-
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.; Garni, 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
Garni, K.8
Hirata, T.9
-
4
-
-
0030747297
-
DNA minor groove binding ligands: A new class of anticancer agents
-
D'Incalci, M.; Sessa, C. DNA minor groove binding ligands: a new class of anticancer agents. 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
-
-
0001699963
-
CC-1065 and the duocarmycins: Synthetic studies
-
Boger, D. L.; Boyce, C. W.; Garbaccio, R. M.; Goldberg, J. A. CC-1065 and the duocarmycins: synthetic studies. Chem. Rev. 1997, 97, 787-828.
-
(1997)
Chem. Rev.
, vol.97
, pp. 787-828
-
-
Boger, D.L.1
Boyce, C.W.2
Garbaccio, R.M.3
Goldberg, J.A.4
-
6
-
-
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
-
7
-
-
0028301328
-
Mapping of DNA alkylation sites induced by adozelesin and bizelesin in human cells by ligation-mediated polymerase chain reaction
-
Lee, C.-S.; Pfeifer, G. P.; Gibson, N. W. Mapping of DNA alkylation sites induced by adozelesin and bizelesin in human cells by ligation-mediated polymerase chain reaction. Biochemistry 1994, 33, 6024-6030.
-
(1994)
Biochemistry
, vol.33
, pp. 6024-6030
-
-
Lee, C.-S.1
Pfeifer, G.P.2
Gibson, N.W.3
-
8
-
-
0031081549
-
Catalysis of the CC-1065 and duocarmycin DNA alkylation reaction: Binding induced conformational change in the agent results in activation
-
Boger, D. L.; Garbaccio, R. M. Catalysis of the CC-1065 and duocarmycin DNA alkylation reaction: binding induced conformational change in the agent results in activation. Bioorg. Med. Chem. 1997, 5, 263-276.
-
(1997)
Bioorg. Med. Chem.
, vol.5
, pp. 263-276
-
-
Boger, D.L.1
Garbaccio, R.M.2
-
9
-
-
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 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 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
-
10
-
-
0021319952
-
Preliminary toxicity studies with the DNA-binding antibiotic CC-1065
-
McGovren, J. P.; Clarke, G. L.; Pratt, E. A.; DeKoning, T. F. Preliminary toxicity studies with the DNA-binding antibiotic CC-1065. J. Antibiot. 1984, 37, 63-70.
-
(1984)
J. Antibiot.
, vol.37
, pp. 63-70
-
-
McGovren, J.P.1
Clarke, G.L.2
Pratt, E.A.3
DeKoning, T.F.4
-
11
-
-
0029608618
-
Phase I trial of adozelesin using the treatment schedule of daily x 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 x 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
-
12
-
-
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
-
13
-
-
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
-
14
-
-
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
-
16
-
-
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
-
17
-
-
0025143478
-
Synthesis and preliminary evaluation of agents incorporating the pharmacophore of the duocarmycin/pyrindamycin alkylating subunit: Identification of CC-1065/duocarmycin common pharmacophore
-
Boger, D. L.; Ishizaki, T.; Zarrinmayeh, H.; Kitos, P. A.; Suntornwat, O. Synthesis and preliminary evaluation of agents incorporating the pharmacophore of the duocarmycin/pyrindamycin alkylating subunit: identification of CC-1065/duocarmycin common pharmacophore. J. Org. Chem. 1990, 55, 4499-4502.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 4499-4502
-
-
Boger, D.L.1
Ishizaki, T.2
Zarrinmayeh, H.3
Kitos, P.A.4
Suntornwat, O.5
-
18
-
-
0025644317
-
Duocarmycin-pyrindamycin DNA alkylation properties and identification, synthesis and evaluation of agents incorporating the pharmacophore of the duocarmycin-pyrindamycin alkylating subunit. Identification of the CC-1065-duocarmycin common pharmacophore
-
Boger, D. L.; Ishizaki, T.; Zarrinmayeh, H.; Munk, S. A.; Kitos, P.A.; Suntornwat, O. Duocarmycin-pyrindamycin DNA alkylation properties and identification, synthesis and evaluation of agents incorporating the pharmacophore of the duocarmycin-pyrindamycin alkylating subunit. Identification of the CC-1065-duocarmycin common pharmacophore. J. Am. Chem. Soc. 1990, 112, 8961-8971.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 8961-8971
-
-
Boger, D.L.1
Ishizaki, T.2
Zarrinmayeh, H.3
Munk, S.A.4
Kitos, P.A.5
Suntornwat, O.6
-
19
-
-
0025980193
-
32P-end-labeled double-stranded DNA for binding studies: Development of a protocol for examination of functional features of (+)-CC-1065 and the duocarmycins that contribute to their sequence-selective DNA alkylation properties
-
32P-end-labeled double-stranded DNA for binding studies: development of a protocol for examination of functional features of (+)-CC-1065 and the duocarmycins that contribute to their sequence-selective DNA alkylation properties. Tetrahedron 1991, 47, 2661-2682.
-
(1991)
Tetrahedron
, vol.47
, pp. 2661-2682
-
-
Boger, D.L.1
Munk, S.A.2
Zarrinmayeh, H.3
Ishizaki, T.4
Haught, J.5
Bina, M.6
-
20
-
-
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
-
21
-
-
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
-
-
Denny, W.A.1
Wilson, W.R.2
-
22
-
-
0030593879
-
A novel nitro-substituted seco-CI: Application as a reductively activated ADEPT prodrug
-
Tercel, M.; Denny, W. A.; Wilson, W. R. A novel nitro-substituted seco-CI: application as a reductively activated ADEPT prodrug. Bioorg. Med. Chem. Lett. 1996, 6, 2741-2744.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 2741-2744
-
-
Tercel, M.1
Denny, W.A.2
Wilson, W.R.3
-
23
-
-
0344058160
-
Cytotoxicity and DNA interaction of the enantiomers of 6-amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)carbonyl]indoline (amino-seco-CI-TMI)
-
Gieseg, M. A.; Fan, J.-Y.; Tercel, M.; Tan, K.; Boyd, M.; Denny, W. A. Cytotoxicity and DNA interaction of the enantiomers of 6-amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)carbonyl]indoline (amino-seco-CI-TMI). Manuscript submitted to Chem. Res. Tox.
-
Chem. Res. Tox.
-
-
Gieseg, M.A.1
Fan, J.-Y.2
Tercel, M.3
Tan, K.4
Boyd, M.5
Denny, W.A.6
-
24
-
-
0005867760
-
Coumarones from o-hydroxyaldehydes and bromomalonic ester
-
Tanaka, S. Coumarones from o-hydroxyaldehydes and bromomalonic ester. J. Am. Chem. Soc. 1951, 73, 872.
-
(1951)
J. Am. Chem. Soc.
, vol.73
, pp. 872
-
-
Tanaka, S.1
-
25
-
-
0025037667
-
Topically active carbonic anhydrase inhibitors. 3. Benzofuran-and indole-2-is sulfonamides
-
Graham, S. L.; Hoffman, J. M.; Gautheron, P.; Michelson, S. R.; Scholz, T. H.; Schwam, H.; Shepard, K. L.; Smith, A. M.; Smith, R. L.; Sondey, J. M.; Sugrue, M. F. Topically active carbonic anhydrase inhibitors. 3. Benzofuran-and indole-2-is sulfonamides. J. Med. Chem. 1990, 33, 749-754.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 749-754
-
-
Graham, S.L.1
Hoffman, J.M.2
Gautheron, P.3
Michelson, S.R.4
Scholz, T.H.5
Schwam, H.6
Shepard, K.L.7
Smith, A.M.8
Smith, R.L.9
Sondey, J.M.10
Sugrue, M.F.11
-
26
-
-
0028790373
-
1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indole-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]indole-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
-
27
-
-
0021678633
-
4-iodophenylcholine: A potential myocardial imaging agent
-
Hunter, D. H.; Ponce, Y. Z.; Brown, G. W.; Chamberlain, M. J.; Driedger, A. A.; Morrissey, G. 4-Iodophenylcholine: a potential myocardial imaging agent Can. J. Chem. 1984, 62, 2015-2018.
-
(1984)
Can. J. Chem.
, vol.62
, pp. 2015-2018
-
-
Hunter, D.H.1
Ponce, Y.Z.2
Brown, G.W.3
Chamberlain, M.J.4
Driedger, A.A.5
Morrissey, G.6
-
28
-
-
0000574395
-
Enazides, part 3: Thermolysis of α-azidocinnamates; synthesis of indole derivatives
-
(a) Hemetsberger, H.; Knittel, D.; Weidmann, H. Enazides, Part 3: Thermolysis of α-azidocinnamates; synthesis of indole derivatives. Monatsh. Chem. 1970, 101, 161-165.
-
(1970)
Monatsh. Chem.
, vol.101
, pp. 161-165
-
-
Hemetsberger, H.1
Knittel, D.2
Weidmann, H.3
-
29
-
-
0000070413
-
Improved synthesis of α-azidocinnamates and 2H-azirines
-
(b) Knittel, D. Improved synthesis of α-azidocinnamates and 2H-azirines. Synthesis 1985, 186-188.
-
(1985)
Synthesis
, pp. 186-188
-
-
Knittel, D.1
-
30
-
-
0344489356
-
7-dimethoxyindoles and related compounds
-
Crohare, R.; Merkuza, M.; Gonzalez, H. A.; Ruveda, E. A. 5,7-Dimethoxyindoles and related compounds. Heterocyclic Chem. 1970, 7, 729-732.
-
(1970)
Heterocyclic Chem.
, vol.7
, pp. 729-732
-
-
Crohare, R.1
Merkuza, M.2
Gonzalez, H.A.3
Ruveda, E.A.4
-
31
-
-
0002646326
-
Research in heterocyclic series. VI. Synthesis of nitro derivatives of N-methylpyrrole. Application of polarographic analyses for the separation of nitro isomers
-
Fournari, P. Research in heterocyclic series. VI. Synthesis of nitro derivatives of N-methylpyrrole. Application of polarographic analyses for the separation of nitro isomers. Bull. Soc. Chim. Fr. 1963, 488-491.
-
(1963)
Bull. Soc. Chim. Fr.
, pp. 488-491
-
-
Fournari, P.1
-
32
-
-
0021166371
-
A semiautomated microculture method for investigating growth inhibitory effects of cytotoxic compounds on exponentially growing carcinoma cells
-
Finlay, G. J.; Baguley, B. C.; Wilson, W. R. A semiautomated microculture method for investigating growth inhibitory effects of cytotoxic compounds on exponentially growing carcinoma cells. Anal. Biochem. 1984, 139, 272-277.
-
(1984)
Anal. Biochem.
, vol.139
, pp. 272-277
-
-
Finlay, G.J.1
Baguley, B.C.2
Wilson, W.R.3
-
33
-
-
0024529829
-
Hypoxia-selective antitumor agents. 2. Electronic effects of 4-substituents on the mechanisms of cytotoxicity and metabolic stability of nitracrine derivatives
-
Wilson, W. R.; Thompson, L. H.; Anderson, R. F.; Denny, W. A. Hypoxia-selective antitumor agents. 2. Electronic effects of 4-substituents on the mechanisms of cytotoxicity and metabolic stability of nitracrine derivatives. J. Med. Chem. 1989, 32, 31-38.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 31-38
-
-
Wilson, W.R.1
Thompson, L.H.2
Anderson, R.F.3
Denny, W.A.4
-
34
-
-
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
-
35
-
-
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
-
36
-
-
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
-
37
-
-
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
-
38
-
-
0028100406
-
2 substituent: Validation of a direct relationship between solvolysis and chemical stability and in vitro biological potency
-
2 substituent: validation of a direct relationship between solvolysis and chemical stability and in vitro biological potency. J. Am. Chem. Soc. 1994, 116, 5523-5524.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 5523-5524
-
-
Boger, D.L.1
Yun, W.2
-
39
-
-
0032582736
-
Synthesis and evaluation of a carboxylic analogue of the CC-1065 and duocarmycin alkylating subunits: Role of the vinologous amide and implications on DNA alkylation catalysis
-
(b) Boger, D. L.; Turnbull, P. Synthesis and evaluation of a carboxylic analogue of the CC-1065 and duocarmycin alkylating subunits: role of the vinologous amide and implications on DNA alkylation catalysis. J. Am. Chem. Soc. 1998, 63, 8004-8011.
-
(1998)
J. Am. Chem. Soc.
, vol.63
, pp. 8004-8011
-
-
Boger, D.L.1
Turnbull, P.2
-
40
-
-
0029915634
-
Design, synthesis, cytotoxic properties and preliminary DNA sequencing evaluation of CPI-N-methylpyrrole hybrids. Enhancing effect of a trans double bond linker and role of the terminal amide functionality on cytotoxic potency
-
Wang, Y.; Gupta, R.; Huang, L.; Luo, W.; Lown, J. W. Design, synthesis, cytotoxic properties and preliminary DNA sequencing evaluation of CPI-N-methylpyrrole hybrids. Enhancing effect of a trans double bond linker and role of the terminal amide functionality on cytotoxic potency. Anti-Cancer Drug Design 1996, 11, 15-34.
-
(1996)
Anti-cancer Drug Design
, vol.11
, pp. 15-34
-
-
Wang, Y.1
Gupta, R.2
Huang, L.3
Luo, W.4
Lown, J.W.5
-
41
-
-
0026769197
-
Entry into 6-methoxy-D(+)-tryptophans. Stereospecific synthesis of 1-benzenesylfonyl-6-methoxy-D(+)-tryptophan ethyl ester
-
Allen, M. S.; Hamaker, L. K.; La Loggia, A. J.; Cook, J. M. Entry into 6-Methoxy-D(+)-tryptophans. Stereospecific synthesis of 1-benzenesylfonyl-6-methoxy-D(+)-tryptophan ethyl ester. Synth. Commun. 1992, 22, 2077-2102.
-
(1992)
Synth. Commun.
, vol.22
, pp. 2077-2102
-
-
Allen, M.S.1
Hamaker, L.K.2
La Loggia, A.J.3
Cook, J.M.4
-
42
-
-
0025973098
-
Analogues of the cyclic hydroxamic acid 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one: Decomposition to benzoxazolinones and reaction with β-mercaptoethanol
-
Atkinson, J.; Morand, P.; Arnason, J. T.; Niemeyer, H. M.; Bravo, H. R. Analogues of the cyclic hydroxamic acid 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one: decomposition to benzoxazolinones and reaction with β-mercaptoethanol. J. Org. Chem. 1991, 56, 1788-1800.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 1788-1800
-
-
Atkinson, J.1
Morand, P.2
Arnason, J.T.3
Niemeyer, H.M.4
Bravo, H.R.5
-
43
-
-
0021871658
-
Preparation of 2-iodotryptamine and 2-iodo-5-methoxytryptamine
-
Kline, T. Preparation of 2-iodotryptamine and 2-iodo-5-methoxytryptamine. J. Heterocyclic Chem. 1985, 22, 505-509.
-
(1985)
J. Heterocyclic Chem.
, vol.22
, pp. 505-509
-
-
Kline, T.1
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