Development of Potent and Selective Indomethacin Analogues for the Inhibition of AKR1C3 (Type 5 17β-Hydroxysteroid Dehydrogenase/Prostaglandin F Synthase) in Castrate-Resistant Prostate Cancer
- Authors:
-
- Departments of Biochemistry, Chemistry, and Pharmacology, Vanderbilt Institute of Chemical Biology, Center in Molecular Toxicology, Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, United States
- Department of Pharmacology and Center of Excellence in Environmental Toxicology, Perelman School of Medicine, University of Pennsylvania, 1315 BRB II/III, 420 Curie Boulevard, Philadelphia, Pennsylvania 19104-6061, United States
- Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States
- Publication Date:
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1123359
- Resource Type:
- Published Article
- Journal Name:
- Journal of Medicinal Chemistry
- Additional Journal Information:
- Journal Name: Journal of Medicinal Chemistry Journal Volume: 56 Journal Issue: 6; Journal ID: ISSN 0022-2623
- Publisher:
- American Chemical Society
- Country of Publication:
- United States
- Language:
- English
Citation Formats
Liedtke, Andy J., Adeniji, Adegoke O., Chen, Mo, Byrns, Michael C., Jin, Yi, Christianson, David W., Marnett, Lawrence J., and Penning, Trevor M. Development of Potent and Selective Indomethacin Analogues for the Inhibition of AKR1C3 (Type 5 17β-Hydroxysteroid Dehydrogenase/Prostaglandin F Synthase) in Castrate-Resistant Prostate Cancer. United States: N. p., 2013.
Web. doi:10.1021/jm3017656.
Liedtke, Andy J., Adeniji, Adegoke O., Chen, Mo, Byrns, Michael C., Jin, Yi, Christianson, David W., Marnett, Lawrence J., & Penning, Trevor M. Development of Potent and Selective Indomethacin Analogues for the Inhibition of AKR1C3 (Type 5 17β-Hydroxysteroid Dehydrogenase/Prostaglandin F Synthase) in Castrate-Resistant Prostate Cancer. United States. https://doi.org/10.1021/jm3017656
Liedtke, Andy J., Adeniji, Adegoke O., Chen, Mo, Byrns, Michael C., Jin, Yi, Christianson, David W., Marnett, Lawrence J., and Penning, Trevor M. Wed .
"Development of Potent and Selective Indomethacin Analogues for the Inhibition of AKR1C3 (Type 5 17β-Hydroxysteroid Dehydrogenase/Prostaglandin F Synthase) in Castrate-Resistant Prostate Cancer". United States. https://doi.org/10.1021/jm3017656.
@article{osti_1123359,
title = {Development of Potent and Selective Indomethacin Analogues for the Inhibition of AKR1C3 (Type 5 17β-Hydroxysteroid Dehydrogenase/Prostaglandin F Synthase) in Castrate-Resistant Prostate Cancer},
author = {Liedtke, Andy J. and Adeniji, Adegoke O. and Chen, Mo and Byrns, Michael C. and Jin, Yi and Christianson, David W. and Marnett, Lawrence J. and Penning, Trevor M.},
abstractNote = {},
doi = {10.1021/jm3017656},
journal = {Journal of Medicinal Chemistry},
number = 6,
volume = 56,
place = {United States},
year = {Wed Mar 13 00:00:00 EDT 2013},
month = {Wed Mar 13 00:00:00 EDT 2013}
}
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https://doi.org/10.1021/jm3017656
https://doi.org/10.1021/jm3017656
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Cited by: 66 works
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