-
1
-
-
0034923502
-
DNA topoisomerases: Structure, function, and mechanism
-
DOI 10.1146/annurev.biochem.70.1.369
-
Champoux, J.J., DNA topoisomerases: structure, function, and mechanism. Annu. Rev. Biochem., 2001, 70, 369-413. (Pubitemid 32662215)
-
(2001)
Annual Review of Biochemistry
, vol.70
, pp. 369-413
-
-
Champoux, J.J.1
-
2
-
-
33745278845
-
Repair of topoisomerase I-mediated DNA damage
-
DOI 10.1016/S0079-6603(06)81005-6, PII S0079660306810056, Progress in Nuclei Acid Research and Molecular Biology
-
Pommier, Y.; Barcelo, J.M.; Rao, V.A.; Sordet, O.; Jobson, A.G.; Thibaut, L.; Miao, Z.H.; Seiler, J.A.; Zhang, H.; Marchand, C.; Agama, K.; Nitiss, J.L.; Redon, C., Repair of topoisomerase I-mediated DNA damage. Prog. Nucleic Acid Res. Mol. Biol., 2006, 81, 179-229. (Pubitemid 44767505)
-
(2006)
Progress in Nucleic Acid Research and Molecular Biology
, vol.81
, pp. 179-229
-
-
Pommier, Y.1
Barcelo, J.M.2
Rao, V.A.3
Sordet, O.4
Jobson, A.G.5
Thibaut, L.6
Miao, Z.7
Seiler, J.A.8
Zhang, H.9
Marchand, C.10
Agama, K.11
Nitiss, J.L.12
Redon, C.13
-
3
-
-
67650682519
-
DNA topoisomerase i inhibitors: Chemistry, biology, and interfacial inhibition
-
Pommier, Y., DNA topoisomerase I inhibitors: chemistry, biology, and interfacial inhibition. Chem. Rev., 2009, 109, 2894-2902.
-
(2009)
Chem. Rev.
, vol.109
, pp. 2894-2902
-
-
Pommier, Y.1
-
4
-
-
33749034730
-
Topoisomerase I inhibitors: Camptothecins and beyond
-
DOI 10.1038/nrc1977, PII NRC1977
-
Pommier, Y., Topoisomerase I inhibitors: camptothecins and beyond. Nat. Rev. Cancer, 2006, 6, 789-802. (Pubitemid 44450467)
-
(2006)
Nature Reviews Cancer
, vol.6
, Issue.10
, pp. 789-802
-
-
Pommier, Y.1
-
5
-
-
64649105115
-
DNA topoisomerase II and its growing repertoire of biological functions
-
Nitiss, J.L., DNA topoisomerase II and its growing repertoire of biological functions. Nat. Rev. Cancer, 2009, 9, 327-337.
-
(2009)
Nat. Rev. Cancer
, vol.9
, pp. 327-337
-
-
Nitiss, J.L.1
-
6
-
-
54349090340
-
Targeting topoisomerase I: Molecular mechanisms and cellular determinants of response to topoisomerase i inhibitors
-
Beretta, G.L.; Perego, P.; Zunino, F., Targeting topoisomerase I: molecular mechanisms and cellular determinants of response to topoisomerase I inhibitors. Expert. Opin. Ther. Targets, 2008, 12, 1243-1256.
-
(2008)
Expert. Opin. Ther. Targets
, vol.12
, pp. 1243-1256
-
-
Beretta, G.L.1
Perego, P.2
Zunino, F.3
-
7
-
-
64649090292
-
Targeting DNA topoisomerase II in cancer chemotherapy
-
Nitiss, J.L., Targeting DNA topoisomerase II in cancer chemotherapy. Nat. Rev. Cancer, 2009, 9, 338-350.
-
(2009)
Nat. Rev. Cancer
, vol.9
, pp. 338-350
-
-
Nitiss, J.L.1
-
8
-
-
0019332581
-
Covalent bonds between protein and DNA. Formation of phosphotyrosine linkage between certain DNA topoisomerases and DNA
-
Tse, Y.C.; Kirkegaard, K.; Wang, J.C., Covalent bonds between protein and DNA. Formation of phosphotyrosine linkage between certain DNA topoisomerases and DNA. J. Biol. Chem., 1980, 255, 5560-5565.
-
(1980)
J. Biol. Chem.
, vol.255
, pp. 5560-5565
-
-
Tse, Y.C.1
Kirkegaard, K.2
Wang, J.C.3
-
9
-
-
0022340594
-
Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I
-
Hsiang, Y.H.; Hertzberg, R.; Hecht, S.; Liu, L.F., Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I. J. Biol. Chem., 1985, 260, 14873-14878. (Pubitemid 16211028)
-
(1985)
Journal of Biological Chemistry
, vol.260
, Issue.27
, pp. 14873-14878
-
-
Hsiang, Y.-H.1
Hertzberg, R.2
Hecht, S.3
Liu, L.F.4
-
10
-
-
7144248725
-
The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca Acuminata
-
Wall, M.E.; Wani, M.C.; Cook, C.E.; Palmer, K.H.; McPhail, A.T.; Sim, G.A., The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca Acuminata. J. Am. Chem. Soc., 1966, 88, 3888-3890.
-
(1966)
J. Am. Chem. Soc.
, vol.88
, pp. 3888-3890
-
-
Wall, M.E.1
Wani, M.C.2
Cook, C.E.3
Palmer, K.H.4
McPhail, A.T.5
Sim, G.A.6
-
11
-
-
0025133118
-
Involvement of nucleic acid synthesis in cell killing mechanisms of topoisomerase poisons
-
D'Arpa, P.; Beardmore, C.; Liu, L.F., Involvement of nucleic acid synthesis in cell killing mechanisms of topoisomerase poisons. Cancer Res., 1990, 50, 6919-6924. (Pubitemid 20361091)
-
(1990)
Cancer Research
, vol.50
, Issue.21
, pp. 6919-6924
-
-
D'Arpa, P.1
Beardmore, C.2
Liu, L.F.3
-
12
-
-
0034509633
-
Mechanism of action of camptothecin
-
Liu, L.F.; Desai, S.D.; Li, T.K.; Mao, Y.; Sun, M.; Sim, S.P., Mechanism of action of camptothecin. Ann. N. Y. Acad. Sci., 2000, 922, 1-10. (Pubitemid 32050237)
-
(2000)
Annals of the New York Academy of Sciences
, vol.922
, pp. 1-10
-
-
Liu, L.F.1
Desai, S.D.2
Li, T.-K.3
Mao, Y.4
Sun, M.5
Sim, S.-P.6
-
13
-
-
0026625512
-
The involvement of active DNA synthesis in camptothecin-induced G2 arrest: Altered regulation of p34cdc2/cyclin B
-
Tsao, Y.P.; D'Arpa, P.; Liu, L.F., The involvement of active DNA synthesis in camptothecin-induced G2 arrest: altered regulation of p34cdc2/cyclin B. Cancer. Res, 1992, 52, 1823-1829.
-
(1992)
Cancer. Res
, vol.52
, pp. 1823-1829
-
-
Tsao, Y.P.1
D'Arpa, P.2
Liu, L.F.3
-
14
-
-
18044378364
-
Synthesis and pharmacology of new camptothecin drugs
-
DOI 10.2174/1389557053765547
-
Driver, R.W.; Yang, L.X., Synthesis and pharmacology of new camptothecin drugs. Mini. Rev. Med. Chem., 2005, 5, 425-439. (Pubitemid 40601634)
-
(2005)
Mini-Reviews in Medicinal Chemistry
, vol.5
, Issue.5
, pp. 425-439
-
-
Driver, R.W.1
Yang, L.-X.2
-
15
-
-
33745737662
-
Review camptothecin: Current perspectives
-
Li, Q.Y.; Zu, Y.G.; Shi, R.Z.; Yao, L.P., Review camptothecin: current perspectives. Curr. Med. Chem., 2006, 13, 2021-2039.
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 2021-2039
-
-
Li, Q.Y.1
Zu, Y.G.2
Shi, R.Z.3
Yao, L.P.4
-
16
-
-
1542507062
-
Camptothecin: Current perspectives
-
DOI 10.1016/j.bmc.2003.11.036, PII S0968089603008848
-
Thomas, C.J.; Rahier, N.J.; Hecht, S.M., Camptothecin: current perspectives. Bioorg. Med. Chem., 2004, 12, 1585-1604. (Pubitemid 38344159)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.7
, pp. 1585-1604
-
-
Thomas, C.J.1
Rahier, N.J.2
Hecht, S.M.3
-
17
-
-
0026099599
-
Synthesis of water-soluble (aminoalkyl)camptothecin analogues: Inhibition of topoisomerase i and antitumor activity
-
Kingsbury, W.D.; Boehm, J.C.; Jakas, D.R.; Holden, K.G.; Hecht, S.M.; Gallagher, G.; Caranfa, M.J.; McCabe, F.L.; Faucette, L.F.; Johnson, R.K., Synthesis of water-soluble (aminoalkyl)camptothecin analogues: inhibition of topoisomerase I and antitumor activity. J. Med. Chem., 1991, 34, 98-107.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 98-107
-
-
Kingsbury, W.D.1
Boehm, J.C.2
Jakas, D.R.3
Holden, K.G.4
Hecht, S.M.5
Gallagher, G.6
Caranfa, M.J.7
McCabe, F.L.8
Faucette, L.F.9
Johnson, R.K.10
-
18
-
-
0036304427
-
Current perspectives on the clinical experience, pharmacology, and continued development of the camptothecins
-
Garcia-Carbonero, R.; Supko, J.G., Current perspectives on the clinical experience, pharmacology, and continued development of the camptothecins. Clin. Cancer Res., 2002, 8, 641-661. (Pubitemid 34742090)
-
(2002)
Clinical Cancer Research
, vol.8
, Issue.3
, pp. 641-661
-
-
Garcia-Carbonero, R.1
Supko, J.G.2
-
19
-
-
0036134605
-
Preclinical evaluation of the anticancer activity and toxicity of 9-nitro-20(S)-camptothecin (Rubitecan)
-
Giovanella, B.C.; Stehlin, J.S.; Hinz, H.R.; Kozielski, A.J.; Harris, N.J.; Vardeman, D.M., Preclinical evaluation of the anticancer activity and toxicity of 9-nitro-20(S)-camptothecin (Rubitecan). Int. J. Oncol., 2002, 20, 81-88.
-
(2002)
Int. J. Oncol.
, vol.20
, pp. 81-88
-
-
Giovanella, B.C.1
Stehlin, J.S.2
Hinz, H.R.3
Kozielski, A.J.4
Harris, N.J.5
Vardeman, D.M.6
-
20
-
-
15644373056
-
Phase I and pharmacokinetic study of GI147211, a water-soluble camptothecin analogue, administered for five consecutive days every three weeks
-
Eckhardt, S.G.; Baker, S.D.; Eckardt, J.R.; Burke, T.G.; Warner, D.L.; Kuhn, J.G.; Rodriguez, G.; Fields, S.; Thurman, A.; Smith, L.; Rothenberg, M.L.; White, L.; Wissel, P.; Kunka, R.; DePee, S.; Littlefield, D.; Burris, H.A.; Von Hoff, D.D.; Rowinsky, E.K., Phase I and pharmacokinetic study of GI147211, a water-soluble camptothecin analogue, administered for five consecutive days every three weeks. Clin. Cancer. Res., 1998, 4, 595-604. (Pubitemid 28193557)
-
(1998)
Clinical Cancer Research
, vol.4
, Issue.3
, pp. 595-604
-
-
Eckhardt, S.G.1
Baker, S.D.2
Eckardt, J.R.3
Burke, T.G.4
Warner, D.L.5
Kuhn, J.G.6
Rodriguez, G.7
Fields, S.8
Thurman, A.9
Smith, L.10
Rothenberg, M.L.11
White, L.12
Wissel, P.13
Kunka, R.14
DePee, S.15
Littlefield, D.16
Burris, H.A.17
Von Hoff, D.D.18
Rowinsky, E.K.19
-
21
-
-
0034796438
-
Phase I and pharmacological study of a new camptothecin derivative, exatecan mesylate (DX-8951f), infused over 30 minutes every three weeks
-
Minami, H.; Fujii, H.; Igarashi, T.; Itoh, K.; Tamanoi, K.; Oguma, T.; Sasaki, Y., Phase I and pharmacological study of a new camptothecin derivative, exatecan mesylate (DX-8951f), infused over 30 minutes every three weeks. Clin. Cancer Res., 2001, 7, 3056-3064. (Pubitemid 32963824)
-
(2001)
Clinical Cancer Research
, vol.7
, Issue.10
, pp. 3056-3064
-
-
Minami, H.1
Fujii, H.2
Igarashi, T.3
Itoh, K.4
Tamanoi, K.5
Oguma, T.6
Sasaki, Y.7
-
22
-
-
4444358344
-
Camptothecins and topoisomerase I: A foot in the door. Targeting the genome beyond topoisomerase I with camptothecins and novel anticancer drugs: Importance of DNA replication, repair and cell cycle checkpoints
-
DOI 10.2174/1568011043352777
-
Pommier, Y., Camptothecins and topoisomerase I: a foot in the door. Targeting the genome beyond topoisomerase I with camptothecins and novel anticancer drugs: importance of DNA replication, repair and cell cycle checkpoints.Curr. Med. Chem. Anticancer Agents, 2004, 4, 429-434. (Pubitemid 39199346)
-
(2004)
Current Medicinal Chemistry - Anti-Cancer Agents
, vol.4
, Issue.5
, pp. 429-434
-
-
Pommier, Y.1
-
23
-
-
71749108179
-
Synthesis and biological evaluation of 14-(aminoalkylaminomethyl) aromathecins as topoisomerase i inhibitors: Investigating the hypothesis of shared structure-activity relationships
-
Cinelli, M.A.; Cordero, B.; Dexheimer, T.S.; Pommier, Y.; Cushman, M., Synthesis and biological evaluation of 14-(aminoalkylaminomethyl) aromathecins as topoisomerase I inhibitors: investigating the hypothesis of shared structure-activity relationships. Bioorg. Med. Chem., 2009, 17, 7145-7155.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7145-7155
-
-
Cinelli, M.A.1
Cordero, B.2
Dexheimer, T.S.3
Pommier, Y.4
Cushman, M.5
-
24
-
-
0030453706
-
Chemistry of the camptothecins in the bloodstream. Drug stabilization and optimization of activity
-
DOI 10.1111/j.1749-6632.1996.tb26373.x
-
Burke, T.G., Chemistry of the camptothecins in the bloodstream. Drug stabilization and optimization of activity. Ann. N. Y. Acad. Sci., 1996, 803, 29-31. (Pubitemid 27057972)
-
(1996)
Annals of the New York Academy of Sciences
, vol.803
, pp. 29-31
-
-
Burke, T.G.1
-
25
-
-
0023924786
-
Identification of mammalian DNA topoisomerase i as an intracellular target of the anticancer drug camptothecin
-
Hsiang, Y.H.; Liu, L.F., Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin. Cancer Res., 1988, 48, 1722-1726.
-
(1988)
Cancer Res.
, vol.48
, pp. 1722-1726
-
-
Hsiang, Y.H.1
Liu, L.F.2
-
26
-
-
0033429542
-
Camptothecin resistance: Role of the ATP-binding cassette (ABC), mitoxantrone-resistance half-transporter (MXR), and potential for glucuronidation in MXR-expressing cells
-
Brangi, M.; Litman, T.; Ciotti, M.; Nishiyama, K.; Kohlhagen, G.; Takimoto, C.; Robey, R.; Pommier, Y.; Fojo, T.; Bates, S.E., Camptothecin resistance: role of the ATP-binding cassette (ABC), mitoxantrone-resistance halftransporter (MXR), and potential for glucuronidation in MXR-expressing cells. Cancer Res., 1999, 59, 5938-5946. (Pubitemid 30004955)
-
(1999)
Cancer Research
, vol.59
, Issue.23
, pp. 5938-5946
-
-
Brangi, M.1
Litman, T.2
Ciotti, M.3
Nishiyama, K.4
Kohlhagen, G.5
Takimoto, C.6
Robey, R.7
Pommier, Y.8
Fojo, T.9
Bates, S.E.10
-
27
-
-
38549161260
-
Reduced expression of DNA topoisomerase I in SF295 human glioblastoma cells selected for resistance to homocamptothecin and diflomotecan
-
DOI 10.1124/mol.107.041178
-
Liao, Z.; Robey, R.W.; Guirouilh-Barbat, J.; To, K.K.; Polgar, O.; Bates, S.E.; Pommier, Y., Reduced expression of DNA topoisomerase I in SF295 human glioblastoma cells selected for resistance to homocamptothecin and diflomotecan. Mol. Pharmacol., 2008, 73, 490-497. (Pubitemid 351159219)
-
(2008)
Molecular Pharmacology
, vol.73
, Issue.2
, pp. 490-497
-
-
Liao, Z.1
Robey, R.W.2
Guirouilh-Barbat, J.3
To, K.K.W.4
Polgar, O.5
Bates, S.E.6
Pommier, Y.7
-
28
-
-
33644755350
-
Molecular modeling of new camptothecin analogues to circumvent ABCG2-mediated drug resistance in cancer
-
DOI 10.1016/j.canlet.2005.05.052, PII S0304383505009286, Pharmacogenomics in Cancer Chemotherapy: Recent Advances in Drug Transporters and Genome Analysis
-
Nakagawa, H.; Saito, H.; Ikegami, Y.; Aida-Hyugaji, S.; Sawada, S.; Ishikawa, T., Molecular modeling of new camptothecin analogues to circumvent ABCG2-mediated drug resistance in cancer. Cancer Lett., 2006, 234, 81-89. (Pubitemid 43343942)
-
(2006)
Cancer Letters
, vol.234
, Issue.1
, pp. 81-89
-
-
Nakagawa, H.1
Saito, H.2
Ikegami, Y.3
Aida-Hyugaji, S.4
Sawada, S.5
Ishikawa, T.6
-
29
-
-
0028957974
-
Mutation at the catalytic site of topoisomerase i in CEM/C2, a human leukemia cell line resistant to camptothecin
-
Fujimori, A.; Harker, W.G.; Kohlhagen, G.; Hoki, Y.; Pommier, Y., Mutation at the catalytic site of topoisomerase I in CEM/C2, a human leukemia cell line resistant to camptothecin. Cancer Res., 1995, 55, 1339-1346.
-
(1995)
Cancer Res.
, vol.55
, pp. 1339-1346
-
-
Fujimori, A.1
Harker, W.G.2
Kohlhagen, G.3
Hoki, Y.4
Pommier, Y.5
-
30
-
-
0035266161
-
Characterization of a novel topoisomerase I mutation from a camptothecin-resistant human prostate cancer cell line
-
Urasaki, Y.; Laco, G.S.; Pourquier, P.; Takebayashi, Y.; Kohlhagen, G.; Gioffre, C.; Zhang, H.; Chatterjee, D.; Pantazis, P.; Pommier, Y., Characterization of a novel topoisomerase I mutation from a camptothecin- resistant human prostate cancer cell line. Cancer Res., 2001, 61, 1964-1969. (Pubitemid 32692014)
-
(2001)
Cancer Research
, vol.61
, Issue.5
, pp. 1964-1969
-
-
Urasaki, Y.1
Laco, G.S.2
Pourquier, P.3
Takebayashi, Y.4
Kohlhagen, G.5
Gioffre, C.6
Zhang, H.7
Chatterjee, D.8
Pantazis, P.9
Pommier, Y.10
-
31
-
-
78651518327
-
3-Arylisoquinolines as novel topoisomerase i inhibitors
-
Khadka, D.B.; Cho, W.J., 3-Arylisoquinolines as novel topoisomerase I inhibitors. Bioorg. Med. Chem., 2011, 19, 724-734.
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 724-734
-
-
Khadka, D.B.1
Cho, W.J.2
-
32
-
-
0038207882
-
Non-camptothecin DNA topoisomerase i inhibitors in cancer therapy
-
Meng, L.H.; Liao, Z.Y.; Pommier, Y., Non-camptothecin DNA topoisomerase I inhibitors in cancer therapy. Curr. Top. Med. Chem., 2003, 3, 305-320.
-
(2003)
Curr. Top. Med. Chem.
, vol.3
, pp. 305-320
-
-
Meng, L.H.1
Liao, Z.Y.2
Pommier, Y.3
-
33
-
-
39749119942
-
Next generation topoisomerase I inhibitors: Rationale and biomarker strategies
-
DOI 10.1016/j.bcp.2007.10.016, PII S0006295207006946
-
Teicher, B.A., Next generation topoisomerase I inhibitors: Rationale and biomarker strategies. Biochem. Pharmacol., 2008, 75, 1262-1271. (Pubitemid 351305209)
-
(2008)
Biochemical Pharmacology
, vol.75
, Issue.6
, pp. 1262-1271
-
-
Teicher, B.A.1
-
34
-
-
0032033603
-
Diversity of DNA topoisomerases I and inhibitors
-
DOI 10.1016/S0300-9084(98)80008-4
-
Pommier, Y., Diversity of DNA topoisomerases I and inhibitors. Biochimie, 1998, 80, 255-270. (Pubitemid 28206041)
-
(1998)
Biochimie
, vol.80
, Issue.3
, pp. 255-270
-
-
Pommier, Y.1
-
35
-
-
33646477959
-
Phase i and pharmacokinetic study of edotecarin, a novel topoisomerase i inhibitor, administered once every 3 weeks in patients with solid tumors
-
Yamada, Y.; Tamura, T.; Yamamoto, N.; Shimoyama, T.; Ueda, Y.; Murakami, H.; Kusaba, H.; Kamiya, Y.; Saka, H.; Tanigawara, Y.; McGovren, J.P.; Natsumeda, Y., Phase I and pharmacokinetic study of edotecarin, a novel topoisomerase I inhibitor, administered once every 3 weeks in patients with solid tumors. Cancer Chemother. Pharmacol., 2006, 58, 173-182.
-
(2006)
Cancer Chemother. Pharmacol.
, vol.58
, pp. 173-182
-
-
Yamada, Y.1
Tamura, T.2
Yamamoto, N.3
Shimoyama, T.4
Ueda, Y.5
Murakami, H.6
Kusaba, H.7
Kamiya, Y.8
Saka, H.9
Tanigawara, Y.10
McGovren, J.P.11
Natsumeda, Y.12
-
36
-
-
0242610818
-
Differential Induction of Topoisomerase I-DNA Cleavage Complexes by the Indenoisoquinoline MJ-III-65 (NSC 706744) and Camptothecin: Base Sequence Analysis and Activity against Camptothecin-Resistant Topoisomerases I
-
Antony, S.; Jayaraman, M.; Laco, G.; Kohlhagen, G.; Kohn, K.W.; Cushman, M.; Pommier, Y., Differential induction of topoisomerase I-DNA cleavage complexes by the indenoisoquinoline MJ-III-65 (NSC 706744) and camptothecin: base sequence analysis and activity against camptothecinresistant topoisomerases I. Cancer Res., 2003, 63, 7428-7435. (Pubitemid 37413485)
-
(2003)
Cancer Research
, vol.63
, Issue.21
, pp. 7428-7435
-
-
Antony, S.1
Jayaraman, M.2
Laco, G.3
Kohlhagen, G.4
Kohn, K.W.5
Cushman, M.6
Pommier, Y.7
-
37
-
-
13444284042
-
Cellular topoisomerase I inhibition and antiproliferative activity by MJ-III-65 (NSC 706744), an indenoisoquinoline topoisomerase I poison
-
DOI 10.1124/mol.104.003889
-
Antony, S.; Kohlhagen, G.; Agama, K.; Jayaraman, M.; Cao, S.; Durrani, F.A.; Rustum, Y.M.; Cushman, M.; Pommier, Y., Cellular topoisomerase I inhibition and antiproliferative activity by MJ-III-65 (NSC 706744), an indenoisoquinoline topoisomerase I poison. Mol. Pharmacol., 2005, 67, 523-530. (Pubitemid 40216745)
-
(2005)
Molecular Pharmacology
, vol.67
, Issue.2
, pp. 523-530
-
-
Antony, S.1
Kohlhagen, G.2
Agama, K.3
Jayaraman, M.4
Cao, S.5
Durrani, F.A.6
Rustum, Y.M.7
Cushman, M.8
Pommier, Y.9
-
38
-
-
0036488643
-
Natural products in cancer chemotherapy: Past, present and future
-
Mann, J., Natural products in cancer chemotherapy: past, present and future. Nat. Rev. Cancer, 2002, 2, 143-148. (Pubitemid 37328801)
-
(2002)
Nature Reviews Cancer
, vol.2
, Issue.2
, pp. 143-148
-
-
Mann, J.1
-
39
-
-
1442334562
-
Camptothecin and taxol: Historic achievements in natural products research
-
DOI 10.1021/np030498t
-
Oberlies, N.H.; Kroll, D.J., Camptothecin and taxol: historic achievements in natural products research. J. Nat. Prod., 2004, 67, 129-135. (Pubitemid 38282896)
-
(2004)
Journal of Natural Products
, vol.67
, Issue.2
, pp. 129-135
-
-
Oberlies, N.H.1
Kroll, D.J.2
-
40
-
-
12444318520
-
DNA topoisomerase I inhibitors from Rinorea anguifera
-
DOI 10.1016/j.bmcl.2004.10.095, PII S0960894X04013344
-
Ma, J.; Jones, S.H.; Marshall, R.; Wu, X.; Hecht, S.M., DNA topoisomerase I inhibitors from Rinorea anguifera. Bioorg. Med. Chem. Lett., 2005, 15, 813-816. (Pubitemid 40143171)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.3
, pp. 813-816
-
-
Ma, J.1
Jones, S.H.2
Marshall, R.3
Wu, X.4
Hecht, S.M.5
-
41
-
-
52149114901
-
DNA topoisomerase i inhibitory alkaloids from Corydalis saxicola
-
Cheng, X.; Wang, D.; Jiang, L.; Yang, D., DNA topoisomerase I inhibitory alkaloids from Corydalis saxicola. Chem. Biodivers., 2008, 5, 1335-1344.
-
(2008)
Chem. Biodivers.
, vol.5
, pp. 1335-1344
-
-
Cheng, X.1
Wang, D.2
Jiang, L.3
Yang, D.4
-
42
-
-
62349140431
-
Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana
-
Wang, P.; Li, S.; Ownby, S.; Zhang, Z.; Yuan, W.; Zhang, W.; Scott Beasley, R., Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana. Phytochemistry, 2009, 70, 430-436.
-
(2009)
Phytochemistry
, vol.70
, pp. 430-436
-
-
Wang, P.1
Li, S.2
Ownby, S.3
Zhang, Z.4
Yuan, W.5
Zhang, W.6
Scott Beasley, R.7
-
43
-
-
78449259383
-
Inhibition of DNA topoisomerases i and II and cytotoxicity of compounds from Ulmus davidiana var. japonica
-
Zheng, M.S.; Lee, Y.K.; Li, Y.; Hwangbo, K.; Lee, C.S.; Kim, J.R.; Lee, S.K.; Chang, H.W.; Son, J.K., Inhibition of DNA topoisomerases I and II and cytotoxicity of compounds from Ulmus davidiana var. japonica. Arch. Pharm. Res., 2010, 33, 1307-1315.
-
(2010)
Arch. Pharm. Res.
, vol.33
, pp. 1307-1315
-
-
Zheng, M.S.1
Lee, Y.K.2
Li, Y.3
Hwangbo, K.4
Lee, C.S.5
Kim, J.R.6
Lee, S.K.7
Chang, H.W.8
Son, J.K.9
-
44
-
-
70450188835
-
Inhibition of DNA topoisomerases i and II and cytotoxicity by lignans from Saururus chinensis
-
Lee, Y.K.; Seo, C.S.; Lee, C.S.; Lee, K.S.; Kang, S.J.; Jahng, Y.; Chang, H.W.; Son, J.K., Inhibition of DNA topoisomerases I and II and cytotoxicity by lignans from Saururus chinensis. Arch. Pharm. Res., 2009, 32, 1409-1415.
-
(2009)
Arch. Pharm. Res.
, vol.32
, pp. 1409-1415
-
-
Lee, Y.K.1
Seo, C.S.2
Lee, C.S.3
Lee, K.S.4
Kang, S.J.5
Jahng, Y.6
Chang, H.W.7
Son, J.K.8
-
45
-
-
33646064109
-
Preparation of yuanhuacine and relative daphne diterpene esters from Daphne genkwa and structure-activity relationship of potent inhibitory activity against DNA topoisomerase i
-
Zhang, S.; Li, X.; Zhang, F.; Yang, P.; Gao, X.; Song, Q., Preparation of yuanhuacine and relative daphne diterpene esters from Daphne genkwa and structure-activity relationship of potent inhibitory activity against DNA topoisomerase I. Bioorg. Med. Chem., 2006, 14, 3888-3895.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 3888-3895
-
-
Zhang, S.1
Li, X.2
Zhang, F.3
Yang, P.4
Gao, X.5
Song, Q.6
-
46
-
-
22544463084
-
Indole alkaloids and other constituents of Rauwolfia serpentina
-
DOI 10.1021/np058007n
-
Itoh, A.; Kumashiro, T.; Yamaguchi, M.; Nagakura, N.; Mizushina, Y.; Nishi, T.; Tanahashi, T., Indole alkaloids and other constituents of Rauwolfia serpentina. J. Nat. Prod., 2005, 68, 848-852. (Pubitemid 41017496)
-
(2005)
Journal of Natural Products
, vol.68
, Issue.6
, pp. 848-852
-
-
Itoh, A.1
Kumashiro, T.2
Yamaguchi, M.3
Nagakura, N.4
Mizushina, Y.5
Nishi, T.6
Tanahashi, T.7
-
47
-
-
33846423855
-
Cucurbitane triterpenes from the fruiting bodies and cultivated mycelia of Leucopaxillus gentianeus
-
DOI 10.1021/np060213n
-
Clericuzio, M.; Tabasso, S.; Bianco, M.A.; Pratesi, G.; Beretta, G.; Tinelli, S.; Zunino, F.; Vidari, G., Cucurbitane triterpenes from the fruiting bodies and cultivated mycelia of Leucopaxillus gentianeus. J. Nat. Prod., 2006, 69, 1796-1799. (Pubitemid 46144979)
-
(2006)
Journal of Natural Products
, vol.69
, Issue.12
, pp. 1796-1799
-
-
Clericuzio, M.1
Tabasso, S.2
Bianco, M.A.3
Pratesi, G.4
Beretta, G.5
Tinelli, S.6
Zunino, F.7
Vidari, G.8
-
48
-
-
65249155938
-
Calothrixins, a new class of human DNA topoisomerase i poisons
-
Khan, Q.A.; Lu, J.; Hecht, S.M., Calothrixins, a new class of human DNA topoisomerase I poisons. J Nat Prod, 2009, 72, (3), 438-442.
-
(2009)
J Nat Prod
, vol.72
, Issue.3
, pp. 438-442
-
-
Khan, Q.A.1
Lu, J.2
Hecht, S.M.3
-
49
-
-
58049199480
-
Steroids, alkaloids, and coumarins from Gelsemium sempervirens
-
Zhang, Z.; Wang, P.; Yuan, W.; Li, S., Steroids, alkaloids, and coumarins from Gelsemium sempervirens. Planta. Med., 2008, 74, 1818-1822.
-
(2008)
Planta. Med.
, vol.74
, pp. 1818-1822
-
-
Zhang, Z.1
Wang, P.2
Yuan, W.3
Li, S.4
-
50
-
-
84954358489
-
The contribution of plukenetione A to the anti-tumoral activity of Cuban propolis
-
Diaz-Carballo, D.; Malak, S.; Bardenheuer, W.; Freistuehler, M.; Peter Reusch, H., The contribution of plukenetione A to the anti-tumoral activity of Cuban propolis. Bioorg. Med. Chem., 2008, 16, 9635-9643.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 9635-9643
-
-
Diaz-Carballo, D.1
Malak, S.2
Bardenheuer, W.3
Freistuehler, M.4
Peter Reusch, H.5
-
51
-
-
0033778305
-
Novel human topoisomerase i inhibitors, topopyrones A, B, C and D. I. Producing strain, fermentation, isolation, physico-chemical properties and biological activity
-
Kanai, Y.; Ishiyama, D.; Senda, H.; Iwatani, W.; Takahashi, H.; Konno, H.; Tokumasu, S.; Kanazawa, S., Novel human topoisomerase I inhibitors, topopyrones A, B, C and D. I. Producing strain, fermentation, isolation, physico-chemical properties and biological activity. J. Antibiot., 2000, 53, 863-872.
-
(2000)
J. Antibiot.
, vol.53
, pp. 863-872
-
-
Kanai, Y.1
Ishiyama, D.2
Senda, H.3
Iwatani, W.4
Takahashi, H.5
Konno, H.6
Tokumasu, S.7
Kanazawa, S.8
-
52
-
-
0033770559
-
Novel human topoisomerase i inhibitors, topopyrones A, B, C and D. II. Structure elucidation
-
Ishiyama, D.; Kanai, Y.; Senda, H.; Iwatani, W.; Konno, H.; Kanazawa, S., Novel human topoisomerase I inhibitors, topopyrones A, B, C and D. II. Structure elucidation. J. Antibiot., 2000, 53, 873-878.
-
(2000)
J. Antibiot.
, vol.53
, pp. 873-878
-
-
Ishiyama, D.1
Kanai, Y.2
Senda, H.3
Iwatani, W.4
Konno, H.5
Kanazawa, S.6
-
53
-
-
0037294445
-
Rebeccamycin analogues as anti-cancer agents
-
DOI 10.1016/S0223-5234(03)00011-4
-
Prudhomme, M., Rebeccamycin analogues as anti-cancer agents. Eur. J. Med. Chem., 2003, 38, 123-140. (Pubitemid 36288468)
-
(2003)
European Journal of Medicinal Chemistry
, vol.38
, Issue.2
, pp. 123-140
-
-
Prudhomme, M.1
-
54
-
-
0035254661
-
Apoptotic response of HL-60 human leukemia cells to the antitumor drug NB-506, a glycosylated indolocarbazole inhibitor of topoisomerase 1
-
DOI 10.1016/S0006-2952(00)00553-0, PII S0006295200005530
-
Facompre, M.; Goossens, J.F.; Bailly, C., Apoptotic response of HL-60 human leukemia cells to the antitumor drug NB-506, a glycosylated indolocarbazole inhibitor of topoisomerase 1. Biochem. Pharmacol., 2001, 61, 299-310. (Pubitemid 32126668)
-
(2001)
Biochemical Pharmacology
, vol.61
, Issue.3
, pp. 299-310
-
-
Facompre, M.1
Goossens, J.-F.2
Bailly, C.3
-
55
-
-
0033519179
-
Synthesis and biological activities of topoisomerase I inhibitors, 6-N- amino analogues of NB-506
-
DOI 10.1016/S0960-894X(99)00188-2, PII S0960894X99001882
-
Ohkubo, M.; Kojiri, K.; Kondo, H.; Tanaka, S.; Kawamoto, H.; Nishimura, T.; Nishimura, I.; Yoshinari, T.; Arakawa, H.; Suda, H.; Morishima, H.; Nishimura, S., Synthesis and biological activities of topoisomerase I inhibitors, 6-N-amino analogues of NB-506. Bioorg. Med. Chem. Lett., 1999, 9, 1219-1224. (Pubitemid 29207435)
-
(1999)
Bioorganic and Medicinal Chemistry Letters
, vol.9
, Issue.9
, pp. 1219-1224
-
-
Ohkubo, M.1
Kojiri, K.2
Kondo, H.3
Tanaka, S.4
Kawamoto, H.5
Nishimura, T.6
Nishimura, I.7
Yoshinari, T.8
Arakawa, H.9
Suda, H.10
Morishima, H.11
Nishimura, S.12
-
56
-
-
0033530871
-
Synthesis and biological activities of NB-506 analogues: Effects of the positions of two hydroxyl groups at the indole rings
-
Ohkubo, M.; Nishimura, T.; Honma, T.; Nishimura, I.; Ito, S.; Yoshinari, T.; Suda, H.A.; Morishima, H.; Nishimura, S., Synthesis and biological activities of NB-506 analogues: Effects of the positions of two hydroxyl groups at the indole rings. Bioorg Med Chem Lett, 1999, 9, (23), 3307-3312.
-
(1999)
Bioorg Med Chem Lett
, vol.9
, Issue.23
, pp. 3307-3312
-
-
Ohkubo, M.1
Nishimura, T.2
Honma, T.3
Nishimura, I.4
Ito, S.5
Yoshinari, T.6
Suda, H.A.7
Morishima, H.8
Nishimura, S.9
-
57
-
-
0034611438
-
Synthesis and biological activities of NB-506 analogues modified at the glucose group
-
DOI 10.1016/S0960-894X(00)00004-4, PII S0960894X00000044
-
Ohkubo, M.; Nishimura, T.; Kawamoto, H.; Nakano, M.; Honma, T.; Yoshinari, T.; Arakawa, H.; Suda, H.; Morishima, H.; Nishimura, S., Synthesis and biological activities of NB-506 analogues modified at the glucose group. Bioorg. Med. Chem. Lett., 2000, 10, 419-422. (Pubitemid 30153604)
-
(2000)
Bioorganic and Medicinal Chemistry Letters
, vol.10
, Issue.5
, pp. 419-422
-
-
Ohkubo, M.1
Nishimura, T.2
Kawamoto, H.3
Nakano, M.4
Honma, T.5
Yoshinari, T.6
Arakawa, H.7
Suda, H.8
Morishima, H.9
Nishimura, S.10
-
58
-
-
21844454211
-
Edotecarin: A novel topoisomerase i inhibitor
-
Saif, M.W.; Diasio, R.B., Edotecarin: a novel topoisomerase I inhibitor. Clin. Colorectal. Cancer, 2005, 5, 27-36.
-
(2005)
Clin. Colorectal. Cancer
, vol.5
, pp. 27-36
-
-
Saif, M.W.1
Diasio, R.B.2
-
59
-
-
33751292216
-
A phase I study of the safety and pharmacokinetics of edotecarin (J-107088), a novel topoisomerase I inhibitor, in patients with advanced solid tumors
-
DOI 10.1007/s00280-006-0267-9
-
Hurwitz, H.I.; Cohen, R.B.; McGovren, J.P.; Hirawat, S.; Petros, W.P.; Natsumeda, Y.; Yoshinari, T., A phase I study of the safety and pharmacokinetics of edotecarin (J-107088), a novel topoisomerase I inhibitor, in patients with advanced solid tumors. Cancer Chemother. Pharmacol., 2007, 59, 139-147. (Pubitemid 44796112)
-
(2007)
Cancer Chemotherapy and Pharmacology
, vol.59
, Issue.1
, pp. 139-147
-
-
Hurwitz, H.I.1
Cohen, R.B.2
McGovren, J.P.3
Hirawat, S.4
Petros, W.P.5
Natsumeda, Y.6
Yoshinari, T.7
-
60
-
-
77954657958
-
A phase i doseescalation study of edotecarin (J-107088) combined with infusional 5-fluorouracil and leucovorin in patients with advanced/metastatic solid tumors
-
Saif, M.W.; Sellers, S.; Diasio, R.B.; Douillard, J.Y., A phase I doseescalation study of edotecarin (J-107088) combined with infusional 5-fluorouracil and leucovorin in patients with advanced/metastatic solid tumors. Anticancer Drugs, 2010, 21, 716-723.
-
(2010)
Anticancer Drugs
, vol.21
, pp. 716-723
-
-
Saif, M.W.1
Sellers, S.2
Diasio, R.B.3
Douillard, J.Y.4
-
61
-
-
12144288796
-
Design and Synthesis of a Fluoroindolocarbazole Series as Selective Topoisomerase I Active Agents. Discovery of Water-Soluble 3,9-Difluoro-12,13- dihydro-13-[6-amino-β-D-glucopyranosyll]-5H,13H-benzo[b] -thienyl[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione (BMS-251873) with Curative Antitumor Activity against Prostate Carcinoma Xenograft Tumor Model
-
DOI 10.1021/jm034197s
-
Balasubramanian, B.N.; St Laurent, D.R.; Saulnier, M.G.; Long, B.H.; Bachand, C.; Beaulieu, F.; Clarke, W.; Deshpande, M.; Eummer, J.; Fairchild, C.R.; Frennesson, D.B.; Kramer, R.; Lee, F.Y.; Mahler, M.; Martel, A.; Naidu, B.N.; Rose, W.C.; Russell, J.; Ruediger, E.; Solomon, C.; Stoffan, K.M.; Wong, H.; Wright, J.J.; Zimmermann, K.; Vyas, D.M., Design and synthesis of a fluoroindolocarbazole series as selective topoisomerase I active agents. Discovery of water-soluble 3,9-difluoro-12,13-dihydro-13-[6-amino-beta-D- glucopyranosyl]-5H,13H-benzo [b]-thienyl[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)- dione (BMS-251873) with curative antitumor activity against prostate carcinoma xenograft tumor model. J. Med. Chem., 2004, 47, 1609-1612. (Pubitemid 38386629)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.7
, pp. 1609-1612
-
-
Balasubramanian, B.N.1
St. Laurent, D.R.2
Saulnier, M.G.3
Long, B.H.4
Bachand, C.5
Beaulieu, F.6
Clarke, W.7
Deshpande, M.8
Eummer, J.9
Fairchild, C.R.10
Frennesson, D.B.11
Kramer, R.12
Lee, F.Y.13
Mahler, M.14
Martel, A.15
Naidu, B.N.16
Rose, W.C.17
Russell, J.18
Ruediger, E.19
Solomon, C.20
Stoffan, K.M.21
Wong, H.22
Zimmermann, K.23
Vyas, D.M.24
more..
-
62
-
-
20244372565
-
Discovery of a fluoroindolo[2,3-a]carbazole clinical candidate with broad spectrum antitumor activity in preclinical tumor models superior to the marketed oncology drug, CPT-11
-
DOI 10.1021/jm049090z
-
Saulnier, M.G.; Balasubramanian, B.N.; Long, B.H.; Frennesson, D.B.; Ruediger, E.; Zimmermann, K.; Eummer, J.T.; St Laurent, D.R.; Stoffan, K.M.; Naidu, B.N.; Mahler, M.; Beaulieu, F.; Bachand, C.; Lee, F.Y.; Fairchild, C.R.; Stadnick, L.K.; Rose, W.C.; Solomon, C.; Wong, H.; Martel, A.; Wright, J.J.; Kramer, R.; Langley, D.R.; Vyas, D.M., Discovery of a fluoroindolo[2,3-a] carbazole clinical candidate with broad spectrum antitumor activity in preclinical tumor models superior to the marketed oncology drug, CPT-11. J. Med. Chem., 2005, 48, 2258-2261. (Pubitemid 40520515)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.7
, pp. 2258-2261
-
-
Saulnier, M.G.1
Balasubramanian, B.N.2
Long, B.H.3
Frennesson, D.B.4
Ruediger, E.5
Zimmermann, K.6
Eummer, J.T.7
St. Laurent, D.R.8
Stoffan, K.M.9
Naidu, B.N.10
Mahler, M.11
Beaulieu, F.12
Bachand, C.13
Lee, F.Y.14
Fairchild, C.R.15
Stadnick, L.K.16
Rose, W.C.17
Solomon, C.18
Wong, H.19
Martel, A.20
Wright, J.J.21
Kramer, R.22
Langley, D.R.23
Vyas, D.M.24
more..
-
63
-
-
20244380623
-
Syntheses and biological activities of rebeccamycin analogues with uncommon sugars
-
DOI 10.1021/jm0493764
-
Zhang, G.; Shen, J.; Cheng, H.; Zhu, L.; Fang, L.; Luo, S.; Muller, M.T.; Lee, G.E.; Wei, L.; Du, Y.; Sun, D.; Wang, P.G., Syntheses and biological activities of rebeccamycin analogues with uncommon sugars. J. Med. Chem., 2005, 48, 2600-2611. (Pubitemid 40516449)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.7
, pp. 2600-2611
-
-
Zhang, G.1
Shen, J.2
Cheng, H.3
Zhu, L.4
Fang, L.5
Luo, S.6
Muller, M.T.7
Lee, G.E.8
Wei, L.9
Du, Y.10
Sun, D.11
Wang, P.G.12
-
64
-
-
14944374500
-
Synthesis and biological evaluation of novel naphthocarbazoles as potential anticancer agents
-
DOI 10.1021/jm049213f
-
Routier, S.; Peixoto, P.; Merour, J.Y.; Coudert, G.; Dias, N.; Bailly, C.; Pierre, A.; Leonce, S.; Caignard, D.H., Synthesis and biological evaluation of novel naphthocarbazoles as potential anticancer agents. J. Med. Chem., 2005, 48, 1401-1413. (Pubitemid 40372209)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.5
, pp. 1401-1413
-
-
Routier, S.1
Peixoto, P.2
Merour, J.-Y.3
Coudert, G.4
Dias, N.5
Bailly, C.6
Pierre, A.7
Leonce, S.8
Caignard, D.-H.9
-
65
-
-
31544479559
-
Synthesis and biological evaluation of novel phenylcarbazoles as potential anticancer agents
-
DOI 10.1021/jm050945x
-
Routier, S.; Merour, J.Y.; Dias, N.; Lansiaux, A.; Bailly, C.; Lozach, O.; Meijer, L., Synthesis and biological evaluation of novel phenylcarbazoles as potential anticancer agents. J. Med. Chem., 2006, 49, 789-799. (Pubitemid 43158444)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.2
, pp. 789-799
-
-
Routier, S.1
Merour, J.-Y.2
Dias, N.3
Lansiaux, A.4
Bailly, C.5
Lozach, O.6
Meijer, L.7
-
66
-
-
17144371295
-
Structures of three classes of anticancer agents bound to the human topoisomerase I-DNA covalent complex
-
DOI 10.1021/jm049146p
-
Staker, B.L.; Feese, M.D.; Cushman, M.; Pommier, Y.; Zembower, D.; Stewart, L.; Burgin, A.B., Structures of three classes of anticancer agents bound to the human topoisomerase I-DNA covalent complex. J. Med. Chem., 2005, 48, 2336-2345. (Pubitemid 40516428)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.7
, pp. 2336-2345
-
-
Staker, B.L.1
Feese, M.D.2
Cushman, M.3
Pommier, Y.4
Zembower, D.5
Stewart, L.6
Burgin, A.B.7
-
67
-
-
66249113962
-
Synthesis and biological activities of topoisomerase i inhibitors, 6-arylmethylamino analogues of edotecarin
-
Sunami, S.; Nishimura, T.; Nishimura, I.; Ito, S.; Arakawa, H.; Ohkubo, M., Synthesis and biological activities of topoisomerase I inhibitors, 6-arylmethylamino analogues of edotecarin. J. Med. Chem., 2009, 52, 3225-3237.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 3225-3237
-
-
Sunami, S.1
Nishimura, T.2
Nishimura, I.3
Ito, S.4
Arakawa, H.5
Ohkubo, M.6
-
68
-
-
43049130352
-
Isoindolo[2,1-a]quinoxaline derivatives, novel potent antitumor agents with dual inhibition of tubulin polymerization and topoisomerase I
-
DOI 10.1021/jm070834t
-
Diana, P.; Martorana, A.; Barraja, P.; Montalbano, A.; Dattolo, G.; Cirrincione, G.; Dall'acqua, F.; Salvador, A.; Vedaldi, D.; Basso, G.; Viola, G., Isoindolo[2,1-a]quinoxaline derivatives, novel potent antitumor agents with dual inhibition of tubulin polymerization and topoisomerase I. J. Med. Chem., 2008, 51, 2387-2399. (Pubitemid 351628500)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.8
, pp. 2387-2399
-
-
Diana, P.1
Martorana, A.2
Barraja, P.3
Montalbano, A.4
Dattolo, G.5
Cirrincione, G.6
Dall'Acqua, F.7
Salvador, A.8
Vedaldi, D.9
Basso, G.10
Viola, G.11
-
69
-
-
3142764930
-
Lamellarins, from A to Z: A family of anticancer marine pyrrole alkaloids
-
DOI 10.2174/1568011043352939
-
Bailly, C., Lamellarins, from A to Z: a family of anticancer marine pyrrole alkaloids. Curr. Med. Chem. Anticancer Agents, 2004, 4, 363-378. (Pubitemid 38923329)
-
(2004)
Current Medicinal Chemistry - Anti-Cancer Agents
, vol.4
, Issue.4
, pp. 363-378
-
-
Bailly, C.1
-
70
-
-
0242526064
-
Lamellarin D: A novel potent inhibitor of topoisomerase I
-
Facompre, M.; Tardy, C.; Bal-Mahieu, C.; Colson, P.; Perez, C.; Manzanares, I.; Cuevas, C.; Bailly, C., Lamellarin D: a novel potent inhibitor of topoisomerase I. Cancer Res., 2003, 63, 7392-7399. (Pubitemid 37413481)
-
(2003)
Cancer Research
, vol.63
, Issue.21
, pp. 7392-7399
-
-
Facompre, M.1
Tardy, C.2
Bal-Mahieu, C.3
Colson, P.4
Perez, C.5
Manzanares, I.6
Cuevas, C.7
Bailly, C.8
-
71
-
-
20144369676
-
Molecular determinants of topoisomerase I poisoning by lamellarins: Comparison with camptothecin and structure-activity relationships
-
DOI 10.1021/jm049060w
-
Marco, E.; Laine, W.; Tardy, C.; Lansiaux, A.; Iwao, M.; Ishibashi, F.; Bailly, C.; Gago, F., Molecular determinants of topoisomerase I poisoning by lamellarins: comparison with camptothecin and structure-activity relationships. J. Med. Chem., 2005, 48, 3796-3807. (Pubitemid 40776854)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.11
, pp. 3796-3807
-
-
Marco, E.1
Laine, W.2
Tardy, C.3
Lansiaux, A.4
Iwao, M.5
Ishibashi, F.6
Bailly, C.7
Gago, F.8
-
72
-
-
12144288129
-
Topoisomerase I-mediated DNA cleavage as a guide to the development of antitumor agents derived from the marine alkaloid lamellarin D: Triester derivatives incorporating amino acid residues
-
DOI 10.1016/j.bmc.2004.01.020, PII S0968089604000550
-
Tardy, C.; Facompre, M.; Laine, W.; Baldeyrou, B.; Garcia-Gravalos, D.; Francesch, A.; Mateo, C.; Pastor, A.; Jimenez, J.A.; Manzanares, I.; Cuevas, C.; Bailly, C., Topoisomerase I-mediated DNA cleavage as a guide to the development of antitumor agents derived from the marine alkaloid lamellarin D: triester derivatives incorporating amino acid residues. Bioorg. Med. Chem., 2004, 12, 1697-1712. (Pubitemid 38340766)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.7
, pp. 1697-1712
-
-
Tardy, C.1
Facompre, M.2
Laine, W.3
Baldeyrou, B.4
Garcia-Gravalos, D.5
Francesch, A.6
Mateo, C.7
Pastor, A.8
Jimenez, J.A.9
Manzanares, I.10
Cuevas, C.11
Bailly, C.12
-
73
-
-
0036241818
-
Synthesis and structure-activity relationship study of lamellarin derivatives
-
DOI 10.1021/np0104525
-
Ishibashi, F.; Tanabe, S.; Oda, T.; Iwao, M., Synthesis and structure-activity relationship study of lamellarin derivatives. J. Nat. Prod., 2002, 65, 500-504. (Pubitemid 34456932)
-
(2002)
Journal of Natural Products
, vol.65
, Issue.4
, pp. 500-504
-
-
Ishibashi, F.1
Tanabe, S.2
Oda, T.3
Iwao, M.4
-
74
-
-
33744796250
-
Synthesis and structure-activity relationship study of potent cytotoxic analogues of the marine alkaloid lamellarin D
-
DOI 10.1021/jm0602458
-
Pla, D.; Marchal, A.; Olsen, C.A.; Francesch, A.; Cuevas, C.; Albericio, F.; Alvarez, M., Synthesis and structure-activity relationship study of potent cytotoxic analogues of the marine alkaloid Lamellarin D. J. Med. Chem., 2006, 49, 3257-3268. (Pubitemid 43830523)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.11
, pp. 3257-3268
-
-
Pla, D.1
Marchal, A.2
Olsen, C.A.3
Francesch, A.4
Cuevas, C.5
Albericio, F.6
Alvarez, M.7
-
75
-
-
70350733553
-
Design and synthesis of lamellarin D analogues targeting topoisomerase i
-
Ohta, T.; Fukuda, T.; Ishibashi, F.; Iwao, M., Design and synthesis of lamellarin D analogues targeting topoisomerase I. J. Org. Chem., 2009, 74, 8143-8153.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 8143-8153
-
-
Ohta, T.1
Fukuda, T.2
Ishibashi, F.3
Iwao, M.4
-
76
-
-
62749137447
-
Cytotoxicities and structure-activity relationships of natural and unnatural lamellarins toward cancer cell lines
-
Chittchang, M.; Batsomboon, P.; Ruchirawat, S.; Ploypradith, P., Cytotoxicities and structure-activity relationships of natural and unnatural lamellarins toward cancer cell lines. ChemMedChem, 2009, 4, 457-465.
-
(2009)
ChemMedChem
, vol.4
, pp. 457-465
-
-
Chittchang, M.1
Batsomboon, P.2
Ruchirawat, S.3
Ploypradith, P.4
-
77
-
-
0029995669
-
Differences in the topoisomerase I cleavage complexes formed by camptothecin and wakayin, a DNA-intercalating marine natural product
-
Kokoshka, J.M.; Capson, T.L.; Holden, J.A.; Ireland, C.M.; Barrows, L.R., Differences in the topoisomerase I cleavage complexes formed by camptothecin and wakayin, a DNA-intercalating marine natural product. Anticancer Drugs, 1996, 7, 758-765. (Pubitemid 26388766)
-
(1996)
Anti-Cancer Drugs
, vol.7
, Issue.7
, pp. 758-765
-
-
Kokoshka, J.M.1
Capson, T.L.2
Holden, J.A.3
Ireland, C.M.4
Barrows, L.R.5
-
78
-
-
0030599249
-
New alkaloids from a South African latrunculid sponge
-
DOI 10.1016/0040-4039(96)01560-2
-
Hooper, G.J.; Davies-Coleman, M.T.; Kelly-Borges, M.; Coetzee, P.S., New alkaloids from South African Latrunculid sponge. Tetrahedron Lett., 1996, 37, 7135-7138. (Pubitemid 26305097)
-
(1996)
Tetrahedron Letters
, vol.37
, Issue.39
, pp. 7135-7138
-
-
Hooper, G.J.1
Davies-Coleman, M.T.2
Kelly-Borges, M.3
Coetzee, P.S.4
-
79
-
-
33646747297
-
Synthesis and antitumor characterization of pyrazolic analogues of the marine pyrroloquinoline alkaloids: Wakayin and tsitsikammamines
-
Legentil, L.; Benel, L.; Bertrand, V.; Lesur, B.; Delfourne, E., Synthesis and antitumor characterization of pyrazolic analogues of the marine pyrroloquinoline alkaloids: wakayin and tsitsikammamines. J. Med. Chem., 2006, 49, 2979-2988.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2979-2988
-
-
Legentil, L.1
Benel, L.2
Bertrand, V.3
Lesur, B.4
Delfourne, E.5
-
80
-
-
27944481173
-
Aza-analogues of the marine pyrroloquinoline alkaloids wakayin and tsitsikammamines: Synthesis and topoisomerase inhibition
-
DOI 10.1016/j.bmcl.2005.09.063, PII S0960894X05012308
-
Legentil, L.; Lesur, B.; Delfourne, E., Aza-analogues of the marine pyrroloquinoline alkaloids wakayin and tsitsikammamines: synthesis and topoisomerase inhibition. Bioorg. Med. Chem. Lett., 2006, 16, 427-429. (Pubitemid 41680640)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.2
, pp. 427-429
-
-
Legentil, L.1
Lesur, B.2
Delfourne, E.3
-
81
-
-
0034691311
-
Human topoisomerase I poisoning by protoberberines: Potential roles for both drug-DNA and drug-enzyme interactions
-
DOI 10.1021/bi000171g
-
Li, T.K.; Bathory, E.; LaVoie, E.J.; Srinivasan, A.R.; Olson, W.K.; Sauers, R.R.; Liu, L.F.; Pilch, D.S., Human topoisomerase I poisoning by protoberberines: potential roles for both drug-DNA and drug-enzyme interactions. Biochemistry, 2000, 39, 7107-7116. (Pubitemid 30413099)
-
(2000)
Biochemistry
, vol.39
, Issue.24
, pp. 7107-7116
-
-
Li, T.-K.1
Bathory, E.2
LaVoie, E.J.3
Srinivasan, A.R.4
Olson, W.K.5
Sauers, R.R.6
Liu, L.F.7
Pilch, D.S.8
-
82
-
-
56049085650
-
Diazoniapolycyclic ions inhibit the activity of topoisomerase i and the growth of certain tumor cell lines
-
Basili, S.; Basso, G.; Faccio, A.; Granzhan, A.; Ihmels, H.; Moro, S.; Viola, G., Diazoniapolycyclic ions inhibit the activity of topoisomerase I and the growth of certain tumor cell lines. ChemMedChem, 2008, 3, 1671-1676.
-
(2008)
ChemMedChem
, vol.3
, pp. 1671-1676
-
-
Basili, S.1
Basso, G.2
Faccio, A.3
Granzhan, A.4
Ihmels, H.5
Moro, S.6
Viola, G.7
-
83
-
-
38949212995
-
Synthesis and cytotoxic activity of a new series of topoisomerase I inhibitors
-
DOI 10.1016/j.bmcl.2007.12.055, PII S0960894X07015144
-
Dallavalle, S.; Gattinoni, S.; Mazzini, S.; Scaglioni, L.; Merlini, L.; Tinelli, S.; Beretta, G.L.; Zunino, F., Synthesis and cytotoxic activity of a new series of topoisomerase I inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 1484-1489. (Pubitemid 351226518)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.4
, pp. 1484-1489
-
-
Dallavalle, S.1
Gattinoni, S.2
Mazzini, S.3
Scaglioni, L.4
Merlini, L.5
Tinelli, S.6
Beretta, G.L.7
Zunino, F.8
-
84
-
-
58549095229
-
Interaction between double helix DNA fragments and a new topopyrone acting as human topoisomerase i poison
-
Scaglioni, L.; Mazzini, S.; Mondelli, R.; Dallavalle, S.; Gattinoni, S.; Tinelli, S.; Beretta, G.L.; Zunino, F.; Ragg, E., Interaction between double helix DNA fragments and a new topopyrone acting as human topoisomerase I poison. Bioorg. Med. Chem., 2009, 17, 484-491.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 484-491
-
-
Scaglioni, L.1
Mazzini, S.2
Mondelli, R.3
Dallavalle, S.4
Gattinoni, S.5
Tinelli, S.6
Beretta, G.L.7
Zunino, F.8
Ragg, E.9
-
85
-
-
0035089487
-
Isoaurostatin, a novel topoisomerase inhibitor produced by Thermomonospora alba
-
DOI 10.1021/np0004606
-
Suzuki, K.; Yahara, S.; Maehata, K.; Uyeda, M., Isoaurostatin, a novel topoisomerase inhibitor produced by Thermomonospora alba. J. Nat. Prod., 2001, 64, 204-207. (Pubitemid 32198347)
-
(2001)
Journal of Natural Products
, vol.64
, Issue.2
, pp. 204-207
-
-
Suzuki, K.1
Yahara, S.2
Maehata, K.3
Uyeda, M.4
-
86
-
-
15944415851
-
Inhibitory activities against topoisomerase I and II by isoaurostatin derivatives and their structure-activity relationships
-
DOI 10.1016/j.bmcl.2005.02.052
-
Suzuki, K.; Okawara, T.; Higashijima, T.; Yokomizo, K.; Mizushima, T.; Otsuka, M., Inhibitory activities against topoisomerase I and II by isoaurostatin derivatives and their structure-activity relationships. Bioorg. Med. Chem. Lett., 2005, 15, 2065-2068. (Pubitemid 40445470)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.8
, pp. 2065-2068
-
-
Suzuki, K.1
Okawara, T.2
Higashijima, T.3
Yokomizo, K.4
Mizushima, T.5
Otsuka, M.6
-
87
-
-
68949086525
-
Synthesis of gibberellin derivatives with anti-tumor bioactivities
-
Chen, J.; Sun, Z.; Zhang, Y.; Zeng, X.; Qing, C.; Liu, J.; Li, L.; Zhang, H., Synthesis of gibberellin derivatives with anti-tumor bioactivities. Bioorg. Med. Chem. Lett., 2009, 19, 5496-5499.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 5496-5499
-
-
Chen, J.1
Sun, Z.2
Zhang, Y.3
Zeng, X.4
Qing, C.5
Liu, J.6
Li, L.7
Zhang, H.8
-
88
-
-
59649105538
-
Camptothecins: A SAR/QSAR study
-
Verma, R.P.; Hansch, C., Camptothecins: a SAR/QSAR study. Chem. Rev., 2009, 109, 213-235.
-
(2009)
Chem. Rev.
, vol.109
, pp. 213-235
-
-
Verma, R.P.1
Hansch, C.2
-
89
-
-
66849113688
-
The indenoisoquinoline noncamptothecin topoisomerase i inhibitors: Update and perspectives
-
Pommier, Y.; Cushman, M., The indenoisoquinoline noncamptothecin topoisomerase I inhibitors: update and perspectives. Mol. Cancer Ther., 2009, 8, 1008-1014.
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 1008-1014
-
-
Pommier, Y.1
Cushman, M.2
-
90
-
-
0007565558
-
Stereoselective oxidation by thionyl chloride leadingto the indeno[1,2-c]isoquinoline system
-
Cushman, M.; Cheng, L., Stereoselective oxidation by thionyl chloride leadingto the indeno[1,2-c]isoquinoline system. J. Org. Chem., 1978, 43, 3781-3783.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 3781-3783
-
-
Cushman, M.1
Cheng, L.2
-
91
-
-
0031815336
-
Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison
-
Kohlhagen, G.; Paull, K.D.; Cushman, M.; Nagafuji, P.; Pommier, Y., Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison. Mol. Pharmacol., 1998, 54, 50-58. (Pubitemid 28337586)
-
(1998)
Molecular Pharmacology
, vol.54
, Issue.1
, pp. 50-58
-
-
Kohlhagen, G.1
Paull, K.D.2
Cushman, M.3
Nagafuji, P.4
Pommier, Y.5
-
92
-
-
7444233119
-
Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings
-
DOI 10.1021/jm040025z
-
Nagarajan, M.; Morrell, A.; Fort, B.C.; Meckley, M.R.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Cushman, M., Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings. J. Med. Chem., 2004, 47, 5651-5661. (Pubitemid 39447262)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.23
, pp. 5651-5661
-
-
Nagarajan, M.1
Morrell, A.2
Fort, B.C.3
Meckley, M.R.4
Antony, S.5
Kohlhagen, G.6
Pommier, Y.7
Cushman, M.8
-
93
-
-
33845955224
-
A systematic study of nitrated indenoisoquinolines reveals a potent topoisomerase I inhibitor
-
DOI 10.1021/jm060974n
-
Morrell, A.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Cushman, M., A systematic study of nitrated indenoisoquinolines reveals a potent topoisomerase I inhibitor. J. Med. Chem., 2006, 49, 7740-7753. (Pubitemid 46033665)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.26
, pp. 7740-7753
-
-
Morrell, A.1
Antony, S.2
Kohlhagen, G.3
Pommier, Y.4
Cushman, M.5
-
94
-
-
34548510839
-
Nitrated indenoisoquinolines as topoisomerase I inhibitors: A systematic study and optimization
-
DOI 10.1021/jm070361q
-
Morrell, A.; Placzek, M.; Parmley, S.; Antony, S.; Dexheimer, T.S.; Pommier, Y.; Cushman, M., Nitrated indenoisoquinolines as topoisomerase I inhibitors: a systematic study and optimization. J. Med. Chem., 2007, 50, 4419-4430. (Pubitemid 47378839)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.18
, pp. 4419-4430
-
-
Morrell, A.1
Placzek, M.2
Parmley, S.3
Antony, S.4
Dexheimer, T.S.5
Pommier, Y.6
Cushman, M.7
-
95
-
-
34548504314
-
Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors
-
DOI 10.1021/jm070307+
-
Morrell, A.; Placzek, M.; Parmley, S.; Grella, B.; Antony, S.; Pommier, Y.; Cushman, M., Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors. J. Med. Chem., 2007, 50, 4388-4404. (Pubitemid 47378837)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.18
, pp. 4388-4404
-
-
Morrell, A.1
Placzek, M.2
Parmley, S.3
Grella, B.4
Antony, S.5
Pommier, Y.6
Cushman, M.7
-
96
-
-
33750142705
-
Synthesis and evaluation of indenoisoquinoline topoisomerase I inhibitors substituted with nitrogen heterocycles
-
DOI 10.1021/jm060564z
-
Nagarajan, M.; Morrell, A.; Ioanoviciu, A.; Antony, S.; Kohlhagen, G.; Agama, K.; Hollingshead, M.; Pommier, Y.; Cushman, M., Synthesis and evaluation of indenoisoquinoline topoisomerase I inhibitors substituted with nitrogen heterocycles. J. Med. Chem., 2006, 49, 6283-6289. (Pubitemid 44595205)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.21
, pp. 6283-6289
-
-
Nagarajan, M.1
Morrell, A.2
Ioanoviciu, A.3
Antony, S.4
Kohlhagen, G.5
Agama, K.6
Hollingshead, M.7
Pommier, Y.8
Cushman, M.9
-
97
-
-
22744438407
-
Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysis
-
DOI 10.1021/jm050076b
-
Ioanoviciu, A.; Antony, S.; Pommier, Y.; Staker, B.L.; Stewart, L.; Cushman, M., Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by Xray crystallographic analysis. J. Med. Chem., 2005, 48, 4803-4814. (Pubitemid 41033123)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.15
, pp. 4803-4814
-
-
Ioanoviciu, A.1
Antony, S.2
Pommier, Y.3
Staker, B.L.4
Stewart, L.5
Cushman, M.6
-
98
-
-
77949357034
-
Structure-based design, syn
-
thesis, and biological studies of new anticancer norindenoisoquinoline topoisomerase I inhibitors
-
Song, Y.; Shao, Z.; Dexheimer, T.S.; Scher, E.S.; Pommier, Y.; Cushman, M., Structure-based design, synthesis, and biological studies of new anticancer norindenoisoquinoline topoisomerase I inhibitors. J. Med. Chem., 2010, 53, 1979-1989.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1979-1989
-
-
Song, Y.1
Shao, Z.2
Dexheimer, T.S.3
Scher, E.S.4
Pommier, Y.5
Cushman, M.6
-
99
-
-
78650395550
-
Design, synthesis, and evaluation of Dibenzo[c,h][1,6]naphthyridines as topoisomerase i inhibitors and potential anticancer agents
-
Kiselev, E.; Dexheimer, T.S.; Pommier, Y.; Cushman, M., Design, synthesis, and evaluation of Dibenzo[c,h][1,6]naphthyridines as topoisomerase I inhibitors and potential anticancer agents. J. Med. Chem., 2010, 53, 8716-8726.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8716-8726
-
-
Kiselev, E.1
Dexheimer, T.S.2
Pommier, Y.3
Cushman, M.4
-
100
-
-
33747470312
-
Synthesis and biological evaluation of bisindenoisoquinolines as topoisomerase I inhibitors
-
DOI 10.1021/jm060046o
-
Nagarajan, M.; Morrell, A.; Antony, S.; Kohlhagen, G.; Agama, K.; Pommier, Y.; Ragazzon, P.A.; Garbett, N.C.; Chaires, J.B.; Hollingshead, M.; Cushman, M., Synthesis and biological evaluation of bisindenoisoquinolines as topoisomerase I inhibitors. J. Med. Chem., 2006, 49, (17), 5129-5140. (Pubitemid 44260209)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.17
, pp. 5129-5140
-
-
Nagarajan, M.1
Morrell, A.2
Antony, S.3
Kohlhagen, G.4
Agama, K.5
Pommier, Y.6
Ragazzon, P.A.7
Garbett, N.C.8
Chaires, J.B.9
Hollingshead, M.10
Cushman, M.11
-
101
-
-
33747600400
-
Bisindenoisoquinoline bis-1,3-{(5,6-dihydro-5,11-diketo-11H-indeno[1,2-c] isoquinoline)-6-propylamino}propane bis(trifluoroacetate) (NSC 727357), a DNA intercalator and topoisomerase inhibitor with antitumor activity
-
DOI 10.1124/mol.106.024372
-
Antony, S.; Agama, K.K.; Miao, Z.H.; Hollingshead, M.; Holbeck, S.L.; Wright, M.H.; Varticovski, L.; Nagarajan, M.; Morrell, A.; Cushman, M.; Pommier, Y., Bisindenoisoquinoline bis-1,3-{(5,6-dihydro-5,11-diketo-11Hindeno[ 1,2-c]isoquinoline) -6-propyla mino}propane bis(trifluoroacetate) (NSC 727357), a DNA intercalator and topoisomerase inhibitor with antitumor activity. Mol. Pharmacol., 2006, 70, 1109-1120. (Pubitemid 44268468)
-
(2006)
Molecular Pharmacology
, vol.70
, Issue.3
, pp. 1109-1120
-
-
Antony, S.1
Agama, K.K.2
Miao, Z.-H.3
Hollingshead, M.4
Holbeck, S.L.5
Wright, M.H.6
Varticovski, L.7
Nagarajan, M.8
Morrell, A.9
Cushman, M.10
Pommier, Y.11
-
102
-
-
0029078874
-
Synthesis and biological evaluation of amino-substituted benzo[f]pyrido[4,3-b] and pyrido[3,4-b]quinoxalines: A new class of antineoplastic agents
-
Nguyen, C.H.; Fan, E.; Riou, J.F.; Bissery, M.C.; Vrignaud, P.; Lavelle, F.; Bisagni, E., Synthesis and biological evaluation of amino-substituted benzo[f]pyrido[4,3-b] and pyrido[3,4-b]quinoxalines: a new class of antineoplastic agents. Anticancer Drug Des., 1995, 10, 277-297.
-
(1995)
Anticancer Drug Des.
, vol.10
, pp. 277-297
-
-
Nguyen, C.H.1
Fan, E.2
Riou, J.F.3
Bissery, M.C.4
Vrignaud, P.5
Lavelle, F.6
Bisagni, E.7
-
103
-
-
79151486288
-
Synthesis and biological activity of novel inhibitors of topoisomerase I: 2-aryl-substituted 2-bis-1H-benzimidazoles
-
Singh, M.; Tandon, V., Synthesis and biological activity of novel inhibitors of topoisomerase I: 2-aryl-substituted 2-bis-1H-benzimidazoles. Eur. J. Med. Chem., 2011, 46, 659-669.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 659-669
-
-
Singh, M.1
Tandon, V.2
-
104
-
-
0032189683
-
Mechanism of action of eukaryotic DNA topoisomerase i and drugs targeted to the enzyme
-
Pommier, Y.; Pourquier, P.; Fan, Y.; Strumberg, D., Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim. Biophys. Acta, 1998, 1400, (1-3), 83-105.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, Issue.1-3
, pp. 83-105
-
-
Pommier, Y.1
Pourquier, P.2
Fan, Y.3
Strumberg, D.4
-
105
-
-
34249018852
-
Synthesis, DNA binding, and Leishmania topoisomerase inhibition activities of a novel series of anthra[1,2-d]imidazole-6,11-dione derivatives
-
DOI 10.1021/jm0610604
-
Chaudhuri, P.; Majumder, H.K.; Bhattacharya, S., Synthesis, DNA binding, and Leishmania topoisomerase inhibition activities of a novel series of anthra[ 1,2-d]imidazole-6,11-dione derivatives. J. Med. Chem., 2007, 50, 2536-2540. (Pubitemid 46799266)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.10
, pp. 2536-2540
-
-
Chaudhuri, P.1
Majumder, H.K.2
Bhattacharya, S.3
-
106
-
-
0035829148
-
Synthesis, topoisomerase I inhibition and antitumor cytotoxicity of 2,2′:6′,2′-, 2,2′:6′,3′- and 2,2′:6′,4′-terpyridine derivatives
-
DOI 10.1016/S0960-894X(01)00531-5, PII S0960894X01005315
-
Zhao, L.X.; Kim, T.S.; Ahn, S.H.; Kim, T.H.; Kim, E.K.; Cho, W.J.; Choi, H.; Lee, C.S.; Kim, J.A.; Jeong, T.C.; Chang, C.J.; Lee, E.S., Synthesis, topoisomerase I inhibition and antitumor cytotoxicity of 2 2′:6′, 2″-, 2,2′:6′,3″- and 2 2′:6′,4″- terpyridine derivatives. Bioorg. Med. Chem. Lett., 2001, 11, 2659-2662. (Pubitemid 32823378)
-
(2001)
Bioorganic and Medicinal Chemistry Letters
, vol.11
, Issue.19
, pp. 2659-2662
-
-
Zhao, L.-X.1
Kim, T.S.2
Ahn, S.-H.3
Kim, T.-H.4
Kim, E.-K.5
Cho, W.-J.6
Choi, H.7
Lee, C.-S.8
Kim, J.-A.9
Jeong, T.C.10
Chang, C.-J.11
Lee, E.-S.12
-
107
-
-
10744227567
-
Synthesis, topoisomerase I inhibition and structure-activity relationship study of 2,4,6-trisubstituted pyridine derivatives
-
DOI 10.1016/j.bmcl.2003.11.084
-
Zhao, L.X.; Moon, Y.S.; Basnet, A.; Kim, E.K.; Jahng, Y.; Park, J.G.; Jeong, T.C.; Cho, W.J.; Choi, S.U.; Lee, C.O.; Lee, S.Y.; Lee, C.S.; Lee, E.S., Synthesis, topoisomerase I inhibition and structure-activity relationship study of 2,4,6-trisubstituted pyridine derivatives. Bioorg. Med. Chem. Lett., 2004, 14, 1333-1337. (Pubitemid 38232668)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.5
, pp. 1333-1337
-
-
Zhao, L.-X.1
Moon, Y.-S.2
Basnet, A.3
Kim, E.-K.4
Jahng, Y.5
Park, J.G.6
Jeong, T.C.7
Cho, W.-J.8
Choi, S.-U.9
Lee, C.O.10
Lee, S.-Y.11
Lee, C.-S.12
Lee, E.-S.13
-
108
-
-
41249098017
-
Synthesis of 2,6-diaryl-substituted pyridines and their antitumor activities
-
DOI 10.1016/j.ejmech.2007.05.002, PII S022352340700222X
-
Son, J.K.; Zhao, L.X.; Basnet, A.; Thapa, P.; Karki, R.; Na, Y.; Jahng, Y.; Jeong, T.C.; Jeong, B.S.; Lee, C.S.; Lee, E.S., Synthesis of 2,6-diarylsubstituted pyridines and their antitumor activities. Eur. J. Med. Chem., 2008, 43, 675-682. (Pubitemid 351446141)
-
(2008)
European Journal of Medicinal Chemistry
, vol.43
, Issue.4
, pp. 675-682
-
-
Son, J.-K.1
Zhao, L.-X.2
Basnet, A.3
Thapa, P.4
Karki, R.5
Na, Y.6
Jahng, Y.7
Jeong, T.C.8
Jeong, B.-S.9
Lee, C.-S.10
Lee, E.-S.11
-
109
-
-
34248633109
-
2,4,6-Trisubstituted pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship
-
DOI 10.1016/j.bmc.2007.04.047, PII S0968089607003756
-
Basnet, A.; Thapa, P.; Karki, R.; Na, Y.; Jahng, Y.; Jeong, B.S.; Jeong, T.C.; Lee, C.S.; Lee, E.S., 2,4,6-Trisubstituted pyridines: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship. Bioorg. Med. Chem., 2007, 15, 4351-4359. (Pubitemid 46777301)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.13
, pp. 4351-4359
-
-
Basnet, A.1
Thapa, P.2
Karki, R.3
Na, Y.4
Jahng, Y.5
Jeong, B.-S.6
Jeong, T.C.7
Lee, C.-S.8
Lee, E.-S.9
-
110
-
-
72049125310
-
2,6-Dithienyl-4-furyl pyridines: Synthesis, topoisomerase i and II inhibition, cytotoxicity, structure-activity relationship, and docking study
-
Basnet, A.; Thapa, P.; Karki, R.; Choi, H.; Choi, J.H.; Yun, M.; Jeong, B.S.; Jahng, Y.; Na, Y.; Cho, W.J.; Kwon, Y.; Lee, C.S.; Lee, E.S., 2,6-Dithienyl-4-furyl pyridines: Synthesis, topoisomerase I and II inhibition, cytotoxicity, structure-activity relationship, and docking study. Bioorg. Med. Chem. Lett., 2010, 20, 42-47.
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 42-47
-
-
Basnet, A.1
Thapa, P.2
Karki, R.3
Choi, H.4
Choi, J.H.5
Yun, M.6
Jeong, B.S.7
Jahng, Y.8
Na, Y.9
Cho, W.J.10
Kwon, Y.11
Lee, C.S.12
Lee, E.S.13
-
111
-
-
72049095310
-
2-Thienyl-4-furyl-6-aryl pyridine derivatives: Synthesis, topoisomerase i and II inhibitory activity, cytotoxicity, and structure-activity relationship study
-
Thapa, P.; Karki, R.; Thapa, U.; Jahng, Y.; Jung, M.J.; Nam, J.M.; Na, Y.; Kwon, Y.; Lee, E.S., 2-Thienyl-4-furyl-6-aryl pyridine derivatives: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study. Bioorg. Med. Chem., 2010, 18, 377-386.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 377-386
-
-
Thapa, P.1
Karki, R.2
Thapa, U.3
Jahng, Y.4
Jung, M.J.5
Nam, J.M.6
Na, Y.7
Kwon, Y.8
Lee, E.S.9
-
112
-
-
77951204579
-
Synthesis, topoisomerase i and II inhibitory activity, cytotoxicity, and structure-activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines
-
Karki, R.; Thapa, P.; Kang, M.J.; Jeong, T.C.; Nam, J.M.; Kim, H.L.; Na, Y.; Cho, W.J.; Kwon, Y.; Lee, E.S., Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines. Bioorg. Med. Chem., 2010, 18, 3066-3077.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 3066-3077
-
-
Karki, R.1
Thapa, P.2
Kang, M.J.3
Jeong, T.C.4
Nam, J.M.5
Kim, H.L.6
Na, Y.7
Cho, W.J.8
Kwon, Y.9
Lee, E.S.10
-
113
-
-
10744221343
-
Benzo[f]azino[2,1-a]phthalazinium cations: Novel DNA intercalating chromophores with antiproliferative activity
-
DOI 10.1021/jm0310434
-
Martinez, V.; Burgos, C.; Alvarez-Builla, J.; Fernandez, G.; Domingo, A.; Garcia-Nieto, R.; Gago, F.; Manzanares, I.; Cuevas, C.; Vaquero, J.J., Benzo[f]azino[2,1-a]phthalazinium cations: novel DNA intercalating chromophores with antiproliferative activity. J. Med. Chem., 2004, 47, 1136-1148. (Pubitemid 38229115)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.5
, pp. 1136-1148
-
-
Martinez, V.1
Burgos, C.2
Alvarez-Builla, J.3
Fernandez, G.4
Domingo, A.5
Garcia-Nieto, R.6
Gago, F.7
Manzanares, I.8
Cuevas, C.9
Vaquero, J.J.10
-
114
-
-
0022530901
-
Streptonigrin. 1. Structure-activity relationships among simple bicyclic analogues. Rate dependence of DNA degradation on quinone reduction potential
-
Shaikh, I.A.; Johnson, F.; Grollman, A.P., Streptonigrin. 1. Structure-activity relationships among simple bicyclic analogues. Rate dependence of DNA degradation on quinone reduction potential. J. Med. Chem., 1986, 29, 1329-1340. (Pubitemid 16034617)
-
(1986)
Journal of Medicinal Chemistry
, vol.29
, Issue.8
, pp. 1329-1340
-
-
Shaikh, I.A.1
Johnson, F.2
Grollman, A.P.3
-
115
-
-
0034800971
-
The 3-D QSAR study of anticancer 1-Nsubstituted imidazo- and pyrrolo-quinoline-4,9-dione derivatives by CoMFA and CoMSIA
-
Suh, M.E.; Kang, M.J.; Park, S.Y., The 3-D QSAR study of anticancer 1-Nsubstituted imidazo- and pyrrolo-quinoline-4,9-dione derivatives by CoMFA and CoMSIA. Bioorg. Med. Chem., 2001, 9, 2987-2991.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 2987-2991
-
-
Suh, M.E.1
Kang, M.J.2
Park, S.Y.3
-
116
-
-
42149147572
-
Synthesis, cytotoxic activities and structure-activity relationships of topoisomerase I inhibitors: Indolizinoquinoline-5,12-dione derivatives
-
DOI 10.1016/j.bmc.2008.02.036, PII S0968089608001570
-
Cheng, Y.; An, L.K.; Wu, N.; Wang, X.D.; Bu, X.Z.; Huang, Z.S.; Gu, L.Q., Synthesis, cytotoxic activities and structure-activity relationships of topoisomerase I inhibitors: indolizinoquinoline-5,12-dione derivatives. Bioorg. Med. Chem., 2008, 16, 4617-4625. (Pubitemid 351539023)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.8
, pp. 4617-4625
-
-
Cheng, Y.1
An, L.-K.2
Wu, N.3
Wang, X.-D.4
Bu, X.-Z.5
Huang, Z.-S.6
Gu, L.-Q.7
-
117
-
-
25844525477
-
Novel synthetic isoquinolino[5,4-ab]phenazines: Inhibition toward topoisomerase I, antitumor and DNA photo-cleaving activities
-
DOI 10.1016/j.bmc.2005.07.029, PII S0968089605006425
-
Yang, P.; Yang, Q.; Qian, X.; Cui, J., Novel synthetic isoquinolino[5,4-ab]phenazines: inhibition toward topoisomerase I, antitumor and DNA photo-cleaving activities. Bioorg. Med. Chem., 2005, 13, 5909-5914. (Pubitemid 41399899)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.21
, pp. 5909-5914
-
-
Yang, P.1
Yang, Q.2
Qian, X.3
Cui, J.4
-
118
-
-
77958000750
-
Novel synthetic 2-amino-10-(3,5-dimethoxy)benzyl-9(10H)-acridinone derivatives as potent DNA-binding antiproliferative agents
-
Gao, C.; Liu, F.; Luan, X.; Tan, C.; Liu, H.; Xie, Y.; Jin, Y.; Jiang, Y., Novel synthetic 2-amino-10-(3,5-dimethoxy)benzyl-9(10H)-acridinone derivatives as potent DNA-binding antiproliferative agents. Bioorg. Med. Chem., 2010, 18, 7507-7514.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 7507-7514
-
-
Gao, C.1
Liu, F.2
Luan, X.3
Tan, C.4
Liu, H.5
Xie, Y.6
Jin, Y.7
Jiang, Y.8
-
119
-
-
28844447055
-
Synthesis, cytotoxicity, and DNA-topoisomerase inhibitory activity of new asymmetric ureas and thioureas
-
DOI 10.1016/j.bmc.2005.08.031, PII S0968089605007856
-
Esteves-Souza, A.; Pissinate, K.; Nascimento Mda, G.; Grynberg, N.F.; Echevarria, A., Synthesis, cytotoxicity, and DNA-topoisomerase inhibitory activity of new asymmetric ureas and thioureas. Bioorg. Med. Chem., 2006, 14, 492-499. (Pubitemid 41767609)
-
(2006)
Bioorganic and Medicinal Chemistry
, vol.14
, Issue.2
, pp. 492-499
-
-
Esteves-Souza, A.1
Pissinate, K.2
Graca Nascimento, M.D.3
Grynberg, N.F.4
Echevarria, A.5
-
120
-
-
33846604114
-
Binding mode and affinity studies of DNA-binding agents using topoisomerase I DNA unwinding assay
-
DOI 10.1016/j.bmcl.2006.11.038, PII S0960894X0601331X
-
McKnight, R.E.; Gleason, A.B.; Keyes, J.A.; Sahabi, S., Binding mode and affinity studies of DNA-binding agents using topoisomerase I DNA unwinding assay. Bioorg. Med. Chem. Lett., 2007, 17, 1013-1017. (Pubitemid 46177615)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.4
, pp. 1013-1017
-
-
McKnight, R.E.1
Gleason, A.B.2
Keyes, J.A.3
Sahabi, S.4
-
121
-
-
0033523672
-
'Scaffold-Hopping' by topological pharmacophore search: A contribution to virtual screening
-
DOI 10.1002/(SICI)1521-3773(19991004)38:19<2894::AID-ANIE2894>3.0. CO;2-F
-
Schneider, G.; Neidhart, W.; Giller, T.; Schmid, G., "Scaffold- Hopping" by Topological Pharmacophore Search: A Contribution to Virtual Screening. Angew. Chem. Int. Ed. Engl., 1999, 38, 2894-2896. (Pubitemid 29479958)
-
(1999)
Angewandte Chemie - International Edition
, vol.38
, Issue.19
, pp. 2894-2896
-
-
Schneider, G.1
Neidhart, W.2
Giller, T.3
Schmid, G.4
-
122
-
-
49449112587
-
Design, synthesis, and biological evaluation of 14-substituted aromathecins as topoisomerase i inhibitors
-
Cinelli, M.A.; Morrell, A.; Dexheimer, T.S.; Scher, E.S.; Pommier, Y.; Cushman, M., Design, synthesis, and biological evaluation of 14-substituted aromathecins as topoisomerase I inhibitors. J. Med. Chem., 2008, 51, 4609-4619.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4609-4619
-
-
Cinelli, M.A.1
Morrell, A.2
Dexheimer, T.S.3
Scher, E.S.4
Pommier, Y.5
Cushman, M.6
-
123
-
-
77955427384
-
The structure-activity relationships of A-ringsubstituted aromathecin topoisomerase i inhibitors strongly support a camptothecin-like binding mode
-
Cinelli, M.A.; Morrell, A.E.; Dexheimer, T.S.; Agama, K.; Agrawal, S.; Pommier, Y.; Cushman, M., The structure-activity relationships of A-ringsubstituted aromathecin topoisomerase I inhibitors strongly support a camptothecin-like binding mode. Bioorg. Med. Chem., 2010, 18, 5535-5552.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 5535-5552
-
-
Cinelli, M.A.1
Morrell, A.E.2
Dexheimer, T.S.3
Agama, K.4
Agrawal, S.5
Pommier, Y.6
Cushman, M.7
-
124
-
-
0037401629
-
5H-Dibenzo[c,h]1,6-naphthyridin-6-ones: Novel topoisomerase I-targeting anticancer agents with potent cytotoxic activity
-
DOI 10.1016/S0968-0896(03)00051-8
-
Ruchelman, A.L.; Singh, S.K.; Ray, A.; Wu, X.H.; Yang, J.M.; Li, T.K.; Liu, A.; Liu, L.F.; LaVoie, E.J., 5H-Dibenzo[c,h]1,6-naphthyridin-6-ones: novel topoisomerase I-targeting anticancer agents with potent cytotoxic activity. Bioorg. Med. Chem., 2003, 11, 2061-2073. (Pubitemid 36379023)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.9
, pp. 2061-2073
-
-
Ruchelman, A.L.1
Singh, S.K.2
Ray, A.3
Wu, X.H.4
Yang, J.-M.5
Li, T.-K.6
Liu, A.7
Liu, L.F.8
LaVoie, E.J.9
-
125
-
-
0037131728
-
Diaza- and triazachrysenes: Potent topoisomerase-targeting agents with exceptional antitumor activity against the human tumor xenograft, MDA-MB-435
-
DOI 10.1016/S0960-894X(02)00737-0, PII S0960894X02007370
-
Ruchelman, A.L.; Singh, S.K.; Wu, X.; Ray, A.; Yang, J.M.; Li, T.K.; Liu, A.; Liu, L.F.; LaVoie, E.J., Diaza- and triazachrysenes: potent topoisomerase-targeting agents with exceptional antitumor activity against the human tumor xenograft, MDA-MB-435. Bioorg. Med. Chem. Lett., 2002, 12, 3333-3336. (Pubitemid 35248243)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.22
, pp. 3333-3336
-
-
Ruchelman, A.L.1
Singh, S.K.2
Wu, X.3
Ray, A.4
Yang, J.-M.5
Li, T.-K.6
Liu, A.7
Liu, L.F.8
LaVoie, E.J.9
-
126
-
-
0346365368
-
Characterization of ARC-111 as a Novel Topoisomerase I-Targeting Anticancer Drug
-
Li, T.K.; Houghton, P.J.; Desai, S.D.; Daroui, P.; Liu, A.A.; Hars, E.S.; Ruchelman, A.L.; LaVoie, E.J.; Liu, L.F., Characterization of ARC-111 as a novel topoisomerase I-targeting anticancer drug. Cancer Res., 2003, 63, 8400-8407. (Pubitemid 37549495)
-
(2003)
Cancer Research
, vol.63
, Issue.23
, pp. 8400-8407
-
-
Li, T.-K.1
Houghton, P.J.2
Desai, S.D.3
Daroui, P.4
Liu, A.A.5
Hars, E.S.6
Ruchelman, A.L.7
LaVoie, E.J.8
Liu, L.F.9
-
127
-
-
34247640293
-
ARC-111 inhibits hypoxia-mediated hypoxia-inducible factor-1α accumulation
-
DOI 10.1097/CAD.0b013e328013ffed, PII 0000181320070400000009
-
Meng, F.; Nguyen, X.T.; Cai, X.; Duan, J.; Matteucci, M.; Hart, C.P., ARC-111 inhibits hypoxia-mediated hypoxia-inducible factor-1alpha accumulation. Anticancer Drugs, 2007, 18, 435-445. (Pubitemid 46712407)
-
(2007)
Anti-Cancer Drugs
, vol.18
, Issue.4
, pp. 435-445
-
-
Meng, F.1
Nguyen, X.-T.2
Cai, X.3
Duan, J.4
Matteucci, M.5
Hart, C.P.6
-
128
-
-
13444291906
-
5-(2-Aminoethyl)dibenzo[c,h][1,6]naphthyridin-6-ones: Variation of N-alkyl substituents modulates sensitivity to efflux transporters associated with multidrug resistance
-
DOI 10.1021/jm049447z
-
Ruchelman, A.L.; Houghton, P.J.; Zhou, N.; Liu, A.; Liu, L.F.; LaVoie, E.J., 5-(2-aminoethyl)dibenzo[c,h][1,6]naphthyridin-6-ones: variation of n-alkyl substituents modulates sensitivity to efflux transporters associated with multidrug resistance. J. Med. Chem., 2005, 48, 792-804. (Pubitemid 40209101)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.3
, pp. 792-804
-
-
Ruchelman, A.L.1
Houghton, P.J.2
Zhou, N.3
Liu, A.4
Liu, L.F.5
LaVoie, E.J.6
-
129
-
-
67650430005
-
Novel topoisomerase I-targeting antitumor agents synthesized from the N,N,N-trimethylammonium derivative of ARC-111, 5H-2,3-dimethoxy-8,9- methylenedioxy-5-[(2-N,N,N-trimethylammonium)ethyl]di benzo[c,h][1,6] naphthyridin-6-one iodide
-
Feng, W.; Satyanarayana, M.; Tsai, Y.C.; Liu, A.A.; Liu, L.F.; LaVoie, E.J., Novel topoisomerase I-targeting antitumor agents synthesized from the N,N,N-trimethylammonium derivative of ARC-111, 5H-2,3-dimethoxy-8,9- methylenedioxy-5-[(2-N,N,N-trimethylammonium)ethyl]di benzo[c,h][1,6] naphthyridin-6-one iodide. Eur. J. Med. Chem., 2009, 44, 3433-3438.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 3433-3438
-
-
Feng, W.1
Satyanarayana, M.2
Tsai, Y.C.3
Liu, A.A.4
Liu, L.F.5
Lavoie, E.J.6
-
130
-
-
49149111130
-
Syntheses and biological evaluation of topoisomerase Itargeting agents related to 11-[2-(N,N-dimethylamino)ethyl]-2,3-dimethoxy-8,9-methylenedioxy-11H- isoqu ino[4,3-c]cinnolin-12-one (ARC-31)
-
Satyanarayana, M.; Feng, W.; Cheng, L.; Liu, A.A.; Tsai, Y.C.; Liu, L.F.;
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 7824-7831
-
-
Satyanarayana, M.1
Feng, W.2
Cheng, L.3
Liu, A.A.4
Tsai, Y.C.5
Liu, L.F.6
Lavoie, E.J.7
-
131
-
-
33644987261
-
6-Substituted 6H-dibenzo[c,h][2,6]naphthyridin-5-ones: Reversed lactam analogues of ARC-111 with potent topoisomerase I-targeting activity and cytotoxicity
-
Zhu, S.; Ruchelman, A.L.; Zhou, N.; Liu, A.; Liu, L.F.; LaVoie, E.J., 6-Substituted 6H-dibenzo[c,h][2,6]naphthyridin-5-ones: reversed lactam analogues of ARC-111 with potent topoisomerase I-targeting activity and cytotoxicity. Bioorg. Med. Chem., 2006, 14, 3131-3143.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 3131-3143
-
-
Zhu, S.1
Ruchelman, A.L.2
Zhou, N.3
Liu, A.4
Liu, L.F.5
Lavoie, E.J.6
-
132
-
-
0842265849
-
11H-Isoquino[4,3-c]cinnolin-12-ones: Novel anticancer agents with potent topoisomerase I-targeting activity and cytotoxicity
-
DOI 10.1016/j.bmc.2003.10.061
-
Ruchelman, A.L.; Singh, S.K.; Ray, A.; Wu, X.; Yang, J.M.; Zhou, N.; Liu, A.; Liu, L.F.; LaVoie, E.J., 11H-Isoquino[4,3-c]cinnolin-12-ones; novel anticancer agents with potent topoisomerase I-targeting activity and cytotoxicity. Bioorg. Med. Chem., 2004, 12, 795-806. (Pubitemid 38173061)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.4
, pp. 795-806
-
-
Ruchelman, A.L.1
Singh, S.K.2
Ray, A.3
Wu, X.4
Yang, J.-M.5
Zhou, N.6
Liu, A.7
Liu, L.F.8
LaVoie, E.J.9
-
133
-
-
62949117616
-
12-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridines as novel topoisomerase I-targeting antitumor agents
-
Feng, W.; Satyanarayana, M.; Tsai, Y.C.; Liu, A.A.; Liu, L.F.; LaVoie, E.J., 12-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridines as novel topoisomerase I-targeting antitumor agents. Bioorg. Med. Chem., 2009, 17, 2877-2885.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 2877-2885
-
-
Feng, W.1
Satyanarayana, M.2
Tsai, Y.C.3
Liu, A.A.4
Liu, L.F.5
Lavoie, E.J.6
-
134
-
-
51449119022
-
11-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridine derivatives as novel topoisomerase I-targeting agents
-
Feng, W.; Satyanarayana, M.; Tsai, Y.C.; Liu, A.A.; Liu, L.F.; LaVoie, E.J., 11-Substituted 2,3-dimethoxy-8,9-methylenedioxybenzo[i]phenanthridine derivatives as novel topoisomerase I-targeting agents. Bioorg. Med. Chem., 2008, 16, 8598-8606.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 8598-8606
-
-
Feng, W.1
Satyanarayana, M.2
Tsai, Y.C.3
Liu, A.A.4
Liu, L.F.5
Lavoie, E.J.6
-
135
-
-
70349410539
-
Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase i inhibitors by scaffold modification
-
You, Q.D.; Li, Z.Y.; Huang, C.H.; Yang, Q.; Wang, X.J.; Guo, Q.L.; Chen, X.G.; He, X.G.; Li, T.K.; Chern, J.W., Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification. J. Med. Chem., 2009, 52, 5649-5661.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5649-5661
-
-
You, Q.D.1
Li, Z.Y.2
Huang, C.H.3
Yang, Q.4
Wang, X.J.5
Guo, Q.L.6
Chen, X.G.7
He, X.G.8
Li, T.K.9
Chern, J.W.10
-
136
-
-
36148947863
-
Novel cyano- and amidino-substituted derivatives of styryl-2- benzimidazoles and benzimidazo[1,2-a]quinolines. Synthesis, photochemical synthesis, DNA binding, and antitumor evaluation, part 3
-
DOI 10.1021/jm070876h
-
Hranjec, M.; Kralj, M.; Piantanida, I.; Sedic, M.; Suman, L.; Pavelic, K.; Karminski-Zamola, G., Novel cyano- and amidino-substituted derivatives of styryl-2-benzimidazoles and benzimidazo[1,2-a]quinolines. Synthesis, photochemical synthesis, DNA binding, and antitumor evaluation, part 3. J. Med. Chem., 2007, 50, 5696-5711. (Pubitemid 350106024)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.23
, pp. 5696-5711
-
-
Hranjec, M.1
Kralj, M.2
Piantanida, I.3
Sedic, M.4
Suman, L.5
Pavelic, K.6
Karminski-Zamola, G.7
-
137
-
-
50249175013
-
Novel amidino-substituted thienyl- and furylvinylbenzimidazole: Derivatives and their photochemical conversion into corresponding diazacyclopenta[ c]fluorenes. synthesis, interactions with DNA and RNA, and antitumor evaluation. 4
-
Hranjec, M.; Piantanida, I.; Kralj, M.; Suman, L.; Pavelic, K.; Karminski-Zamola, G., Novel amidino-substituted thienyl- and furylvinylbenzimidazole: derivatives and their photochemical conversion into corresponding diazacyclopenta[ c]fluorenes. synthesis, interactions with DNA and RNA, and antitumor evaluation. 4. J. Med. Chem., 2008, 51, 4899-4910.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4899-4910
-
-
Hranjec, M.1
Piantanida, I.2
Kralj, M.3
Suman, L.4
Pavelic, K.5
Karminski-Zamola, G.6
-
138
-
-
33847667574
-
Naphthoindole-based analogues of tryptophan and tryptamine: Synthesis and cytotoxic properties
-
DOI 10.1016/j.bmc.2007.01.034, PII S0968089607000600
-
Shchekotikhin, A.E.; Dezhenkova, L.G.; Susova, O.Y.; Glazunova, V.A.; Luzikov, Y.N.; Sinkevich, Y.B.; Buyanov, V.N.; Shtil, A.A.; Preobrazhenskaya, M.N., Naphthoindole-based analogues of tryptophan and tryptamine: synthesis and cytotoxic properties. Bioorg. Med. Chem., 2007, 15, 2651-2659. (Pubitemid 46367701)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.7
, pp. 2651-2659
-
-
Shchekotikhin, A.E.1
Dezhenkova, L.G.2
Susova, O.Yu.3
Glazunova, V.A.4
Luzikov, Y.N.5
Sinkevich, Y.B.6
Buyanov, V.N.7
Shtil, A.A.8
Preobrazhenskaya, M.N.9
-
139
-
-
78650723189
-
Cytotoxicity and topoisomerase I/II inhibition of glycosylated 2-phenyl-indoles, 2-phenyl-benzo[b]thiophenes and 2-phenyl-benzo[b]furans
-
Shi, W.; Marcus, S.L.; Lowary, T.L., Cytotoxicity and topoisomerase I/II inhibition of glycosylated 2-phenyl-indoles, 2-phenyl-benzo[b]thiophenes and 2-phenyl-benzo[b]furans. Bioorg. Med. Chem., 2011, 19, 603-612.
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 603-612
-
-
Shi, W.1
Marcus, S.L.2
Lowary, T.L.3
-
140
-
-
38949162250
-
New insight for fluoroquinophenoxazine derivatives as possibly new potent topoisomerase I inhibitor
-
DOI 10.1016/j.bmcl.2007.12.053, PII S0960894X07015120
-
Kang, D.H.; Kim, J.S.; Jung, M.J.; Lee, E.S.; Jahng, Y.; Kwon, Y.; Na, Y., New insight for fluoroquinophenoxazine derivatives as possibly new potent topoisomerase I inhibitor. Bioorg. Med. Chem. Lett., 2008, 18, 1520-1524. (Pubitemid 351227458)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.4
, pp. 1520-1524
-
-
Kang, D.-H.1
Kim, J.-S.2
Jung, M.-J.3
Lee, E.-S.4
Jahng, Y.5
Kwon, Y.6
Na, Y.7
-
141
-
-
33745601106
-
Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity
-
DOI 10.1016/j.bmc.2006.04.044, PII S0968089606003440
-
Goodell, J.R.; Madhok, A.A.; Hiasa, H.; Ferguson, D.M., Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity. Bioorg. Med. Chem., 2006, 14, 5467-5480. (Pubitemid 43994481)
-
(2006)
Bioorganic and Medicinal Chemistry
, vol.14
, Issue.16
, pp. 5467-5480
-
-
Goodell, J.R.1
Madhok, A.A.2
Hiasa, H.3
Ferguson, D.M.4
-
142
-
-
38349194792
-
Acridine-based agents with topoisomerase II activity inhibit pancreatic cancer cell proliferation and induce apoptosis
-
Goodell, J.R.; Ougolkov, A.V.; Hiasa, H.; Kaur, H.; Remmel, R.; Billadeau, D.D.; Ferguson, D.M., Acridine-based agents with topoisomerase II activity inhibit pancreatic cancer cell proliferation and induce apoptosis. J. Med. Chem., 2008, 51, 179-182.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 179-182
-
-
Goodell, J.R.1
Ougolkov, A.V.2
Hiasa, H.3
Kaur, H.4
Remmel, R.5
Billadeau, D.D.6
Ferguson, D.M.7
-
143
-
-
67649996706
-
On the role of topoisomerase i in mediating the cytotoxicity of 9-aminoacridine-based anticancer agents
-
Galvez-Peralta, M.; Hackbarth, J.S.; Flatten, K.S.; Kaufmann, S.H.; Hiasa, H.; Xing, C.; Ferguson, D.M., On the role of topoisomerase I in mediating the cytotoxicity of 9-aminoacridine-based anticancer agents. Bioorg. Med. Chem. Lett., 2009, 19, 4459-4462.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4459-4462
-
-
Galvez-Peralta, M.1
Hackbarth, J.S.2
Flatten, K.S.3
Kaufmann, S.H.4
Hiasa, H.5
Xing, C.6
Ferguson, D.M.7
-
144
-
-
0038615843
-
Dual topoisomerase I/II inhibitors in cancer therapy
-
Denny, W.A.; Baguley, B.C., Dual topoisomerase I/II inhibitors in cancer therapy. Curr. Top. Med. Chem., 2003, 3, 339-353.
-
(2003)
Curr. Top. Med. Chem.
, vol.3
, pp. 339-353
-
-
Denny, W.A.1
Baguley, B.C.2
-
145
-
-
0023243267
-
Potential antitumor agents. 51. Synthesis and antitumor activity of substituted phenazine-1-carboxamides
-
Rewcastle, G.W.; Denny, W.A.; Baguley, B.C., Potential antitumor agents. 51. Synthesis and antitumor activity of substituted phenazine-1-carboxamides. J. Med. Chem., 1987, 30, 843-851. (Pubitemid 17119530)
-
(1987)
Journal of Medicinal Chemistry
, vol.30
, Issue.5
, pp. 843-851
-
-
Rewcastle, G.W.1
Denny, W.A.2
Baguley, B.C.3
-
146
-
-
0037204017
-
Novel angular benzophenazines: Dual topoisomerase I and topoisomerase II inhibitors as potential anticancer agents
-
DOI 10.1021/jm010329a
-
Vicker, N.; Burgess, L.; Chuckowree, I.S.; Dodd, R.; Folkes, A.J.; Hardick, D.J.; Hancox, T.C.; Miller, W.; Milton, J.; Sohal, S.; Wang, S.; Wren, S.P.; Charlton, P.A.; Dangerfield, W.; Liddle, C.; Mistry, P.; Stewart, A.J.; Denny, W.A., Novel angular benzophenazines: dual topoisomerase I and topoisomerase II inhibitors as potential anticancer agents. J. Med. Chem., 2002, 45, 721-739. (Pubitemid 34145719)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.3
, pp. 721-739
-
-
Vicker, N.1
Burgess, L.2
Chuckowree, I.S.3
Dodd, R.4
Folkes, A.J.5
Hardick, D.J.6
Hancox, T.C.7
Miller, W.8
Milton, J.9
Sohal, S.10
Wang, S.11
Wren, S.P.12
Charlton, P.A.13
Dangerfield, W.14
Liddle, C.15
Mistry, P.16
Stewart, A.J.17
Denny, W.A.18
-
147
-
-
0037130278
-
Self-association and unique DNA binding properties of the anti-cancer agent TAS-103, a dual inhibitor of topoisomerases I and II
-
DOI 10.1016/S0925-4439(02)00078-9, PII S0925443902000789
-
Ishida, K.; Asao, T., Self-association and unique DNA binding properties of the anti-cancer agent TAS-103, a dual inhibitor of topoisomerases I and II. Biochim. Biophys. Acta, 2002, 1587, 155-163. (Pubitemid 34655785)
-
(2002)
Biochimica et Biophysica Acta - Molecular Basis of Disease
, vol.1587
, Issue.2-3
, pp. 155-163
-
-
Ishida, K.1
Asao, T.2
-
148
-
-
0034666698
-
An investigation into the formation of N- [2-(dimethylamino)ethyl] acridine-4-carboxamide (DACA) and 6-[2-(dimethylamino)ethylamino]- 3-hydroxy-7H-indeno[2,1-C]quinolin-7-one dihydrochloride (TAS-103) stabilised DNA topoisomerase I and II cleavable complexes in human leukaemia cells
-
DOI 10.1016/S0006-2952(00)00402-0, PII S0006295200004020
-
Padget, K.; Stewart, A.; Charlton, P.; Tilby, M.J.; Austin, C.A., An investigation into the formation of N-[2-(dimethylamino)ethyl]acridine-4- carboxamide (DACA) and 6-[2-(dimethylamino)ethylamino]-3-hydroxy-7Hindeno[ 2, 1-C]quinolin-7-one dihydrochloride (TAS-103) stabilised DNA topoisomerase I and II cleavable complexes in human leukaemia cells. Biochem. Pharmacol., 2000, 60, 817-821. (Pubitemid 30621666)
-
(2000)
Biochemical Pharmacology
, vol.60
, Issue.6
, pp. 817-821
-
-
Padget, K.1
Stewart, A.2
Charlton, P.3
Tilby, M.J.4
Austin, C.A.5
-
149
-
-
79551474302
-
Benzoquinazoline derivatives as new agents affecting DNA processing
-
Marzaro, G.; Dalla Via, L.; Toninello, A.; Guiotto, A.; Chilin, A., Benzoquinazoline derivatives as new agents affecting DNA processing. Bioorg. Med. Chem., 2011, 19, 1197-1204.
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 1197-1204
-
-
Marzaro, G.1
Dalla Via, L.2
Toninello, A.3
Guiotto, A.4
Chilin, A.5
-
150
-
-
8844263666
-
Synthesis and anticancer evaluation of certain indolo[2,3-b]quinoline derivatives
-
Chen, Y.L.; Hung, H.M.; Lu, C.M.; Li, K.C.; Tzeng, C.C., Synthesis and anticancer evaluation of certain indolo[2,3-b]quinoline derivatives. Bioorg. Med. Chem., 2004, 12,6539-6546.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 6539-6546
-
-
Chen, Y.L.1
Hung, H.M.2
Lu, C.M.3
Li, K.C.4
Tzeng, C.C.5
-
151
-
-
77249129333
-
Synthesis and antiproliferative evaluation of certain indolo[3,2-c]quinoline derivatives
-
Lu, C.M.; Chen, Y.L.; Chen, H.L.; Chen, C.A.; Lu, P.J.; Yang, C.N.; Tzeng, C.C., Synthesis and antiproliferative evaluation of certain indolo[3,2-c]quinoline derivatives. Bioorg. Med. Chem., 2010, 18, 1948-1957.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 1948-1957
-
-
Lu, C.M.1
Chen, Y.L.2
Chen, H.L.3
Chen, C.A.4
Lu, P.J.5
Yang, C.N.6
Tzeng, C.C.7
-
152
-
-
73949126608
-
Synthesis and antiproliferative evaluation of 6-arylindeno[1,2-c] quinoline derivatives
-
Tseng, C.H.; Chen, Y.L.; Chung, K.Y.; Cheng, C.M.; Wang, C.H.; Tzeng, C.C., Synthesis and antiproliferative evaluation of 6-arylindeno[1,2-c]quinoline derivatives. Bioorg. Med. Chem., 2009, 17, 7465-7476.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7465-7476
-
-
Tseng, C.H.1
Chen, Y.L.2
Chung, K.Y.3
Cheng, C.M.4
Wang, C.H.5
Tzeng, C.C.6
-
153
-
-
40949138412
-
Synthesis and antiproliferative evaluation of certain indeno[1,2-c]quinoline derivatives
-
Tseng, C.H.; Chen, Y.L.; Lu, P.J.; Yang, C.N.; Tzeng, C.C., Synthesis and antiproliferative evaluation of certain indeno[1,2-c]quinoline derivatives. Bioorg. Med. Chem., 2008, 16, 3153-3162.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 3153-3162
-
-
Tseng, C.H.1
Chen, Y.L.2
Lu, P.J.3
Yang, C.N.4
Tzeng, C.C.5
-
154
-
-
77955894751
-
Synthesis and antiproliferative evaluation of certain indeno[1,2-c]quinoline derivatives. Part 2
-
Tseng, C.H.; Tzeng, C.C.; Yang, C.L.; Lu, P.J.; Chen, H.L.; Li, H.Y.; Chuang, Y.C.; Yang, C.N.; Chen, Y.L., Synthesis and antiproliferative evaluation of certain indeno[1,2-c]quinoline derivatives. Part 2. J. Med. Chem., 2010, 53, 6164-6179.
-
(2010)
J. Med. Chem.
, Issue.53
, pp. 6164-6179
-
-
Tseng, C.H.1
Tzeng, C.C.2
Yang, C.L.3
Lu, P.J.4
Chen, H.L.5
Li, H.Y.6
Chuang, Y.C.7
Yang, C.N.8
Chen, Y.L.9
-
155
-
-
66149149851
-
Structure-based discovery of beta2-adrenergic receptor ligands
-
Kolb, P.; Rosenbaum, D.M.; Irwin, J.J.; Fung, J.J.; Kobilka, B.K.; Shoichet, B.K., Structure-based discovery of beta2-adrenergic receptor ligands. Proc. Natl. Acad. Sci. U S A., 2009, 106, 6843-6848.
-
(2009)
Proc. Natl. Acad. Sci. U S A.
, vol.106
, pp. 6843-6848
-
-
Kolb, P.1
Rosenbaum, D.M.2
Irwin, J.J.3
Fung, J.J.4
Kobilka, B.K.5
Shoichet, B.K.6
-
156
-
-
68549087091
-
Identification of novel falcipain-2 inhibitors as potential antimalarial agents through structure-based virtual screening
-
Li, H.; Huang, J.; Chen, L.; Liu, X.; Chen, T.; Zhu, J.; Lu, W.; Shen, X.; Li, J.; Hilgenfeld, R.; Jiang, H., Identification of novel falcipain-2 inhibitors as potential antimalarial agents through structure-based virtual screening. J. Med. Chem., 2009, 52, 4936-4940.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4936-4940
-
-
Li, H.1
Huang, J.2
Chen, L.3
Liu, X.4
Chen, T.5
Zhu, J.6
Lu, W.7
Shen, X.8
Li, J.9
Hilgenfeld, R.10
Jiang, H.11
-
157
-
-
11144323163
-
Virtual screening of chemical libraries
-
DOI 10.1038/nature03197
-
Shoichet, B.K., Virtual screening of chemical libraries. Nature, 2004, 432, 862-865. (Pubitemid 40037142)
-
(2004)
Nature
, vol.432
, Issue.7019
, pp. 862-865
-
-
Shoichet, B.K.1
-
158
-
-
0032489634
-
Crystal structures of human topoisomerase I in covalent and noncovalent complexes with DNA
-
DOI 10.1126/science.279.5356.1504
-
Redinbo, M.R.; Stewart, L.; Kuhn, P.; Champoux, J.J.; Hol, W.G., Crystal structures of human topoisomerase I in covalent and noncovalent complexes with DNA. Science, 1998, 279, 1504-1513. (Pubitemid 28217069)
-
(1998)
Science
, vol.279
, Issue.5356
, pp. 1504-1513
-
-
Redinbo, M.R.1
Stewart, L.2
Kuhn, P.3
Champoux, J.J.4
Hol, W.G.J.5
-
159
-
-
0037180432
-
The mechanism of topoisomerase I poisoning by a camptothecin analog
-
DOI 10.1073/pnas.242259599
-
Staker, B.L.; Hjerrild, K.; Feese, M.D.; Behnke, C.A.; Burgin, A.B., Jr.; Stewart, L., The mechanism of topoisomerase I poisoning by a camptothecin analog. Proc. Natl. Acad. Sci. U S A., 2002, 99, 15387-15392. (Pubitemid 35403944)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.24
, pp. 15387-15392
-
-
Staker, B.L.1
Hjerrild, K.2
Feese, M.D.3
Behnke, C.A.4
Burgin Jr., A.B.5
Stewart, L.6
-
160
-
-
78149253942
-
Selection of evodiamine as a novel topoisomerase i inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents
-
Dong, G.; Sheng, C.; Wang, S.; Miao, Z.; Yao, J.; Zhang, W., Selection of evodiamine as a novel topoisomerase I inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents. J. Med. Chem., 2010, 53, 7521-7531.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 7521-7531
-
-
Dong, G.1
Sheng, C.2
Wang, S.3
Miao, Z.4
Yao, J.5
Zhang, W.6
-
161
-
-
0031552362
-
Development and validation of a genetic algorithm for flexible docking
-
DOI 10.1006/jmbi.1996.0897
-
Jones, G.; Willett, P.; Glen, R.C.; Leach, A.R.; Taylor, R., Development and validation of a genetic algorithm for flexible docking. J. Mol. Biol., 1997, 267, 727-748. (Pubitemid 27170693)
-
(1997)
Journal of Molecular Biology
, vol.267
, Issue.3
, pp. 727-748
-
-
Jones, G.1
Willett, P.2
Glen, R.C.3
Leach, A.R.4
Taylor, R.5
-
162
-
-
37549023863
-
Structural basis for gate-DNA recognition and bending by type IIA topoisomerases
-
Dong, K.C.; Berger, J.M., Structural basis for gate-DNA recognition and bending by type IIA topoisomerases. Nature, 2007, 450, 1201-1205.
-
(2007)
Nature
, vol.450
, pp. 1201-1205
-
-
Dong, K.C.1
Berger, J.M.2
-
163
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
DOI 10.1016/S0169-409X(00)00129-0, PII S0169409X00001290
-
Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J., Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev., 2001, 46, 3-26. (Pubitemid 33653411)
-
(2000)
Advanced Drug Delivery Reviews
, vol.46
, Issue.1-3
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
164
-
-
0141726877
-
A 'rule of three' for fragmentbased lead discovery?
-
Congreve, M.; Carr, R.; Murray, C.; Jhoti, H., A 'rule of three' for fragmentbased lead discovery? Drug Discov. Today, 2003, 8, 876-877.
-
(2003)
Drug Discov. Today
, vol.8
, pp. 876-877
-
-
Congreve, M.1
Carr, R.2
Murray, C.3
Jhoti, H.4
-
165
-
-
0037364162
-
ADMET in silico modelling: Towards prediction paradise?
-
DOI 10.1038/nrd1032
-
van de Waterbeemd, H.; Gifford, E., ADMET in silico modelling: towards prediction paradise? Nat. Rev. Drug Discov., 2003, 2, 192-204. (Pubitemid 37361664)
-
(2003)
Nature Reviews Drug Discovery
, vol.2
, Issue.3
, pp. 192-204
-
-
Van De Waterbeemd, H.1
Gifford, E.2
-
166
-
-
0042330313
-
ADME-Tox in drug discovery: Integration of experimental and computational technologies
-
DOI 10.1016/S1359-6446(03)02828-9, PII S1359644603028289
-
Yu, H.; Adedoyin, A., ADME-Tox in drug discovery: integration of experimental and computational technologies. Drug Discov. Today, 2003, 8, 852-861. (Pubitemid 37083343)
-
(2003)
Drug Discovery Today
, vol.8
, Issue.18
, pp. 852-861
-
-
Yu, H.1
Adedoyin, A.2
-
167
-
-
71749084307
-
Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase i inhibitors
-
Cho, H.J.; Jung, M.J.; Kwon, Y.; Na, Y., Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase I inhibitors. Bioorg. Med. Chem. Lett., 2009, 19, 6766-6769.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6766-6769
-
-
Cho, H.J.1
Jung, M.J.2
Kwon, Y.3
Na, Y.4
-
168
-
-
79952189620
-
Cytotoxic 3,6-bis((imidazolidinone)imino)acridines: Synthesis, DNA binding and molecular modeling
-
Janovec, L.; Kozurkova, M.; Sabolova, D.; Ungvarsky, J.; Paulikova, H.; Plsikova, J.; Vantova, Z.; Imrich, J., Cytotoxic 3,6-bis((imidazolidinone)imino) acridines: Synthesis, DNA binding and molecular modeling. Bioorg. Med. Chem., 2011, 19, 1790-1801.
-
(2011)
Bioorg. Med. Chem.
, Issue.19
, pp. 1790-1801
-
-
Janovec, L.1
Kozurkova, M.2
Sabolova, D.3
Ungvarsky, J.4
Paulikova, H.5
Plsikova, J.6
Vantova, Z.7
Imrich, J.8
|