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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14N5O7P
Molecular Weight 347.2212
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2'-DEOXYGUANOSINE 5'-PHOSPHATE

SMILES

NC1=NC2=C(N=CN2[C@H]3C[C@H](O)[C@@H](COP(O)(O)=O)O3)C(=O)N1

InChI

InChIKey=LTFMZDNNPPEQNG-KVQBGUIXSA-N
InChI=1S/C10H14N5O7P/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)/t4-,5+,6+/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H14N5O7P
Molecular Weight 347.2212
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Antiviral Activity of 4'-thioIDU and Thymidine Analogs against Orthopoxviruses.
2010-09
Guanosine quadruplexes in solution: a small-angle x-ray scattering analysis of temperature effects on self-assembling of deoxyguanosine monophosphate.
2010-06-21
Guanine nucleotides: base-centered and phosphate-centered valence-bound radical anions in aqueous solution.
2010-01-21
Dependence of deformability of geometries and characteristics of intramolecular hydrogen bonds in canonical 2'-deoxyribonucleotides on DNA conformations.
2009-04
Infrared absorption detection of metal ion-deoxyguanosine monophosphate binding: experimental and theoretical study.
2009-01-08
Recent development of nano-materials used in DNA biosensors.
2009
The exceptional properties of Plasmodium deoxyguanylate pathways as a potential area for metabolic and drug discovery studies.
2009
Interaction of the DNA bases and their mononucleotides with pyridine-2-carbaldehyde thiosemicarbazonecopper(II) complexes. Structure of the cytosine derivative.
2008-10
Radicals produced by gamma-irradiation of hyperquenched glassy water containing 2'-deoxyguanosine-5'-monophosphate.
2008-09-18
Systems analysis of metabolism in the pathogenic trypanosomatid Leishmania major.
2008
A new crystal form of bovine pancreatic RNase A in complex with 2'-deoxyguanosine-5'-monophosphate.
2007-09-01
Using gene expression data and network topology to detect substantial pathways, clusters and switches during oxygen deprivation of Escherichia coli.
2007-05-08
The role of metal ion binding in generating 8-hydroxy-2'-deoxyguanosine from the nucleoside 2'-deoxyguanosine and the nucleotide 2'-deoxyguanosine-5'-monophosphate.
2007-03
Intramolecular hydrogen bonds in canonical 2'-deoxyribonucleotides: an atoms in molecules study.
2006-03-09
Cloning of deoxynucleoside monophosphate kinase genes and biosynthesis of deoxynucleoside diphosphates.
2006-02-20
Dietary nucleotides and human immune cells. II. Modulation of PBMC growth and cytokine secretion.
2005-10
Single-molecule detection of biomolecules by surface-enhanced coherent anti-Stokes Raman scattering.
2005-05-01
A deoxynucleotide derivatization methodology for improving LC-ESI-MS detection.
2005-04-15
Synthesis and biological activity of water-soluble maleimide derivatives of the anticancer drug carboplatin designed as albumin-binding prodrugs.
2004-11-18
Conformational analysis of canonical 2-deoxyribonucleotides. 2. Purine nucleotides.
2004-10
Antibodies to guanosine triphosphate misidentified as anti-double-stranded DNA antibodies in a patient with antinuclear antibody-negative lupus, due to buckling of insolubilized assay DNA.
2004-05
Heat shock protein 70 stimulation of the deoxyribonucleic acid base excision repair enzyme polymerase beta.
2003
Key role of template sequence for primer synthesis by the herpes simplex virus 1 helicase-primase.
2002-12-10
Separation of N2-ethyl-2'-deoxyguanosine-5'-monophosphate and four native deoxyribonucleoside monophosphates using capillary zone electrophoresis with polyethylene glycol as buffer additive.
2001-01
Specificity of mouse hybridoma antibodies to DNA. III. Antigenic determinants of nucleic acids recognized by poly(dG) specific monoclonal antibodies.
1985-05
Molecular and crystal structure of deoxyguanosine 5'-phosphate.
1974-11-08
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:35:52 GMT 2025
Edited
by admin
on Mon Mar 31 22:35:52 GMT 2025
Record UNII
7EAM4TG712
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-82626
Preferred Name English
2'-DEOXYGUANOSINE 5'-PHOSPHATE
Common Name English
5'-GUANYLIC ACID, 2'-DEOXY-
Common Name English
DEOXYGUANOSINE 5'-MONOPHOSPHATE
Systematic Name English
2'-DEOXY-5'-GMP
Common Name English
DGMP
Common Name English
2'-DEOXYGUANOSINE 5'-MONOPHOSPHATE
Systematic Name English
Code System Code Type Description
CHEBI
16192
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
CAS
902-04-5
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
NSC
82626
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-988-2
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
PUBCHEM
135398597
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
CHEBI
57673
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
FDA UNII
7EAM4TG712
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
WIKIPEDIA
Deoxyguanosine monophosphate
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
EPA CompTox
DTXSID20896947
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY
DRUG BANK
DB04457
Created by admin on Mon Mar 31 22:35:52 GMT 2025 , Edited by admin on Mon Mar 31 22:35:52 GMT 2025
PRIMARY