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NADPH - ≥93%, high purity , CAS No.2646-71-1

    Grade & Purity:
  • ≥93%
In stock
Item Number
N276326
Grouped product items
SKU Size
Availability
Price Qty
N276326-50mg
50mg
4
$48.90
N276326-100mg
100mg
5
$79.90
N276326-250mg
250mg
Available within 1-2 weeks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$159.90

Coenzyme.

Basic Description

Synonyms NADPH Na4 | TPNH2 Na4 | AS-10522 | C21H26N7O17P3Na4 | A-NADPH | HB4469 | C74369 | MFCD00036263 | beta-Nicotinamide adenine dinucleotide phosphate reduced tetrasodium salt | NADPH tetrasodium salt (reduced form) | Dihydronicotinamide-adenine dinucleotide p
Specifications & Purity ≥93%
Biochemical and Physiological Mechanisms Ubiquitous coenzyme and biological reducing agent that acts as an electron donor for many redox enzymes including nitric oxide synthetase. Generated by reduction of the electron acceptor NADP+.
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.
Note 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

Store at -20°C. It is important to note that this product is reported to be light sensitive. Store In the Dark. Store under desiccating conditions.

Taxonomic Classification

Taxonomy Tree

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

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488201525
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488201525
IUPAC Name tetrasodium;[(2R,3R,4R,5R)-2-(6-aminopurin-9-yl)-5-[[[[(2R,3S,4R,5R)-5-(3-carbamoyl-4H-pyridin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl]oxymethyl]-4-hydroxyoxolan-3-yl] phosphate
INCHI InChI=1S/C21H30N7O17P3.4Na/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;;;;/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35);;;;/q;4*+1/p-4/t10-,11-,13-,14-,15-,16-,20-,21-;;;;/m1..../s1
InChIKey WYWWVJHQDVCHKF-ITGWJZMWSA-J
Smiles [Na+].[Na+].[Na+].[Na+].NC(=O)C1=CN(C=CC1)[C@H]2O[C@@H](COP([O-])(=O)OP([O-])(=O)OC[C@H]3O[C@H]([C@H](OP([O-])([O-])=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@H](O)[C@@H]2O
Isomeric SMILES C1C=CN(C=C1C(=O)N)[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.[Na+].[Na+].[Na+].[Na+]
Molecular Weight 833.35 (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.

31 results found

Lot Number Certificate Type Date Item
F2528107 Certificate of Analysis Jul 04, 2025 N276326
I2424105 Certificate of Analysis Oct 09, 2024 N276326
G2423030 Certificate of Analysis Jul 30, 2024 N276326
G2419064 Certificate of Analysis Jul 29, 2024 N276326
G2419065 Certificate of Analysis Jul 29, 2024 N276326
F2413087 Certificate of Analysis Jun 18, 2024 N276326
G2403036 Certificate of Analysis Jun 18, 2024 N276326
F2404214 Certificate of Analysis Jun 05, 2024 N276326
F2404215 Certificate of Analysis Jun 05, 2024 N276326
F2404216 Certificate of Analysis Jun 05, 2024 N276326
D2415018 Certificate of Analysis Apr 19, 2024 N276326
D2415020 Certificate of Analysis Apr 19, 2024 N276326
D2415019 Certificate of Analysis Apr 19, 2024 N276326
A2305301 Certificate of Analysis Mar 07, 2024 N276326
D2327022 Certificate of Analysis Jan 31, 2024 N276326
L2306104 Certificate of Analysis Dec 08, 2023 N276326
K2309008 Certificate of Analysis Nov 14, 2023 N276326
J2316011 Certificate of Analysis Oct 25, 2023 N276326
H2331025 Certificate of Analysis Sep 08, 2023 N276326
H2331024 Certificate of Analysis Sep 07, 2023 N276326
D2327018 Certificate of Analysis May 02, 2023 N276326
D2327019 Certificate of Analysis May 02, 2023 N276326
D2327020 Certificate of Analysis Apr 29, 2023 N276326
D2327021 Certificate of Analysis Apr 29, 2023 N276326
A2305351 Certificate of Analysis Jan 12, 2023 N276326
A2305299 Certificate of Analysis Jan 12, 2023 N276326
A2305352 Certificate of Analysis Jan 12, 2023 N276326
J2220037 Certificate of Analysis Nov 03, 2022 N276326
J2220038 Certificate of Analysis Nov 03, 2022 N276326
C2212546 Certificate of Analysis Jun 01, 2022 N276326
C2212542 Certificate of Analysis Jun 01, 2022 N276326

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Chemical and Physical Properties

Solubility 10 mM NaOH: soluble 50 mg/mL, clear
Sensitivity light sensitive;Heat sensitive
Molecular Weight 833.300 g/mol
XLogP3
Hydrogen Bond Donor Count 5
Hydrogen Bond Acceptor Count 22
Rotatable Bond Count 12
Exact Mass 833.019 Da
Monoisotopic Mass 833.019 Da
Topological Polar Surface Area 375.000 Ų
Heavy Atom Count 52
Formal Charge 0
Complexity 1380.000
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 5

Citations of This Product

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