Foroozesh M - Search Results

1

Development of flavone propargyl ethers as potent and selective inhibitors of cytochrome P450 enzymes 1A1 and 1A2.

Sridhar J, Ellis J, Dupart P, Liu J, Stevens CL, Foroozesh M. Sridhar J, et al. Among authors: foroozesh m. Drug Metab Lett. 2012;6(4):275-84. doi: 10.2174/1872312811206040007. Drug Metab Lett. 2012. PMID: 23506553 Free PMC article.

2

Suicide inhibitors of cytochrome P450 1A1 and P450 2B1.

Hopkins NE, Foroozesh MK, Alworth WL. Hopkins NE, et al. Among authors: foroozesh mk. Biochem Pharmacol. 1992 Aug 18;44(4):787-96. doi: 10.1016/0006-2952(92)90417-h. Biochem Pharmacol. 1992. PMID: 1510726

3

Aryl acetylenes as mechanism-based inhibitors of cytochrome P450-dependent monooxygenase enzymes.

Foroozesh M, Primrose G, Guo Z, Bell LC, Alworth WL, Guengerich FP. Foroozesh M, et al. Chem Res Toxicol. 1997 Jan;10(1):91-102. doi: 10.1021/tx960064g. Chem Res Toxicol. 1997. PMID: 9074808

4

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. Among authors: foroozesh m. 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.

5

Design, synthesis, and biological activity of a family of novel ceramide analogues in chemoresistant breast cancer cells.

Antoon JW, Liu J, Gestaut MM, Burow ME, Beckman BS, Foroozesh M. Antoon JW, et al. Among authors: foroozesh m. J Med Chem. 2009 Sep 24;52(18):5748-52. doi: 10.1021/jm9009668. J Med Chem. 2009. PMID: 19694470

6

In silico studies of polyaromatic hydrocarbon inhibitors of cytochrome P450 enzymes 1A1, 1A2, 2A6, and 2B1.

Sridhar J, Jin P, Liu J, Foroozesh M, Stevens CL. Sridhar J, et al. Among authors: foroozesh m. Chem Res Toxicol. 2010 Mar 15;23(3):600-7. doi: 10.1021/tx900348v. Chem Res Toxicol. 2010. PMID: 20078084 Free PMC article.

7

Novel D: -erythro N-octanoyl sphingosine analogs as chemo- and endocrine-resistant breast cancer therapeutics.

Antoon JW, Liu J, Ponnapakkam AP, Gestaut MM, Foroozesh M, Beckman BS. Antoon JW, et al. Among authors: foroozesh m. Cancer Chemother Pharmacol. 2010 May;65(6):1191-5. doi: 10.1007/s00280-009-1233-0. Epub 2010 Feb 14. Cancer Chemother Pharmacol. 2010. PMID: 20155475

8

Ethynyl and Propynylpyrene Inhibitors of Cytochrome P450.

Zhu N, Lightsey D, Liu J, Foroozesh M, Morgan KM, Stevens ED, Klein Stevens CL. Zhu N, et al. Among authors: foroozesh m. J Chem Crystallogr. 2010 Apr 1;40(4):343-352. doi: 10.1007/s10870-009-9659-0. J Chem Crystallogr. 2010. PMID: 20473363 Free PMC article.

9

Novel anti-viability ceramide analogs: design, synthesis, and structure-activity relationship studies of substituted (S)-2-(benzylideneamino)-3-hydroxy-N-tetradecylpropanamides.

Liu J, Antoon JW, Ponnapakkam A, Beckman BS, Foroozesh M. Liu J, et al. Among authors: foroozesh m. Bioorg Med Chem. 2010 Jul 15;18(14):5316-22. doi: 10.1016/j.bmc.2010.05.044. Epub 2010 Jun 8. Bioorg Med Chem. 2010. PMID: 20639111

10

QSAR models of cytochrome P450 enzyme 1A2 inhibitors using CoMFA, CoMSIA and HQSAR.

Sridhar J, Foroozesh M, Stevens CL. Sridhar J, et al. Among authors: foroozesh m. SAR QSAR Environ Res. 2011 Oct;22(7-8):681-97. doi: 10.1080/1062936X.2011.623320. Epub 2011 Oct 17. SAR QSAR Environ Res. 2011. PMID: 22004550 Free PMC article.

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