Small Molecule Regulators Targeting NAD+ Biosynthetic Enzymes

被引:3
作者
Curry, Alyson [1 ]
White, Dawanna [1 ]
Cen, Yana [1 ,2 ]
机构
[1] Virginia Commonwealth Univ, Dept Med Chem, Richmond, VA 23219 USA
[2] Virginia Commonwealth Univ, Inst Struct Biol Drug Discovery & Dev, Richmond, VA 23219 USA
关键词
Nicotinamide adenine dinucleotide (NAD(+)); metabolic pathways; electrons; redox reactions; enzymatic transformations; therapeutic potentials; NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE NAMPT; PERMEABILITY TRANSITION PORE; NEURONAL CELL-DEATH; INDOLEAMINE 2,3-DIOXYGENASE; CRYSTAL-STRUCTURE; ACID PHOSPHORIBOSYLTRANSFERASE; KYNURENINE; 3-MONOOXYGENASE; ADENINE-DINUCLEOTIDE; POTENT INHIBITOR; SALVAGE PATHWAY;
D O I
10.2174/0929867328666210531144629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nicotinamide adenine dinucleotide (NAD(+)) is a key player in many metabolic pathways as an activated carrier of electrons. In addition to being the cofactor for redox reactions, NAD(+) also serves as the substrate for various enzymatic transformations such as adenylation and ADP-ribosylation. Maintaining cellular NAD(+) homeostasis has been suggested as an effective anti-aging strategy. Given the importance of NAD(+) in regulating a broad spectrum of cellular events, small molecules targeting NAD+ metabolism have been pursued as therapeutic interventions for the treatment of mitochondrial disorders and age-related diseases. In this article, small molecule regulators of NAD(+) biosynthetic enzymes will be reviewed. The focus will be given to the discovery and development of these molecules, the mechanism of action as well as their therapeutic potentials.
引用
收藏
页码:1718 / 1738
页数:21
相关论文
共 150 条
  • [91] Anticancer agent CHS-828 inhibits cellular synthesis of NAD
    Olesen, Uffe Hogh
    Christensen, Mette Knak
    Bjorkling, Fredrik
    Jaattela, Marja
    Jensen, Peter Buhl
    Sehested, Maxwell
    Nielsen, Soren Jensby
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 367 (04) : 799 - 804
  • [92] Expression patterns of nicotinamide phosphoribosyltransferase and nicotinic acid phosphoribosyltransferase in human malignant lymphomas
    Olesen, Uffe Hogh
    Hastrup, Nina
    Sehested, Maxwell
    [J]. APMIS, 2011, 119 (4-5) : 296 - 303
  • [93] The NAD+ synthesizing enzyme nicotinamide mononucleotide adenylyltransferase 2 (NMNAT-2) is a p53 downstream target
    Pan, Lu-Zhe
    Ahn, Dae-Gyun
    Sharif, Tanveer
    Clements, Derek
    Gujar, Shashi A.
    Lee, Patrick W. K.
    [J]. CELL CYCLE, 2014, 13 (06) : 1041 - 1048
  • [94] Pellicciari R, 2003, ADV EXP MED BIOL, V527, P621
  • [95] MODULATION OF THE KYNURENINE PATHWAY IN SEARCH FOR NEW NEUROPROTECTIVE AGENTS - SYNTHESIS AND PRELIMINARY EVALUATION OF (M-NITROBENZOYL)ALANINE, A POTENT INHIBITOR OF KYNURENINE-3-HYDROXYLASE
    PELLICCIARI, R
    NATALINI, B
    COSTANTINO, G
    MAHMOUD, MR
    MATTOLI, L
    SADEGHPOUR, BM
    MORONI, F
    CHIARUGI, A
    CARPENEDO, R
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (05) : 647 - 655
  • [96] AN IONTOPHORETIC INVESTIGATION OF THE ACTIONS OF CONVULSANT KYNURENINES AND THEIR INTERACTION WITH THE ENDOGENOUS EXCITANT QUINOLINIC ACID
    PERKINS, MN
    STONE, TW
    [J]. BRAIN RESEARCH, 1982, 247 (01) : 184 - 187
  • [97] Pevarello P., 1999, Tricyclic 3-oxo-propanenitrile Compounds, Patent No. [WO1999/016753A2, 1999016753]
  • [98] Modulation of Enzyme Activity in the Kynurenine Pathway by Kynurenine Monooxygenase Inhibition
    Phillips, Robert S.
    Iradukunda, Emma Carine
    Hughes, Tamera
    Bowen, J. Phillip
    [J]. FRONTIERS IN MOLECULAR BIOSCIENCES, 2019, 6
  • [99] Structure and mechanism of kynureninase
    Phillips, Robert S.
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2014, 544 : 69 - 74
  • [100] STEREOCHEMISTRY AND MECHANISM OF ALDOL REACTIONS CATALYZED BY KYNURENINASE
    PHILLIPS, RS
    DUA, RK
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (19) : 7385 - 7388