Basic Description

Synonyms	Guanosine 5'-triphosphate disodium salt \| 56001-37-7 \| GUANOSINE-5'-TRIPHOSPHATE DISODIUM SALT \| Guanosine-5'-triphosphoric aicd disodium salt \| disodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphono p
Specifications & Purity	≥98%
Storage Temp	Protected from light,Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Guanosine-5'-triphosphate disodium salt is a phosphoryl donor in protein synthesis and in signal transduction. A phosphoryl donor in protein synthesis and signal transduction.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Purine nucleotides
    - Subclass Purine ribonucleotides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Purine nucleotides
Subclass	Purine ribonucleotides
Intermediate Tree Nodes	Not available
Direct Parent	Purine ribonucleoside triphosphates
Alternative Parents	Purine ribonucleoside monophosphates Pentose phosphates Glycosylamines 6-oxopurines Hypoxanthines Monosaccharide phosphates Pyrimidones Aminopyrimidines and derivatives Alkyl phosphates N-substituted imidazoles Tetrahydrofurans Vinylogous amides Heteroaromatic compounds Secondary alcohols 1,2-diols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic zwitterions Primary amines Organopnictogen compounds Organic sodium salts Organic oxides
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Purine ribonucleoside triphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Pyrimidine - Monosaccharide - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic alkali metal salt - Amine - Organic sodium salt - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organic salt - Organic zwitterion - Primary amine - Organic oxygen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as purine ribonucleoside triphosphates. These are purine ribobucleotides with a triphosphate group linked to the ribose moiety.
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	504773348
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504773348
IUPAC Name	disodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphono phosphate
INCHI	InChI=1S/C10H16N5O14P3.2Na/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(27-9)1-26-31(22,23)29-32(24,25)28-30(19,20)21;;/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H2,19,20,21)(H3,11,13,14,18);;/q;2*+1/p-2/t3-,5-,6-,9-;;/m1../s1
InChIKey	FIZIYLKEXVIRHJ-LGVAUZIVSA-L
Smiles	C1=NC2=C(N1C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)O)O)O)N=C(NC2=O)N.[Na+].[Na+]
Isomeric SMILES	C1=NC2=C(N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)O)O)O)N=C(NC2=O)N.[Na+].[Na+]
PubChem CID	135465086
Molecular Weight	567.15
Beilstein	4113439

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.

9 results found

Lot Number	Certificate Type	Date	Item
G2501048	Certificate of Analysis	Aug 23, 2023	G419147
H2330451	Certificate of Analysis	Aug 23, 2023	G419147
H2330487	Certificate of Analysis	Aug 23, 2023	G419147
H2330486	Certificate of Analysis	Aug 23, 2023	G419147
H2330444	Certificate of Analysis	Aug 23, 2023	G419147
H2330335	Certificate of Analysis	Aug 23, 2023	G419147
F2523093	Certificate of Analysis	Aug 23, 2023	G419147
H2330488	Certificate of Analysis	Aug 23, 2023	G419147
H2330334	Certificate of Analysis	Aug 23, 2023	G419147

Chemical and Physical Properties

Sensitivity	Heat sensitive；Moisture sensitive；Light sensitive
Molecular Weight	567.140 g/mol
XLogP3
Hydrogen Bond Donor Count	6
Hydrogen Bond Acceptor Count	16
Rotatable Bond Count	8
Exact Mass	566.955 Da
Monoisotopic Mass	566.955 Da
Topological Polar Surface Area	300.000 Å²
Heavy Atom Count	34
Formal Charge	0
Complexity	910.000
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	3

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Ting Zeng, Jie Yin, Ziwen Liu, Zhaoxing Li, Yu Zhang, Yang Lv, Mei-Ling Lu, Min Luo, Meirong Chen, Yibei Xiao. (2023) Mechanistic insights into transposon cleavage and integration by TnsB of ShCAST system. Cell Reports, 42 (112698).
2. Ying Ding, Qingyan Jia, Yongmei Wen, Weimin Liu, Jiechao Ge, Jiasheng Wu, Hongyan Zhang, Pengfei Wang. (2018) New detection method for nucleoside triphosphates based on carbon dots: The distance-dependent singlet oxygen trapping. ANALYTICA CHIMICA ACTA, 1031 (145).
3. Qu Fei, Mao Beibei, Xue Fangfang, Xia Lian, You Jinmao, Song Cuihua. (2018) Photoinduced electron transfer from polymer-templated Ag nanoclusters to G-quadruplex-hemin complexes for the construction of versatile biosensors and logic gate applications. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 410 (8): (2211-2219).
4. Jie Lv,Shuangling Wang,Cong Zhang,Yulong Lin,Yan Fu,Meng Li. (2020-07-14) ATP induced alteration in the peroxidase-like properties of hollow Prussian blue nanocubes: a platform for alkaline phosphatase detection.. The Analyst, 145 ((14)): (5032-5040).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

=

Concentration

x

Volume

x

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

x

Volume 1 (V1)

=

Concentration 2 (C2)

x

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

=

Mass (in vial)

÷

Desired Reconstitution Concentration

SKU	Size	Availability	Price
G419147-50mg	50mg	3	$90.90
G419147-250mg	250mg	3	$309.90
G419147-1g	1g	2	$859.90
G419147-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$3,022.90

Guanosine-5'-triphosphate disodium salt - 98%, high purity , CAS No.56001-37-7