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Huiping Zhao, Ph.D.

Affiliations: 
2008 Department of Chemistry Kansas State University, Manhattan, KS, United States 
Area:
Organic Chemistry, Polymer Chemistry
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Duy Hua grad student 2008 Kansas State University
 (I. Total synthesis of (+/-)ovalicin and its analogues. II. Bio-based polymers from vegetable oil. III. New synthetic methods of diacetylene fatty acids.)

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Publications

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Garg G, Zhao H, Blagg BS. (2016) Design, synthesis and biological evaluation of alkylamino biphenylamides as Hsp90 C-terminal inhibitors. Bioorganic & Medicinal Chemistry
Hall J, Seedarala S, Zhao H, et al. (2016) Novobiocin Analogs That Inhibit the MAPK Pathway. Journal of Medicinal Chemistry
White PT, Subramanian C, Zhu Q, et al. (2015) Novel HSP90 inhibitors effectively target functions of thyroid cancer stem cell preventing migration and invasion. Surgery
Liu W, Vielhauer GA, Holzbeierlein JM, et al. (2015) KU675, a Concomitant Heat-Shock Protein Inhibitor of Hsp90 and Hsc70 that Manifests Isoform Selectivity for Hsp90α in Prostate Cancer Cells. Molecular Pharmacology. 88: 121-30
Garg G, Zhao H, Blagg BS. (2015) Design, synthesis, and biological evaluation of ring-constrained novobiocin analogues as hsp90 C-terminal inhibitors. Acs Medicinal Chemistry Letters. 6: 204-9
Zhao H, Garg G, Zhao J, et al. (2015) Design, synthesis and biological evaluation of biphenylamide derivatives as Hsp90 C-terminal inhibitors. European Journal of Medicinal Chemistry. 89: 442-66
Zhao J, Zhao H, Hall JA, et al. (2014) Triazole Containing Novobiocin and Biphenyl Amides as Hsp90 C-Terminal Inhibitors. Medchemcomm. 5: 1317-1323
Zhao H, Anyika M, Girgis A, et al. (2014) Novologues containing a benzamide side chain manifest anti-proliferative activity against two breast cancer cell lines. Bioorganic & Medicinal Chemistry Letters. 24: 3633-7
Zhao H, Moroni E, Colombo G, et al. (2014) Identification of a new scaffold for hsp90 C-terminal inhibition. Acs Medicinal Chemistry Letters. 5: 84-8
Ma J, Farmer KL, Pan P, et al. (2014) Heat shock protein 70 is necessary to improve mitochondrial bioenergetics and reverse diabetic sensory neuropathy following KU-32 therapy. The Journal of Pharmacology and Experimental Therapeutics. 348: 281-92
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