Zobrazeno 1 - 10
of 82
pro vyhledávání: '"O. Michael Colvin"'
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 57:110-114
The prodrugs cyclophosphamide (CP) and ifosfamide (IF) each metabolize to an active alkylating agent through a cytochrome P450-mediated oxidation at the C-4 position. Competing with this activation pathway are enzymatic oxidations at the exocyclic α
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 50:115-122
A variety of deuterated 3-amino-1-propanols were made by the LiAlD 4 or AlD 3 reduction of nitrile or ester precursors. The labeled aminopropanols and/or deuterated bis(2-chloroethyl)amines were used to synthesize [4,4- 2 H 2 ]-, [6,6- 2 H 2 ]-, [α,
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 50:79-84
Reduction of diethyliminodiacetate with [ 3 H]-LiAlH 4 and then reaction with SOCl 2 gave bis(2-chloro-2-[ 3 H] ethyl)amine hydrochloride. This compound, together with [ 33 P]-phosphorus oxychloride, provided for the synthesis of [ 3 H, 33 P]-phospho
Preclinical Evaluation of Gemcitabine Combination Regimens for Application in Acute Myeloid Leukemia
Publikováno v:
Clinical Cancer Research. 11:4225-4233
The DNA antimetabolite gemcitabine is an anticancer agent with shown preclinical and clinical utility and a low toxicity profile. In this study, we sought to identify and optimize drug partners for binary and tertiary combinations with gemcitabine fo
Autor:
Paul S. Miller, Mateus Webba da Silva, Christopher J. Wilds, Michael P. Gamcsik, Anne M. Noronha, O. Michael Colvin
Publikováno v:
Biochemistry. 43:12549-12554
The solution structure of the undecamer d(CGAAATTTTCG)(2), where T represents a N(3)T-ethyl-N(3)T interstrand cross link, was elucidated using molecular dynamics calculations restrained by NOE and dihedral data obtained from NMR spectroscopy. The eth
Autor:
Henry S. Friedman, O. Michael Colvin, Tsung Yen Cheng, Elizabeth G. Grubbs, Zeinab Abdel-Wahab, Bercedis Peterson, Scott K. Pruitt, Omar Abdel-Wahab, Douglas S. Tyler
Publikováno v:
Journal of the American College of Surgeons. 199:419-427
Background Regional perfusion treatments for melanoma, using the alkylating agent melphalan, show variable responses in magnitude and duration. Surprisingly, the potential contribution of alkylating-agent resistance mechanisms to diminish tumor respo
Autor:
Manny D. Bacolod, Stewart P. Johnson, Anthony E. Pegg, M. Eileen Dolan, Robert C. Moschel, Nancy S. Bullock, Qingming Fang, O. Michael Colvin, Paul Modrich, Darell D. Bigner, Henry S. Friedman
Publikováno v:
Molecular Cancer Therapeutics. 3:1127-1135
The chemotherapeutic activity of 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU or carmustine) may be improved by the addition of O6-benzylguanine (O6-BG). The reaction of O6-BG with O6-alkylguanine-DNA alkyltransferase (AGT) prevents the repair of O6-ch
Autor:
Drazen Raucher, Narayanan Balu, Susan M. Ludeman, Matthew R. Dreher, Ashutosh Chilkoti, O. Michael Colvin
Publikováno v:
Journal of Controlled Release. 91:31-43
Thermally responsive elastin-like polypeptides (ELPs) were synthesized by recombinant DNA techniques and conjugated to doxorubicin through an acid-labile hydrazone bond to enable release of the drug in the acidic environment of lysosomes. The thermal
Autor:
Paul S. Miller, Mateus Webba da Silva, Anne M. Noronha, David M. Noll, Michael P. Gamcsik, O. Michael Colvin
Publikováno v:
Biochemistry. 41:15181-15188
The solution structure of an interstrand cross-linked self-complementary oligodeoxynucleotide containing directly opposed alkylated N(4)C-ethyl-N(4)C cytosine bases was determined by molecular dynamics calculations guided by NMR-derived restraints. T
Autor:
Michael E. Colvin, O. Michael Colvin, S. M. Ludeman, Michael P. Gamcsik, Narayanan Balu, M. Eileen Dolan
Publikováno v:
Chemical Research in Toxicology. 15:380-387
Alkylation of DNA by acrolein and/or chloroacetaldehyde may result in the mutations that lead to the therapy-induced leukemia associated with cyclophosphamide (and ifosfamide) treatment. O(6)-(n-Propanalyl)guanine (O(6)-PAG) and O(6)-(ethanalyl)guani