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Structure-based design of lipophilic quinazoline inhibitors of thymidylate synthase.
J Med Chem. 1996 Feb 16;39(4):904-17. doi: 10.1021/jm9502652.
J Med Chem. 1996.
PMID: 8632414
Design of thymidylate synthase inhibitors using protein crystal structures: the synthesis and biological evaluation of a novel class of 5-substituted quinazolinones.
Webber SE, Bleckman TM, Attard J, Deal JG, Kathardekar V, Welsh KM, Webber S, Janson CA, Matthews DA, Smith WW, et al.
Webber SE, et al. Among authors: kathardekar v.
J Med Chem. 1993 Mar 19;36(6):733-46. doi: 10.1021/jm00058a010.
J Med Chem. 1993.
PMID: 8459400
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Structure-based design of substituted diphenyl sulfones and sulfoxides as lipophilic inhibitors of thymidylate synthase.
Jones TR, Webber SE, Varney MD, Reddy MR, Lewis KK, Kathardekar V, Mazdiyasni H, Deal J, Nguyen D, Welsh KM, Webber S, Johnston A, Matthews DA, Smith WW, Janson CA, Bacquet RJ, Howland EF, Booth CL, Herrmann SM, Ward RW, White J, Bartlett CA, Morse CA.
Jones TR, et al. Among authors: kathardekar v.
J Med Chem. 1997 Feb 28;40(5):677-83. doi: 10.1021/jm960613f.
J Med Chem. 1997.
PMID: 9057854
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Inactivation of yeast alcohol dehydrogenase by nitrilopropionamides.
Shiao GC, Kathardekar V, Viola RE.
Shiao GC, et al. Among authors: kathardekar v.
J Enzyme Inhib. 1994;8(2):133-46. doi: 10.3109/14756369409020196.
J Enzyme Inhib. 1994.
PMID: 7539073
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