Mechanisms of in situ activation for DNA-targeting antitumor agents
SE Wolkenberg, DL Boger - Chemical reviews, 2002 - ACS Publications
CC-1065 and the duocarmycins are the parent members of a potent class of naturally
occurring antitumor antibiotics that exert their biological properties through the sequence …
occurring antitumor antibiotics that exert their biological properties through the sequence …
Fundamental relationships between structure, reactivity, and biological activity for the duocarmycins and CC-1065
KS MacMillan, DL Boger - Journal of medicinal chemistry, 2009 - ACS Publications
The duocarmycins (1 and 2) 1 belong to a small family of natural products (Figure 1) that
also include yatakemycin (3) 2 and CC-1065 (4). 3 Their exceptionally potent cytotoxic …
also include yatakemycin (3) 2 and CC-1065 (4). 3 Their exceptionally potent cytotoxic …
The difference a single atom can make: synthesis and design at the chemistry–biology interface
DL Boger - The Journal of organic chemistry, 2017 - ACS Publications
A Perspective of work in our laboratory on the examination of biologically active compounds,
especially natural products, is presented. In the context of individual programs and along …
especially natural products, is presented. In the context of individual programs and along …
Recent anticancer cytotoxic agents
P Cozzi, N Mongelli, A Suarato - Current Medicinal Chemistry …, 2004 - ingentaconnect.com
In spite of the impressive progress in diagnosis, surgery and therapy that occurred since the
Sixties, the overall cancer mortality is still high and the medical need is largely unmet. A …
Sixties, the overall cancer mortality is still high and the medical need is largely unmet. A …
Cross-bridged cyclen or cyclam Co (III) complexes containing cytotoxic ligands as hypoxia-activated prodrugs
JYC Chang, GL Lu, RJ Stevenson, PJ Brothers… - Inorganic …, 2013 - ACS Publications
A series of cobalt (III) complexes of the potent DNA minor groove alkylator (1-(chloromethyl)-
5-hydroxy-1 H-pyrrolo [3, 2-f] quinolin-3 (2 H)-yl)(5, 6, 7-trimethoxy-1 H-indol-2-yl) …
5-hydroxy-1 H-pyrrolo [3, 2-f] quinolin-3 (2 H)-yl)(5, 6, 7-trimethoxy-1 H-indol-2-yl) …
Anti-cancer 2, 3-dihydro-1H-pyrrolo [3, 2-f] quinoline complexes of cobalt and chromium
This invention relates to a class of heterocycles and their metal complexes, and is
particularly concerned with the use of these compounds in the preparation of prodrugs or as …
particularly concerned with the use of these compounds in the preparation of prodrugs or as …
Establishment of substituent effects in the DNA binding subunit of CBI analogues of the duocarmycins and CC-1065
JP Parrish, DB Kastrinsky, F Stauffer… - Bioorganic & medicinal …, 2003 - Elsevier
An extensive series of CBI analogues of the duocarmycins and CC-1065 exploring
substituent effects within the first indole DNA binding subunit is detailed. In general …
substituent effects within the first indole DNA binding subunit is detailed. In general …
Metal-stabilized phenoxonium cation
A Vigalok, B Rybtchinski, Y Gozin… - Journal of the …, 2003 - ACS Publications
An unprecedented metal-stabilized phenoxonium cation was prepared by a process
involving dearomatization of a phenoxy complex. The unique η2 CO− metal (iridium) …
involving dearomatization of a phenoxy complex. The unique η2 CO− metal (iridium) …
Parallel Synthesis and Evaluation of 132 (+)-1,2,9,9a-Tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) Analogues of CC-1065 and the Duocarmycins Defining the …
DL Boger, HW Schmitt, BE Fink… - The Journal of Organic …, 2001 - ACS Publications
The solution-phase, parallel synthesis and evaluation of a library of 132 (+)-1, 2, 9, 9a-
tetrahydrocyclopropa [c] benz [e] indol-4-one (CBI) analogues of CC-1065 and the …
tetrahydrocyclopropa [c] benz [e] indol-4-one (CBI) analogues of CC-1065 and the …
Remarkable acceleration of a DNA/RNA inter-strand functionality transfer reaction to modify a cytosine residue: the proximity effect via complexation with a metal …
D Jitsuzaki, K Onizuka, A Nishimoto… - Nucleic acids …, 2014 - academic.oup.com
Modified nucleosides in natural RNA molecules are essential for their functions. Non-natural
nucleoside analogues have been introduced into RNA to manipulate its structure and …
nucleoside analogues have been introduced into RNA to manipulate its structure and …