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Journal of Medicinal Chemistry|July 24, 2009
Triazole inhibitors of Cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseSushil K Maurya, Deviprasad R Gollapalli, Shivapriya Kirubakaran, et al.
Journal of Medicinal Chemistry|September 7, 2012
Selective and potent urea inhibitors of cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseSuresh Kumar Gorla, Mandapati Kavitha, Minjia Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2013
Phthalazinone inhibitors of inosine-5'-monophosphate dehydrogenase from Cryptosporidium parvumCorey R Johnson, Suresh Kumar Gorla, Mandapati Kavitha, et al.
Molecular Pharmacology|December 23, 2008
A juxtamembrane mutation in the N terminus of the dopamine transporter induces preference for an inward-facing conformationBipasha Guptaroy, Minjia Zhang, Erica Bowton, et al.
Bioorganic & Medicinal Chemistry Letters|February 8, 2012
Structure-activity relationship study of selective benzimidazole-based inhibitors of Cryptosporidium parvum IMPDHSivapriya Kirubakaran, Suresh Kumar Gorla, Lisa Sharling, et al.
The Journal of Biological Chemistry|January 10, 2015
A novel cofactor-binding mode in bacterial IMP dehydrogenases explains inhibitor selectivityMagdalena Makowska-Grzyska, Youngchang Kim, Natalia Maltseva, et al.
Journal of Medicinal Chemistry|May 15, 2013
Optimization of benzoxazole-based inhibitors of Cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseSuresh Kumar Gorla, Mandapati Kavitha, Minjia Zhang, et al.
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