Basic Description

Synonyms	β-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate \| beta-Nicotinamide adenine dinucleotide phosphate sodium salt hydrate \| Triphosphopyridine nucleotide sodium salt hydrate \| β-NADP
Specifications & Purity	≥98%(HPLC)
Storage Temp	Protected from light,Store at -20°C,Desiccated
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Acts as an electron acceptor commonly used by cells. This is used in vitro to study NADP and how it accepts electrons, among other applications. An endogenous electron acceptor and the common form of NADP Application： β-Nicotinamide adenine dinucleotide 2′-phosphate (NADP+) and β-Nicotinamide adenine dinucleotide 2′-phosphate, reduced (NADPH) comprise a coenzyme redox pair (NADP+:NADPH) involved in a wide range of enzyme catalyzed oxidation reduction reactions. The NADP+/NADPH redox pair facilitates electron transfer in anabolic reactions such as lipid and cholesterol biosynthesis and fatty acyl chain elongation. The NADP+/NADPH redox pair is used in a variety of antioxidation mechanism where it protects agains reactive oxidation species accumulation. NADPH is generated in vivio by the pentose phosphate pathway (PPP).

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class (5'->5')-dinucleotides

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 2',5'-bisphosphates Nicotinamide nucleotides Pentose phosphates Glycosylamines 6-aminopurines Monosaccharide phosphates Organic pyrophosphates Nicotinamides Aminopyrimidines and derivatives Monoalkyl phosphates Pyridinium derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Vinylogous amides Secondary alcohols Primary carboxylic acid amides Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives Organopnictogen compounds Organic sodium salts Organic zwitterions
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	(5'->5')-dinucleotide - Purine nucleotide sugar - Purine ribonucleoside diphosphate - Purine ribonucleoside bisphosphate - Purine ribonucleoside 2',5'-bisphosphate - Nicotinamide-nucleotide - Pyridine nucleotide - Pentose-5-phosphate - Pentose phosphate - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Organic pyrophosphate - Pyridine carboxylic acid or derivatives - Imidazopyrimidine - Purine - Nicotinamide - Monoalkyl phosphate - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyrimidine - Pyridine - Pyridinium - Oxolane - Azole - Vinylogous amide - Imidazole - Heteroaromatic compound - Primary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Organic alkali metal salt - Azacycle - Oxacycle - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - Organic salt - Organic zwitterion - Organonitrogen compound - Organooxygen compound - Organic sodium salt - 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
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

Names and Identifiers

Pubchem Sid	504772594
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504772594
IUPAC Name	sodium;[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate;hydrate
INCHI	InChI=1S/C21H28N7O17P3.Na.H2O/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32;;/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39);;1H2/q;+1;/p-1/t10-,11-,13-,14-,15-,16-,20-,21-;;/m1../s1
InChIKey	CYQLUFJYVTUUFN-WUEGHLCSSA-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)OP(=O)(O)O)O)O)O)C(=O)N.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)OP(=O)(O)O)O)O)O)C(=O)N.O.[Na+]
WGK Germany	3
Alternate CAS	1184-16-3
PubChem CID	90475149
Molecular Weight	765.39 (anhydrous basis)

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

26 results found

Lot Number	Certificate Type	Date	Item
K2412564	Certificate of Analysis	Nov 04, 2024	T140491
K2412565	Certificate of Analysis	Nov 04, 2024	T140491
K2412566	Certificate of Analysis	Nov 04, 2024	T140491
K2412571	Certificate of Analysis	Nov 04, 2024	T140491
K2412573	Certificate of Analysis	Nov 04, 2024	T140491
F2404129	Certificate of Analysis	May 11, 2024	T140491
L2318456	Certificate of Analysis	Dec 11, 2023	T140491
J2312279	Certificate of Analysis	Oct 08, 2023	T140491
J2312308	Certificate of Analysis	Oct 08, 2023	T140491
J2312278	Certificate of Analysis	Oct 08, 2023	T140491
J2312280	Certificate of Analysis	Oct 08, 2023	T140491
J2312282	Certificate of Analysis	Oct 08, 2023	T140491
J2312348	Certificate of Analysis	Oct 08, 2023	T140491
J2312277	Certificate of Analysis	Oct 08, 2023	T140491
J2312281	Certificate of Analysis	Oct 08, 2023	T140491
I1521131	Certificate of Analysis	Jun 05, 2023	T140491
L2205632	Certificate of Analysis	Nov 01, 2022	T140491
I2326003	Certificate of Analysis	Nov 01, 2022	T140491
L2205784	Certificate of Analysis	Nov 01, 2022	T140491
L2205633	Certificate of Analysis	Nov 01, 2022	T140491
L2205607	Certificate of Analysis	Nov 01, 2022	T140491
D2221034	Certificate of Analysis	Feb 28, 2022	T140491
D2221024	Certificate of Analysis	Feb 28, 2022	T140491
D2221021	Certificate of Analysis	Feb 28, 2022	T140491
B2210132	Certificate of Analysis	Feb 14, 2022	T140491
B2210176	Certificate of Analysis	Feb 14, 2022	T140491

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Chemical and Physical Properties

Solubility	Soluble in water (50 mg/ml).
Sensitivity	Light and heat sensitive
Melt Point(°C)	175-178°C
Molecular Weight	783.400 g/mol
XLogP3
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	22
Rotatable Bond Count	13
Exact Mass	783.068 Da
Monoisotopic Mass	783.068 Da
Topological Polar Surface Area	371.000 Å²
Heavy Atom Count	50
Formal Charge	0
Complexity	1290.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	8
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	3

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SKU	Size	Availability	Price
T140491-25mg	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
T140491-100mg	100mg	2	$16.90
T140491-500mg	500mg	2	$39.90
T140491-1g	1g	2	$65.90
T140491-5g	5g	2	$209.90

Triphosphopyridine nucleotide sodium salt hydrate - ≥98% (HPLC), high purity , CAS No.698999-85-8