β-Nicotinamide Mononucleotide (NMN) - 10mM in Water, high purity

6 Citations
  • 10mM in Water
Item Number
N420568
Grouped product items
SKUSizeAvailabilityPrice Qty
N420568-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$182.90

Key NAD+ intermediate

Basic Description

Synonyms1094-61-7 | beta-Nicotinamide mononucleotide | nicotinamide mononucleotide | NMN zwitterion | beta-NMN | Nicotinamide ribotide | nicotinamide nucleotide | NMN | beta-nicotinamide D-ribonucleotide | nicotinamide ribonucleotide | nicotinamide D-ribonucleotide | beta-Nicotinamide
Specifications & Purity10mM in Water
Biochemical and Physiological MechanismsProduct of the NAMPT reaction and\xa0a key intermediate in the biosynthesis of nicotinamide adenine dinucleotide (NAD + ). Ameliorates glucose intolerance by restoring NAD + levels in high-fat diet (HFD)-induced T2D mice. Enhances hepatic insulin sensitiv
Storage TempStore at -80°C
Shipped InIce chest + Ice pads
Product Description

A product of the eNAMPT reaction and a NAD+ intermediate

β-Nicotinamide mononucleotide (NMN) is used to study binding motifs within RNA aptamers and ribozyme activation processes involving β-nicotinamide mononucleotide (β-NMN)-activated RNA fragments.

β-Nicotinamide mononucleotide is a product of the extracellular Nicotinamide phosphoribosyltransferase (eNAMPT) reaction and a key NAD+ intermediate. It ameliorates glucose intolerance by restoring NAD+ levels in HFD-induced T2D mice. It also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation.

Associated Targets(Human)

GLUD1 Tbio Glutamate dehydrogenase 1, mitochondrial (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GAPDH Tchem Glyceraldehyde-3-phosphate dehydrogenase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
LDHB Tchem L-lactate dehydrogenase B chain (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MDH1 Tchem Malate dehydrogenase, cytoplasmic (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
LDHB Tchem L-lactate dehydrogenase B chain (463 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDH1 Tchem Malate dehydrogenase cytoplasmic (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GAPDH Tchem Glyceraldehyde-3-phosphate dehydrogenase liver (1284 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADH1A Tclin Alcohol dehydrogenase (35 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

GLUD1 Glutamate dehydrogenase (27 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
panE Ketopantoate reductase (28 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name [(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl hydrogen phosphate
INCHI InChI=1S/C11H15N2O8P/c12-10(16)6-2-1-3-13(4-6)11-9(15)8(14)7(21-11)5-20-22(17,18)19/h1-4,7-9,11,14-15H,5H2,(H3-,12,16,17,18,19)/t7-,8-,9-,11-/m1/s1
InChi Key DAYLJWODMCOQEW-TURQNECASA-N
Canonical SMILES C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)(O)[O-])O)O)C(=O)N
Isomeric SMILES C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)[O-])O)O)C(=O)N
WGK Germany 3
PubChem CID 14180
Molecular Weight 334.22
Beilstein 3570187

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

Sensitivityheat sensitive
Specific Rotation[α]-24° (C=2,H2O)
Melt Point(°C)166 °C

Safety and Hazards(GHS)

WGK Germany 3
Merck Index 6663

Related Documents

Citations of This Product

1. Jiyan Xu, Xinlu Chen, Shuai Liu, Ziqi Wei, Minhui Xu, Linhao Jiang, Xue Han, Liangyu Peng, Xiaoping Gu, Tianjiao Xia.  (2023)  Nicotinamide mononucleotide pretreatment improves long-term isoflurane anesthesia-induced cognitive impairment in mice.  BEHAVIOURAL BRAIN RESEARCH,    (14): (114738).  [PMID:37931707]
2. Qi Shen, Shi-Jia Zhang, Bin-Hui Xu, Zhi-Yu Chen, Feng Peng, Neng Xiong, Ya-Ping Xue, Yu-Guo Zheng.  (2023)  Semirational engineering of Cytophaga hutchinsonii polyphosphate kinase for developing a cost-effective, robust, and efficient adenosine 5′-triphosphate regeneration system.  APPLIED AND ENVIRONMENTAL MICROBIOLOGY,      [PMID:37902313]
3. Ruixue Duan, Yueping Li, Ruru Zhang, Xuelan Hu, Yi wang, Jianfeng Zeng, Mingyuan Gao.  (2023)  Reversing Acute Kidney Injury Through Coordinated Interplay of Anti-inflammation and Iron Supplementation.  ADVANCED MATERIALS,    (2301283).  [PMID:37029662]
4. Zhuhui Chen, Yue Xiong, Ranran Ma, Pei Chen, Le Duan, Shuying Yang, Ineza Urujeni Gisèle, Linjun You, Deli Xiao.  (2023)  A novel magnetic fluid for ultra-fast and highly efficient extraction of N1-methylnicotinamide in urine samples.  NEW JOURNAL OF CHEMISTRY,  47  (16): (7862-7872).  [PMID:]
5. Wu Yue, Yang Jingjuan, Xu Chengmei, Li Qiuqi, Ma Yage, Zhao Shenglan, Zhuang Jiachen, Shen Fei, Wang Qianqian, Feng Fengqin, Zhang Xi.  (2022)  Sea cucumber (Acaudina leucoprocta) peptides extended the lifespan and enhanced antioxidant capacity via DAF-16/DAF-2/SOD-3/OLD-1/PEPT-1 in Caenorhabditis elegans.  Frontiers in Nutrition,    [PMID:36483922]
6. Zhongshi Huang, Ning Li, Shiqin Yu, Weiping Zhang, Tianmeng Zhang, Jingwen Zhou.  (2022)  Systematic Engineering of Escherichia coli for Efficient Production of Nicotinamide Mononucleotide From Nicotinamide.  ACS Synthetic Biology,  11  (9): (2979–2988).  [PMID:35977419]

References

1. Jiyan Xu, Xinlu Chen, Shuai Liu, Ziqi Wei, Minhui Xu, Linhao Jiang, Xue Han, Liangyu Peng, Xiaoping Gu, Tianjiao Xia.  (2023)  Nicotinamide mononucleotide pretreatment improves long-term isoflurane anesthesia-induced cognitive impairment in mice.  BEHAVIOURAL BRAIN RESEARCH,    (14): (114738).  [PMID:37931707]
2. Qi Shen, Shi-Jia Zhang, Bin-Hui Xu, Zhi-Yu Chen, Feng Peng, Neng Xiong, Ya-Ping Xue, Yu-Guo Zheng.  (2023)  Semirational engineering of Cytophaga hutchinsonii polyphosphate kinase for developing a cost-effective, robust, and efficient adenosine 5′-triphosphate regeneration system.  APPLIED AND ENVIRONMENTAL MICROBIOLOGY,      [PMID:37902313]
3. Ruixue Duan, Yueping Li, Ruru Zhang, Xuelan Hu, Yi wang, Jianfeng Zeng, Mingyuan Gao.  (2023)  Reversing Acute Kidney Injury Through Coordinated Interplay of Anti-inflammation and Iron Supplementation.  ADVANCED MATERIALS,    (2301283).  [PMID:37029662]
4. Zhuhui Chen, Yue Xiong, Ranran Ma, Pei Chen, Le Duan, Shuying Yang, Ineza Urujeni Gisèle, Linjun You, Deli Xiao.  (2023)  A novel magnetic fluid for ultra-fast and highly efficient extraction of N1-methylnicotinamide in urine samples.  NEW JOURNAL OF CHEMISTRY,  47  (16): (7862-7872).  [PMID:]
5. Wu Yue, Yang Jingjuan, Xu Chengmei, Li Qiuqi, Ma Yage, Zhao Shenglan, Zhuang Jiachen, Shen Fei, Wang Qianqian, Feng Fengqin, Zhang Xi.  (2022)  Sea cucumber (Acaudina leucoprocta) peptides extended the lifespan and enhanced antioxidant capacity via DAF-16/DAF-2/SOD-3/OLD-1/PEPT-1 in Caenorhabditis elegans.  Frontiers in Nutrition,    [PMID:36483922]
6. Zhongshi Huang, Ning Li, Shiqin Yu, Weiping Zhang, Tianmeng Zhang, Jingwen Zhou.  (2022)  Systematic Engineering of Escherichia coli for Efficient Production of Nicotinamide Mononucleotide From Nicotinamide.  ACS Synthetic Biology,  11  (9): (2979–2988).  [PMID:35977419]

Solution Calculators