-
1
-
-
0024996602
-
Duocarmycin SA, A New Antitumor Antibiotic from Streptomyces sp
-
Ichimura, M.; Ogawa, T.; Takahashi, K.; Kobayashi, E.; Kawamoto, I.; Yasuzawa, T.; Takahashi, I.; Nakano, H. Duocarmycin SA, A New Antitumor Antibiotic From Streptomyces sp J. Antibiot. 1990, 43, 1037-1038
-
(1990)
J. Antibiot.
, vol.43
, pp. 1037-1038
-
-
Ichimura, M.1
Ogawa, T.2
Takahashi, K.3
Kobayashi, E.4
Kawamoto, I.5
Yasuzawa, T.6
Takahashi, I.7
Nakano, H.8
-
2
-
-
0019769681
-
CC-1065 (NSC 298223), A Potent New Antitumor Agent. Improved Production and Isolation, Characterization and Antitumor Activity
-
Martin, D. G.; Biles, C.; Gerpheide, S. A.; Hanka, L. J.; Krueger, W. C.; McGovren, J. P.; Mizsak, S. A.; Neil, G. L.; Stewart, J. C.; Visser, J. CC-1065 (NSC 298223), A Potent New Antitumor Agent. Improved Production and Isolation, Characterization and Antitumor Activity J. Antibiot. 1981, 34, 1119-1125
-
(1981)
J. Antibiot.
, vol.34
, pp. 1119-1125
-
-
Martin, D.G.1
Biles, C.2
Gerpheide, S.A.3
Hanka, L.J.4
Krueger, W.C.5
McGovren, J.P.6
Mizsak, S.A.7
Neil, G.L.8
Stewart, J.C.9
Visser, J.10
-
3
-
-
0024261683
-
Duocarmycin, A New Antitumor Antibiotic from Streptomyces
-
Takahashi, I.; Takahashi, K.; Ichimura, M.; Morimoto, M.; Asano, K.; Kawamoto, I.; Tomita, F.; Nakano, H. Duocarmycin, A New Antitumor Antibiotic From Streptomyces J. Antibiot. 1988, 41, 1915-1917
-
(1988)
J. Antibiot.
, vol.41
, pp. 1915-1917
-
-
Takahashi, I.1
Takahashi, K.2
Ichimura, M.3
Morimoto, M.4
Asano, K.5
Kawamoto, I.6
Tomita, F.7
Nakano, H.8
-
4
-
-
0344837276
-
Yatakemycin, A Novel Antifungal Antibiotic Produced by Streptomyces sp. TP-A0356
-
Igarashi, Y.; Futamata, K.; Fujita, T.; Sekine, A.; Senda, H.; Naoki, H.; Furumai, T. Yatakemycin, A Novel Antifungal Antibiotic Produced by Streptomyces sp. TP-A0356 J. Antibiot. 2003, 56, 107-113
-
(2003)
J. Antibiot.
, vol.56
, pp. 107-113
-
-
Igarashi, Y.1
Futamata, K.2
Fujita, T.3
Sekine, A.4
Senda, H.5
Naoki, H.6
Furumai, T.7
-
5
-
-
0028095610
-
(+)- and ent -(-)-Duocarmycin SA and (+)- and ent -(-)-N-BOC-DSA DNA Alkylation Properties. Alkylation Site Models That 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 (+)- and ent -(-)-N-BOC-DSA DNA Alkylation Properties. Alkylation Site Models That 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
-
6
-
-
0041733260
-
DNA Alkylation Properties of Yatakemycin
-
Parrish, J. P.; Kastrinsky, D. B.; Wolkenberg, S. E.; Igarashi, Y.; Boger, D. L. DNA Alkylation Properties of Yatakemycin J. Am. Chem. Soc. 2003, 125, 10971-10976
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 10971-10976
-
-
Parrish, J.P.1
Kastrinsky, D.B.2
Wolkenberg, S.E.3
Igarashi, Y.4
Boger, D.L.5
-
7
-
-
33644847729
-
Alkylation of Duplex DNA in Nucleosome Core Particles by Duocarmycin SA and Yatakemycin
-
Trzupek, J. D.; Gottesfeld, J. M.; Boger, D. L. Alkylation of Duplex DNA in Nucleosome Core Particles by Duocarmycin SA and Yatakemycin Nat. Chem. Biol. 2006, 2, 79-82
-
(2006)
Nat. Chem. Biol.
, vol.2
, pp. 79-82
-
-
Trzupek, J.D.1
Gottesfeld, J.M.2
Boger, D.L.3
-
8
-
-
34848834561
-
Systematic Exploration of the Structural Features of Yatakemycin Impacting DNA Alkylation and Biological Activity
-
Tichenor, M. S.; MacMillan, K. S.; Trzupek, J. D.; Rayl, T. J.; Hwang, I.; Boger, D. L. Systematic Exploration of the Structural Features of Yatakemycin Impacting DNA Alkylation and Biological Activity J. Am. Chem. Soc. 2007, 129, 10858-10869
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 10858-10869
-
-
Tichenor, M.S.1
MacMillan, K.S.2
Trzupek, J.D.3
Rayl, T.J.4
Hwang, I.5
Boger, D.L.6
-
9
-
-
0024290406
-
Molecular Basis for Sequence-Specific DNA Alkylation by CC-1065
-
Hurley, L. H.; Lee, C.-S.; McGovren, J. P.; Warpehoski, M. A.; Mitchell, M. A.; Kelly, R. C.; Aristoff, P. A. Molecular Basis for Sequence-Specific DNA Alkylation by CC-1065 Biochemistry 1988, 27, 3886-3892
-
(1988)
Biochemistry
, vol.27
, pp. 3886-3892
-
-
Hurley, L.H.1
Lee, C.-S.2
McGovren, J.P.3
Warpehoski, M.A.4
Mitchell, M.A.5
Kelly, R.C.6
Aristoff, P.A.7
-
10
-
-
0028376605
-
Molecular Basis for Sequence Selective DNA Alkylation by (+)- and ent -(-)-CC-1065 and Related Agents: Alkylation Site Models that Accommodate the Offset AT-Rich Adenine N3 Alkylation Selectivity
-
Boger, D. L.; Johnson, D. S.; Yun, W.; Tarby, C. M. Molecular Basis for Sequence Selective DNA Alkylation by (+)- and ent -(-)-CC-1065 and Related Agents: Alkylation Site Models that Accommodate the Offset AT-Rich Adenine N3 Alkylation Selectivity Bioorg. Med. Chem. 1994, 2, 115-135
-
(1994)
Bioorg. Med. Chem.
, vol.2
, pp. 115-135
-
-
Boger, D.L.1
Johnson, D.S.2
Yun, W.3
Tarby, C.M.4
-
11
-
-
0025900895
-
(+)-CC-1065-DNA Alkylation: Key Studies Demonstrating a Noncovalent Binding Selectivity Contribution to the Alkylation Selectivity
-
Boger, D. L.; Munk, S. A.; Zarrinmayeh, H. (+)-CC-1065-DNA Alkylation: Key Studies Demonstrating a Noncovalent Binding Selectivity Contribution to the Alkylation Selectivity J. Am. Chem. Soc. 1991, 113, 3980-3983
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 3980-3983
-
-
Boger, D.L.1
Munk, S.A.2
Zarrinmayeh, H.3
-
12
-
-
0026092765
-
Demonstration of a Pronounced Effect of Noncovalent Binding Selectivity on the (+)-CC-1065 DNA Alkylation and Identification of the Pharmacophore of the Alkylation Subunit
-
Boger, D. L.; Zarrinmayeh, H.; Munk, S. A.; Kitos, P. A.; Suntornwat, O. Demonstration of a Pronounced Effect of Noncovalent Binding Selectivity on the (+)-CC-1065 DNA Alkylation and Identification of the Pharmacophore of the Alkylation Subunit Proc. Natl. Acad. Sci. U.S.A 1991, 88, 1431-1435
-
(1991)
Proc. Natl. Acad. Sci. U.S.A
, vol.88
, pp. 1431-1435
-
-
Boger, D.L.1
Zarrinmayeh, H.2
Munk, S.A.3
Kitos, P.A.4
Suntornwat, O.5
-
13
-
-
0025111222
-
3. Preparation of Key Partial Structures and Definition of an Additional Functional Role of the CC-1065 Central and Right-Hand Subunits
-
3. Preparation of Key Partial Structures and Definition of an Additional Functional Role of the CC-1065 Central and Right-Hand Subunits J. Am. Chem. Soc. 1990, 112, 4623-4632
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 4623-4632
-
-
Boger, D.L.1
Coleman, R.S.2
Invergo, B.J.3
Sakya, S.M.4
Ishizaki, T.5
Munk, S.A.6
Zarrinmayeh, H.7
Kitos, P.A.8
Thompson, S.C.9
-
14
-
-
0025900895
-
(+)-CC-1065 DNA Alkylation: Key Studies Demonstrating a Noncovalent Binding Selectivity Contribution to the Alkylation Selectivity
-
Boger, D. L.; Munk, S. A.; Zarrinmayeh, H. (+)-CC-1065 DNA Alkylation: Key Studies Demonstrating a Noncovalent Binding Selectivity Contribution to the Alkylation Selectivity J. Am. Chem. Soc. 1991, 113, 3980-3983
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 3980-3983
-
-
Boger, D.L.1
Munk, S.A.2
Zarrinmayeh, H.3
-
15
-
-
0025644317
-
Duocarmycin-Pyrindamycin DNA Alkylation Properties and Identification, Synthesis, and Evaluation of Agents Incorporating the Pharmacophore of the Duocarmycin-Pyrindamycin Alkylation 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 Alkylation 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
-
16
-
-
0025773799
-
Isolation and Characterization of the Duocarmycin-Adenine DNA Adduct
-
Boger, D. L.; Ishizaki, T.; Zarrinmayeh, H. Isolation and Characterization of the Duocarmycin-Adenine DNA Adduct J. Am. Chem. Soc. 1991, 113, 6645-6649
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6645-6649
-
-
Boger, D.L.1
Ishizaki, T.2
Zarrinmayeh, H.3
-
17
-
-
0026646153
-
DNA Alkylation Properties of the Duocarmycins: (+)-Duocarmycin A, epi -(+)-Duocarmycin A, ent -(-)-Duocarmycin A and epi, ent -(-)-Duocarmycin A
-
Boger, D. L.; Yun, W.; Terashima, S.; Fukuda, Y.; Nakatani, K.; Kitos, P. A.; Jin, Q. DNA Alkylation Properties of the Duocarmycins: (+)-Duocarmycin A, epi -(+)-Duocarmycin A, ent -(-)-Duocarmycin A and epi, ent -(-)-Duocarmycin A Bioorg. Med. Chem. Lett. 1992, 2, 759-765
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 759-765
-
-
Boger, D.L.1
Yun, W.2
Terashima, S.3
Fukuda, Y.4
Nakatani, K.5
Kitos, P.A.6
Jin, Q.7
-
18
-
-
0027367893
-
Reversibility of the Duocarmycin A and SA DNA Alkylation Reaction
-
Boger, D. L.; Yun, W. Reversibility of the Duocarmycin A and SA DNA Alkylation Reaction J. Am. Chem. Soc. 1993, 115, 9872-9873
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9872-9873
-
-
Boger, D.L.1
Yun, W.2
-
19
-
-
0025021874
-
A Demonstration of the Intrinsic Importance of Stabilizing Hydrophobic Binding and Noncovalent van der Waals Contacts Dominant in the Noncovalent CC-1065/B-DNA Binding
-
Boger, D. L.; Invergo, B. J.; Coleman, R. S.; Zarrinmayeh, H.; Kitos, P. A.; Thompson, S. C.; Leong, T.; McLaughlin, L. W. A Demonstration of the Intrinsic Importance of Stabilizing Hydrophobic Binding and Noncovalent van der Waals Contacts Dominant in the Noncovalent CC-1065/B-DNA Binding Chem.-Biol. Interact. 1990, 73, 29-52
-
(1990)
Chem.-Biol. Interact.
, vol.73
, pp. 29-52
-
-
Boger, D.L.1
Invergo, B.J.2
Coleman, R.S.3
Zarrinmayeh, H.4
Kitos, P.A.5
Thompson, S.C.6
Leong, T.7
McLaughlin, L.W.8
-
20
-
-
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
-
21
-
-
0002631330
-
The Duocarmycins: Synthetic and Mechanistic Studies
-
Boger, D. L. The Duocarmycins: Synthetic and Mechanistic Studies Acc. Chem. Res. 1995, 28, 20-29
-
(1995)
Acc. Chem. Res.
, vol.28
, pp. 20-29
-
-
Boger, D.L.1
-
22
-
-
0029053550
-
CC-1065 and the Duocarmycins: Unraveling the Keys to a New Class of Naturally Derived DNA Alkylating Agents
-
Boger, D. L.; Johnson, D. S. CC-1065 and the Duocarmycins: Unraveling the Keys to a New Class of Naturally Derived DNA Alkylating Agents Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 3642-3649
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 3642-3649
-
-
Boger, D.L.1
Johnson, D.S.2
-
23
-
-
0033377095
-
Shape-Dependent Catalysis: Insights into the Source of Catalysis for the CC-1065 and Duocarmycin DNA Alkylation Reaction
-
Boger, D. L.; Garbaccio, R. M. Shape-Dependent Catalysis: Insights into the Source of Catalysis for the CC-1065 and Duocarmycin DNA Alkylation Reaction Acc. Chem. Res. 1999, 32, 1043-1052
-
(1999)
Acc. Chem. Res.
, vol.32
, pp. 1043-1052
-
-
Boger, D.L.1
Garbaccio, R.M.2
-
24
-
-
41749095626
-
Yatakemycin: Total Synthesis, DNA Alkylation, and Biological Properties
-
Tichenor, M. S.; Boger, D. L. Yatakemycin: Total Synthesis, DNA Alkylation, and Biological Properties Natural Prod. Rep 2008, 25, 220-226
-
(2008)
Natural Prod. Rep
, vol.25
, pp. 220-226
-
-
Tichenor, M.S.1
Boger, D.L.2
-
25
-
-
70349641991
-
Fundamental Relationships between Structure, Reactivity, and Biological Activity for the Duocarmycins and CC-1065
-
MacMillan, K. S.; Boger, D. L. Fundamental Relationships Between Structure, Reactivity, and Biological Activity for the Duocarmycins and CC-1065 J. Med. Chem. 2009, 52, 5771-5780
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5771-5780
-
-
MacMillan, K.S.1
Boger, D.L.2
-
26
-
-
0036015565
-
Duocarmycins: Nature's Prodrugs?
-
Searcey, M. Duocarmycins: Nature's Prodrugs? Curr. Pharm. Des 2002, 8, 1375-1389
-
(2002)
Curr. Pharm. des
, vol.8
, pp. 1375-1389
-
-
Searcey, M.1
-
27
-
-
10644249279
-
Sequence-Selective DNA Recognition: Natural Products and Nature's Lessons
-
Tse, W. C.; Boger, D. L. Sequence-Selective DNA Recognition: Natural Products and Nature's Lessons Chem. Biol. 2004, 11, 1607-1617
-
(2004)
Chem. Biol.
, vol.11
, pp. 1607-1617
-
-
Tse, W.C.1
Boger, D.L.2
-
28
-
-
0023858516
-
Total Synthesis of (+)-CC-1065 and ent -(-)-CC-1065
-
Boger, D. L.; Coleman, R. S. Total Synthesis of (+)-CC-1065 and ent -(-)-CC-1065 J. Am. Chem. Soc. 1988, 110, 1321-1323
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 1321-1323
-
-
Boger, D.L.1
Coleman, R.S.2
-
30
-
-
0027067027
-
Total Synthesis of (+)-Duocarmycin SA
-
Boger, D. L.; Machiya, K. Total Synthesis of (+)-Duocarmycin SA J. Am. Chem. Soc. 1992, 114, 10056-10058
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10056-10058
-
-
Boger, D.L.1
MacHiya, K.2
-
31
-
-
0027442101
-
Total Synthesis and Preliminary Evaluation of (+)- and ent -(-)-Duocarmycin SA
-
Boger, D. L.; Machiya, K.; Hertzog, D. L.; Kitos, P. A.; Holmes, D. Total Synthesis and Preliminary Evaluation of (+)- and ent -(-)-Duocarmycin SA J. Am. Chem. Soc. 1993, 115, 9025-9036
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 9025-9036
-
-
Boger, D.L.1
MacHiya, K.2
Hertzog, D.L.3
Kitos, P.A.4
Holmes, D.5
-
32
-
-
0029871620
-
Enantioselective Total Synthesis of (+)-Duocarmycin A, epi -(+)-Duocarmycin A, and Their Unnatural Enantiomers
-
Boger, D. L.; McKie, J. A.; Nishi, T.; Ogiku, T. Enantioselective Total Synthesis of (+)-Duocarmycin A, epi -(+)-Duocarmycin A, and Their Unnatural Enantiomers J. Am. Chem. Soc. 1996, 118, 2301-2302
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 2301-2302
-
-
Boger, D.L.1
McKie, J.A.2
Nishi, T.3
Ogiku, T.4
-
33
-
-
0031055494
-
Total Synthesis of (+)-Duocarmycin A and epi -(+)-Duocarmycin A and Their Unnatural Enantiomers: Assessment of Chemical and Biological Properties
-
Boger, D. L.; McKie, J. A.; Nishi, T.; Ogiku, T. Total Synthesis of (+)-Duocarmycin A and epi -(+)-Duocarmycin A and Their Unnatural Enantiomers: Assessment of Chemical and Biological Properties J. Am. Chem. Soc. 1997, 119, 311-325
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 311-325
-
-
Boger, D.L.1
McKie, J.A.2
Nishi, T.3
Ogiku, T.4
-
34
-
-
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
-
35
-
-
3142723437
-
Total Synthesis, Structure Revision, and Absolute Configuration of (+)-Yatakemycin
-
Tichenor, M. S.; Kastrinsky, D. B.; Boger, D. L. Total Synthesis, Structure Revision, and Absolute Configuration of (+)-Yatakemycin J. Am. Chem. Soc. 2004, 126, 8396-8398
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8396-8398
-
-
Tichenor, M.S.1
Kastrinsky, D.B.2
Boger, D.L.3
-
36
-
-
33845402161
-
Asymmetric Total Synthesis of (+)- and ent -(-)-Yatakemycin and Duocarmycin SA. Evaluation of Yatakemycin Key Partial Structures and Its Unnatural Enantiomer
-
Tichenor, M. S.; Trzupek, J. D.; Kastrinsky, D. B.; Shiga, F.; Hwang, I.; Boger, D. L. Asymmetric Total Synthesis of (+)- and ent -(-)-Yatakemycin and Duocarmycin SA. Evaluation of Yatakemycin Key Partial Structures and Its Unnatural Enantiomer J. Am. Chem. Soc. 2006, 128, 15683-15696
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 15683-15696
-
-
Tichenor, M.S.1
Trzupek, J.D.2
Kastrinsky, D.B.3
Shiga, F.4
Hwang, I.5
Boger, D.L.6
-
37
-
-
61749099637
-
Total Synthesis and Evaluation of iso -Duocarmycin SA and iso -Yatakemycin
-
MacMillan, K. S.; Nguyen, T.; Hwang, I.; Boger, D. L. Total Synthesis and Evaluation of iso -Duocarmycin SA and iso -Yatakemycin J. Am. Chem. Soc. 2009, 131, 1187-1194
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 1187-1194
-
-
MacMillan, K.S.1
Nguyen, T.2
Hwang, I.3
Boger, D.L.4
-
38
-
-
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
-
39
-
-
0030904168
-
Reversed and Sandwiched Analogs of Duocarmycin SA: Establishment of the Origin of the Sequence-Selective Alkylation of DNA and New Insights into the Source of Catalysis
-
Boger, D. L.; Bollinger, B.; Hertzog, D. L.; Johnson, D. S.; Cai, H.; Mesini, P.; Garbaccio, R. M.; Jin, Q.; Kitos, P. A. Reversed and Sandwiched Analogs of Duocarmycin SA: Establishment of the Origin of the Sequence-Selective Alkylation of DNA and New Insights into the Source of Catalysis J. Am. Chem. Soc. 1997, 119, 4987-4998
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 4987-4998
-
-
Boger, D.L.1
Bollinger, B.2
Hertzog, D.L.3
Johnson, D.S.4
Cai, H.5
Mesini, P.6
Garbaccio, R.M.7
Jin, Q.8
Kitos, P.A.9
-
40
-
-
0031081549
-
Catalysis of the CC-1065 and Duocarmycin DNA Alkylation Reaction: DNA 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: DNA 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
-
41
-
-
0024393748
-
2: CC-1065 Functional Agents Incorporating the Equivalent 1,2,9,9a-Tetrahydrocyclopropa[1,2- c ]benz[1,2- e ]indol-4-one (CBI) Left-Hand Subunit
-
2: CC-1065 Functional Agents Incorporating the Equivalent 1,2,9,9a-Tetrahydrocyclopropa[1,2- c ]benz[1,2- e ]indol-4-one (CBI) Left-Hand Subunit J. Am. Chem. Soc. 1989, 111, 6461-6463
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 6461-6463
-
-
Boger, D.L.1
Ishizaki, T.2
Wysocki Jr., R.J.3
Munk, S.A.4
Kitos, P.A.5
Suntornwat, O.6
-
42
-
-
0025119357
-
2: Enhanced Functional Analogs of CC-1065 Incorporating the 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI) Left-Hand Subunit
-
2: Enhanced Functional Analogs 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
-
43
-
-
0025099719
-
2: Enhanced Functional Analogs of (+)-CC-1065. A Critical Appraisal of a Proposed Relationship between Electrophile Reactivity, DNA Binding Properties, and Cytotoxic Potency
-
2: Enhanced Functional Analogs of (+)-CC-1065. A Critical Appraisal of a Proposed Relationship Between Electrophile Reactivity, DNA Binding Properties, and Cytotoxic Potency Tetrahedron Lett. 1990, 31, 793-796
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 793-796
-
-
Boger, D.L.1
Ishizaki, T.2
-
44
-
-
0025907919
-
A Potent, Simple Derivative of an Analog of the CC-1065 Alkylation Subunit
-
Boger, D. L.; Ishizaki, T.; Zarrinmayeh, H.; Kitos, P. A.; Suntornwat, O. A Potent, Simple Derivative of an Analog of the CC-1065 Alkylation Subunit Bioorg. Med. Chem. Lett. 1991, 1, 55-58
-
(1991)
Bioorg. Med. Chem. Lett.
, vol.1
, pp. 55-58
-
-
Boger, D.L.1
Ishizaki, T.2
Zarrinmayeh, H.3
Kitos, P.A.4
Suntornwat, O.5
-
45
-
-
11944251378
-
DNA Alkylation Properties of Enhanced Functional Analogs of CC-1065 Incorporating the 1,2,9,9a-Tetrahydrocyclopropa[1,2- c ]benz[1,2- e ]indol-4-one (CBI) Alkylation Subunit
-
Boger, D. L.; Munk, S. A. DNA Alkylation Properties of Enhanced Functional Analogs of CC-1065 Incorporating the 1,2,9,9a-Tetrahydrocyclopropa[1, 2- c ]benz[1,2- e ]indol-4-one (CBI) Alkylation Subunit J. Am. Chem. Soc. 1992, 114, 5487-5496
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 5487-5496
-
-
Boger, D.L.1
Munk, S.A.2
-
46
-
-
0028100406
-
2 Substituent: Validation of a Direct Relationship between Solvolysis Chemical Stability and in vitro Biological Potency
-
2 Substituent: Validation of a Direct Relationship Between Solvolysis 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
-
47
-
-
0029065554
-
1: CC-1065 Analogs Containing Deep-Seated Modifications in the DNA Binding Subunit
-
1: CC-1065 Analogs Containing Deep-Seated Modifications in the DNA Binding Subunit Bioorg. Med. Chem. 1995, 3, 761-775
-
(1995)
Bioorg. Med. Chem.
, vol.3
, pp. 761-775
-
-
Boger, D.L.1
Yun, W.2
Cai, H.3
Han, N.4
-
48
-
-
0028036453
-
CBI-TMI: Synthesis and Evaluation of a Key Analog of the Duocarmycins. Validation of a Direct Relationship between Chemical Solvolytic Stability and Cytotoxic Potency and Confirmation of the Structural Features Responsible for the Distinguishing Behavior of Enantiomeric Pairs of Agents
-
Boger, D. L.; Yun, W. CBI-TMI: Synthesis and Evaluation of a Key Analog of the Duocarmycins. Validation of a Direct Relationship between Chemical Solvolytic Stability and Cytotoxic Potency and Confirmation of the Structural Features Responsible for the Distinguishing Behavior 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
-
49
-
-
0043123409
-
Establishment of Substituent Effects in the DNA Binding Subunit of CBI Analogues of the Duocarmycins and CC-1065
-
Parrish, J. P.; Katrinsky, D. B.; Stauffer, F.; Hedrick, M. P.; Hwang, I.; Boger, D. L. Establishment of Substituent Effects in the DNA Binding Subunit of CBI Analogues of the Duocarmycins and CC-1065 Bioorg. Med. Chem. 2003, 11, 3815-3838
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 3815-3838
-
-
Parrish, J.P.1
Katrinsky, D.B.2
Stauffer, F.3
Hedrick, M.P.4
Hwang, I.5
Boger, D.L.6
-
50
-
-
0025045711
-
Synthesis of N-(Phenylsulfonyl)-CI, N-(tert-Butyloxy carbonyl-CI, CI-CDPI1, and CI-CDPI2: CC-1065 Functional Analogs Incorporating the Parent 1,2,7,7a-Tetrahydrocycloprop[1,2- c ]indol-4-one (CI) Left-Hand Subunit
-
Boger, D. L.; Wysocki, R. J.; Ishizaki, T. Synthesis of N-(Phenylsulfonyl)-CI, N-(tert-Butyloxy carbonyl-CI, CI-CDPI1, and CI-CDPI2: CC-1065 Functional Analogs Incorporating the Parent 1,2,7,7a- Tetrahydrocycloprop[1,2- c ]indol-4-one (CI) Left-Hand Subunit J. Am. Chem. Soc. 1990, 112, 5230-5240
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 5230-5240
-
-
Boger, D.L.1
Wysocki, R.J.2
Ishizaki, T.3
-
51
-
-
0026638104
-
An Improved Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI): A Simplified Analog of the CC-1065 Alkylation Subunit
-
Boger, D. L.; Yun, W.; Teegarden, B. R. An Improved Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI): A Simplified Analog of the CC-1065 Alkylation Subunit J. Org. Chem. 1992, 57, 2873-2876
-
(1992)
J. Org. Chem.
, vol.57
, pp. 2873-2876
-
-
Boger, D.L.1
Yun, W.2
Teegarden, B.R.3
-
52
-
-
0028920020
-
An Efficient Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI): An Enhanced and Simplified Analog of the CC-1065 and Duocarmycin Alkylation Subunits
-
Boger, D. L.; McKie, J. A. An Efficient Synthesis of 1,2,9,9a- Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI): An Enhanced and Simplified Analog of the CC-1065 and Duocarmycin Alkylation Subunits J. Org. Chem. 1995, 60, 1271-1275
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1271-1275
-
-
Boger, D.L.1
McKie, J.A.2
-
53
-
-
0002617056
-
Asymmetric Synthesis of the 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI) Alkylation Subunit of CC-1065 and Duocarmycin Analogues
-
Boger, D. L.; McKie, J. A.; Boyce, C. W. Asymmetric Synthesis of the 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI) Alkylation Subunit of CC-1065 and Duocarmycin Analogues Synlett 1997, 515-517
-
(1997)
Synlett
, pp. 515-517
-
-
Boger, D.L.1
McKie, J.A.2
Boyce, C.W.3
-
54
-
-
1842505068
-
Effective Asymmetric Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ e ]benz[ e ]indol-4-one (CBI)
-
Kastrinsky, D. B.; Boger, D. L. Effective Asymmetric Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ e ]benz[ e ]indol-4-one (CBI) J. Org. Chem. 2004, 69, 2284-2289
-
(2004)
J. Org. Chem.
, vol.69
, pp. 2284-2289
-
-
Kastrinsky, D.B.1
Boger, D.L.2
-
55
-
-
78651499016
-
Asymmetric Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI)
-
Lajiness, J. P.; Boger, D. L. Asymmetric Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI) J. Org. Chem. 2010, 76, 583-587
-
(2010)
J. Org. Chem.
, vol.76
, pp. 583-587
-
-
Lajiness, J.P.1
Boger, D.L.2
-
56
-
-
0025732318
-
A Photochemically Based Synthesis of the Benzannelated Analog of the CC-1065 A Unit
-
Drost, K. J.; Cava, M. P. A Photochemically Based Synthesis of the Benzannelated Analog of the CC-1065 A Unit J. Org. Chem. 1991, 56, 2240-2244
-
(1991)
J. Org. Chem.
, vol.56
, pp. 2240-2244
-
-
Drost, K.J.1
Cava, M.P.2
-
57
-
-
0026677093
-
Synthesis of CBI-PDE-I-Dimer, the Benzannelated Analog of CC-1065
-
Aristoff, P. A.; Johnson, P. D. Synthesis of CBI-PDE-I-Dimer, the Benzannelated Analog of CC-1065 J. Org. Chem. 1992, 57, 6234-6239
-
(1992)
J. Org. Chem.
, vol.57
, pp. 6234-6239
-
-
Aristoff, P.A.1
Johnson, P.D.2
-
58
-
-
0028009270
-
Total Synthesis and Biological Properties of Novel Antineoplastic (Chloromethyl)furanoindolines. An Asymmetric Hydroboration Mediated Synthesis of the Alkylation Subunits
-
Mohamadi, F.; Speez, M. M.; Staten, G. S.; Marder, P.; Kipka, J. K.; Johnson, D. A.; Boger, D. L.; Zarrinmayeh, H. Total Synthesis and Biological Properties of Novel Antineoplastic (Chloromethyl)furanoindolines. An Asymmetric Hydroboration Mediated Synthesis of the Alkylation Subunits J. Med. Chem. 1994, 37, 232-239
-
(1994)
J. Med. Chem.
, vol.37
, pp. 232-239
-
-
Mohamadi, F.1
Speez, M.M.2
Staten, G.S.3
Marder, P.4
Kipka, J.K.5
Johnson, D.A.6
Boger, D.L.7
Zarrinmayeh, H.8
-
59
-
-
0031323470
-
A Practical Route to Optically Active CBI, A Potent Analog of the CC-1065 Alkylation Subunit
-
Ling, L.; Xie, Y.; Lown, J. W. A Practical Route to Optically Active CBI, A Potent Analog of the CC-1065 Alkylation Subunit Heterocycl. Commun. 1997, 3, 405-408
-
(1997)
Heterocycl. Commun.
, vol.3
, pp. 405-408
-
-
Ling, L.1
Xie, Y.2
Lown, J.W.3
-
60
-
-
0028790373
-
1,2,9,9a-Tetrahydrocyclopropa[ c ]benz[ e ]indol-4-one (CBI) Analogs 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) Analogs 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
-
61
-
-
0025891696
-
2: An Enhanced Functional Analog of CC-1065
-
2: An Enhanced Functional Analog of CC-1065 Bioorg. Med. Chem. Lett. 1991, 1, 115-120
-
(1991)
Bioorg. Med. Chem. Lett.
, vol.1
, pp. 115-120
-
-
Boger, D.L.1
Ishizaki, T.2
Sakya, S.3
Munk, S.A.4
Kitos, P.A.5
Jin, Q.6
Besterman, J.M.7
-
62
-
-
0026786973
-
Cytotoxicity and Antitumor Activity of Carzelesin, a Prodrug Cyclopropylpyrroloindole Analogue
-
Li, L.; 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.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
-
63
-
-
0032101165
-
Comparative Pharmacology of the Novel Cyclopropylpyrroloindole-Prodrug Carzelesin in Mice, Rats, and Humans
-
van Tellingen, O.; Nooijen, W. J.; Schaaf, L. J.; van der Valk, M.; van Asperen, J.; Henrar, R. E. C.; Beijnen, J H. Comparative Pharmacology of the Novel Cyclopropylpyrroloindole-Prodrug Carzelesin in Mice, Rats, and Humans Cancer Res. 1998, 58, 2410-2416
-
(1998)
Cancer Res.
, vol.58
, pp. 2410-2416
-
-
Van Tellingen, O.1
Nooijen, W.J.2
Schaaf, L.J.3
Van Der Valk, M.4
Van Asperen, J.5
Henrar, R.E.C.6
Beijnen, J.H.7
-
64
-
-
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
-
65
-
-
0028840445
-
Synthesis and Antitumor Activity of Duocarmycin Derivatives
-
Nagamura, S.; Kanda, Y.; Kobayashi, E.; Gomi, K.; Saito, H. Synthesis and Antitumor Activity of Duocarmycin Derivatives Chem. Pharm. Bull. 1995, 43, 1530-1535
-
(1995)
Chem. Pharm. Bull.
, vol.43
, pp. 1530-1535
-
-
Nagamura, S.1
Kanda, Y.2
Kobayashi, E.3
Gomi, K.4
Saito, H.5
-
66
-
-
0032813670
-
CBI Prodrug Analogs of CC-1065 and the Duocarmycins
-
Boger, D. L.; Boyce, C. W.; Garbaccio, R. M.; Searcey, M.; Jin, Q. CBI Prodrug Analogs of CC-1065 and the Duocarmycins Synthesis 1999, 1505-1509
-
(1999)
Synthesis
, pp. 1505-1509
-
-
Boger, D.L.1
Boyce, C.W.2
Garbaccio, R.M.3
Searcey, M.4
Jin, Q.5
-
67
-
-
33750083620
-
Synthesis and Antitumor Activity of CBI-Bearing Ester and Carbamate Prodrugs of CC-1065
-
Wang, Y.; Li, L.; Tian, Z.; Jiang, W.; Larrick, J. Synthesis and Antitumor Activity of CBI-Bearing Ester and Carbamate Prodrugs of CC-1065 Bioorg. Med. Chem. 2006, 14, 7854-7861
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 7854-7861
-
-
Wang, Y.1
Li, L.2
Tian, Z.3
Jiang, W.4
Larrick, J.5
-
68
-
-
65249102262
-
Studies Toward the Duocarmycin Prodrugs for the Antibody Prodrug Therapy Approach
-
Li, L. S.; Sinha, S. C. Studies Toward the Duocarmycin Prodrugs for the Antibody Prodrug Therapy Approach Tetrahedron Lett. 2009, 50, 2932-2935
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 2932-2935
-
-
Li, L.S.1
Sinha, S.C.2
-
69
-
-
84863084739
-
A Novel, Unusually Efficacious Duocarmycin Carbamate Prodrug that Releases No Residual Byproduct
-
Wolfe, A. L.; Duncan, K. K.; Parelkar, N. K.; Weir, S. J.; Vielhauer, G. A.; Boger, D. L. A Novel, Unusually Efficacious Duocarmycin Carbamate Prodrug that Releases No Residual Byproduct J. Med. Chem. 2012, 55, 5878-5886
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5878-5886
-
-
Wolfe, A.L.1
Duncan, K.K.2
Parelkar, N.K.3
Weir, S.J.4
Vielhauer, G.A.5
Boger, D.L.6
-
70
-
-
0034945043
-
A Strategy for Tumor-Selective Chemotherapy by Enzymatic Liberation of seco-duocarmycin SA-derivatives from Nontoxic Prodrugs
-
Tietze, L. F.; Lieb, M.; Herzig, T.; Haunert, F.; Schuberth, I. A Strategy for Tumor-Selective Chemotherapy by Enzymatic Liberation of seco-duocarmycin SA-derivatives from Nontoxic Prodrugs Bioorg. Med. Chem. 2001, 9, 1929-1939
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 1929-1939
-
-
Tietze, L.F.1
Lieb, M.2
Herzig, T.3
Haunert, F.4
Schuberth, I.5
-
71
-
-
33749843662
-
Antitumor Agents: Development of Highly Potent Glycosidic Duocarmycin Analogues for Selective Cancer Therapy
-
Tietze, L. F.; Major, F.; Schuberth, I. Antitumor Agents: Development of Highly Potent Glycosidic Duocarmycin Analogues for Selective Cancer Therapy Angew. Chem., Int. Ed. 2006, 45, 6574-6577
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 6574-6577
-
-
Tietze, L.F.1
Major, F.2
Schuberth, I.3
-
72
-
-
44649194513
-
Duocarmycin-based Prodrugs for Cancer Prodrug Monotherapy
-
Tietze, L. F.; Schuster, H. J.; Schmuck, K.; Schuberth, I.; Alves, F. Duocarmycin-based Prodrugs for Cancer Prodrug Monotherapy Bioorg. Med. Chem. 2008, 16, 6312-6318
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 6312-6318
-
-
Tietze, L.F.1
Schuster, H.J.2
Schmuck, K.3
Schuberth, I.4
Alves, F.5
-
73
-
-
0344118703
-
Synthesis and Evaluation of Nitroheterocyclic Carbamate Prodrugs for Use with Nitroreductase-Mediated Gene-Directed Enzyme Prodrug Therapy
-
Hay, M. P.; Anderson, R. F.; Ferry, D. M.; Wilson, W. R.; Denny, W. A. Synthesis and Evaluation of Nitroheterocyclic Carbamate Prodrugs for Use with Nitroreductase-Mediated Gene-Directed Enzyme Prodrug Therapy J. Med. Chem. 2003, 46, 5533-5545
-
(2003)
J. Med. Chem.
, vol.46
, pp. 5533-5545
-
-
Hay, M.P.1
Anderson, R.F.2
Ferry, D.M.3
Wilson, W.R.4
Denny, W.A.5
-
74
-
-
0033516908
-
A 2-Nitroimidazole Carbamate Prodrug of 5-Amino-1-(chloromethyl)-3-[(5,6, 7-trimethoxyindol-2-yl)carbonyl]-1,2-dihydro-3 H -benz[ e ]indole (Amino-seco-CBI-TMI) for Use with ADEPT and GDEPT
-
Hay, M. P.; Sykes, B. M.; Denny, W. A.; Wilson, W. R. A 2-Nitroimidazole Carbamate Prodrug of 5-Amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl) carbonyl]-1,2-dihydro-3 H -benz[ e ]indole (Amino-seco-CBI-TMI) for Use With ADEPT and GDEPT Bioorg. Med. Chem. Lett. 1999, 9, 2237-2242
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2237-2242
-
-
Hay, M.P.1
Sykes, B.M.2
Denny, W.A.3
Wilson, W.R.4
-
75
-
-
79952253984
-
Selective Treatment of Hypoxic Tumor Cells in Vivo: Phosphate Pre-Prodrugs of Nitro Analogues of the Duocarmycins
-
Tercel, M.; Atwell, G. J.; Yang, S.; Ashoorzadeh, A.; Stevenson, R. J.; Botting, K. J.; Gu, Y.; Mehta, S. Y.; Denny, W. A.; Wilson, W. R.; Pruijn, F. B. Selective Treatment of Hypoxic Tumor Cells In Vivo: Phosphate Pre-Prodrugs of Nitro Analogues of the Duocarmycins Angew. Chem., Int. Ed. 2011, 50, 2606-2609
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 2606-2609
-
-
Tercel, M.1
Atwell, G.J.2
Yang, S.3
Ashoorzadeh, A.4
Stevenson, R.J.5
Botting, K.J.6
Gu, Y.7
Mehta, S.Y.8
Denny, W.A.9
Wilson, W.R.10
Pruijn, F.B.11
-
76
-
-
0036437483
-
Investigation of a Novel Reductively-Activatable Anticancer Prodrug of seco -CBI-TMI, an Analog of Duocarmycin SA
-
Townes, H.; Summerville, K.; Purnell, B.; Hooker, M.; Madsen, E.; Hudson, S.; Lee, M. Investigation of a Novel Reductively-Activatable Anticancer Prodrug of seco -CBI-TMI, an Analog of Duocarmycin SA Med. Chem. Res. 2002, 11, 248-253
-
(2002)
Med. Chem. Res.
, vol.11
, pp. 248-253
-
-
Townes, H.1
Summerville, K.2
Purnell, B.3
Hooker, M.4
Madsen, E.5
Hudson, S.6
Lee, M.7
-
77
-
-
0033615631
-
A Novel Class of CC-1065 and Duocarmycin Analogues Subject to Mitomycin-Related Reductive Activation
-
Boger, D. L.; Garbaccio, R. M. A Novel Class of CC-1065 and Duocarmycin Analogues Subject to Mitomycin-Related Reductive Activation J. Org. Chem. 1999, 64, 8350-8362
-
(1999)
J. Org. Chem.
, vol.64
, pp. 8350-8362
-
-
Boger, D.L.1
Garbaccio, R.M.2
-
78
-
-
84856373074
-
Synthesis and Biological Evaluation of Antibody Conjugates of Phosphate Prodrugs of Cytotoxic DNA Alkylators for the Targeted Treatment of Cancer
-
Zhao, R. H.; Erickson, H. K.; Leece, B. A.; Reid, E. E.; Goldmacher, V. S.; Lambert, J. M.; Chari, R. V. J. Synthesis and Biological Evaluation of Antibody Conjugates of Phosphate Prodrugs of Cytotoxic DNA Alkylators for the Targeted Treatment of Cancer J. Med. Chem. 2012, 55, 766-782
-
(2012)
J. Med. Chem.
, vol.55
, pp. 766-782
-
-
Zhao, R.H.1
Erickson, H.K.2
Leece, B.A.3
Reid, E.E.4
Goldmacher, V.S.5
Lambert, J.M.6
Chari, R.V.J.7
-
79
-
-
80155209663
-
Modification of the Duocarmycin Pharmacophore Enables CYP1A1 Targeting for Biological Activity
-
Pors, K.; Loadman, P. M.; Shnyder, S. D.; Sutherland, M.; Sheldrake, H. M.; Guino, M.; Kiakos, K.; Hartley, J. A.; Searcey, M.; Patterson, L. H. Modification of the Duocarmycin Pharmacophore Enables CYP1A1 Targeting for Biological Activity Chem. Commun. 2011, 47, 12062-12064
-
(2011)
Chem. Commun.
, vol.47
, pp. 12062-12064
-
-
Pors, K.1
Loadman, P.M.2
Shnyder, S.D.3
Sutherland, M.4
Sheldrake, H.M.5
Guino, M.6
Kiakos, K.7
Hartley, J.A.8
Searcey, M.9
Patterson, L.H.10
-
80
-
-
0036628558
-
Mechanisms of in situ Activation for DNA Targeting Antitumor Agents
-
Wolkenberg, S. E.; Boger, D. L. Mechanisms of in situ Activation for DNA Targeting Antitumor Agents Chem. Rev. 2002, 102, 2477-2495
-
(2002)
Chem. Rev.
, vol.102
, pp. 2477-2495
-
-
Wolkenberg, S.E.1
Boger, D.L.2
-
81
-
-
37049036373
-
A Unique Class of Duocarmycin and CC-1065 Analogues Subject to Reductive Activation
-
Jin, W.; Trzupek, J. D.; Rayl, T. J.; Broward, M. A.; Vielhauer, G. A.; Weir, S. J.; Hwang, I.; Boger, D. L. A Unique Class of Duocarmycin and CC-1065 Analogues Subject to Reductive Activation J. Am. Chem. Soc. 2007, 129, 15391-15397
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 15391-15397
-
-
Jin, W.1
Trzupek, J.D.2
Rayl, T.J.3
Broward, M.A.4
Vielhauer, G.A.5
Weir, S.J.6
Hwang, I.7
Boger, D.L.8
-
82
-
-
78149236204
-
Design, Synthesis, and Evaluation of Duocarmycin O -Amino Phenol Prodrugs Subject to Tunable Reductive Activation
-
Lajiness, J. P.; Robertson, W. M.; Dunwiddie, I.; Broward, M. A.; Vielhauer, G. A.; Weir, S. J.; Boger, D. L. Design, Synthesis, and Evaluation of Duocarmycin O -Amino Phenol Prodrugs Subject to Tunable Reductive Activation J. Med. Chem. 2010, 53, 7731-7738
-
(2010)
J. Med. Chem.
, vol.53
, pp. 7731-7738
-
-
Lajiness, J.P.1
Robertson, W.M.2
Dunwiddie, I.3
Broward, M.A.4
Vielhauer, G.A.5
Weir, S.J.6
Boger, D.L.7
-
83
-
-
0023626542
-
Elevation of Glutathione in Phenylalanine Mustard-resistant Murine L1210 Leukemia Cells
-
Ahmad, S.; Okine, L.; Le, B.; Najarian, P.; Vistica, D. T. Elevation of Glutathione in Phenylalanine Mustard-resistant Murine L1210 Leukemia Cells J. Biol. Chem. 1987, 262, 15048-15053
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 15048-15053
-
-
Ahmad, S.1
Okine, L.2
Le, B.3
Najarian, P.4
Vistica, D.T.5
-
84
-
-
8744226622
-
The Role of Glutathione in Cancer
-
Balendiran, G. K.; Dabur, R.; Fraser, D. The Role of Glutathione in Cancer Cell Biochem. Func 2004, 22, 343-352
-
(2004)
Cell Biochem. Func
, vol.22
, pp. 343-352
-
-
Balendiran, G.K.1
Dabur, R.2
Fraser, D.3
-
85
-
-
0030848358
-
DNA-DNA Interstrand Crosslinking by FR66979: Intermediates in the Activation Cascade
-
Paz, M. M; Hopkins, P. B. DNA-DNA Interstrand Crosslinking by FR66979: Intermediates in the Activation Cascade J. Am. Chem. Soc. 1997, 119, 5999-6005
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 5999-6005
-
-
Paz, M.M.1
Hopkins, P.B.2
-
86
-
-
0031079664
-
FR 900482, A Close Cousin of Mitomycin C that Exploits Mitosene-based DNA Crosslinking
-
Williams, R. M.; Rajski, S. R.; Rollins, S. B. FR 900482, A Close Cousin of Mitomycin C that Exploits Mitosene-based DNA Crosslinking Chem. Biol. 1997, 4, 127-137
-
(1997)
Chem. Biol.
, vol.4
, pp. 127-137
-
-
Williams, R.M.1
Rajski, S.R.2
Rollins, S.B.3
-
87
-
-
0037193103
-
DNA Interstrand Cross-link Formation by Reductive Activation of Dehydropyrrolizidine Progenitors
-
Tepe, J. J.; Kosogof, C.; Williams, R. M. DNA Interstrand Cross-link Formation by Reductive Activation of Dehydropyrrolizidine Progenitors Tetrahedron 2002, 58, 3553-3559
-
(2002)
Tetrahedron
, vol.58
, pp. 3553-3559
-
-
Tepe, J.J.1
Kosogof, C.2
Williams, R.M.3
-
88
-
-
0025980193
-
An Alternative and Convenient Strategy for Generation of Substantial Quantities of Singly 5′-P32-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
-
Boger, D. L.; Munk, S. A.; Zarrinmayeh, H.; Ishizaki, T.; Haught, J.; Bina, M. An Alternative and Convenient Strategy for Generation of Substantial Quantities of Singly 5′-P32-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
-
89
-
-
0034833710
-
A Simple High-Resolution Method for Establishing DNA Binding Affinity and Sequence Selectivity
-
Boger, D. L.; Fink, B. E.; Brunette, S. R.; Tse, W. C.; Hedrick, M. P. A Simple High-Resolution Method for Establishing DNA Binding Affinity and Sequence Selectivity J. Am. Chem. Soc. 2001, 123, 5878-5891
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 5878-5891
-
-
Boger, D.L.1
Fink, B.E.2
Brunette, S.R.3
Tse, W.C.4
Hedrick, M.P.5
|