2′-Deoxyguanosine 5′-monophosphate disodium salt hydrate - ≥98% , CAS No.33430-61-4

CAS: 33430-61-4 Cat. No.: D588762 Molecular Weight: 391.18 (anhydrous basis) EC Number: 251-517-5 PubChem CID: 135742695

GRADE & PURITY ≥98%

Synonyms

2'-Deoxyguanosine 5'-Phosphate Disodium Salt | 5'-Guanylic acid, 2'-deoxy-, disodium salt | AKOS015896903 | 2'-DEOXYGUANOSINE-5'-MONOPHOSPHATE DISODIUM | HG1088 | AC-32419 | SCHEMBL543082 | 2'-Deoxyguanosine-5'-monophosphoric acid disodium salt | disodium

Storage

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

Shipped In

Ice chest + Ice pads

Overview

Product Application
As reactants, participate in the following reactions:
1. Analysis of self-assembly and G-quadruplex nucleation/growth in solution
2. Nucleophilic capture
3. Reductive alkylation

Specifications

Synonyms

2'-Deoxyguanosine 5'-Phosphate Disodium Salt | 5'-Guanylic acid, 2'-deoxy-, disodium salt | AKOS015896903 | 2'-DEOXYGUANOSINE-5'-MONOPHOSPHATE DISODIUM | HG1088 | AC-32419 | SCHEMBL543082 | 2'-Deoxyguanosine-5'-monophosphoric acid disodium salt | disodium

Specifications & Purity

≥98%

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

≥98%

Names and Identifiers

• Canonical Smiles: C1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)COP(=O)([O-])[O-])O.[Na+].[Na+]
• IUPAC Name: disodium;[(2R,3S,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl phosphate
• InChIKey: CTPAMSRBXKGZCJ-FVALZTRZSA-L
• INCHI: 1S/C10H14N5O7P.2Na/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(22-6)2-21-23(18,19)20;;/h3-6,16H,1-2H2,(H2,18,19,20)(H3,11,13,14,17);;/q;2*+1/p-2/t4-,5+,6+;;/m0../s1
• Isomeric SMILES: C1[C@@H]([C@H](O[C@H]1N2C=NC3=C2N=C(NC3=O)N)COP(=O)([O-])[O-])O.[Na+].[Na+]
• WGK Germany: 3
• PubChem CID: 135742695
• Molecular Weight: 391.18 (anhydrous basis)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Class Purine nucleotides
      • Subclass Purine deoxyribonucleotides
        • Level5 Purine deoxyribonucleoside monophosphates
          • Level6 Purine 2'-deoxyribonucleoside monophosphates

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Class: Purine nucleotides
• Subclass: Purine deoxyribonucleotides
• Intermediate Tree Nodes: Purine deoxyribonucleoside monophosphates
• Direct Parent: Purine 2'-deoxyribonucleoside monophosphates
• Alternative Parents: 6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives Alkyl phosphates N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Hydrocarbon derivatives Organic oxides Organic sodium salts Organic zwitterions
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Purine 2'-deoxyribonucleoside monophosphate - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Pyrimidone - Aminopyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Pyrimidine - Alkyl phosphate - Oxolane - Imidazole - Heteroaromatic compound - Vinylogous amide - Azole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Organic alkali metal salt - Oxacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Primary amine - Organic oxide - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organic zwitterion - Organic salt - Amine - Organic sodium salt - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.
• 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

• Sensitivity: Light sensitive，Moisture sensitive
• Melt Point(°C): >245°C
• Molecular Weight: 391.190 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 3
• Exact Mass: 391.027 Da
• Monoisotopic Mass: 391.027 Da
• Topological Polar Surface Area: 187.000 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 556.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• 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

1. Yangcenzi Xie, Mingyang Chen, Xinyu Liu, Xiaoming Su, Ming Li.  (2023)  Artificial Intelligence-Assisted Label-Free Spectroscopic Quantification of Global DNA Cytosine Methylation in a Miniature Plasmonic Pickering Emulsion.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202307091]