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P1,P5-Di(adenosine-5′) pentaphosphate pentasodium - 96%, high purity , CAS No.4097-04-5

    Grade & Purity:
  • ≥96%
In stock
Item Number
P113572
Grouped product items
SKU Size
Availability
Price Qty
P113572-1mg
1mg
2
$103.90
P113572-5mg
5mg
2
$378.90
P113572-10mg
10mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$754.90
View related series
Metabolite (5307)

Basic Description

Synonyms 4097-04-5 | Adenosine 5'-(hexahydrogen pentaphosphate), 5'.5'-ester with adenosine, pentasodium salt | EINECS 223-852-7 | P1,P5-Di(adenosine-5') pentaphosphate pentasodium salt | pentasodium;bis[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]metho
Specifications & Purity ≥96%
Biochemical and Physiological Mechanisms Polyphosphate diphosphate is stored in the secretory vesicles of platelets, chromaffin cells and nerve cells. When it is released into extracellular matrix, it will affect many biological activities in many target tissues. In the nervous system, it plays
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.
Product Description

A diadenosine polyphosphate stored in secretory granules of chromaffin and neuronal cells and thrombocytes. After release into the extracellular space, the compound affects a variety of biological activities in a wide range of target tissues. In the nervous system it acts through various purinergic receptors. It also activates 5'-nucleotidase and inhibits adenosine kinase activity in vitro. Ap5A is metabolized by soluble enzymes in the blood plasma and by membrane-bound ectoenzymes of a number of cell types including endothelial and smooth muscle cells.

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 ribonucleoside polyphosphates  Purine nucleotide sugars  Purine ribonucleoside monophosphates  Pentose phosphates  Glycosylamines  6-aminopurines  Monosaccharide phosphates  Aminopyrimidines and derivatives  Alkyl phosphates  N-substituted imidazoles  Imidolactams  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  Oxacyclic compounds  Azacyclic compounds  Hydrocarbon derivatives  Organic oxides  Organic sodium salts  Organic zwitterions  Organopnictogen compounds  Primary amines  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents (5'->5')-dinucleotide - Purine ribonucleoside polyphosphate - Purine nucleotide sugar - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - Monosaccharide - Alkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Azole - Imidazole - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Organic alkali metal salt - Azacycle - Organic oxide - Amine - Organonitrogen compound - Organic zwitterion - Alcohol - Organic salt - Organic sodium salt - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organopnictogen compound - 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

Names and Identifiers

IUPAC Name pentasodium;bis[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] phosphate
INCHI InChI=1S/C20H29N10O22P5.5Na/c21-15-9-17(25-3-23-15)29(5-27-9)19-13(33)11(31)7(47-19)1-45-53(35,36)49-55(39,40)51-57(43,44)52-56(41,42)50-54(37,38)46-2-8-12(32)14(34)20(48-8)30-6-28-10-16(22)24-4-26-18(10)30;;;;;/h3-8,11-14,19-20,31-34H,1-2H2,(H,35,36)(H,37,38)(H,39,40)(H,41,42)(H,43,44)(H2,21,23,25)(H2,22,24,26);;;;;/q;5*+1/p-5/t7-,8-,11-,12-,13-,14-,19-,20-;;;;;/m1...../s1
InChIKey NNMFUJJMJIYTSP-CSMIRWGRSA-I
Smiles C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OCC4C(C(C(O4)N5C=NC6=C(N=CN=C65)N)O)O)O)O)N.[Na+].[Na+].[Na+].[Na+].[Na+]
Isomeric SMILES C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=NC6=C(N=CN=C65)N)O)O)O)O)N.[Na+].[Na+].[Na+].[Na+].[Na+]
WGK Germany 3
Alternate CAS 41708-91-2
PubChem CID 16219241
Molecular Weight 1026.28
Beilstein 4949216

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.

11 results found

Lot Number Certificate Type Date Item
F2108216 Certificate of Analysis Mar 04, 2025 P113572
F23301156 Certificate of Analysis May 05, 2023 P113572
F23301164 Certificate of Analysis May 05, 2023 P113572
F23301161 Certificate of Analysis Jan 04, 2023 P113572
F2330500 Certificate of Analysis Jan 04, 2023 P113572
D2304007 Certificate of Analysis Jan 04, 2023 P113572
D23031311 Certificate of Analysis Jan 04, 2023 P113572
D2304014 Certificate of Analysis Jan 04, 2023 P113572
H2211473 Certificate of Analysis Jul 30, 2022 P113572
H2211472 Certificate of Analysis Jul 30, 2022 P113572
H2211471 Certificate of Analysis Jul 30, 2022 P113572

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Chemical and Physical Properties

Solubility Soluble in water (50 mg/ml.clear,Slightly yellow
Molecular Weight 1026.300 g/mol
XLogP3
Hydrogen Bond Donor Count 6
Hydrogen Bond Acceptor Count 30
Rotatable Bond Count 16
Exact Mass 1025.92 Da
Monoisotopic Mass 1025.92 Da
Topological Polar Surface Area 495.000 Ų
Heavy Atom Count 62
Formal Charge 0
Complexity 1540.000
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 6

Solution Calculators

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