PMID

Data

Article Title

Organization

Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylase based on a cinnamic hydroxamic acid core structure.

University of Minnesota

Structure-activity relationship study of selective benzimidazole-based inhibitors of Cryptosporidium parvum IMPDH.

Brandeis University

Triazole inhibitors of Cryptosporidium parvum inosine 5'-monophosphate dehydrogenase.

Brandeis University

Novel mycophenolic adenine bis(phosphonate) analogues as potential differentiation agents against human leukemia.

Pharmasset

Synthesis of a methylenebis(phosphonate) analogue of mycophenolic adenine dinucleotide: a glucuronidation-resistant MAD analogue of NAD.

Codon Pharmaceuticals

Isosteric analogues of nicotinamide adenine dinucleotide derived from furanfurin, thiophenfurin, and selenophenfurin as mammalian inosine monophosphate dehydrogenase (type I and II) inhibitors.

Universit£

Cofactor-type inhibitors of inosine monophosphate dehydrogenase via modular approach: targeting the pyrophosphate binding sub-domain.

University of Minnesota

Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase and differentiation induction of K562 cells among the mycophenolic acid derivatives.

Hokkaido University

Triazole-linked inhibitors of inosine monophosphate dehydrogenase from human and Mycobacterium tuberculosis.

University of Minnesota

Mycophenolic acid analogs with a modified metabolic profile.

University of Minnesota

Bis(sulfonamide) isosters of mycophenolic adenine dinucleotide analogues: inhibition of inosine monophosphate dehydrogenase.

University of Minnesota

Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylases for cancer treatment.

University of Minnesota

Methylenebis(sulfonamide) linked nicotinamide adenine dinucleotide analogue as an inosine monophosphate dehydrogenase inhibitor.

University of Minnesota

Novel methylenephosphophosphonate analogues of mycophenolic adenine dinucleotide. Inhibition of inosine monophosphate dehydrogenase.

University of Minnesota

Phosphonic acid-containing analogues of mycophenolic acid as inhibitors of IMPDH.

Gilead Sciences

Novel indole-based inhibitors of IMPDH: introduction of hydrogen bond acceptors at indole C-3.

Bristol-Myers Squibb Pri

Novel inhibitors of IMPDH: a highly potent and selective quinolone-based series.

Bristol-Myers Squibb Pri

Novel amide-based inhibitors of inosine 5'-monophosphate dehydrogenase.

Bristol-Myers Squibb Pri

Synthesis and immunosuppressive activity of some side-chain variants of mycophenolic acid.

Syntex Research