Guanosine-5'-triphosphate disodium salt（5′-GTP-Na2） - ≥90% , CAS No.56001-37-7

CAS: 56001-37-7 Cat. No.: G122989 Molecular Weight: 567.15 Beilstein Registry Number: 4113439 EC Number: 259-940-7 PubChem CID: 135465086

GRADE & PURITY ≥90%

Synonyms

Guanosine 5'-triphosphate disodium salt | Guanosine-5,-triphosphoric aicd disodium | Guanosine-5/'-triphosphoric aicd disodium salt | 5'-GTP disodium salt | disodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidopho

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Overview

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

Specifications

Synonyms

Guanosine 5'-triphosphate disodium salt | Guanosine-5, -triphosphoric aicd disodium | Guanosine-5/'-triphosphoric aicd disodium salt | 5'-GTP disodium salt | disodium;[[(2R, 3S, 4R, 5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3, 4-dihydroxyoxolan-2-yl]methoxy-oxidopho

Specifications & Purity

≥90%

Storage

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.

Purity

≥90%

Names and Identifiers

• Canonical 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+]
• 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
• InChIKey: FIZIYLKEXVIRHJ-LGVAUZIVSA-L
• 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
• 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

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

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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water, Soluble in water
• Sensitivity: Heat & moisture & light sensitive
• Molecular Weight: 567.140 g/mol
• 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 Ų
• 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

XLogP3

References

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6. Fan Huahua, Wang Runjia, Zhang Li, Liu Minghua.  (2025)  Amplified circularly polarized luminescence in assembly of terpyridine-ZnII and GTP induced by silver(I) ion.  Science China-Chemistry,      [PMID:] [10.1007/s11426-024-2571-3]

7. Jie Lv, Shuangling Wang, Cong Zhang, Yulong Lin, Yan Fu, Meng Li.  (2020)  ATP induced alteration in the peroxidase-like properties of hollow Prussian blue nanocubes: a platform for alkaline phosphatase detection.  ANALYST,  145  (14): (5032-5040).  [PMID:32658942] [10.1039/D0AN00405G]

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