer
, vol.9
, pp. 242
-
-
Boumendjel, A.1
McLeer-Florin, A.2
Champelovier, P.3
Allegro, D.4
Muhammad, D.5
Souard, F.6
Derouazi, M.7
Peyrot, V.8
Toussaint, B.9
Boutonnat, J.10
-
31
-
-
77954102352
-
Resveratrol as cardioprotective agent: Evidence from bench and bedside
-
eds. B. B. Aggarwal and S. Shishodia, London, U.K.: Taylor & Francis
-
Burjonroppa, S. and K. Fujise. 2006. Resveratrol as cardioprotective agent: Evidence from bench and bedside. In Resveratrol in Health and Disease, eds. B. B. Aggarwal and S. Shishodia, pp. 539-555. London, U.K.: Taylor & Francis.
-
(2006)
Resveratrol in Health and Disease
, pp. 539-555
-
-
Burjonroppa, S.1
Fujise, K.2
-
32
-
-
42949169386
-
Stilbene derivatives that are colchicine site microtubule inhibitors have antileuke¬mic activity and minimal systemic toxicity
-
Cao, T. M., D. Durrant, A. Tripathi, J. Liu, S. Tsai, G. E. Kellogg, D. Simoni, and R. M. Lee. 2008. Stilbene derivatives that are colchicine site microtubule inhibitors have antileuke¬mic activity and minimal systemic toxicity. Am. J. Hematol. 83: 390-397.
-
(2008)
Am. J. Hematol
, vol.83
, pp. 390-397
-
-
Cao, T.M.1
Durrant, D.2
Tripathi, A.3
Liu, J.4
Tsai, S.5
Kellogg, G.E.6
Simoni, D.7
Lee, R.M.8
-
33
-
-
33644975749
-
Antitumor activity of some natural flavonoids and synthetic derivatives on various human and murine can¬cer cell lines
-
Cardenas, M., M. Marder, V. C. Blank, L. P. Roguin, and P. Leonor. 2006. Antitumor activity of some natural flavonoids and synthetic derivatives on various human and murine can¬cer cell lines. Bioorg. Med. Chem. 14: 2966-2971.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 2966-2971
-
-
Cardenas, M.1
Marder, M.2
Blank, V.C.3
Roguin, L.P.4
Leonor, P.5
-
34
-
-
34547411544
-
Antiproliferative activity of methylated analogues of E- and Z-resveratrol
-
Cardile, V., R. Chillemi, L. Lombardo, S. Sciuto, C. Spatafora, and C. Tringali. 2007. Antiproliferative activity of methylated analogues of E- and Z-resveratrol. Z. Naturforsch. 62c: 189-195.
-
(2007)
Z. Naturforsch
, vol.62C
, pp. 189-195
-
-
Cardile, V.1
Chillemi, R.2
Lombardo, L.3
Sciuto, S.4
Spatafora, C.5
Tringali, C.6
-
35
-
-
12844261092
-
Chemo-enzymatic synthesis and antiproliferative activity of resveratrol analogues
-
Cardile, V., L. Lombardo, C. Spatafora, and C. Tringali. 2005. Chemo-enzymatic synthesis and antiproliferative activity of resveratrol analogues. Bioorg. Chem. 33: 22-33.
-
(2005)
Bioorg. Chem
, vol.33
, pp. 22-33
-
-
Cardile, V.1
Lombardo, L.2
Spatafora, C.3
Tringali, C.4
-
36
-
-
33750134570
-
2-Amino and 2′-aminocombretastatin derivatives as potent antimitotic agents
-
Chang, J.-Y., M.-F. Yang, C.-Y. Chang, C.-M. Chen, C.-C. Kuo, and J.-P. Liou. 2006. 2-Amino and 2′-aminocombretastatin derivatives as potent antimitotic agents. J. Med. Chem. 49: 6412-6415.
-
(2006)
J. Med. Chem
, vol.49
, pp. 6412-6415
-
-
Chang, J.-Y.1
Yang, M.-F.2
Chang, C.-Y.3
Chen, C.-M.4
Kuo, C.-C.5
Liou, J.-P.6
-
37
-
-
37349083149
-
Combretastatin A-4 analogs as anticancer agents
-
Chaudhary, A., S. N. Pandeya, P. Kumar, P. P. Sharma, S. Gupta, N. Soni, K. K. Verma, and G. Bhardwaj. 2007. Combretastatin A-4 analogs as anticancer agents. Mini Rev. Med. Chem. 7: 1186-1205.
-
(2007)
Mini Rev. Med. Chem
, vol.7
, pp. 1186-1205
-
-
Chaudhary, A.1
Pandeya, S.N.2
Kumar, P.3
Sharma, P.P.4
Gupta, S.5
Soni, N.6
Verma, K.K.7
Bhardwaj, G.8
-
38
-
-
34249884856
-
Cancer preventive mechanisms of the green tea polyphenol (-)-epigallocatechin-3-gallate
-
Chen, L. and H.-Y. Zhang. 2007. Cancer preventive mechanisms of the green tea polyphenol (-)-epigallocatechin-3-gallate. Molecules 12: 946-957.
-
(2007)
Molecules
, vol.12
, pp. 946-957
-
-
Chen, L.1
Zhang, H.-Y.2
-
39
-
-
55549143327
-
Novel syn¬thetic luteolin analogue-caused sensitization of tumor necrosis factor-α-induced apopto¬sis in human tumor cells
-
Cheng, L., H. Tan, X. Wu, R. Hu, C. Aw, M. Zhao, H.-M. Shen, and Y. Lu. 2008. Novel syn¬thetic luteolin analogue-caused sensitization of tumor necrosis factor-α-induced apopto¬sis in human tumor cells. Org. Biom. Chem. 6: 4102-4104.
-
(2008)
Org. Biom. Chem
, vol.6
, pp. 4102-4104
-
-
Cheng, L.1
Tan, H.2
Wu, X.3
Hu, R.4
Aw, C.5
Zhao, M.6
Shen, H.-M.7
Lu, Y.8
-
40
-
-
84864983865
-
Anti-tumor properties of stilbene-based resveratrol analogues: Recent results
-
Chillemi, R., S. Sciuto, C. Spatafora, and C. Tringali. 2007. Anti-tumor properties of stilbene-based resveratrol analogues: Recent results. Nat. Prod. Comm. 2: 499-513.
-
(2007)
Nat. Prod. Comm
, vol.2
, pp. 499-513
-
-
Chillemi, R.1
Sciuto, S.2
Spatafora, C.3
Tringali, C.4
-
41
-
-
0026047751
-
Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential antican¬cer agents that inhibit tubulin polymerization
-
Cushman, M., D. Nagarathnam, D. Gopal, A. K. Chakraborti, C. M. Lin, and E. Hamel. 1991. Synthesis and evaluation of stilbene and dihydrostilbene derivatives as potential antican¬cer agents that inhibit tubulin polymerization. J. Med. Chem. 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
-
42
-
-
71849101048
-
Biomimetic synthesis of natu¬ral and “unnatural” lignans by oxidative coupling of caffeic esters
-
Daquino, C., A. Rescifina, C. Spatafora, and C. Tringali. 2009. Biomimetic synthesis of natu¬ral and “unnatural” lignans by oxidative coupling of caffeic esters. Eur. J. Org. Chem. 6289-6300.
-
(2009)
Eur. J. Org. Chem
, pp. 6289-6300
-
-
Daquino, C.1
Rescifina, A.2
Spatafora, C.3
Tringali, C.4
-
43
-
-
0034829143
-
Effects of soy phytoestrogens genistein and daidzein on breast cancer growth
-
De Lemos, M. L. 2001. Effects of soy phytoestrogens genistein and daidzein on breast cancer growth. Ann. Pharmacother. 35: 1118-1121.
-
(2001)
Ann. Pharmacother
, vol.35
, pp. 1118-1121
-
-
De Lemos, M.L.1
-
44
-
-
33646068410
-
Resveratrol as a chemopre¬ventive agent: A promising molecule for fighting cancer
-
Delmas, D., A. Lançon, D. Colin, B. Jannin, and N. Latruffe. 2006. Resveratrol as a chemopre¬ventive agent: A promising molecule for fighting cancer. Curr. Drug Targets 7: 423-442.
-
(2006)
Curr. Drug Targets
, vol.7
, pp. 423-442
-
-
Delmas, D.1
Lançon, A.2
Colin, D.3
Jannin, B.4
Latruffe, N.5
-
46
-
-
79251517428
-
Structural basis for the potential antitumor activity of DNA-interacting Benzo[kl]xanthene lignans
-
Di Micco, S., C. Daquino, C. Spatafora, F. Mazué, D. Delmas, N. Latruffe, C. Tringali, R. Riccio, and G. Bifulco. 2011. Structural basis for the potential antitumor activity of DNA-interacting Benzo[kl]xanthene lignans. Org. Biomol. Chem. 9: 701-710.
-
(2011)
Org. Biomol. Chem
, vol.9
, pp. 701-710
-
-
Di Micco, S.1
Daquino, C.2
Spatafora, C.3
Mazué, F.4
Delmas, D.5
Latruffe, N.6
Tringali, C.7
Riccio, R.8
Bifulco, G.9
-
47
-
-
56449125983
-
The design, synthesis, and evaluation of coumarin ring deriva¬tives of the novobiocin scaffold that exhibit antiproliferative activity
-
Donnelly, A. C., J. R. Mays, J. A. Burlison, J. T. Nelson, G. Vielhauer, J. Holzbeierlein, and B. S. J. Blagg. 2008. The design, synthesis, and evaluation of coumarin ring deriva¬tives of the novobiocin scaffold that exhibit antiproliferative activity. J. Org. Chem. 73: 8901-8920.
-
(2008)
J. Org. Chem
, vol.73
, pp. 8901-8920
-
-
Donnelly, A.C.1
Mays, J.R.2
Burlison, J.A.3
Nelson, J.T.4
Vielhauer, G.5
Holzbeierlein, J.6
Blagg, B.S.J.7
-
48
-
-
72049105856
-
Combretastatin-like chalcones as inhibitors of microtubule polymerisation. Part 2: Structure-based discovery of alpha-aryl chalcones
-
Ducki, S., G. MacKenzie, B. Greedy, S. Armitage, J. Fournier Dit Chabert, E. Bennett, J. Nettles, J. P. Snyder, and N. J. Lawrence. 2009a. Combretastatin-like chalcones as inhibitors of microtubule polymerisation. Part 2: Structure-based discovery of alpha-aryl chalcones. Bioorg. Med. Chem. 17: 7711-7722.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 7711-7722
-
-
Ducki, S.1
MacKenzie, G.2
Greedy, B.3
Armitage, S.4
Fournier Dit Chabert, J.5
Bennett, E.6
Nettles, J.7
Snyder, J.P.8
Lawrence, N.J.9
-
49
-
-
12344286977
-
Quantitative structure-activity relationship (5D-QSAR) study of combretastatin-like analogues as inhibitors of tubulin assembly
-
Ducki, S., G. Mackenzie, N. J. Lawrence, and J. P. Snyder. 2005. Quantitative structure-activity relationship (5D-QSAR) study of combretastatin-like analogues as inhibitors of tubulin assembly. J. Med. Chem. 48: 457-465.
-
(2005)
J. Med. Chem
, vol.48
, pp. 457-465
-
-
Ducki, S.1
Mackenzie, G.2
Lawrence, N.J.3
Snyder, J.P.4
-
50
-
-
72049087235
-
Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 1: Synthesis and biological evaluation of antivascular activity
-
Ducki, S., D. Rennison, M. Woo, A. Kendall, J. Fournier Dit Chabert, A. T. McGown, and N. J. Lawrence. 2009b. Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 1: Synthesis and biological evaluation of antivascular activity. Bioorg. Med. Chem. 17: 7698-7710.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 7698-7710
-
-
Ducki, S.1
Rennison, D.2
Woo, M.3
Kendall, A.4
Fournier Dit Chabert, J.5
McGown, A.T.6
Lawrence, N.J.7
-
51
-
-
37049126973
-
Natural occurrence of 3-aryl-4-hydroxycou¬marins. I. Phytochemical examination of Derris robusta
-
East, A. J., W. D. Ollis, and R. E. Wheeler. 1969. Natural occurrence of 3-aryl-4-hydroxycou¬marins. I. Phytochemical examination of Derris robusta. J. Chem. Soc. C 3: 365-374.
-
(1969)
J. Chem. Soc. C
, vol.3
, pp. 365-374
-
-
East, A.J.1
Ollis, W.D.2
Wheeler, R.E.3
-
52
-
-
77953542272
-
Inhibitory effect of caffeic acid phenethyl ester on mice bearing tumor involving angiostatic and apoptotic activities
-
El-Refaei, M. F. and M. M. El-Naa. 2010. Inhibitory effect of caffeic acid phenethyl ester on mice bearing tumor involving angiostatic and apoptotic activities. Chem. Bio. Interact. 186: 152-156.
-
(2010)
Chem. Bio. Interact
, vol.186
, pp. 152-156
-
-
El-Refaei, M.F.1
El-Naa, M.M.2
-
53
-
-
0035192121
-
Mechanism of toxicity of esters of caffeic and dihydrocaffeic acids
-
Etzenhouser, B., C. Hansch, S. Kapur, and C. D. Selassie. 2001. Mechanism of toxicity of esters of caffeic and dihydrocaffeic acids. Bioorg. Med. Chem. 9: 199-209.
-
(2001)
Bioorg. Med. Chem
, vol.9
, pp. 199-209
-
-
Etzenhouser, B.1
Hansch, C.2
Kapur, S.3
Selassie, C.D.4
-
54
-
-
33750696293
-
Interaction between doxorubicin and the resistance modifier stilbene on multidrug resistant mouse lymphoma and human breast cancer cells
-
Ferreira, M.-J. U., N. Duarte, N. Gyémánt, R. Radics, G. Cherepnev, A. Varga, and J. Molnar. 2006. Interaction between doxorubicin and the resistance modifier stilbene on multidrug resistant mouse lymphoma and human breast cancer cells. Anticancer Res. 26: 3541-3546.
-
(2006)
Anticancer Res
, vol.26
, pp. 3541-3546
-
-
Ferreira, M.-J.U.1
Duarte, N.2
Gyémánt, N.3
Radics, R.4
Cherepnev, G.5
Varga, A.6
Molnar, J.7
-
55
-
-
2942612898
-
Phenolic acid derivatives with potential antican¬cer properties: A structure-activity relationship study. Part 1: Methyl, propyl and octyl esters of caffeic and gallic acids
-
Fiuza, S. M., C. Gomes, L. J. Teixeira, M. T. Girao da Cruz, M. N. D. S. Cordeiro, N. Milhazes, F. Borges, and M. P. M. Marques. 2004. Phenolic acid derivatives with potential antican¬cer properties: A structure-activity relationship study. Part 1: Methyl, propyl and octyl esters of caffeic and gallic acids. Bioorg. Med. Chem. 12: 3581-3589.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 3581-3589
-
-
Fiuza, S.M.1
Gomes, C.2
Teixeira, L.J.3
Girao da Cruz, M.T.4
Cordeiro, M.N.D.S.5
Milhazes, N.6
Borges, F.7
Marques, M.P.M.8
-
56
-
-
43049130754
-
1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogues of combretastatin A-4: Synthesis, molecular modelling and evaluation as cytotoxic agents and inhibitors of tubulin
-
Flørenesd, V. A. and T. V. Hansen. 2008. 1,5-Disubstituted 1,2,3-triazoles as cis-restricted analogues of combretastatin A-4: Synthesis, molecular modelling and evaluation as cytotoxic agents and inhibitors of tubulin. Bioorg. Med. Chem. 16: 4829-4838.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 4829-4838
-
-
Flørenesd, V.A.1
Hansen, T.V.2
-
57
-
-
0037114363
-
Green tea: Cancer preventive bever¬age and/or drug
-
Fujiki, H., M. Suganuma, K. Imai, and K. Nakachi. 2002. Green tea: Cancer preventive bever¬age and/or drug. Cancer Lett. 188: 9-13.
-
(2002)
Cancer Lett
, vol.188
, pp. 9-13
-
-
Fujiki, H.1
Suganuma, M.2
Imai, K.3
Nakachi, K.4
-
58
-
-
20144367578
-
Chalcones: An update on cytotoxic and chemopreven¬tive properties
-
Go, M. L., X. Wu, and X. L. Liu. 2005. Chalcones: An update on cytotoxic and chemopreven¬tive properties. Curr. Med. Chem. 12: 483-499.
-
(2005)
Curr. Med. Chem
, vol.12
, pp. 483-499
-
-
Go, M.L.1
Wu, X.2
Liu, X.L.3
-
59
-
-
0033662352
-
Antitumor properties of podophyllotoxin and related compounds
-
Gordaliza, M., M. A. Castro, J. M. Miguel del Corral, and A. San Feliciano. 2000. Antitumor properties of podophyllotoxin and related compounds. Curr. Pharm. Des. 6: 1811-1839.
-
(2000)
Curr. Pharm. Des
, vol.6
, pp. 1811-1839
-
-
Gordaliza, M.1
Castro, M.A.2
Miguel del Corral, J.M.3
San Feliciano, A.4
-
60
-
-
37549000584
-
Dragon’s blood: Botany, chemistry and thera¬peutic uses
-
Gupta, D., B. Bleakley, and R. K. Gupta. 2008. Dragon’s blood: Botany, chemistry and thera¬peutic uses. J. Ethnopharmacol. 115: 361-380.
-
(2008)
J. Ethnopharmacol
, vol.115
, pp. 361-380
-
-
Gupta, D.1
Bleakley, B.2
Gupta, R.K.3
-
61
-
-
19444374982
-
Synthesis and characteriza¬tion of azole isoflavone inhibitors of aromatase
-
Hackett, J. C., Y.-W. Kim, B. Su, and R. W. Brueggemeier. 2005. Synthesis and characteriza¬tion of azole isoflavone inhibitors of aromatase. Bioorg. Med. Chem. 13: 4063-4070.
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 4063-4070
-
-
Hackett, J.C.1
Kim, Y.-W.2
Su, B.3
Brueggemeier, R.W.4
-
62
-
-
38349059089
-
Derrubone, an inhibitor of the Hsp90 protein folding machinery
-
Hadden, M. K., L. Galam, R. L. Matts, and B. S. J. Blagg. 2007. Derrubone, an inhibitor of the Hsp90 protein folding machinery. J. Nat. Prod. 70: 2014-2018.
-
(2007)
J. Nat. Prod
, vol.70
, pp. 2014-2018
-
-
Hadden, M.K.1
Galam, L.2
Matts, R.L.3
Blagg, B.S.J.4
-
63
-
-
19544367790
-
Synthesis and evaluation of double bond substituted combretastatins
-
Hadfield, J. A., K. Gaukroger, N. Hirst, A. P. Weston, N. J. Lawrence, and A. T. McGown. 2005. Synthesis and evaluation of double bond substituted combretastatins. Eur. J. Med.Chem. 40: 529-541.
-
(2005)
Eur. J. Med.Chem
, vol.40
, pp. 529-541
-
-
Hadfield, J.A.1
Gaukroger, K.2
Hirst, N.3
Weston, A.P.4
Lawrence, N.J.5
McGown, A.T.6
-
65
-
-
33845921591
-
Synthesis and pre¬liminary anticancer activity studies of C4 and C8-modified derivatives of catechin gal¬late (CG) and epicatechin gallate (ECG)
-
Hayes, C. J., B. P. Whittaker, S. A. Watson, and A. M. Grabowska. 2006. Synthesis and pre¬liminary anticancer activity studies of C4 and C8-modified derivatives of catechin gal¬late (CG) and epicatechin gallate (ECG). J. Org. Chem. 71: 9701-9712.
-
(2006)
J. Org. Chem
, vol.71
, pp. 9701-9712
-
-
Hayes, C.J.1
Whittaker, B.P.2
Watson, S.A.3
Grabowska, A.M.4
-
66
-
-
0036324914
-
Preclinical evaluation of the antitumor activity of the novel vascular-targeting agent Oxi 4503
-
Hill, S. A., G. M. Tozer, G. R. Pettit, and D. J. Chaplin. 2002. Preclinical evaluation of the antitumor activity of the novel vascular-targeting agent Oxi 4503. Anticancer Res. 22: 1453-1458. http://www.groupepolyphenols.com
-
(2002)
Anticancer Res
, vol.22
, pp. 1453-1458
-
-
Hill, S.A.1
Tozer, G.M.2
Pettit, G.R.3
Chaplin, D.J.4
-
67
-
-
33847161756
-
Synthesis and cytotoxic evaluation of a series of resveratrol derivatives modified in C2 position
-
Huang, X.-F., B.-F. Ruan, X.-T. Wang, C. Xu, H.-M. Ge, H.-L. Zhu, and R.-X. Tan. 2007. Synthesis and cytotoxic evaluation of a series of resveratrol derivatives modified in C2 position. Eur. J. Med. Chem. 42: 263-267.
-
(2007)
Eur. J. Med. Chem
, vol.42
, pp. 263-267
-
-
Huang, X.-F.1
Ruan, B.-F.2
Wang, X.-T.3
Xu, C.4
Ge, H.-M.5
Zhu, H.-L.6
Tan, R.-X.7
-
68
-
-
58149113002
-
The challenge of developing green tea polyphenols as therapeutic agents
-
Huo, C., S. B. Wan, W. H. Lam, L. Li, Z. Wang, K. R. Landis-Piwowar, D. Chen, Q. P. Dou, and T. H. Chan. 2008. The challenge of developing green tea polyphenols as therapeutic agents. Inflammopharmacology 16: 248-252.
-
(2008)
Inflammopharmacology
, vol.16
, pp. 248-252
-
-
Huo, C.1
Wan, S.B.2
Lam, W.H.3
Li, L.4
Wang, Z.5
Landis-Piwowar, K.R.6
Chen, D.7
Dou, Q.P.8
Chan, T.H.9
-
69
-
-
0030689057
-
Cancer-preventive effects of drinking green tea among a Japanese population
-
Imai, K., K. Suga, and K. Nakachi. 1997. Cancer-preventive effects of drinking green tea among a Japanese population. Prev. Med. 26: 769-775.
-
(1997)
Prev. Med
, vol.26
, pp. 769-775
-
-
Imai, K.1
Suga, K.2
Nakachi, K.3
-
70
-
-
0032033637
-
Discovery of podophyllotoxins
-
Imbert, T. F. 1998. Discovery of podophyllotoxins. Biochimie 80: 207-222.
-
(1998)
Biochimie
, vol.80
, pp. 207-222
-
-
Imbert, T.F.1
-
71
-
-
55649088513
-
Recent advances in the investigation of curcuminoids
-
Itokawa, H., Q. Shi, T. Akiyama, S. L. Morris-Natschke, and K.-H. Lee. 2008. Recent advances in the investigation of curcuminoids. Chin. Med. 3: 11.
-
(2008)
Chin. Med
, vol.3
, pp. 11
-
-
Itokawa, H.1
Shi, Q.2
Akiyama, T.3
Morris-Natschke, S.L.4
Lee, K.-H.5
-
72
-
-
0031561513
-
Cancer chemopreventive activity of resveratrol, a natural product derived from grapes
-
Jang, M., L. Cai, G. O. Udeani et al. 1997. Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. Science 275: 218-220.
-
(1997)
Science
, vol.275
, pp. 218-220
-
-
Jang, M.1
Cai, L.2
Udeani, G.O.3
-
73
-
-
33746869949
-
Impact of alkyl esters of caffeic and ferulic acids on tumor cell proliferation, cyclooxygenase enzyme, and lipid peroxidation
-
Jayaprakasam, B., M. Vanisree, Y. Zhang, D. L. Dewitt, and M. G. Nair. 2006. Impact of alkyl esters of caffeic and ferulic acids on tumor cell proliferation, cyclooxygenase enzyme, and lipid peroxidation. J. Agric. Food Chem. 54: 5375-5381.
-
(2006)
J. Agric. Food Chem
, vol.54
, pp. 5375-5381
-
-
Jayaprakasam, B.1
Vanisree, M.2
Zhang, Y.3
Dewitt, D.L.4
Nair, M.G.5
-
74
-
-
77954138804
-
Resveratrol as a sensitizer to apoptosis-inducing stimuli
-
eds. B. B. Aggarwal and S. Shishodia, London, U.K.: Taylor & Francis
-
Jazirehi, A. R. and B. Bonavida. 2006. Resveratrol as a sensitizer to apoptosis-inducing stimuli. In Resveratrol in Health and Disease, eds. B. B. Aggarwal and S. Shishodia, pp. 399-421. London, U.K.: Taylor & Francis.
-
(2006)
Resveratrol in Health and Disease
, pp. 399-421
-
-
Jazirehi, A.R.1
Bonavida, B.2
-
75
-
-
62749159928
-
A novel resveratrol derivative, HS1793, overcomes the resistance conferred by Bcl-2 in human leukemic U937 cells
-
Jeong, S. H., W. S. Jo, S. Song, H. Suh, S.-Y. Seol, S.-H. Leem, T. K. Kwon, and Y. H. Yoo. 2009. A novel resveratrol derivative, HS1793, overcomes the resistance conferred by Bcl-2 in human leukemic U937 cells. Biochem. Pharmacol. 77: 1337-1347.
-
(2009)
Biochem. Pharmacol
, vol.77
, pp. 1337-1347
-
-
Jeong, S.H.1
Jo, W.S.2
Song, S.3
Suh, H.4
Seol, S.-Y.5
Leem, S.-H.6
Kwon, T.K.7
Yoo, Y.H.8
-
76
-
-
36749043820
-
Tumor targeting by microtubule-depolymerising vascular disrupting agents
-
Kanthou, C. and G. M. Tozer. 2007. Tumor targeting by microtubule-depolymerising vascular disrupting agents. Expert Opin. Ther. Targets 11: 1443-1457.
-
(2007)
Expert Opin. Ther. Targets
, vol.11
, pp. 1443-1457
-
-
Kanthou, C.1
Tozer, G.M.2
-
77
-
-
70350755731
-
Polyphenolic profile, antioxidant properties and antimicrobial activity of grape skin extracts of 14 Vitis vinifera varieties grown in Dalmatia (Croatia)
-
Katalinic, V., S. S. Mozina, D. Skroza, I. Generalic, H. Abramovic, M. Milos, I. Ljubenkov et al. 2009. Polyphenolic profile, antioxidant properties and antimicrobial activity of grape skin extracts of 14 Vitis vinifera varieties grown in Dalmatia (Croatia). Food Chem. 119: 715-723.
-
(2009)
Food Chem
, vol.119
, pp. 715-723
-
-
Katalinic, V.1
Mozina, S.S.2
Skroza, D.3
Generalic, I.4
Abramovic, H.5
Milos, M.6
Ljubenkov, I.7
-
78
-
-
65649105091
-
Chalcones in cancer: Understanding their role in terms of QSAR
-
Katsori, A. M. and D. Hadjipavlou-Litina. 2009. Chalcones in cancer: Understanding their role in terms of QSAR. Curr. Med. Chem. 16: 1062-1081.
-
(2009)
Curr. Med. Chem
, vol.16
, pp. 1062-1081
-
-
Katsori, A.M.1
Hadjipavlou-Litina, D.2
-
79
-
-
3242794236
-
Synthesis and aromatase inhibitory activity of novel pyridine-containing isoflavones
-
Kim, Y. W., J. C. Hackett, and R. W. Brueggemeier. 2004. Synthesis and aromatase inhibitory activity of novel pyridine-containing isoflavones. J. Med. Chem. 47: 4032-4040.
-
(2004)
J. Med. Chem
, vol.47
, pp. 4032-4040
-
-
Kim, Y.W.1
Hackett, J.C.2
Brueggemeier, R.W.3
-
80
-
-
65349097586
-
Tubulin-interactive natural products as anticancer agents
-
Kingston, D. G. I. 2009. Tubulin-interactive natural products as anticancer agents. J. Nat. Prod. 72: 507-515.
-
(2009)
J. Nat. Prod
, vol.72
, pp. 507-515
-
-
Kingston, D.G.I.1
-
81
-
-
25144434945
-
Structure-based discovery of a boronic acid bioisostere of combre¬tastatin A-4
-
Kong, Y., J. Grembecka, M. C. Edler, E. Hamel, S. L. Mooberry, M. Sabat, J. Rieger, and M. L. Brown. 2005. Structure-based discovery of a boronic acid bioisostere of combre¬tastatin A-4. Chem. Biol. 12: 1007-1014.
-
(2005)
Chem. Biol
, vol.12
, pp. 1007-1014
-
-
Kong, Y.1
Grembecka, J.2
Edler, M.C.3
Hamel, E.4
Mooberry, S.L.5
Sabat, M.6
Rieger, J.7
Brown, M.L.8
-
82
-
-
76649133808
-
A boronic acid chalcone analog of combretastatin A-4 as a potent anti-proliferation agent
-
Kong, Y., K. Wang, M. C. Edler, E. Hamel, S. L. Mooberry, M. A. Paigeand, and M. L. Brown. 2010. A boronic acid chalcone analog of combretastatin A-4 as a potent anti-proliferation agent. Bioorg. Med. Chem. 18: 971-977.
-
(2010)
Bioorg. Med. Chem
, vol.18
, pp. 971-977
-
-
Kong, Y.1
Wang, K.2
Edler, M.C.3
Hamel, E.4
Mooberry, S.L.5
Paigeand, M.A.6
Brown, M.L.7
-
83
-
-
0037784028
-
Design, synthesis, and evaluation of novel boronic-chalcone derivatives as antitumor agents
-
Kumar, S. K., E. Hager, C. Pettit, H. Gurulingappa, N. E. Davidson, and S. R. Khan. 2003. Design, synthesis, and evaluation of novel boronic-chalcone derivatives as antitumor agents. J. Med. Chem. 46: 2813-2815.
-
(2003)
J. Med. Chem
, vol.46
, pp. 2813-2815
-
-
Kumar, S.K.1
Hager, E.2
Pettit, C.3
Gurulingappa, H.4
Davidson, N.E.5
Khan, S.R.6
-
84
-
-
61649094969
-
Curcumin as a possible lead compound against hormone-independent, multidrug-resistant breast cancer. Steroid enzymes and cancer
-
Labbozzetta, M., M. Notarbartolo, P. Poma, A. Maurici, L. Inguglia, P. Marchetti, M. Rizzi, R. Baruchello, D. Simoni, and N. D’Alessandro. 2009. Curcumin as a possible lead compound against hormone-independent, multidrug-resistant breast cancer. Steroid enzymes and cancer. Ann. N. Y. Acad. Sci. 1155: 278-283.
-
(2009)
Ann. N. Y. Acad. Sci
, vol.1155
, pp. 278-283
-
-
Labbozzetta, M.1
Notarbartolo, M.2
Poma, P.3
Maurici, A.4
Inguglia, L.5
Marchetti, P.6
Rizzi, M.7
Baruchello, R.8
Simoni, D.9
D’Alessandro, N.10
-
85
-
-
33751517433
-
Peracetylation as a means of enhancing in vitro bioactivity and bioavailability of epigal¬locatechin-3-gallate
-
Lambert, J. D., S. Sang, J. Hong, S.-J. Kwon, M.-J. Lee, C.-T. Ho, and C. S. Yang. 2006. Peracetylation as a means of enhancing in vitro bioactivity and bioavailability of epigal¬locatechin-3-gallate. Drug Metab. Dispos. 34: 2111-2116.
-
(2006)
Drug Metab. Dispos
, vol.34
, pp. 2111-2116
-
-
Lambert, J.D.1
Sang, S.2
Hong, J.3
Kwon, S.-J.4
Lee, M.-J.5
Ho, C.-T.6
Yang, C.S.7
-
86
-
-
0037081274
-
Green tea catechins inhibit vascular endothelial growth factor receptor phosphorylation
-
Lamy, S., D. Gingras, and R. Béliveau. 2002. Green tea catechins inhibit vascular endothelial growth factor receptor phosphorylation. Cancer Res. 62: 381-385.
-
(2002)
Cancer Res
, vol.62
, pp. 381-385
-
-
Lamy, S.1
Gingras, D.2
Béliveau, R.3
-
87
-
-
34247399158
-
Resveratrol in human hepatoma HepG2 cells: Metabolism and inducibility of detoxifying enzymes
-
Lançon, A., N. Hanet, B. Jannen, D. Delmas, J.-M. Heyuel, G. Lizard, M.-C. Chagnot, Y. Artur, and N. Latruffe. 2007. Resveratrol in human hepatoma HepG2 cells: Metabolism and inducibility of detoxifying enzymes. Drug Metab. Dispos. 35: 699-703.
-
(2007)
Drug Metab. Dispos
, vol.35
, pp. 699-703
-
-
Lançon, A.1
Hanet, N.2
Jannen, B.3
Delmas, D.4
Heyuel, J.-M.5
Lizard, G.6
Chagnot, M.-C.7
Artur, Y.8
Latruffe, N.9
-
88
-
-
34249299083
-
A novel prodrug of the green tea polyphenol (-)-epigallocatechin-3-gallate as a poten¬tial anticancer agent
-
Landis-Piwowar, K. R., C. Huo, D. Chen, V. Milacic, G. Shi, T. H. Chan, and Q. P. Dou. 2007. A novel prodrug of the green tea polyphenol (-)-epigallocatechin-3-gallate as a poten¬tial anticancer agent. Cancer Res. 67: 4303-4310.
-
(2007)
Cancer Res
, vol.67
, pp. 4303-4310
-
-
Landis-Piwowar, K.R.1
Huo, C.2
Chen, D.3
Milacic, V.4
Shi, G.5
Chan, T.H.6
Dou, Q.P.7
-
89
-
-
0034684958
-
Intake of flavonoids and lung cancer
-
Le Marchand, L., S. P. Murphy, J. H. Hankin, L. R. Wilkens, and L. N. Kolonel. 2000. Intake of flavonoids and lung cancer. J. Natl. Cancer Inst. 92: 154-160.
-
(2000)
J. Natl. Cancer Inst
, vol.92
, pp. 154-160
-
-
Le Marchand, L.1
Murphy, S.P.2
Hankin, J.H.3
Wilkens, L.R.4
Kolonel, L.N.5
-
90
-
-
0034729308
-
Preferential cytotoxicity of caffeic acid phenethyl ester analogues on oral cancer cells
-
Lee, Y. J., P. H. Liao, W. K. Chen, and C. Y. Yang. 2000. Preferential cytotoxicity of caffeic acid phenethyl ester analogues on oral cancer cells. Cancer Lett. 153: 51-56.
-
(2000)
Cancer Lett
, vol.153
, pp. 51-56
-
-
Lee, Y.J.1
Liao, P.H.2
Chen, W.K.3
Yang, C.Y.4
-
91
-
-
23844529912
-
Lignans in treatment of cancer and other diseases
-
Lee, K.-H. and Z. Xiao. 2003. Lignans in treatment of cancer and other diseases. Phytochem. Rev. 2: 341-362.
-
(2003)
Phytochem. Rev
, vol.2
, pp. 341-362
-
-
Lee, K.-H.1
Xiao, Z.2
-
92
-
-
21044436229
-
3′,4-Di-O-methylcedrusin: Synthesis, resolution and absolute configuration
-
Lemiere, G., M. Gao, A. De Groot, R. Dommisse, J. Lepoivre, L. Pieters, and V. Buss. 1995. 3′,4-Di-O-methylcedrusin: Synthesis, resolution and absolute configuration. J. Chem. Society, Perkin Trans. 18: 11775-11779.
-
(1995)
J. Chem. Society, Perkin Trans.
, vol.18
, pp. 11775-11779
-
-
Lemiere, G.1
Gao, M.2
De Groot, A.3
Dommisse, R.4
Lepoivre, J.5
Pieters, L.6
Buss, V.7
-
93
-
-
33646228155
-
Synthesis and cytotoxic evaluation of a series of genistein derivatives
-
Li, H.-Q., H.-M. Ge, Y.-X. Chen, C. Xu, L. Shi, H. Ding, H.-L. Zhu, and R.-X. Tan. 2006. Synthesis and cytotoxic evaluation of a series of genistein derivatives. Chem. Biodivers. 3: 463-472.
-
(2006)
Chem. Biodivers
, vol.3
, pp. 463-472
-
-
Li, H.-Q.1
Ge, H.-M.2
Chen, Y.-X.3
Xu, C.4
Shi, L.5
Ding, H.6
Zhu, H.-L.7
Tan, R.-X.8
-
94
-
-
59049087195
-
A rapid HPLC method for the quantification of 3,5,4′-trime¬thoxy-trans-stilbene (TMS) in rat plasma and its application in pharmacokinetic study
-
Lin, H. S. and P. C. Ho. 2009. A rapid HPLC method for the quantification of 3,5,4′-trime¬thoxy-trans-stilbene (TMS) in rat plasma and its application in pharmacokinetic study. J. Pharm. Biomed. Anal. 49: 387-392.
-
(2009)
J. Pharm. Biomed. Anal
, vol.49
, pp. 387-392
-
-
Lin, H.S.1
Ho, P.C.2
-
95
-
-
73349096649
-
Phase II study of flavopiridol in relapsed chronic lymphocytic leukemia demon¬strating high response rates in genetically high-risk disease
-
Lin, T. S., A. S. Ruppert, A. J. Johnson, B. Fischer, N. A. Heerema, L. A. Andritsos, K. A. Blum et al. 2009. Phase II study of flavopiridol in relapsed chronic lymphocytic leukemia demon¬strating high response rates in genetically high-risk disease. J. Clin. Oncol. 27: 6012-6018.
-
(2009)
J. Clin. Oncol
, vol.27
, pp. 6012-6018
-
-
Lin, T.S.1
Ruppert, A.S.2
Johnson, A.J.3
Fischer, B.4
Heerema, N.A.5
Andritsos, L.A.6
Blum, K.A.7
-
96
-
-
33745642485
-
Antitumor agents. 250. Design and synthesis of new curcumin analogues as poten¬tial anti-prostate cancer agents
-
Lin, L., Q. Shi, A. K. Nyarko, F. Kenneth, C.-C. Wu, C.-Y. Su, C. C.-Y. Shih, and K.-H. Lee. 2006a. Antitumor agents. 250. Design and synthesis of new curcumin analogues as poten¬tial anti-prostate cancer agents. J. Med. Chem. 49: 3963-3972.
-
(2006)
J. Med. Chem
, vol.49
, pp. 3963-3972
-
-
Lin, L.1
Shi, Q.2
Nyarko, A.K.3
Kenneth, F.4
Wu, C.-C.5
Su, C.-Y.6
Shih, C.C.-Y.7
Lee, K.-H.8
-
97
-
-
33644780779
-
Antitumor agents 247. New 4-ethoxycarbonylethyl curcumin analogs as potential antiandrogenic agents
-
Lin, L., Q. Shi, C.-Y. Su, C. C.-Y. Shih, and K.-H. Lee. 2006b. Antitumor agents 247. New 4-ethoxycarbonylethyl curcumin analogs as potential antiandrogenic agents. Bioorg. Med. Chem. 14: 2527-2534.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 2527-2534
-
-
Lin, L.1
Shi, Q.2
Su, C.-Y.3
Shih, C.C.-Y.4
Lee, K.-H.5
-
98
-
-
78149416440
-
LC determination of trans-3,5,3′,4′,5′-pentamethoxystilbene in rat plasma
-
Lin, H.-S., C. Tringali, C. Spatafora, Q.-Y. Choo, and P. C. Ho. 2010. LC determination of trans-3,5,3′,4′,5′-pentamethoxystilbene in rat plasma. Chromatographia 72: 827-832.
-
(2010)
Chromatographia
, vol.72
, pp. 827-832
-
-
Lin, H.-S.1
Tringali, C.2
Spatafora, C.3
Choo, Q.-Y.4
Ho, P.C.5
-
100
-
-
0028176485
-
Potent inhibition of CDC2 kinase activity by the flavonoid L86-8275
-
Losiewicz, M. D., B. A. Carlson, G. Kaur, E. A. Sausville, and P. J. Worland. 1994. Potent inhibition of CDC2 kinase activity by the flavonoid L86-8275. Biochem. Biophys. Res. Commun. 201: 589-595.
-
(1994)
Biochem. Biophys. Res. Commun
, vol.201
, pp. 589-595
-
-
Losiewicz, M.D.1
Carlson, B.A.2
Kaur, G.3
Sausville, E.A.4
Worland, P.J.5
-
101
-
-
75149149892
-
Design, synthesis and biological evaluation of chrysin long-chain derivatives as potential anticancer agents
-
Lv, P.-C., K.-R. Wang, Q.-S. Li, J. Chen, J. Sun, and H.-L. Zhu. 2010. Design, synthesis and biological evaluation of chrysin long-chain derivatives as potential anticancer agents. Bioorg. Med. Chem. 18: 1117-1123.
-
(2010)
Bioorg. Med. Chem
, vol.18
, pp. 1117-1123
-
-
Lv, P.-C.1
Wang, K.-R.2
Li, Q.-S.3
Chen, J.4
Sun, J.5
Zhu, H.-L.6
-
102
-
-
0000604731
-
Non-alkaloidal constituents of Virola elongate bark
-
MacRae, W. D. and G. H. N. Towers. 1985. Non-alkaloidal constituents of Virola elongate bark. Phytochemistry 24: 561-566.
-
(1985)
Phytochemistry
, vol.24
, pp. 561-566
-
-
MacRae, W.D.1
Towers, G.H.N.2
-
103
-
-
33846934752
-
Structural simplification of bio¬active natural products with multicomponent synthesis: Dihydropyridopyrazole ana¬logues of podophyllotoxin
-
Magedov, I. V., M. Manpadi, E. Rozhkova, N. M. Przheval’skii, S. Rogelj, S. T. Shors, W. F. A. Steelant, S. Van Slambrouck, and A. Kornienko. 2007. Structural simplification of bio¬active natural products with multicomponent synthesis: Dihydropyridopyrazole ana¬logues of podophyllotoxin. Bioorg. Med. Chem. Lett. 17: 1381-1385.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 1381-1385
-
-
Magedov, I.V.1
Manpadi, M.2
Rozhkova, E.3
Przheval’skii, N.M.4
Rogelj, S.5
Shors, S.T.6
Steelant, W.F.A.7
Van Slambrouck, S.8
Kornienko, A.9
-
104
-
-
0037048763
-
Antiproliferative activities of Citrus flavonoids against six human cancer cell lines
-
Manthey, J. A. and N. Guthrie. 2002. Antiproliferative activities of Citrus flavonoids against six human cancer cell lines. J. Agric. Food Chem. 50: 5837-5843.
-
(2002)
J. Agric. Food Chem
, vol.50
, pp. 5837-5843
-
-
Manthey, J.A.1
Guthrie, N.2
-
105
-
-
33947146587
-
Epicatechin conjugated with fatty acid is a potent inhibitor of DNA polymerase and angiogenesis
-
Matsubara, K., A. Saito, A. Tanaka, N. Nakajima, R. Akagi, M. Mori, and Y. Mizushina. 2007. Epicatechin conjugated with fatty acid is a potent inhibitor of DNA polymerase and angiogenesis. Life Sci. 80: 1578-1585.
-
(2007)
Life Sci
, vol.80
, pp. 1578-1585
-
-
Matsubara, K.1
Saito, A.2
Tanaka, A.3
Nakajima, N.4
Akagi, R.5
Mori, M.6
Mizushina, Y.7
-
106
-
-
56349124695
-
Enhanced antitumor activities of (-)-epigallocatechin-3-O-gallate fatty acid monoester derivatives in vitro and in vivo
-
Matsumura, K., K. Kaihatsu, S. Mori, H. H. Cho, N. Kato, and S. H. Hyon. 2008. Enhanced antitumor activities of (-)-epigallocatechin-3-O-gallate fatty acid monoester derivatives in vitro and in vivo. Biochem. Biophys. Res. Comm. 377: 1118-1122.
-
(2008)
Biochem. Biophys. Res. Comm
, vol.377
, pp. 1118-1122
-
-
Matsumura, K.1
Kaihatsu, K.2
Mori, S.3
Cho, H.H.4
Kato, N.5
Hyon, S.H.6
-
107
-
-
77954349704
-
Structural determinants of resveratrol for cell proliferation inhibition potency: Experimental and docking studies of new analogs
-
Mazué, F., D. Colin, J. Gobbo, M. Wegner, A. Rescifina, C. Spatafora, D. Fasseur et al. 2010. Structural determinants of resveratrol for cell proliferation inhibition potency: Experimental and docking studies of new analogs. Eur. J. Med. Chem. 45: 2972-2980.
-
(2010)
Eur. J. Med. Chem
, vol.45
, pp. 2972-2980
-
-
Mazué, F.1
Colin, D.2
Gobbo, J.3
Wegner, M.4
Rescifina, A.5
Spatafora, C.6
Fasseur, D.7
-
108
-
-
27444446522
-
Synthesis of a resveratrol analogue with high ceramide-mediated proapoptotic activity on human breast cancer cells
-
Minutolo, F., G. Sala, A. Bagnacani, S. Bertini, I. Carboni, G. Placanica, G. Prota et al. 2005. Synthesis of a resveratrol analogue with high ceramide-mediated proapoptotic activity on human breast cancer cells. J. Med. Chem. 48: 6783-6786.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6783-6786
-
-
Minutolo, F.1
Sala, G.2
Bagnacani, A.3
Bertini, S.4
Carboni, I.5
Placanica, G.6
Prota, G.7
-
109
-
-
33645885368
-
Anticancer activities of novel chalcone and bis-chalcone derivatives
-
Modzelewska, A., C. Pettit, G. Achanta, N. E. Davidson, P. Huang, and S. R. Khan. 2006. Anticancer activities of novel chalcone and bis-chalcone derivatives. Bioorg. Med. Chem. 14: 3491-3495.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 3491-3495
-
-
Modzelewska, A.1
Pettit, C.2
Achanta, G.3
Davidson, N.E.4
Huang, P.5
Khan, S.R.6
-
110
-
-
72549111088
-
Dysoxylum binectariferum Hook.f (Meliaceae), a rich source of rohitukine
-
Mohanakumara, P., N. Sreejayan, V. Priti, B. T. Ramesha, G. Ravikanth, K. N. Ganeshaiah, R. Vasudeva et al. 2010. Dysoxylum binectariferum Hook.f (Meliaceae), a rich source of rohitukine. Fitoterapia 81: 145-148.
-
(2010)
Fitoterapia
, vol.81
, pp. 145-148
-
-
Mohanakumara, P.1
Sreejayan, N.2
Priti, V.3
Ramesha, B.T.4
Ravikanth, G.5
Ganeshaiah, K.N.6
Vasudeva, R.7
-
111
-
-
66449085994
-
Synthesis, structural characterisation and biological evalua¬tion of fluorinated analogues of resveratrol
-
Moran, B. W., F. P. Anderson, A. Devery, S. Cloonan, W. E. Butler, S. Varughese, S. M. Draper, and P. T. M. Kenny. 2009. Synthesis, structural characterisation and biological evalua¬tion of fluorinated analogues of resveratrol. Bioorg. Med. Chem. 17: 4510-4522.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 4510-4522
-
-
Moran, B.W.1
Anderson, F.P.2
Devery, A.3
Cloonan, S.4
Butler, W.E.5
Varughese, S.6
Draper, S.M.7
Kenny, P.T.M.8
-
113
-
-
61749102591
-
A review of coumarin derivatives in pharmacotherapy of breast cancer
-
Musa, M. A., J. S. Cooperwood, and M. O. F. Khan. 2008. A review of coumarin derivatives in pharmacotherapy of breast cancer. Curr. Med. Chem. 15: 2664-2679.
-
(2008)
Curr. Med. Chem
, vol.15
, pp. 2664-2679
-
-
Musa, M.A.1
Cooperwood, J.S.2
Khan, M.O.F.3
-
114
-
-
33747877987
-
Epigallocatechin-3-gallate (EGCG): Chemical and biomedical perspectives
-
Nagle, D. G., D. Ferreira, and Y.-D. Zhou. 2006. Epigallocatechin-3-gallate (EGCG): Chemical and biomedical perspectives. Phytochemistry 67: 1849-1855.
-
(2006)
Phytochemistry
, vol.67
, pp. 1849-1855
-
-
Nagle, D.G.1
Ferreira, D.2
Zhou, Y.-D.3
-
115
-
-
33644617730
-
A review of the effects and mechanisms of polyphenolics in cancer
-
Nichenametla, S. N., T. G. Taruscio, D. L. Barney, and J. H. Exon. 2006. A review of the effects and mechanisms of polyphenolics in cancer. Crit. Rev. Food Sci. Nutr. 46: 161-183.
-
(2006)
Crit. Rev. Food Sci. Nutr
, vol.46
, pp. 161-183
-
-
Nichenametla, S.N.1
Taruscio, T.G.2
Barney, D.L.3
Exon, J.H.4
-
117
-
-
1642323740
-
Protein kinase inhibitors: Insights into drug design from structure
-
Noble, M. E. M., J. A. Endicott, and L. N. Johnson. 2004. Protein kinase inhibitors: Insights into drug design from structure. Science 303: 1800-1805.
-
(2004)
Science
, vol.303
, pp. 1800-1805
-
-
Noble, M.E.M.1
Endicott, J.A.2
Johnson, L.N.3
-
118
-
-
78651141309
-
Chemical constituents of polygona¬ceous plants. I. Studies on the components of Ko-jo-kon (Polygonum cuspidatum Sieb. et Zucc.)
-
Nonomura, S., H. Kanagawa, and A. Makimoto. 1963. Chemical constituents of polygona¬ceous plants. I. Studies on the components of Ko-jo-kon (Polygonum cuspidatum Sieb. et Zucc.). Yakugaku Zasshi 83: 988-990.
-
(1963)
Yakugaku Zasshi
, vol.83
, pp. 988-990
-
-
Nonomura, S.1
Kanagawa, H.2
Makimoto, A.3
-
119
-
-
77956338346
-
1,2,3-Triazole analogs of combretastatin A-4 as potential microtubule-binding agents
-
Odlo, K., J. Fournier-Dit-Chabert, S. Ducki, O. A. B. S. M. Gani, I. Sylte, and T. V. Hansen. 2010. 1,2,3-Triazole analogs of combretastatin A-4 as potential microtubule-binding agents. Bioorg. Med. Chem. 18: 6874-6885.
-
(2010)
Bioorg. Med. Chem
, vol.18
, pp. 6874-6885
-
-
Odlo, K.1
Fournier-Dit-Chabert, J.2
Ducki, S.3
Gani, O.A.B.S.M.4
Sylte, I.5
Hansen, T.V.6
-
120
-
-
33750489699
-
Synthesis and biological analysis of new curcumin analogues bearing an enhanced potential for the medicinal treatment of cancer
-
Ohori, H., H. Yamakoshi, M. Tomizawa, M. Shibuya, Y. Kakudo, A. Takahashi, and S. Takahashi. 2006. Synthesis and biological analysis of new curcumin analogues bearing an enhanced potential for the medicinal treatment of cancer. Mol. Cancer Ther. 5: 2563-2571.
-
(2006)
Mol. Cancer Ther
, vol.5
, pp. 2563-2571
-
-
Ohori, H.1
Yamakoshi, H.2
Tomizawa, M.3
Shibuya, M.4
Kakudo, Y.5
Takahashi, A.6
Takahashi, S.7
-
121
-
-
70349500532
-
An update on lignans: Natural products and synthesis
-
Pan, J.-Y., S.-L. Chen, M.-H. Yang, J. Wu, J. Sinkkonen, and K. Zous. 2009. An update on lignans: Natural products and synthesis. Nat. Prod. Rep. 26: 1251-1292.
-
(2009)
Nat. Prod. Rep
, vol.26
, pp. 1251-1292
-
-
Pan, J.-Y.1
Chen, S.-L.2
Yang, M.-H.3
Wu, J.4
Sinkkonen, J.5
Zous, K.6
-
122
-
-
75249101052
-
3,5,3′,4′,5′-Pentamethoxystilbene (MR-5), a synthetically methoxylated analogue of resveratrol, inhibits growth and induces G1 cell cycle arrest of human breast carcinoma MCF-7 cells
-
Pan, M.-H., C.-L. Lin, J.-H. Tsai, C.-T. Ho, and W.-J. Chen. 2010. 3,5,3′,4′,5′-Pentamethoxystilbene (MR-5), a synthetically methoxylated analogue of resveratrol, inhibits growth and induces G1 cell cycle arrest of human breast carcinoma MCF-7 cells. J. Agric. Food Chem. 58: 226-334.
-
(2010)
J. Agric. Food Chem
, vol.58
, pp. 226-334
-
-
Pan, M.-H.1
Lin, C.-L.2
Tsai, J.-H.3
Ho, C.-T.4
Chen, W.-J.5
-
123
-
-
70349481489
-
Antineoplastic agents. 579. Synthesis and cancer cell growth evaluation of E-stilstatin 3: A resveratrol structural modification
-
Pettit, G. R., N. Melody, A. Thornhill, J. C. Knight, T. L. Groy, and C. L. Herald. 2009a. Antineoplastic agents. 579. Synthesis and cancer cell growth evaluation of E-stilstatin 3: A resveratrol structural modification. J. Nat. Prod. 72: 1637-1642.
-
(2009)
J. Nat. Prod
, vol.72
, pp. 1637-1642
-
-
Pettit, G.R.1
Melody, N.2
Thornhill, A.3
Knight, J.C.4
Groy, T.L.5
Herald, C.L.6
-
124
-
-
69349102810
-
E-Combretastatin and E-resveratrol structural modifications: Antimicrobial and cancer cell growth inhibitory β-E-nitrostyrenes
-
Pettit, R. K., G. R. Pettit, E. Hamel, F. Hogan, B. R. Moser, S. Wolf, S. Pon, J.-C. Chapuis, and J. M. Schmidt. 2009b. E-Combretastatin and E-resveratrol structural modifications: Antimicrobial and cancer cell growth inhibitory β-E-nitrostyrenes. Bioorg. Med. Chem. 17: 6606-6612.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 6606-6612
-
-
Pettit, R.K.1
Pettit, G.R.2
Hamel, E.3
Hogan, F.4
Moser, B.R.5
Wolf, S.6
Pon, S.7
Chapuis, J.-C.8
Schmidt, J.M.9
-
125
-
-
0024513175
-
-
Pettit, G. R., S. B. Singh, E. Hamel, C. M. Lin, D. S. Alberts, and K. D. Garcia. 1989. Experientia 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, K.D.6
-
126
-
-
54149093135
-
Antineoplastic agents. 552. Oxidation of combretastatin A-1: Trapping the o-quinone intermediate considered the metabolic product of the corresponding phosphate prodrug
-
Pettit, G. R., A. J. Thornhill, B. R. Moser, and F. Hogan. 2008. Antineoplastic agents. 552. Oxidation of combretastatin A-1: Trapping the o-quinone intermediate considered the metabolic product of the corresponding phosphate prodrug. J. Nat. Prod. 71: 1561-1563.
-
(2008)
J. Nat. Prod
, vol.71
, pp. 1561-1563
-
-
Pettit, G.R.1
Thornhill, A.J.2
Moser, B.R.3
Hogan, F.4
-
127
-
-
0033619997
-
Synthesis and biological evaluation of dihydrobenzofuran lignans and related com¬pounds as potential antitumor agents that inhibit tubulin polymerization
-
Pieters, L., S. Van Dyck, M. Gao, R. Bai, E. Hamel, A. Vlietinck, and G. Lemiere. 1999. Synthesis and biological evaluation of dihydrobenzofuran lignans and related com¬pounds as potential antitumor agents that inhibit tubulin polymerization. J. Med. Chem. 42: 5475-5481.
-
(1999)
J. Med. Chem
, vol.42
, pp. 5475-5481
-
-
Pieters, L.1
Van Dyck, S.2
Gao, M.3
Bai, R.4
Hamel, E.5
Vlietinck, A.6
Lemiere, G.7
-
128
-
-
85008389252
-
The discovery and development of the combrestatins
-
eds. G. M. Cragg, D. G. I. Kingston, and D. J. Newman, Boca Raton, FL: CRC Press
-
Pinney, K. G., C. Jelinek, K. Edvardsen, D. J. Chaplin, and G. R. Pettit. 2005. The discovery and development of the combrestatins. In Anticancer Agents from Natural Products, eds. G. M. Cragg, D. G. I. Kingston, and D. J. Newman, pp. 23-46. Boca Raton, FL: CRC Press.
-
(2005)
Anticancer Agents from Natural Products
, pp. 23-46
-
-
Pinney, K.G.1
Jelinek, C.2
Edvardsen, K.3
Chaplin, D.J.4
Pettit, G.R.5
-
129
-
-
33747514168
-
Synthesis and cytotoxic evaluation of combretafurans, potential scaffolds for dual-action antitumoral agents
-
Pirali, T., S. Busacca, L. Beltrami, D. Imovilli, F. Pagliai, G. Miglio, A. Massarotti et al. 2006. Synthesis and cytotoxic evaluation of combretafurans, potential scaffolds for dual-action antitumoral agents. J. Med. Chem. 49: 5372-5376.
-
(2006)
J. Med. Chem
, vol.49
, pp. 5372-5376
-
-
Pirali, T.1
Busacca, S.2
Beltrami, L.3
Imovilli, D.4
Pagliai, F.5
Miglio, G.6
Massarotti, A.7
-
130
-
-
79955011823
-
Why bother with polyphenols?
-
Quideau, S. 2006. Why bother with polyphenols? Polyphénols Actualités 24: 10-14.
-
(2006)
Polyphénols Actualités
, vol.24
, pp. 10-14
-
-
Quideau, S.1
-
131
-
-
66349088189
-
Semisynthesis and antiprolifer¬ative evaluation of a series of 3′- aminoflavones
-
Quintin, J., D. Buisson, S. Thoret, T. Cresteil, and G. Lewin. 2009. Semisynthesis and antiprolifer¬ative evaluation of a series of 3′- aminoflavones. Bioorg. Med. Chem. Lett. 19: 3502-3506.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 3502-3506
-
-
Quintin, J.1
Buisson, D.2
Thoret, S.3
Cresteil, T.4
Lewin, G.5
-
132
-
-
48649095089
-
Cancer chemoprevention and chemotherapy: Dietary polyphenols and signal¬ling pathways
-
Ramos, S. 2008. Cancer chemoprevention and chemotherapy: Dietary polyphenols and signal¬ling pathways. Mol. Nutr. Food Res. 52: 507-526.
-
(2008)
Mol. Nutr. Food Res
, vol.52
, pp. 507-526
-
-
Ramos, S.1
-
133
-
-
0026651085
-
Wine, alcohol, platelets, and the French paradox for coronary heart disease
-
Renaud, S. and M. de Lorgeril. 1992. Wine, alcohol, platelets, and the French paradox for coronary heart disease. Lancet 339: 1523-1526.
-
(1992)
Lancet
, vol.339
, pp. 1523-1526
-
-
Renaud, S.1
de Lorgeril, M.2
-
134
-
-
77950643074
-
Coumarins: Old compounds with novel promising therapeutic perspectives
-
Riveiro, M. E., N. De Kimpe, A. Moglioni, R. Vazquez, F. Monczor, C. Shayo, and C. Davio. 2010. Coumarins: Old compounds with novel promising therapeutic perspectives. Curr. Med. Chem. 17: 1325-1338.
-
(2010)
Curr. Med. Chem
, vol.17
, pp. 1325-1338
-
-
Riveiro, M.E.1
De Kimpe, N.2
Moglioni, A.3
Vazquez, R.4
Monczor, F.5
Shayo, C.6
Davio, C.7
-
135
-
-
48849103277
-
Novel resveratrol analogs induce apoptosis and cause cell cycle arrest in HT29 human colon cancer cells: Inhibition of ribonucleo¬tide reductase activity
-
Saiko, M., Z. Pemberger, I. Horvath, I. Savinc, M. Grusch, N. Handler, T. Erker, W. Jaeger, M. Fritzer-Szekeres, and T. Szekeres. 2008. Novel resveratrol analogs induce apoptosis and cause cell cycle arrest in HT29 human colon cancer cells: Inhibition of ribonucleo¬tide reductase activity. Oncol. Rep. 19: 1621-1626.
-
(2008)
Oncol. Rep
, vol.19
, pp. 1621-1626
-
-
Saiko, M.1
Pemberger, Z.2
Horvath, I.3
Savinc, I.4
Grusch, M.5
Handler, N.6
Erker, T.7
Jaeger, W.8
Fritzer-Szekeres, M.9
Szekeres, T.10
-
136
-
-
41849135027
-
Synthesis and biological activity of a 3,4,5-trimethoxybenzoyl ester analogue of epicatechin-3-gallate
-
Sánchez-del-Campo, L., F. Otón, A. Tárraga, J. Cabezas-Herrera, S. Chazarra, and J. Neptuno Rodríguez-López. 2008. Synthesis and biological activity of a 3,4,5-trimethoxybenzoyl ester analogue of epicatechin-3-gallate. J. Med. Chem. 51: 2018-2026.
-
(2008)
J. Med. Chem
, vol.51
, pp. 2018-2026
-
-
Sánchez-del-Campo, L.1
Otón, F.2
Tárraga, A.3
Cabezas-Herrera, J.4
Chazarra, S.5
Neptuno Rodríguez-López, J.6
-
137
-
-
67249125885
-
Melanoma activation of 3-O-(3,4,5-trimethoxybenzoyl)-(-)-epicatechin to a potent irreversible inhibitor of dihydrofolate reductase
-
Sánchez-del-Campo, L., A. Tarraga, M. F. Montenegro, J. Cabezas-Herrera, and J. N. Rodriguez-Lopez. 2009. Melanoma activation of 3-O-(3,4,5-trimethoxybenzoyl)-(-)-epicatechin to a potent irreversible inhibitor of dihydrofolate reductase. Mol. Pharm. 6: 883-894.
-
(2009)
Mol. Pharm
, vol.6
, pp. 883-894
-
-
Sánchez-del-Campo, L.1
Tarraga, A.2
Montenegro, M.F.3
Cabezas-Herrera, J.4
Rodriguez-Lopez, J.N.5
-
138
-
-
0141857816
-
Resveratrol analog (Z)-3,5,4′-trimethoxystilbene is a potent anti-mitotic drug inhibiting tubulin polymerization
-
Schneider, Y., P. Chabert, J. Stutzmann, D. Coelho, A. Fougerousse, F. Gosse, J.-F. Launay, R. Brouillard, and F. Raul. 2003. Resveratrol analog (Z)-3,5,4′-trimethoxystilbene is a potent anti-mitotic drug inhibiting tubulin polymerization. Int. J. Cancer 107: 189-196.
-
(2003)
Int. J. Cancer
, vol.107
, pp. 189-196
-
-
Schneider, Y.1
Chabert, P.2
Stutzmann, J.3
Coelho, D.4
Fougerousse, A.5
Gosse, F.6
Launay, J.-F.7
Brouillard, R.8
Raul, F.9
-
139
-
-
22844450866
-
Resveratrol as an anticancer nutrient: Molecular basis, open questions and promises
-
Signorelli, P. and R. Ghidoni. 2005. Resveratrol as an anticancer nutrient: Molecular basis, open questions and promises. J. Nutr. Biochem. 16: 449-466.
-
(2005)
J. Nutr. Biochem
, vol.16
, pp. 449-466
-
-
Signorelli, P.1
Ghidoni, R.2
-
140
-
-
58549083941
-
Design, synthesis and biological evaluation of novel stilbene-based antitu¬mor agents
-
Simoni, D., F. P. Invidiata, M. Eleopra, P. Marchetti, R. Rondanin, R. Baruchello, G. Grisolia et al. 2009. Design, synthesis and biological evaluation of novel stilbene-based antitu¬mor agents. Bioorg. Med. Chem. 17: 512-522.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 512-522
-
-
Simoni, D.1
Invidiata, F.P.2
Eleopra, M.3
Marchetti, P.4
Rondanin, R.5
Baruchello, R.6
Grisolia, G.7
-
141
-
-
38149112614
-
Antitumor effects of curcumin and structurally β-diketone modified analogs on multidrug resistant cancer cells
-
Simoni, D., M. Rizzi, R. Rondanin, R. Baruchello, P. Marchetti, F. P. Invidiata, M. Labbozzetta et al. 2008. Antitumor effects of curcumin and structurally β-diketone modified analogs on multidrug resistant cancer cells. Bioorg. Med. Chem. Lett. 18: 845-849.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, pp. 845-849
-
-
Simoni, D.1
Rizzi, M.2
Rondanin, R.3
Baruchello, R.4
Marchetti, P.5
Invidiata, F.P.6
Labbozzetta, M.7
-
142
-
-
33646171087
-
Stilbene-based anticancer agents: Resveratrol analogues active toward HL60 leuke¬mic cells with a non-specific phase mechanism
-
Simoni, D., M. Roberti, F. P. Invidiata, E. Aiello, S. Aiello, P. Marchetti, R. Baruchello et al. 2006. Stilbene-based anticancer agents: Resveratrol analogues active toward HL60 leuke¬mic cells with a non-specific phase mechanism. Bioorg. Med. Chem. Lett. 16: 3245-3248.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 3245-3248
-
-
Simoni, D.1
Roberti, M.2
Invidiata, F.P.3
Aiello, E.4
Aiello, S.5
Marchetti, P.6
Baruchello, R.7
-
143
-
-
69749086697
-
Advances in synthetic approaches for the preparation of combre¬tastatin-based anti-cancer agents
-
Singh, R. and H. Kaur. 2009. Advances in synthetic approaches for the preparation of combre¬tastatin-based anti-cancer agents. Synthesis 15: 2471-2491.
-
(2009)
Synthesis
, vol.15
, pp. 2471-2491
-
-
Singh, R.1
Kaur, H.2
-
144
-
-
37549048120
-
A new arylnaphthalene type lignan from Cordia rufescens A. DC (Boraginaceas)
-
Souza da Silva, S. A., A. L. Souto, M. de Fatima Agra et al. 2004. A new arylnaphthalene type lignan from Cordia rufescens A. DC (Boraginaceas). Arkivok 6: 54-58.
-
(2004)
Arkivok
, vol.6
, pp. 54-58
-
-
Souza da Silva, S.A.1
Souto, A.L.2
de Fatima Agra, M.3
-
145
-
-
66849129572
-
Antiangiogenic resveratrol analogues by mild m-CPBA aromatic hydroxylation of 3,5-dimethoxystil¬benes
-
Spatafora, C., G. Basini, L. Baioni, F. Grasselli, A. Sofia, and C. Tringali. 2009. Antiangiogenic resveratrol analogues by mild m-CPBA aromatic hydroxylation of 3,5-dimethoxystil¬benes. Nat. Prod. Comm. 4: 239-246.
-
(2009)
Nat. Prod. Comm
, vol.4
, pp. 239-246
-
-
Spatafora, C.1
Basini, G.2
Baioni, L.3
Grasselli, F.4
Sofia, A.5
Tringali, C.6
-
146
-
-
84984711470
-
Phenolic oxidative coupling in the biomimetic synthesis of heterocyclic lignans, neolignans and related compounds
-
eds. O. A. Attanasi and D. Spinelli, Roma, Italy: Società Chimica Italiana
-
Spatafora, C. and C. Tringali. 2007. Phenolic oxidative coupling in the biomimetic synthesis of heterocyclic lignans, neolignans and related compounds. In Targets in Heterocyclic Systems. Chemistry and Properties, Vol. 11, eds. O. A. Attanasi and D. Spinelli, pp. 284-312. Roma, Italy: Società Chimica Italiana.
-
(2007)
Targets in Heterocyclic Systems. Chemistry and Properties
, vol.11
, pp. 284-312
-
-
Spatafora, C.1
Tringali, C.2
-
147
-
-
0017136711
-
Prevention of chemical car¬cinogenesis by vitamin A and its synthetic analogs (retinoids)
-
Sporn, M. B., N. M. Dunlop, D. L. Newton, and J. M. Smith. 1976. Prevention of chemical car¬cinogenesis by vitamin A and its synthetic analogs (retinoids). Fed. Proc. 35: 1332-1338.
-
(1976)
Fed. Proc
, vol.35
, pp. 1332-1338
-
-
Sporn, M.B.1
Dunlop, N.M.2
Newton, D.L.3
Smith, J.M.4
-
148
-
-
0041367221
-
Flavonoids from Caesalpinia pulcherrima
-
Srinivas, K. V., R. Y. Koteswara, I. Mahender, B. Das, K. V. S. Rama Krishna, K. Hara Kishore, and U. S. N. Murty. 2003. Flavonoids from Caesalpinia pulcherrima. Phytochemistry 63: 789-793.
-
(2003)
Phytochemistry
, vol.63
, pp. 789-793
-
-
Srinivas, K.V.1
Koteswara, R.Y.2
Mahender, I.3
Das, B.4
Rama Krishna, K.V.S.5
Hara Kishore, K.6
Murty, U.S.N.7
-
149
-
-
54949136123
-
Curcumin in cancer management: Recent results of analogue design and clinical studies and desirable future research
-
Steward, W. P. and A. J. Gescher. 2008. Curcumin in cancer management: Recent results of analogue design and clinical studies and desirable future research. Mol. Nutr. Food Res. 52: 1005-1009.
-
(2008)
Mol. Nutr. Food Res
, vol.52
, pp. 1005-1009
-
-
Steward, W.P.1
Gescher, A.J.2
-
150
-
-
71749096442
-
Curcumin analog cytotoxicity against breast cancer cells: Exploitation of a redox-dependent mechanism
-
Sun, A., Y. J. Lu, H. Hu, M. Shoji, D. C. Liotta, and J. P. Snyder. 2009. Curcumin analog cytotoxicity against breast cancer cells: Exploitation of a redox-dependent mechanism. Bioorg. Med. Chem. Lett. 19: 6627-6631.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 6627-6631
-
-
Sun, A.1
Lu, Y.J.2
Hu, H.3
Shoji, M.4
Liotta, D.C.5
Snyder, J.P.6
-
151
-
-
0032813348
-
Molecular mechanisms of chemopreventive effects of selected dietary and medicinal phenolic substances
-
Surh, Y. 1999. Molecular mechanisms of chemopreventive effects of selected dietary and medicinal phenolic substances. Mutat. Res. 428: 305-327.
-
(1999)
Mutat. Res
, vol.428
, pp. 305-327
-
-
Surh, Y.1
-
152
-
-
0142166328
-
Cancer chemoprevention with dietary phytochemicals
-
Surh, Y. J. 2003. Cancer chemoprevention with dietary phytochemicals. Nat. Rev. Cancer 3: 768-780.
-
(2003)
Nat. Rev. Cancer
, vol.3
, pp. 768-780
-
-
Surh, Y.J.1
-
153
-
-
0041675753
-
Of the phenolic substances of white hellebore (Veratrum grandiflorum Loes. fil.)
-
Takaoka, M. J. 1940. Of the phenolic substances of white hellebore (Veratrum grandiflorum Loes. fil.). J. Fac. Agric. Hokkaido 3: 1-16.
-
(1940)
J. Fac. Agric. Hokkaido
, vol.3
, pp. 1-16
-
-
Takaoka, M.J.1
-
154
-
-
33845705480
-
Dietary polyphenolic phytochemicals-Promising cancer chemopreventive agents in humans? A review of their clinical properties
-
Thomasset, S. C., D. P. Berry, G. Garcea, T. Marczylo, W. P. Steward, and A. J. Gescher. 2006. Dietary polyphenolic phytochemicals-Promising cancer chemopreventive agents in humans? A review of their clinical properties. Int. J. Cancer 120: 451-458.
-
(2006)
Int. J. Cancer
, vol.120
, pp. 451-458
-
-
Thomasset, S.C.1
Berry, D.P.2
Garcea, G.3
Marczylo, T.4
Steward, W.P.5
Gescher, A.J.6
-
156
-
-
33744820579
-
Medicinal chem¬istry of combretastatin A4: Present and future directions
-
Tron, G. C., T. Pirali, G. Sorba, F. Pagliai, S. Busacca, and A. A. Genazzani. 2006. Medicinal chem¬istry of combretastatin A4: Present and future directions. J. Med. Chem. 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
-
157
-
-
42149180752
-
Natural and non-natural prenylated chalcones: Synthesis, cytotoxicity and anti-oxidative activity
-
Vogel, S., S. Ohmayer, G. Brunner, and J. Heilmann. 2008. Natural and non-natural prenylated chalcones: Synthesis, cytotoxicity and anti-oxidative activity. Bioorg. Med. Chem. 16: 4286-4293.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 4286-4293
-
-
Vogel, S.1
Ohmayer, S.2
Brunner, G.3
Heilmann, J.4
-
158
-
-
34548423695
-
Methoxylated flavones, a superior cancer chemopreventive flavonoid subclass?
-
Walle, T. 2007. Methoxylated flavones, a superior cancer chemopreventive flavonoid subclass? Semin. Cancer Biol. 17: 354-362.
-
(2007)
Semin. Cancer Biol
, vol.17
, pp. 354-362
-
-
Walle, T.1
-
159
-
-
32844463364
-
Activation of NF kappa B is inhibited by cur¬cumin and related enones
-
Weber, W. M., L. A. Hunsaker, C. N. B.-M. Roybal, V. Ekaterina, S. F. Abcouwer, R. E. Royer, L. M. Deck, and D. L. Vander Jagt. 2006. Activation of NF kappa B is inhibited by cur¬cumin and related enones. Bioorg. Med. Chem. 14: 2450-2461.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 2450-2461
-
-
Weber, W.M.1
Hunsaker, L.A.2
Roybal, C.N.B.-M.3
Ekaterina, V.4
Abcouwer, S.F.5
Royer, R.E.6
Deck, L.M.7
Vander Jagt, D.L.8
-
160
-
-
67649158904
-
Mechanisms of apoptotic effects induced by resveratrol, dibenzoylmethane, and their analogues on human lung carci¬noma cells
-
Weng, C. J., Y. T. Yang, C. T. Ho, and G. C. Yen. 2009. Mechanisms of apoptotic effects induced by resveratrol, dibenzoylmethane, and their analogues on human lung carci¬noma cells. J. Agric. Food. Chem. 57: 5235-5243.
-
(2009)
J. Agric. Food. Chem
, vol.57
, pp. 5235-5243
-
-
Weng, C.J.1
Yang, Y.T.2
Ho, C.T.3
Yen, G.C.4
-
161
-
-
61649113744
-
Molecular targets for cancer chemoprevention
-
William, N. W. Jr., J. V. Heymach, E. S. Kim, and S. M. Lippman. 2009. Molecular targets for cancer chemoprevention. Nat. Rev. Drug Discov. 8: 213-223.
-
(2009)
Nat. Rev. Drug Discov
, vol.8
, pp. 213-223
-
-
William, N.W.1
Heymach, J.V.2
Kim, E.S.3
Lippman, S.M.4
-
162
-
-
56249087269
-
Synthesis of trans-caffeate analogues and their bioactivities against HIV-1 integrase and cancer cell lines
-
Xia, C., L. H. Li, L. Feng, and W. -X. Hu. 2008. Synthesis of trans-caffeate analogues and their bioactivities against HIV-1 integrase and cancer cell lines. Bioorg. Med. Chem. Lett. 18: 6553-6557.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, pp. 6553-6557
-
-
Xia, C.1
Li, L.H.2
Feng, L.3
Hu, W.-X.4
-
163
-
-
75149160541
-
Structure-activity relationship of C5-curcuminoids and synthesis of their molecular probes thereof
-
Yamakoshi, H., H. Ohori, C. Kudo et al. 2010. Structure-activity relationship of C5-curcuminoids and synthesis of their molecular probes thereof. Bioorg. Med. Chem. 18: 1083-1092.
-
(2010)
Bioorg. Med. Chem
, vol.18
, pp. 1083-1092
-
-
Yamakoshi, H.1
Ohori, H.2
Kudo, C.3
-
164
-
-
0033039112
-
Inhibition of carcinogenesis by tea: Bioavailability of tea polyphenols and mechanisms of actions
-
Yang, C. S., S. Kim, G. Y. Yang, M.-J. Lee, J. Liao, J. Y. Chung, and C.-T. Ho. 1999. Inhibition of carcinogenesis by tea: Bioavailability of tea polyphenols and mechanisms of actions. Proc. Soc. Exp. Biol. Med. 220: 213-217.
-
(1999)
Proc. Soc. Exp. Biol. Med
, vol.220
, pp. 213-217
-
-
Yang, C.S.1
Kim, S.2
Yang, G.Y.3
Lee, M.-J.4
Liao, J.5
Chung, J.Y.6
Ho, C.-T.7
-
165
-
-
71849101913
-
Synthesis and biological evaluation of 3′, 4′, 5′-trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation
-
Yerra, K. R., F. Shih-Hua, and T. Yew-Min. 2009. Synthesis and biological evaluation of 3′, 4′, 5′-trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation. Bioorg. Med. Chem. 17: 7909-7914.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 7909-7914
-
-
Yerra, K.R.1
Shih-Hua, F.2
Yew-Min, T.3
-
166
-
-
45749149086
-
Design, synthesis and cytotoxicity of novel podophyllotoxin derivatives
-
Yu, P.-F., H. Chen, J. Wang, C.-X. He, B. Cao, M. Li, N. Yang, Z.-Y. Lei, and M.-S. Cheng. 2008a. Design, synthesis and cytotoxicity of novel podophyllotoxin derivatives. Chem. Pharm. Bull. 56: 831-834.
-
(2008)
Chem. Pharm. Bull
, vol.56
, pp. 831-834
-
-
Yu, P.-F.1
Chen, H.2
Wang, J.3
He, C.-X.4
Cao, B.5
Li, M.6
Yang, N.7
Lei, Z.-Y.8
Cheng, M.-S.9
-
167
-
-
46749091209
-
Prodrugs of fluoro-substituted benzoates of EGC as tumor cellular proteasome inhibi¬tors and apoptosis inducers
-
Yu, Z., X. L. Qin, Y. Y. Gu, C. Di, Q. C. Cui, T. Jiang, S. B. Wan, and Q. P. Dou. 2008b. Prodrugs of fluoro-substituted benzoates of EGC as tumor cellular proteasome inhibi¬tors and apoptosis inducers. Int. J. Mol. Sci. 9: 951-961.
-
(2008)
Int. J. Mol. Sci
, vol.9
, pp. 951-961
-
-
Yu, Z.1
Qin, X.L.2
Gu, Y.Y.3
Di, C.4
Cui, Q.C.5
Jiang, T.6
Wan, S.B.7
Dou, Q.P.8
-
168
-
-
33644928754
-
Green tea and its polyphenolic catechins: Medicinal uses in cancer and noncancer applications
-
Zaveri, N. T. 2006. Green tea and its polyphenolic catechins: Medicinal uses in cancer and noncancer applications. Life Sci. 78: 2073-2080.
-
(2006)
Life Sci
, vol.78
, pp. 2073-2080
-
-
Zaveri, N.T.1
|