Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Janice L. Hyatt"'
Publikováno v:
Chemico-Biological Interactions. 203:226-230
Carboxylesterases (CEs) are ubiquitously expressed proteins that are responsible for the detoxification of xenobiotics. They tend to be expressed in tissues likely to be exposed to such agents (e.g., lung and gut epithelia, liver) and can hydrolyze n
Autor:
Bing Yan, Lyudmila Tsurkan, Janice L. Hyatt, Cynthia Jeffries, Andrew Lemoff, Carol C. Edwards, Philip M. Potter, M. Jason Hatfield
Publikováno v:
Journal of Natural Products. 76:36-44
The roots of Salvia miltiorrhiza ("Danshen") are used in traditional Chinese medicine for the treatment of numerous ailments including cardiovascular disease, hypertension, and ischemic stroke. Extracts of S. miltiorrhiza roots in the formulation "Co
Autor:
M. J. Hatfield, Xiaozhen Yu, Randy M. Wadkins, Philip M. Potter, Carol C. Edwards, Janice L. Hyatt, Latorya D. Hicks, Lyudmila Tsurkan
Publikováno v:
British Journal of Pharmacology. 160:1916-1928
Background and purpose: Carboxylesterases (CEs) metabolize a wide range of xenobiotic substrates including heroin, cocaine, meperidine and the anticancer agent CPT-11. In this study, we have purified to homogeneity human liver and intestinal CEs and
Autor:
Janice L. Hyatt, Carol C. Edwards, Philip M. Potter, M. Jason Hatfield, Tad H. Koch, Benjamin L. Barthel, Renee C Torres
Publikováno v:
Journal of Medicinal Chemistry. 51:298-304
Doxazolidine (Doxaz), a formaldehyde-doxorubicin (Dox) conjugate, exhibits markedly increased tumor toxicity with respect to Dox without a concurrent increase in toxicity to cardiomyocytes. Pentyl PABC-Doxaz (PPD) is a Doxaz carbamate prodrug that is
Autor:
Janice L. Hyatt, Lyudmila Tsurkan, Charles R. Ross, Guy Crundwell, R. Kip Guy, Philip M. Potter, M. Jason Hatfield, Randy M. Wadkins, Stephanie A. Cantalupo, Mary K. Danks, Latorya D. Hicks, Carol C. Edwards
Publikováno v:
Journal of Medicinal Chemistry. 50:5727-5734
Carboxylesterases (CE) are ubiquitous enzymes responsible for the detoxification of xenobiotics, including numerous clinically used drugs. Therefore, the selective inhibition of these proteins may prove useful in modulating drug half-life and bioavai
Autor:
Lyudmila Tsurkan, Carol C. Edwards, Monika Wierdl, Antonio M. Ferreira, Janice L. Hyatt, Latorya D. Hicks, Teri Moak, Philip M. Potter, Randy M. Wadkins
Publikováno v:
Bioorganic & Medicinal Chemistry. 15:3801-3817
We have synthesized and assessed the ability of symmetrical fluorobenzoins and fluorobenzils to inhibit mammalian carboxylesterases (CE). The majority of the latter were excellent inhibitors of CEs however unexpectedly, the fluorobenzoins were very g
Autor:
Monika Wierdl, Carol C. Edwards, Lyudmila Tsurkan, Michael R. Taylor, Janice L. Hyatt, Robyn A. Umans, Philip M. Potter, M. Jason Hatfield
Publikováno v:
Chemico-biological interactions. 259
Carboxylesterases (CE) are members of the esterase family of enzymes, and as their name suggests, they are responsible for the hydrolysis of carboxylesters into the corresponding alcohol and carboxylic acid. To date, no endogenous CE substrates have
Autor:
Janice L. Hyatt, Matthew R. Redinbo, Randy M. Wadkins, Paul D. Jones, Carol C. Edwards, Bruce D. Hammock, Lyudmila Tsurkan, Craig E. Wheelock, Philip M. Potter
Publikováno v:
Molecular Pharmacology. 71:713-723
Carboxylesterases (CE) are ubiquitous enzymes that hydrolyze numerous ester-containing xenobiotics, including complex molecules, such as the anticancer drugs irinotecan (CPT-11) and capecitabine and the pyrethroid insecticides. Because of the role of
Autor:
Janice L. Hyatt, Carol C. Edwards, Monika Wierdl, Philip M. Potter, Lyudmila Tsurkan, Mary K. Danks
Publikováno v:
Molecular Cancer Therapeutics. 5:2281-2288
Carboxylesterases are ubiquitous proteins responsible for the detoxification of xenobiotics. However, these enzymes also activate prodrugs, such as the anticancer agents capecitabine and CPT-11. As a consequence, overexpression of carboxylesterases w
Autor:
Allen D Hunter, Randy M. Wadkins, Vanessa Stacy, Kyoung Jin P. Yoon, Janice L. Hyatt, Mary K. Danks, Monika Wierdl, Guy Crundwell, Carol C. Edwards, Matthias Zeller, Philip M. Potter
Publikováno v:
Journal of Medicinal Chemistry. 48:5543-5550
Benzil has been identified as a potent selective inhibitor of carboxylesterases (CEs). Essential components of the molecule required for inhibitory activity include the dione moiety and the benzene rings, and substitution within the rings affords inc