Nicotinamide riboside chloride - ≥98% , CAS No.23111-00-4

CAS: 23111-00-4 Cat. No.: N303138 Peso molecular: 290.7 Número EC: 807-820-5

GRADE & PURITY ≥98%

Synonyms

Nicotinamide riboside chloride | 8XM2XT8VWI | Nicotinamide ribose chloride | 3-Carbamoyl-1-((2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium chloride | Nicotinamide riboside (chloride) | 23111-00-4 | 烟酰胺核糖氯酸盐

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

Nicotinamide riboside is involved in nicotinate and nicotinamide metabolism. Nicotinamide riboside was originally identified as a nutrient in milk and later discovered to be a NAD(+) precursor.

Specifications

Sinónimos

Nicotinamide riboside chloride | 8XM2XT8VWI | Nicotinamide ribose chloride | 3-Carbamoyl-1-((2r, 3r, 4s, 5r)-3, 4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium chloride | Nicotinamide riboside (chloride) | 23111-00-4 | 烟酰胺核糖氯酸盐

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504772599
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504772599
• Sonrisas canónicas: C1=CC(=C[N+](=C1)C2C(C(C(O2)CO)O)O)C(=O)N.[Cl-]
• IUPAC Name: 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyridin-1-ium-3-carboxamide;chloride
• InChIKey: YABIFCKURFRPPO-IVOJBTPCSA-N
• INCHI: 1S/C11H14N2O5.ClH/c12-10(17)6-2-1-3-13(4-6)11-9(16)8(15)7(5-14)18-11;/h1-4,7-9,11,14-16H,5H2,(H-,12,17);1H/t7-,8-,9-,11-;/m1./s1
• Isómeros SMILES: C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O)C(=O)N.[Cl-]
• Peso molecular: 290.7
• Reaxy-Rn: 48663754
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=48663754&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 Glycosylamines

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: Glycosylamines
• Alternative Parents: Pentoses Nicotinamides Pyridinium derivatives Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Primary carboxylic acid amides Azacyclic compounds Oxacyclic compounds Organic oxides Organic chloride salts Primary alcohols Hydrocarbon derivatives Organic zwitterions Organonitrogen compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: N-glycosyl compound - Pentose monosaccharide - Nicotinamide - Pyridine carboxylic acid or derivatives - Monosaccharide - Pyridine - Pyridinium - Vinylogous amide - Heteroaromatic compound - Oxolane - Secondary alcohol - Carboxamide group - Primary carboxylic acid amide - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Organic salt - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - Organic oxide - Alcohol - Organic nitrogen compound - Organic chloride salt - Organic zwitterion - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive；Heat sensitive；light sensitive
• Peso molecular: 290.700 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 290.067 Da
• Monoisotopic Mass: 290.067 Da
• Topological Polar Surface Area: 117.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 314.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Referencias

1. Seongsu Kang, Jiwon Park, Eunbyul Cho, Dohyun Kim, Sanghyun Ye, Eui Taek Jeong, Seung-Hyun Jun, Nae-Gyu Kang.  (2025)  Distinctive Gene Expression Profiles and Biological Responses of Skin Fibroblasts to Nicotinamide Mononucleotide: Implications for Longevity Effects on Skin.  Biomedicines,  13  (10): (2395).  [PMID:41153679] [10.3390/biomedicines13102395]

2. Yi Zhang, Ying Guo, Wenxi He, Yaping Zhao, Zhaode Feng, Mengjiao Shi, Xinyan Li, Liangwen Yan, Jiayi Xu, Kailing Hu, Rongrong Liu, Yinggang Zhang, Gang Wang, Hao Li, Pengfei Liu.  (2025)  Deciphering the rules of disulfidptosis: a genome-wide signature for identifying disulfidptosis-related genes and analyzing hepatocellular carcinoma chemotherapy sensitivities.  FREE RADICAL BIOLOGY AND MEDICINE,      [PMID:41138962] [10.1016/j.freeradbiomed.2025.10.278]