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Year | Number of Results |
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2008 | 1 |
2012 | 2 |
2013 | 1 |
2015 | 1 |
2024 | 0 |
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Development of flavone propargyl ethers as potent and selective inhibitors of cytochrome P450 enzymes 1A1 and 1A2.
Drug Metab Lett. 2012;6(4):275-84. doi: 10.2174/1872312811206040007.
Drug Metab Lett. 2012.
PMID: 23506553
Free PMC article.
Pyranoflavones: a group of small-molecule probes for exploring the active site cavities of cytochrome P450 enzymes 1A1, 1A2, and 1B1.
Liu J, Taylor SF, Dupart PS, Arnold CL, Sridhar J, Jiang Q, Wang Y, Skripnikova EV, Zhao M, Foroozesh M.
Liu J, et al.
J Med Chem. 2013 May 23;56(10):4082-92. doi: 10.1021/jm4003654. Epub 2013 May 2.
J Med Chem. 2013.
PMID: 23600958
Free PMC article.
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Differential inhibition of cytochromes P450 3A4 and 3A5 by the newly synthesized coumarin derivatives 7-coumarin propargyl ether and 7-(4-trifluoromethyl)coumarin propargyl ether.
Sridar C, Kent UM, Noon K, McCall A, Alworth B, Foroozesh M, Hollenberg PF.
Sridar C, et al.
Drug Metab Dispos. 2008 Nov;36(11):2234-43. doi: 10.1124/dmd.108.021493. Epub 2008 Jul 24.
Drug Metab Dispos. 2008.
PMID: 18653744
Free PMC article.
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A Ligand-Based Drug Design. Discovery of 4-Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2.
Liu J, Pham PT, Skripnikova EV, Zheng S, Lovings LJ, Wang Y, Goyal N, Bellow SM, Mensah LM, Chatters AJ, Bratton MR, Wiese TE, Zhao M, Wang G, Foroozesh M.
Liu J, et al.
J Med Chem. 2015 Aug 27;58(16):6481-93. doi: 10.1021/acs.jmedchem.5b00494. Epub 2015 Aug 10.
J Med Chem. 2015.
PMID: 26222195
Free PMC article.
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7-Ethynylcoumarins: selective inhibitors of human cytochrome P450s 1A1 and 1A2.
Liu J, Nguyen TT, Dupart PS, Sridhar J, Zhang X, Zhu N, Stevens CL, Foroozesh M.
Liu J, et al.
Chem Res Toxicol. 2012 May 21;25(5):1047-57. doi: 10.1021/tx300023p. Epub 2012 Apr 10.
Chem Res Toxicol. 2012.
PMID: 22443586
Free PMC article.
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