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Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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SKU | Size | Availability | Price | Qty |
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N131850-25mg | 25mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $9.90 | |
N131850-100mg | 100mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $19.90 | |
N131850-500mg | 500mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $29.90 | |
N131850-1g | 1g | In stock | $39.90 | |
N131850-5g | 5g | In stock | $72.90 | |
N131850-25g | 25g | In stock | $216.90 | |
N131850-100g | 100g | In stock | $519.90 |
Key NAD+ intermediate
Synonyms | nicotinamide ribonucleotide | NMN zwitterion | beta-Nicotinamide mononucleotide | Nicotinamide ribotide | nicotinamide D-ribonucleotide | nicotinamide mononucleotide | beta-nicotinamide D-ribonucleotide | beta-NMN | nicotinamide nucleotide | NMN |
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Specifications & Purity | ≥95% |
Biochemical and Physiological Mechanisms | Product 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 Temp | Store at -20°C,Argon charged |
Shipped In | Ice chest + Ice pads |
Note | 25mg/200mg 中国和美国售完停产 Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
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. |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Pubchem Sid | 488181949 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181949 |
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 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
K2421511 | Certificate of Analysis | Nov 08, 2024 | N131850 |
K2421508 | Certificate of Analysis | Nov 08, 2024 | N131850 |
K2421504 | Certificate of Analysis | Nov 08, 2024 | N131850 |
K2421499 | Certificate of Analysis | Nov 08, 2024 | N131850 |
H2231896 | Certificate of Analysis | Jun 19, 2024 | N131850 |
H2231705 | Certificate of Analysis | Jun 19, 2024 | N131850 |
H2231626 | Certificate of Analysis | Jun 19, 2024 | N131850 |
J2425770 | Certificate of Analysis | Apr 23, 2024 | N131850 |
J2425769 | Certificate of Analysis | Apr 23, 2024 | N131850 |
J2425643 | Certificate of Analysis | Apr 23, 2024 | N131850 |
L2107071 | Certificate of Analysis | Sep 19, 2023 | N131850 |
L2106810 | Certificate of Analysis | Sep 19, 2023 | N131850 |
L2106693 | Certificate of Analysis | Sep 19, 2023 | N131850 |
G2321649 | Certificate of Analysis | Jun 13, 2023 | N131850 |
I2405021 | Certificate of Analysis | Jun 13, 2023 | N131850 |
G2321642 | Certificate of Analysis | Jun 13, 2023 | N131850 |
G2321634 | Certificate of Analysis | Jun 13, 2023 | N131850 |
G2321628 | Certificate of Analysis | Jun 13, 2023 | N131850 |
G2321302 | Certificate of Analysis | Jun 13, 2023 | N131850 |
G2321285 | Certificate of Analysis | Jun 13, 2023 | N131850 |
G2109284 | Certificate of Analysis | Apr 18, 2023 | N131850 |
G2109283 | Certificate of Analysis | Apr 18, 2023 | N131850 |
G2109282 | Certificate of Analysis | Apr 18, 2023 | N131850 |
B2328602 | Certificate of Analysis | Feb 16, 2023 | N131850 |
B2328606 | Certificate of Analysis | Feb 16, 2023 | N131850 |
B2328607 | Certificate of Analysis | Feb 16, 2023 | N131850 |
B2328608 | Certificate of Analysis | Feb 16, 2023 | N131850 |
B2328936 | Certificate of Analysis | Feb 16, 2023 | N131850 |
B2328601 | Certificate of Analysis | Feb 16, 2023 | N131850 |
H2231700 | Certificate of Analysis | Jun 18, 2022 | N131850 |
H2231625 | Certificate of Analysis | Jun 18, 2022 | N131850 |
H2231624 | Certificate of Analysis | Jun 18, 2022 | N131850 |
C2226312 | Certificate of Analysis | Feb 17, 2022 | N131850 |
C2226284 | Certificate of Analysis | Feb 17, 2022 | N131850 |
C2226321 | Certificate of Analysis | Feb 17, 2022 | N131850 |
Solubility | Soluble in PBS (10 mg/ml). |
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Sensitivity | heat sensitive |
Specific Rotation[α] | -24° (C=2,H2O) |
Melt Point(°C) | 166 °C |
WGK Germany | 3 |
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Merck Index | 6663 |
Starting at $182.90
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] [10.1016/j.bbr.2023.114738] |
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] [10.1128/aem.01106-23] |
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] [10.1002/adma.202301283] |
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:] [10.1039/D3NJ00488K] |
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, 9 [PMID:36483922] [10.3389/fnut.2022.1065145] |
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] [10.1021/acssynbio.2c00100] |
7. Jinhui Hu, Ting Wang, Lin Zhou, Shaohua Wei. (2020) A ROS responsive nanomedicine with enhanced photodynamic therapy via dual mechanisms: GSH depletion and biosynthesis inhibition. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 209 (111955). [PMID:32653858] [10.1016/j.jphotobiol.2020.111955] |
8. Zhang Weihong, Wang Dan, Wang Jie-Xin, Pu Yuan, Chen Jian-Feng. (2020) High-gravity-assisted emulsification for continuous preparation of waterborne polyurethane nanodispersion with high solids content. Frontiers of Chemical Science and Engineering, 14 (6): (1087-1099). [PMID:] [10.1007/s11705-019-1895-z] |
9. Guohan Sun, Shiqiao Wang, Jianfeng Zhou, Jianbin Pan, Yanli Tong, Qinghua Mei, Haiyun Zhai. (2020) Constructing a simple and sensitive electrochemical sensor for the determination of NMN based on p-m-ABSA film modified glassy carbon electrode. MICROCHEMICAL JOURNAL, 152 (104438). [PMID:] [10.1016/j.microc.2019.104438] |
10. Dengcheng Huang, Yu Zhou, Yuan Xiang, Meijie Shu, Hongxiang Chen, Bing Yang, Xinghua Liao. (2018) Polyurethane/doxorubicin nanoparticles based on electrostatic interactions as pH-sensitive drug delivery carriers. POLYMER INTERNATIONAL, 67 (9): (1186-1193). [PMID:] [10.1002/pi.5618] |
11. Ma Le, Song Lina, Li Fang, Wang Heng, Liu Baohua. (2017) Preparation and properties of poly (propylene carbonate)-based waterborne polyurethane-acrylate composite emulsion. COLLOID AND POLYMER SCIENCE, 295 (12): (2299-2307). [PMID:] [10.1007/s00396-017-4198-2] |
12. Caideng Yuan, Mengyao Wang, Haitao Li, Zhongwei Wang. (2017) Preparation and properties of UV-curable waterborne polyurethane–acrylate emulsion. JOURNAL OF APPLIED POLYMER SCIENCE, 134 (34): (45208). [PMID:] [10.1002/app.45208] |
13. Di Liu, Guo-Min Wu, Zhen-Wu Kong. (2016) Preparation and characterization of a polydimethylsiloxane-modified, epoxy-resin-based polyol dispersion and its crosslinked films. JOURNAL OF APPLIED POLYMER SCIENCE, 134 (1): [PMID:] [10.1002/app.44342] |
14. Sude Ma, Guolin Song, Ningbo Feng. (2012) Preparation and characterization of self-emulsified waterborne nitrocellulose. CARBOHYDRATE POLYMERS, 89 (36). [PMID:24750600] [10.1016/j.carbpol.2012.02.029] |
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] [10.1016/j.bbr.2023.114738] |
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] [10.1128/aem.01106-23] |
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] [10.1002/adma.202301283] |
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:] [10.1039/D3NJ00488K] |
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, 9 [PMID:36483922] [10.3389/fnut.2022.1065145] |
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] [10.1021/acssynbio.2c00100] |
7. Jinhui Hu, Ting Wang, Lin Zhou, Shaohua Wei. (2020) A ROS responsive nanomedicine with enhanced photodynamic therapy via dual mechanisms: GSH depletion and biosynthesis inhibition. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 209 (111955). [PMID:32653858] [10.1016/j.jphotobiol.2020.111955] |
8. Zhang Weihong, Wang Dan, Wang Jie-Xin, Pu Yuan, Chen Jian-Feng. (2020) High-gravity-assisted emulsification for continuous preparation of waterborne polyurethane nanodispersion with high solids content. Frontiers of Chemical Science and Engineering, 14 (6): (1087-1099). [PMID:] [10.1007/s11705-019-1895-z] |
9. Guohan Sun, Shiqiao Wang, Jianfeng Zhou, Jianbin Pan, Yanli Tong, Qinghua Mei, Haiyun Zhai. (2020) Constructing a simple and sensitive electrochemical sensor for the determination of NMN based on p-m-ABSA film modified glassy carbon electrode. MICROCHEMICAL JOURNAL, 152 (104438). [PMID:] [10.1016/j.microc.2019.104438] |
10. Dengcheng Huang, Yu Zhou, Yuan Xiang, Meijie Shu, Hongxiang Chen, Bing Yang, Xinghua Liao. (2018) Polyurethane/doxorubicin nanoparticles based on electrostatic interactions as pH-sensitive drug delivery carriers. POLYMER INTERNATIONAL, 67 (9): (1186-1193). [PMID:] [10.1002/pi.5618] |
11. Ma Le, Song Lina, Li Fang, Wang Heng, Liu Baohua. (2017) Preparation and properties of poly (propylene carbonate)-based waterborne polyurethane-acrylate composite emulsion. COLLOID AND POLYMER SCIENCE, 295 (12): (2299-2307). [PMID:] [10.1007/s00396-017-4198-2] |
12. Caideng Yuan, Mengyao Wang, Haitao Li, Zhongwei Wang. (2017) Preparation and properties of UV-curable waterborne polyurethane–acrylate emulsion. JOURNAL OF APPLIED POLYMER SCIENCE, 134 (34): (45208). [PMID:] [10.1002/app.45208] |
13. Di Liu, Guo-Min Wu, Zhen-Wu Kong. (2016) Preparation and characterization of a polydimethylsiloxane-modified, epoxy-resin-based polyol dispersion and its crosslinked films. JOURNAL OF APPLIED POLYMER SCIENCE, 134 (1): [PMID:] [10.1002/app.44342] |
14. Sude Ma, Guolin Song, Ningbo Feng. (2012) Preparation and characterization of self-emulsified waterborne nitrocellulose. CARBOHYDRATE POLYMERS, 89 (36). [PMID:24750600] [10.1016/j.carbpol.2012.02.029] |