Ashish P. Vartak, PhD
Academic Title
Research Associate
Center for Drug Design
Education
Bachelor's
Bachelor of Pharmacy, University of Pune, India (2000)
Ph.D.
Medicinal Chemistry, University of Minnesota, Minneapolis, MN (2006)
Contact Info
Email
vart0006@umn.edu
Phone
612-624-2146
Office Address
8-125 Weaver-Densford Hall
308 Harvard Street SE
Minneapolis, MN 55455
Mailing Address
MMC 204 Mayo
Campus delivery code 8204 A
Peptidomimetics:
Design of secondary structure mimics
Development of chemical methodology
Applications to the design of therapeutic agents
Organic Process Research:
Development of scalable, economic and environmentally acceptable processes for valuable small-molecules
Design of Nerve-growth Modulators
Recent Publications (For detailed publication list: Click Here)
Vartak, A.P.; Skoblenick, K.; Thomas, N.; Mishra, R.K.; Johnson, R.L. Allosteric Modulation of the Dopamine Receptor by Conformationally Constrained Type VI β -Turn Peptidomimetics of Pro-Leu-Gly-NH2. Journal of Medicinal Chemistry, 2007, 50, 6725.
Vartak, A.P.; Dwoskin, L.P.; Crooks, P.A.Synthesis of symmetrical 1,5-disubstituted granatanines. Tetrahedron Letters, 2008, 49, 6330.
Vartak, A.P.; Nickell, J.R.; Chagkutip, J.; Dwoskin, L.P.; Crooks, P.A. Pyrrolidine Analogues of Lobelane: Relationship of Affinity for the Dihydrotetrabenazine Binding Site with Function of the Vesicular Monoamine Transporter 2 (VMAT2). Journal of Medicinal Chemistry, 2009, 52, 7878. Selected for publication in the Centennial Issue of the Journal of Medicinal Chemistry.
Vartak, A.P. Crooks, P.A. A Scalable, Enantioselective Synthesis of the α2-Adrenergic Agonist, Lofexidine. Organic Process Research & Development, 2009,13, 415. Highlighted in Noteworthy Chemistry, June 29, 2009 release.
Vartak, A.P.; Sonar, V; Crooks, P.A. Rac- and S-(+)-[4,4',5,5'-2H4]-2-(1'-[2'',6''-dichlorophenoxy]-ethyl)-Δ2-imidazoline (lofexidine). Journal of Labelled Compounds and Radiopharmaceuticals, 2009, 52, 431.
Vartak, A.P.; Deaciuc, A.G.; Dwoskin, L.P.; Crooks, P.A. Quinlobelane: a water-soluble lobelane analogue and inhibitor of VMAT2. Bioorganic and Medicinal Chemistry Letters, 2010, 20, 3584
Peter A. Crooks, Guangrong Zheng, Ashish Vartak, John Culver, Fang Zheng, A. Gabi Deaciuc, and Linda P. Dwoskin. Design, Synthesis and VMAT2 Binding of Lobeline Analogs as Potential Therapeutic Agents for Treating Psychostimulant Abuse. Current Topics in Medicinal Chemistry, 2010, 9, Bentham Science, in press, 2010
Beckmann, J.S.; Siripurapu, K.B.; Nickell, J.R.; Horton, D.B.; Denehy, E.D.; Vartak, A.P.; Crooks, P.A.; Dwoskin, L.P.; Bardo, M.T. The Novel Pyrrolidine nor-Lobelane Analog, UKCP-110 (cis-2,5-di-(2-Phenethyl)-pyrrolidine Hydrochloride) Inhibits VMAT2 Function, Methamphetamine-evoked Dopamine Release, and Methamphetamine Self-administration in Rats. Journal of Pharmacology and Experimental Therapeutics, 2010, In press doi:10.1124/jpet.110.172742
Nasim, S.; Vartak, A.P.; Pierce, W.M.; Taylor, G.K.; Smith, N.; Crooks, P.A. 3-O-Phosphate ester conjugates of 17-β-O-{1-[2-carboxy-(2-hydroxy-4-methoxy-3-carboxamido)anilido]ethyl}1,3,5(10)-estratriene as novel bone targeting agents, Bioorganic and Medicinal Chemistry Letters, 2010, In press doi: 10.1016/j.bmcl.2010.10.023
Nasim, S.; Vartak, A.P.; Pierce, W.M., Jr.; Grant, T.K.; Crooks, P.A. Improved and Scalable Synthetic Route to the Synthon 17-β -(2-Carboxyethyl)-1,3,5(10)-Estratriene: An Important Intermediate in the Synthesis of Bone-Targeting Estrogens. Synthetic Communications, 2010, 40, 772.