Maryam Foroozesh PhD

Maryam Foroozesh PhD

Times-Picayune/Samuel Newhouse Foundation Endowed Professor in Scientific Research

Dr. Foroozesh's research group is involved in the design, synthesis and biological studies of new selective inhibitors of P450 enzymes involved in carcinogenesis, and ceramides with the potential of causing reversal of chemoresistance and endocrine resistance in breast cancer.

Selected Publications


Inhibition of Cytochrome P450 6D1 by Alkynylarenes, Methylenedioxy Substituted Aromatics and other Aromatics'Äù, J.G. Scott, M. Foroozesh, N.E. Hopkins, and W.L. Alworth, Pesticide Biochemistry and Physiology, Vol. 67, pp. 63-71, 2000.

1-Adamantyl Propargyl Ether'Äù, J.T. Mague, W.L. Alworth, and M. Foroozesh, Acta Cryst., E57: 220-221, 2001.

Synthesis of a Family of Adamantyl Propargyl Ethers as Potential Cytochrome P450 Inhibitors'Äù, A. Robinson, J. Mesbah, T. Smith, and M. Foroozesh, J. Undergraduate Chemistry Research, Vol. 4, pp. 155-157, 2002.

Metabolic Fate of the AH Receptor Ligand 6-Formylindolo[3,2-b]carbazole'Äù, L. Bergander, A. Rannug, E. Wincent, M. Foroozesh, W. Alworth, and U. Rannug, Chem. Biol. Interact., 149: 151-64, 2004.

Synthesis of a Family of Naphthyl Propargyl Ethers as Potential Cytochrome P450 Inhibitors'Äù, A.T. Kelley, J.Y. Mesbah, M.E. McKendall, T.P. Smith, and M. Foroozesh, J. Undergraduate Chemistry Research, Vol. 3, pp. 103-105, 2004.

Synthesis of a Family of Biphenylpropargyl Ethers as Potential Inhibitors of P450 Enzymes. X-Ray Crystal Structure of 2,2'Äô-Biphenyldipropargyl Ether'Äù, B. Bowman, D. Lightsey, M. McKendall, T. Smith, N. Zhu, C. L. Klein Stevens, and M. Foroozesh, J. Undergraduate Chemistry Research, Vol. 2, pp. 57-61, 2005.

Naphthoflavone Propargyl Ether Inhibitors of Cytochrome P450'Äù, N. Zhu, D. Lightsey, M. Foroozesh, W. Alworth, A. Chaudhary, K. L. Willet, and C.K. Stevens, J. Chemical Crystallography, Vol. 36, No. 5, pp. 289-295, 2006.

Methoxyflavone Inhibitors of Cytochrome P450'Äù, M. McKendall, T. Smith, K. Ahn, J. Ellis, T. McGee, M. Foroozesh, N. Zhu, and C.L. Klein Stevens, Journal of Chemical Crystallography, Vol. 38, No. 4, pp. 231-237, 2008.

Differential Inhibition of P450s 3A4 and 3A5 By the Newly Synthesized Coumarin Derivatives, 7-Coumarin Propargyl Ether and 7-(4-Trifluoromethyl)coumarin Propargyl Ether'Äù, C. Sridar, U.M. Kent, A. McCall, W.L. Alworth, M. Foroozesh, and P. Hollenberg, Drug Metabolism and Disposition, Vol. 36, pp. 2234-2243, 2008.

Interaction of Polycyclic Aromatic Hydrocarbons with Human Cytochrome P450 1B1 in Inhibiting Catalytic Activity'Äù, T. Shimada, N. Murayama, K. Tanaka, S. Takenaka, Y. Imai, N.E. Hopkins, M.K. Foroozesh, W.L. Alworth, H. Yamazaki, F.P. Guengerich, and M. Komori, Chemical Research in Toxicology, Vol. 21, No.12, pp. 2313-2323, 2008.

Reverse Type I Binding Spectra of Human Cytochrome P450 1B1 Induced by Flavonoid, Stilbene, Pyrene, Naphthalene, Phenanthrene, and Biphenyl Derivatives that Inhibit Catalytic Activity: A Structure-Function Relationship Study'Äù, T. Shimada, K. Tanaka, S. Takenaka, M.K. Foroozesh, N. Murayama, H. Yamazaki, F.P. Guengerich, and M. Komori, Chemical Research in Toxicology, Vol. 22, No. 7, pp. 1325-1333, 2009.

Design, Synthesis, and Biological Activity of a Family of Novel Ceramide Analogs in Chemoresistant Breast Cancer Cells'Äù, J.W. Antoon, J. Liu, M.M. Gestaut, M.E. Burow, B.S. Beckman, and M. Foroozesh, Journal of Medicinal Chemistry, Vol.52, No. 18, pp. 5748'Äì5752, 2009.

Ethynyl and Propynyl Pyrene Inhibitors of Cytochrome P450'Äù, N. Zhu, D. Lightsey, J. Liu, M. Foroozesh, K.M. Morgan, E. D. Stevens, and C.L.K. Stevens, Journal of Chemical Crystallography, Vol. 40, pp. 343-352, 2010.

In Silico Studies to Determine Structural Features Influencing Polyaromatic Hydrocarbon Inhibition Potency of Cytochrome P450 enzymes 1A1, 1A2, 2A6 and 2B1'Äù, J. Sridhar, P. Jin, J. Liu, M. Foroozesh, and C. Stevens, Chemical Research in Toxicology, Vol. 23, No. 3, pp. 600'Äì607, 2010.

Novel D-erythro N-Octanoyl Sphingosine Analogues As Chemo- and Endocrine Resistant Breast Cancer Therapeutics'Äù, J. Antoon, J. Liu, A. Ponnapakkam, M. Foroozesh, and B. Beckman, Cancer Chemotherapy and Pharmacology, Vol. 65, No. 6, pp. 1191-1195, 2010.

Novel Anti-Proliferative Ceramide Analogs: Design, Synthesis, and Structure-Activity Relationship Studies of Substituted (S)-2-(Benzylideneamino)-3-hydroxy-N-tetradecylpropanamides'Äù, J. Liu, J.W. Antoon, A. Ponnapakkam, B.S. Beckman, and Maryam Foroozesh, accepted for publication in Bioorganic and Medicinal Chemistry, May 2010.

LCRC Faculty

Asim Abdel-Mageed DVM PhD
Therapeutics & Diagnostics
Tulane University School of Medicine
Suresh K. Alahari PhD
Therapeutics & Diagnostics
LSU Health - New Orleans
Wayne L. Backes PhD
Tumor Biology
LSU Health - New Orleans
Victoria P. Belancio PhD
Genes & Environment
Tulane University School of Medicine
Earl "Nupsius" Benjamin-Robinson DrHSc CPH
Population Sciences
Louisiana Cancer Research Center
Tom Bishop PhD
Genes & Environment
Louisiana Tech University
David Blask MD PhD
Tumor Biology
Tulane University School of Medicine
Levon Bostanian PhD
Therapeutics & Diagnostics
Xavier University
J. Quincy Brown PhD
Therapeutics & Diagnostics
Tulane University School of Medicine