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Nicotinic acid adenine dinucleotide sodium salt - ≥98%, high purity , CAS No.104809-30-5
Basic Description
Synonyms
NAAD sodium salt | AKOS040753193 | Deamido Nad sodium salt | NAAD (sodium) | CS-0063527 | NAAD Na, NaAD | Sodium;[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3S,4R,5R)-5-(3-carboxypyridin-1-ium-1-yl)-3,4-dih
Specifications & Purity
Moligand™, ≥98%
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Product Description
Nicotinic acid adenine dinucleotide sodium salt is used to study the structure of nicotinate mononucleotide adenylyltransferases. It is used as a substrate to study the specificity and kinetics of nicotinamide adenine dinucleotide synthetases. It can also be used as a cosubstrate to study mechanisms of members of the Sir2 class of NAD(+)-dependent deacetylases.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
(5'->5')-dinucleotides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
(5'->5')-dinucleotides
Alternative Parents
Purine nucleotide sugars Purine ribonucleoside diphosphates Purine ribonucleoside monophosphates Nicotinic acid nucleotides Pentose phosphates Glycosylamines 6-aminopurines Monosaccharide phosphates Organic pyrophosphates Pyridinecarboxylic acids Aminopyrimidines and derivatives Alkyl phosphates Pyridinium derivatives Imidolactams N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Amino acids Secondary alcohols Oxacyclic compounds Carboxylic acids Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Primary amines Organic zwitterions Organic sodium salts Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
(5'->5')-dinucleotide - Purine nucleotide sugar - Purine ribonucleoside diphosphate - Purine ribonucleoside monophosphate - Nicotinic-acid-nucleotide - Pyridine nucleotide - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Organic pyrophosphate - Imidazopyrimidine - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - Purine - Aminopyrimidine - Imidolactam - Alkyl phosphate - Monosaccharide - N-substituted imidazole - Pyrimidine - Pyridinium - Pyridine - Organic phosphoric acid derivative - Phosphoric acid ester - Vinylogous amide - Azole - Imidazole - Oxolane - Heteroaromatic compound - Amino acid or derivatives - Amino acid - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Carboxylic acid - Organic alkali metal salt - Organic salt - Alcohol - Organic zwitterion - Organic sodium salt - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Amine - Organonitrogen compound - Organooxygen compound - Organic oxide - Primary amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as (5'->5')-dinucleotides. These are dinucleotides where the two bases are connected via a (5'->5')-phosphodiester linkage.
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.
Names and Identifiers
Pubchem Sid
504772685
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504772685
IUPAC Name
sodium;[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3S,4R,5R)-5-(3-carboxypyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
INCHI
InChI=1S/C21H26N6O15P2.Na/c22-17-12-18(24-7-23-17)27(8-25-12)20-16(31)14(29)11(41-20)6-39-44(36,37)42-43(34,35)38-5-10-13(28)15(30)19(40-10)26-3-1-2-9(4-26)21(32)33;/h1-4,7-8,10-11,13-16,19-20,28-31H,5-6H2,(H4-,22,23,24,32,33,34,35,36,37);/q;+1/p-1/t10-,11-,13-,14-,15-,16-,19-,20-;/m1./s1
InChIKey
LFHLUTZTSGEADU-RHANTIMGSA-M
Smiles
C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OCC3C(C(C(O3)N4C=NC5=C(N=CN=C54)N)O)O)O)O)C(=O)O.[Na+]
Isomeric SMILES
C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])OC[C@@H]3[C@H]([C@H]([C@@H](O3)N4C=NC5=C(N=CN=C54)N)O)O)O)O)C(=O)O.[Na+]
WGK Germany
3
PubChem CID
91872645
Molecular Weight
686.4
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water (50 mg/ml).
Sensitivity
Moisture sensitive
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J2425231