Literature DB >> 18336280

Nicotinamide adenine dinucleotide based therapeutics.

L Chen1, R Petrelli, K Felczak, G Gao, L Bonnac, J S Yu, E M Bennett, K W Pankiewicz.   

Abstract

Nicotinamide adenine dinucleotide (NAD), generally considered a key component involved in redox reactions, has been found to participate in an increasingly diverse range of cellular processes, including signal transduction, DNA repair, and post-translational protein modifications. In recent years, medicinal chemists have become interested in the therapeutic potential of molecules affecting interactions of NAD with NAD-dependent enzymes. Also, enzymes involved in de novo biosynthesis, salvage pathways, and down-stream utilization of NAD have been extensively investigated and implicated in a wide variety of diseases. These studies have bolstered NAD-based therapeutics as a new avenue for the discovery and development of novel treatments for medical conditions ranging from cancer to aging. Industrial and academic groups have produced structurally diverse molecules which target NAD metabolic pathways, with some candidates advancing into clinical trials. However, further intensive structural, biological, and medical studies are needed to facilitate the design and evaluation of new generations of NAD-based therapeutics. At this time, the field of NAD-therapeutics is most likely at a stage similar to that of the early successful development of protein kinase inhibitors, where analogs of ATP (a more widely utilized metabolite than NAD) began to show selectivity against target enzymes. This review focuses on key representative opportunities for research in this area, which extends beyond the scope of this article.

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Year:  2008        PMID: 18336280     DOI: 10.2174/092986708783885282

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  14 in total

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Review 2.  IMP dehydrogenase: structure, mechanism, and inhibition.

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3.  Emissive Synthetic Cofactors: Enzymatic Interconversions of tz A Analogues of ATP, NAD+ , NADH, NADP+ , and NADPH.

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Journal:  Angew Chem Int Ed Engl       Date:  2017-12-21       Impact factor: 15.336

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Authors:  Liqiang Chen; Daniel J Wilson; Yanli Xu; Courtney C Aldrich; Krzysztof Felczak; Yuk Y Sham; Krzysztof W Pankiewicz
Journal:  J Med Chem       Date:  2010-06-24       Impact factor: 7.446

5.  Effects of glutathione reductase inhibition on cellular thiol redox state and related systems.

Authors:  Yong Zhao; Teresa Seefeldt; Wei Chen; Xiuqing Wang; Duane Matthees; Yueshan Hu; Xiangming Guan
Journal:  Arch Biochem Biophys       Date:  2009-03-09       Impact factor: 4.013

6.  Targeting NAD biosynthesis in bacterial pathogens: Structure-based development of inhibitors of nicotinate mononucleotide adenylyltransferase NadD.

Authors:  Leonardo Sorci; Yongping Pan; Yvonne Eyobo; Irina Rodionova; Nian Huang; Oleg Kurnasov; Shijun Zhong; Alexander D MacKerell; Hong Zhang; Andrei L Osterman
Journal:  Chem Biol       Date:  2009-08-28

7.  The small molecule GMX1778 is a potent inhibitor of NAD+ biosynthesis: strategy for enhanced therapy in nicotinic acid phosphoribosyltransferase 1-deficient tumors.

Authors:  Mark Watson; Anne Roulston; Laurent Bélec; Xavier Billot; Richard Marcellus; Dominique Bédard; Cynthia Bernier; Stéphane Branchaud; Helen Chan; Kenza Dairi; Karine Gilbert; Daniel Goulet; Michel-Olivier Gratton; Henady Isakau; Anne Jang; Abdelkrim Khadir; Elizabeth Koch; Manon Lavoie; Michael Lawless; Mai Nguyen; Denis Paquette; Emilie Turcotte; Alvin Berger; Matthew Mitchell; Gordon C Shore; Pierre Beauparlant
Journal:  Mol Cell Biol       Date:  2009-08-24       Impact factor: 4.272

8.  A versatile strategy for the design and synthesis of novel ADP conjugates and their evaluation as potential poly(ADP-ribose) polymerase 1 inhibitors.

Authors:  Yuliya V Sherstyuk; Alexandra L Zakharenko; Mikhail M Kutuzov; Polina V Chalova; Maria V Sukhanova; Olga I Lavrik; Vladimir N Silnikov; Tatyana V Abramova
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9.  Targeting NAD+ salvage pathway induces autophagy in multiple myeloma cells via mTORC1 and extracellular signal-regulated kinase (ERK1/2) inhibition.

Authors:  Michele Cea; Antonia Cagnetta; Mariateresa Fulciniti; Yu-Tzu Tai; Teru Hideshima; Dharminder Chauhan; Aldo Roccaro; Antonio Sacco; Teresa Calimeri; Francesca Cottini; Jana Jakubikova; Sun-Young Kong; Franco Patrone; Alessio Nencioni; Marco Gobbi; Paul Richardson; Nikhil Munshi; Kenneth C Anderson
Journal:  Blood       Date:  2012-09-05       Impact factor: 22.113

10.  Novel synthetic route to the C-nucleoside, 2-deoxy benzamide riboside.

Authors:  Rebecca R Midtkandal; Philip Redpath; Samuel A J Trammell; Simon J F Macdonald; Charles Brenner; Marie E Migaud
Journal:  Bioorg Med Chem Lett       Date:  2012-06-28       Impact factor: 2.823

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