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2′-Deoxyguanosine 5′-monophosphate sodium salt hydrate_Molecular_structure_CAS_)
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2′-Deoxyguanosine 5′-monophosphate sodium salt hydrate

Catalog No. D9500 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C10H15N5NaO8P Telephone 1-800-521-8956
M. W. 387.218331 Fax
Purity ≥99% (HPLC) Email
Storage Chembase ID: 155099

SYNONYMS

IUPAC name
sodium hydrate [(2R,3S,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl hydrogen phosphate
IUPAC Traditional name
sodium hydrate [(2R,3S,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl hydrogen phosphate
Synonyms
dGMP
5′-Deoxyguanylic acid

DATABASE IDS

MDL Number MFCD00150780
PubChem SID 24894297
EC Number 251-517-5

PROPERTIES

Empirical Formula (Hill Notation) C10H14N5O7P · xNa+ · yH2O
Purity ≥99% (HPLC)
MSDS Link Download
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Application
2′-Deoxyguanosine 5′-monophosphate (dGMP) is used as a substrate of guanylate kinase(s) (EC 2.7.4.8) to form dGDP which upon phosphorylation to dGTP supports DNA biosynthesis. dGMP is use to study physiochemical characteristics of guanine based molecules.
Description (简体中文)
Application
2′-Deoxyguanosine 5′-monophosphate (dGMP) is used as a substrate of guanylate kinase(s) (EC 2.7.4.8) to form dGDP which upon phosphorylation to dGTP supports DNA biosynthesis. dGMP is use to study physiochemical characteristics of guanine based molecules.

REFERENCES