-
1
-
-
0022586257
-
The chemistry, mechanism of action, and biological properties of CC-1065, a potent antitumor antibiotic
-
Reynolds, V. L.; McGovren, J. P.; Hurley, L. H. The chemistry, mechanism of action, and biological properties of CC-1065, a potent antitumor antibiotic J. Antibiot. 1986, 34, 319-334.
-
(1986)
J. Antibiot.
, vol.34
, pp. 319-334
-
-
Reynolds, V.L.1
McGovren, J.P.2
Hurley, L.H.3
-
2
-
-
0028937557
-
Duocarmycins, potent antitumor antibiotics produced by Streptomyces sp. structures and chemistry
-
Yasuzawa, T.; Muroi, K.; Ichimura, M.; Takahashi, I.; Ogawa, T.; Takahashi, K.; Sano, H.; Saitoh, Y. Duocarmycins, potent antitumor antibiotics produced by Streptomyces sp. structures and chemistry. Chem. Pharm. Bull. 1995, 43, 378-391.
-
(1995)
Chem. Pharm. Bull.
, vol.43
, pp. 378-391
-
-
Yasuzawa, T.1
Muroi, K.2
Ichimura, M.3
Takahashi, I.4
Ogawa, T.5
Takahashi, K.6
Sano, H.7
Saitoh, Y.8
-
3
-
-
0028198475
-
Characteristics of antitumor activity of KW-2189, a novel water-soluble derivative of duocarmycin, against murine and human tumors
-
Kobayashi, E.; Okamoto, A.; Asada, M.; Okabe, M.; Nagamura, S.; Asai, A.; Saito, H.; Gomi, K.; Hirata, T. Characteristics of antitumor activity of KW-2189, a novel water-soluble derivative of duocarmycin, against murine and human tumors. Cancer Res. 1994, 54, 2404-2410.
-
(1994)
Cancer Res.
, vol.54
, pp. 2404-2410
-
-
Kobayashi, E.1
Okamoto, A.2
Asada, M.3
Okabe, M.4
Nagamura, S.5
Asai, A.6
Saito, H.7
Gomi, K.8
Hirata, T.9
-
4
-
-
0030747297
-
DNA minor groove binding ligands: A new class of anticancer drugs
-
D'Incalci, M.; Sessa, C. DNA minor groove binding ligands: a new class of anticancer drugs. Exp. Opin. Invest. Drugs 1997, 6, 875-884.
-
(1997)
Exp. Opin. Invest. Drugs
, vol.6
, pp. 875-884
-
-
D'Incalci, M.1
Sessa, C.2
-
5
-
-
0029782488
-
CC-1065 and the duocarmycins: Understanding their biological function through mechanistic studies
-
Boger, D. L.; Johnson, D. S. CC-1065 and the duocarmycins: understanding their biological function through mechanistic studies. Angew. Chem., Int. Ed. Engl. 1996, 35, 1438-1474.
-
(1996)
Angew. Chem., Int. Ed. Engl.
, vol.35
, pp. 1438-1474
-
-
Boger, D.L.1
Johnson, D.S.2
-
6
-
-
0030970599
-
Duocarmycin SA shortened, simplified and extended agents: A systematic examination of the role of the DNA binding subunit
-
Boger, D. L.; Hertzog, D. L.; Bollinger, B.; Johnson, D. S.; Cai, H.; Goldberg, J.; Turnbull, P. Duocarmycin SA shortened, simplified and extended agents: a systematic examination of the role of the DNA binding subunit. J. Am. Chem. Soc. 1997, 119, 4977-4986.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 4977-4986
-
-
Boger, D.L.1
Hertzog, D.L.2
Bollinger, B.3
Johnson, D.S.4
Cai, H.5
Goldberg, J.6
Turnbull, P.7
-
7
-
-
0028036453
-
CBI-TMI: Synthesis and evaluation of a key analogue of the duocarmycins. Validation of a direct relationship between chemical solvolytic stability and cytotoxic potency and confirmation of the structural features responsible for distinguishing behaviour of the enantiomeric pairs of agents
-
Boger, D. L.; Yun, W. CBI-TMI: synthesis and evaluation of a key analogue of the duocarmycins. Validation of a direct relationship between chemical solvolytic stability and cytotoxic potency and confirmation of the structural features responsible for distinguishing behaviour of the enantiomeric pairs of agents. J. Am. Chem. Soc. 1994, 116, 7996-8006.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 7996-8006
-
-
Boger, D.L.1
Yun, W.2
-
8
-
-
0025119357
-
2: Enhanced functional analogues of CC-1065 incorporating the 1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) left-hand subunit
-
2: enhanced functional analogues of CC-1065 incorporating the 1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) left-hand subunit. J. Org. Chem. 1990, 55, 5823-5832.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 5823-5832
-
-
Boger, D.L.1
Ishizaki, T.2
Kitos, P.A.3
Suntornwat, O.4
-
9
-
-
0028095610
-
(+)- and ent-(-)-duocarmycin SA and ent-(-)-N-BOC-DSA DNA alkylating properties. Alkylation site models ther accommodate the offset AT-rich adenine N3 alkylation selectivity of the enantiomeric agents
-
Boger, D. L.; Johnson. D. S.; Yun, W. (+)- and ent-(-)-duocarmycin SA and ent-(-)-N-BOC-DSA DNA alkylating properties. Alkylation site models ther accommodate the offset AT-rich adenine N3 alkylation selectivity of the enantiomeric agents. J. Am. Chem. Soc. 1994, 116, 1635-1656.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 1635-1656
-
-
Boger, D.L.1
Johnson, D.S.2
Yun, W.3
-
10
-
-
0029608618
-
Phase I trial of adozelesin using the treatment schedule of daily ×5 every 3 weeks
-
(a) Foster, B. J.; LoRusso, P. M.; Poplin, E.; Zalupski, M.; Valdivieso, M.; Wozniak, A.; Flaherty, L.; Kasunic, D. A.; Earhart, R. H.; Baker, L. H. Phase I trial of adozelesin using the treatment schedule of daily ×5 every 3 weeks. Invest. New Drugs. 1996, 13, 321-326.
-
(1996)
Invest. New Drugs.
, vol.13
, pp. 321-326
-
-
Foster, B.J.1
LoRusso, P.M.2
Poplin, E.3
Zalupski, M.4
Valdivieso, M.5
Wozniak, A.6
Flaherty, L.7
Kasunic, D.A.8
Earhart, R.H.9
Baker, L.H.10
-
11
-
-
8544261171
-
Phase I study with the DNA sequence-specific agent adozelesin
-
(b) Burris, H. A.; Dieras, V. C.; Tunca, M.; Earhart, R. H.; Eckardt, J. R.; Rodriguez, G. I.; Shaffer, D. S.; Fields, S. M.; Campbell, E.; Schaaf, L.; Kasunic, D.; Von Hoff, D. D. Phase I study with the DNA sequence-specific agent adozelesin. Anti-Cancer Drugs 1997, 8, 588-596.
-
(1997)
Anti-Cancer Drugs
, vol.8
, pp. 588-596
-
-
Burris, H.A.1
Dieras, V.C.2
Tunca, M.3
Earhart, R.H.4
Eckardt, J.R.5
Rodriguez, G.I.6
Shaffer, D.S.7
Fields, S.M.8
Campbell, E.9
Schaaf, L.10
Kasunic, D.11
Von Hoff, D.D.12
-
12
-
-
0026786973
-
Cytotoxicity and antitumor activity of carzelesin, a prodrug cyclopropylpyrroloindole analogue
-
Li, L. H.; DeKoning, T. F.; Kelly, R. C.; Krueger, W. C.; McGovren, J. P.; Padbury, G. E.; Petzold, G. L.; Wallace, T. L.; Ouding, R. J.; Prairie, M. D.; Gebhard, I. Cytotoxicity and antitumor activity of carzelesin, a prodrug cyclopropylpyrroloindole analogue. Cancer Res. 1992, 52, 4904-4913.
-
(1992)
Cancer Res.
, vol.52
, pp. 4904-4913
-
-
Li, L.H.1
Dekoning, T.F.2
Kelly, R.C.3
Krueger, W.C.4
McGovren, J.P.5
Padbury, G.E.6
Petzold, G.L.7
Wallace, T.L.8
Ouding, R.J.9
Prairie, M.D.10
Gebhard, I.11
-
13
-
-
0028333762
-
A novel antitumor antibiotic, KW-2189 is activated by carboxyl esterase and induces DNA strand breaks in human small cell lung cancer cells
-
Ogasawara, H.; Nishio, K.; Takeda, Y.; Ohmori, T.; Kubota, N.; Funayama, Y.; Ohira, T.; Kuraishi, Y.; Isogai, Y.; Saijo, N. A novel antitumor antibiotic, KW-2189 is activated by carboxyl esterase and induces DNA strand breaks in human small cell lung cancer cells. Jpn. J. Cancer Res. 1994, 85, 418-425.
-
(1994)
Jpn. J. Cancer Res.
, vol.85
, pp. 418-425
-
-
Ogasawara, H.1
Nishio, K.2
Takeda, Y.3
Ohmori, T.4
Kubota, N.5
Funayama, Y.6
Ohira, T.7
Kuraishi, Y.8
Isogai, Y.9
Saijo, N.10
-
14
-
-
0001687859
-
The design of selectively activated prodrugs for cancer chemotherapy
-
Denny, W. A. The design of selectively activated prodrugs for cancer chemotherapy. Curr. Pharm. Des. 1996, 2, 281-294.
-
(1996)
Curr. Pharm. Des.
, vol.2
, pp. 281-294
-
-
Denny, W.A.1
-
15
-
-
0028149793
-
A prodrug approach to increasing the oral potency of a phenolic drug. 1. Synthesis, characterization, and stability of an O-(imidomethyl) derivative of 17 beta-estradiol
-
Patel, J. U.; Prankerd, R. J.; Sloan, K. B. A prodrug approach to increasing the oral potency of a phenolic drug. 1. Synthesis, characterization, and stability of an O-(imidomethyl) derivative of 17 beta-estradiol. J. Pharm. Sci. 1994, 83, 1477-1481.
-
(1994)
J. Pharm. Sci.
, vol.83
, pp. 1477-1481
-
-
Patel, J.U.1
Prankerd, R.J.2
Sloan, K.B.3
-
16
-
-
0030593869
-
Nitrogen and sulfur analogues of the seco-CI alkyating agent: Synthesis and cytotoxicity
-
Tercel, M.; Denny, W. A.; Wilson, W. R. Nitrogen and sulfur analogues of the seco-CI alkyating agent: synthesis and cytotoxicity. Bioorg. Med. Chem. Lett. 1996, 6, 2735-2740.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 2735-2740
-
-
Tercel, M.1
Denny, W.A.2
Wilson, W.R.3
-
17
-
-
33748666900
-
Synthesis of nitrogen and sulfur analogues of the seco-CI alkylating agent
-
Tercel, M.; Denny, W. A. Synthesis of nitrogen and sulfur analogues of the seco-CI alkylating agent. J. Chem. Soc., Perkin Trans, 1 1998, 509-519.
-
(1998)
J. Chem. Soc., Perkin Trans, 1
, pp. 509-519
-
-
Tercel, M.1
Denny, W.A.2
-
18
-
-
0033602220
-
Synthesis of 1-substituted 3-(chloromethyl)-6-aminoindoline (6-amino-seco-CI) DNA minor groove alkylating agents and structure-activity relationships for the cytotoxicity
-
Milbank, J. B. J.; Tercel, M.; Atwell, G. J.; Wilson, W. R.; Hogg, A.; Denny, W. A. Synthesis of 1-substituted 3-(chloromethyl)-6-aminoindoline (6-amino-seco-CI) DNA minor groove alkylating agents and structure-activity relationships for the cytotoxicity. J. Med. Chem. 1999, 42, 649-658.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 649-658
-
-
Milbank, J.B.J.1
Tercel, M.2
Atwell, G.J.3
Wilson, W.R.4
Hogg, A.5
Denny, W.A.6
-
19
-
-
0030916634
-
Synthesis and cytotoxicity of amino analogues of the potent DNA alkylating agent seco-CBI-TMI
-
Atwell, G. J.; Wilson, W. R.; Denny, W. A. Synthesis and cytotoxicity of amino analogues of the potent DNA alkylating agent seco-CBI-TMI. Bioorg. Med. Chem. Lett. 1997, 7, 1493-1496.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 1493-1496
-
-
Atwell, G.J.1
Wilson, W.R.2
Denny, W.A.3
-
20
-
-
0032509496
-
Synthesis and cytotoxicity of 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1,2-dihydro- 3H-benz[e]indole (amino-seco-CBI-TMI) and related 5-alkylamino analogues: New DNA minor groove alkylating agents
-
Atwell, G. J.; Tercel, M.; Boyd, M.; Wilson, W. R.; Denny, W. A. Synthesis and cytotoxicity of 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1,2-dihydro- 3H-benz[e]indole (amino-seco-CBI-TMI) and related 5-alkylamino analogues: new DNA minor groove alkylating agents. J. Org. Chem. 1998, 63, 9414-9420.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 9414-9420
-
-
Atwell, G.J.1
Tercel, M.2
Boyd, M.3
Wilson, W.R.4
Denny, W.A.5
-
21
-
-
0023906926
-
Stereoelectronic factors influencing the biological activity and DNA interaction of synthetic antitumor agents modeled on CC-1065
-
Warpehoski, M. A.; Gebhard, I.; Kelly, R. C.; Krueger, W. C.; Li, L. H.; McGovren, J. P.; Prairie, M. D.; Wicnienski, N.; Wierenga, W. Stereoelectronic factors influencing the biological activity and DNA interaction of synthetic antitumor agents modeled on CC-1065. J. Med. Chem. 1988, 31, 590-603.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 590-603
-
-
Warpehoski, M.A.1
Gebhard, I.2
Kelly, R.C.3
Krueger, W.C.4
Li, L.H.5
McGovren, J.P.6
Prairie, M.D.7
Wicnienski, N.8
Wierenga, W.9
-
22
-
-
0026337788
-
Pyrazole analogues of the bispyrrolecarboxamide antitumour antibiotics: Synthesis, DNA binding and antitumour properties
-
Lee, H. H.; Boyd, M.; Gravatt, G. L.; Denny, W. A. Pyrazole analogues of the bispyrrolecarboxamide antitumour antibiotics: synthesis, DNA binding and antitumour properties. Anti-Cancer Drug Des. 1991, 6, 501-517.
-
(1991)
Anti-Cancer Drug Des.
, vol.6
, pp. 501-517
-
-
Lee, H.H.1
Boyd, M.2
Gravatt, G.L.3
Denny, W.A.4
-
23
-
-
0000007628
-
Synthesis and characterization of masked aminopyrazolecarboxylic acid synthons
-
Lee, H. H.; Cain, B. F.; Denny, W. A.; Buckleton, J.; Clark, G. R. Synthesis and characterization of masked aminopyrazolecarboxylic acid synthons. J. Org. Chem. 1989, 54, 428-431.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 428-431
-
-
Lee, H.H.1
Cain, B.F.2
Denny, W.A.3
Buckleton, J.4
Clark, G.R.5
-
24
-
-
0023572188
-
Modulation of the antitumor activity by methyl substitution in the series of 7H-pyridocarbazole monomers and dimers
-
Leon, P.; Garbay-Jaureguiberry, C.; Barsi, M. C.; Le Pecq, J. B.; Roques, P. B. Modulation of the antitumor activity by methyl substitution in the series of 7H-pyridocarbazole monomers and dimers. J. Med. Chem. 1987, 30, 2074-2080.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 2074-2080
-
-
Leon, P.1
Garbay-Jaureguiberry, C.2
Barsi, M.C.3
Le Pecq, J.B.4
Roques, P.B.5
-
25
-
-
0021207993
-
Rapid detection of DNA-damaging agents using repair-deficient CHO cells
-
Hoy, C. A.; Salazar, E. P.; Thompson. L. H. Rapid detection of DNA-damaging agents using repair-deficient CHO cells. Mutat. Res. 1984, 130, 321-332.
-
(1984)
Mutat. Res.
, vol.130
, pp. 321-332
-
-
Hoy, C.A.1
Salazar, E.P.2
Thompson, L.H.3
-
26
-
-
0021824209
-
Defective DNA cross-link removal in Chinese hamster cell mutants hypersensitive to bifunctional alkylating agents
-
Hoy, C. A.; Thompson, L. H.; Mooney, C. L.; Salazar, E. P. Defective DNA cross-link removal in Chinese hamster cell mutants hypersensitive to bifunctional alkylating agents. Cancer Res. 1985, 45, 1737-1743.
-
(1985)
Cancer Res.
, vol.45
, pp. 1737-1743
-
-
Hoy, C.A.1
Thompson, L.H.2
Mooney, C.L.3
Salazar, E.P.4
-
27
-
-
0032957259
-
Comparison of the patterns of DNA alkylation by phenol and amino seco-CBI-TMI compounds: Use of a PCR method for the facile preparation of single end-labeled double stranded DNA
-
in press
-
Gieseg, M. A.; Matejovic, J.; Denny, W. A. Comparison of the patterns of DNA alkylation by phenol and amino seco-CBI-TMI compounds: use of a PCR method for the facile preparation of single end-labeled double stranded DNA. Anti-Cancer Drug Des., in press.
-
Anti-Cancer Drug Des.
-
-
Gieseg, M.A.1
Matejovic, J.2
Denny, W.A.3
-
28
-
-
0030591690
-
Examination of the role of the duocarmycin SA methoxy substituents: Identification of the minimum, fully potent DNA binding subunit
-
Boger, D. L.; Bollinger, B.; Johnson, D. S. Examination of the role of the duocarmycin SA methoxy substituents: identification of the minimum, fully potent DNA binding subunit. Bioorg. Med. Chem. Lett. 1996, 6, 2207-2210.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 2207-2210
-
-
Boger, D.L.1
Bollinger, B.2
Johnson, D.S.3
-
30
-
-
0030998113
-
Synthesis and antitumor activity of duocarmycin derivatives: A-ring pyrrole compounds bearing cinnamoyl groups
-
Nagamura, S.; Asai, A.; Amishiro, N.; Kobayashi, E.; Gomi, K.; Saito, H. Synthesis and antitumor activity of duocarmycin derivatives: A-ring pyrrole compounds bearing cinnamoyl groups. J. Med. Chem. 1997, 40, 972-979.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 972-979
-
-
Nagamura, S.1
Asai, A.2
Amishiro, N.3
Kobayashi, E.4
Gomi, K.5
Saito, H.6
-
31
-
-
0000544068
-
The synthesis of 4-nitro, 6-nitro and 7-nitroindole
-
Parmerter, S. M.; Cook, A. G.; Dixon, W. B. The synthesis of 4-nitro, 6-nitro and 7-nitroindole. J. Am. Chem. Soc. 1958, 80, 4621-4622.
-
(1958)
J. Am. Chem. Soc.
, vol.80
, pp. 4621-4622
-
-
Parmerter, S.M.1
Cook, A.G.2
Dixon, W.B.3
-
32
-
-
0028790373
-
1,2,9,9a-Tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins: Synthesis and evaluation
-
Boger D. L.; Yun, W.; Han, N. 1,2,9,9a-Tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins: synthesis and evaluation. Bioorg. Med. Chem. 1995, 3, 1429-1453.
-
(1995)
Bioorg. Med. Chem.
, vol.3
, pp. 1429-1453
-
-
Boger, D.L.1
Yun, W.2
Han, N.3
-
33
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan, P.; Storeng, R.; Scuderio, D.; Monks, A.; McMahon, J.; Vistica, D.; Warren, J. T.; Bokesch, H.; Kenney, S.; Boyd, M. R. New colorimetric cytotoxicity assay for anticancer-drug screening. J. Natl. Cancer Inst. 1990, 82, 1107-1112.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scuderio, D.3
Monks, A.4
McMahon, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, H.8
Kenney, S.9
Boyd, M.R.10
|