| Weight | 347.224 g/mol |
|---|---|
| Formula | C10H14N5O7P |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Deoxyguanylic acid (902-04-5, 25656-92-2)
dGMP · deoxyguanosine 5'-monophosphate · 2'-deoxyguanosine 5'-monophosphate
Score:
#1545 in Physics
,
#1615 in Biochemistry
,
#4623 in Chemistry
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- Pulse radiolytic study of the interaction of thiols and ascorbate with OH adducts of dGMP and dG: implications for DNA repair processes (Radiation Research, 1983)
- Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine (Nucleic Acids Research, 1999)
- Potential repair of free radical adducts of dGMP and dG by a series of reductants. A pulse radiolytic study (International Journal of Radiation Biology, 1985)
- CZE-ICP-MS as a tool for studying the hydrolysis of ruthenium anticancer drug candidates and their reactivity towards the DNA model compound dGMP (Journal of Inorganic Biochemistry, 2008)
- Interaction of dGMP radical with cysteamine and promethazine as possible model of DNA repair (Nature, 1974)
- Alkylation by propylene oxide of deoxyribonucleic acid, adenine, guanosine and deoxyguanylic acid. (Biochemical Journal, 1972)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dGMP
- deoxyguanosine 5'-monophosphate
- 2'-deoxyguanosine 5'-monophosphate
- 2'-deoxyguanosine 5'-phosphate, ion (1+)
- 2'-deoxyguanosine 5'-phosphate, disodium salt
- 2'-dG-5'-MP
- 2'-deoxyguanosine 5'-phosphate
-
SMILESC1C(C(OC1N2C=NC3=C2NC(=NC3=O)N)COP(=O)(O)O)O
-
InChIKeyLTFMZDNNPPEQNG-UHFFFAOYSA-N
- Pubchem - Deoxyguanylic acid
- Wikipedia - deoxyguanosine monophosphate
Deoxyguanosine monophosphate (dGMP), also known as deoxyguanylic acid or deoxyguanylate in its conjugate acid and conjugate base forms, respectively, is a derivative of the common nucleic acid guanosine triphosphate (GTP), in which the OH (hydroxyl) group on the 2' carbon on the nucleotide's pentose has been reduced to just a hydrogen atom (hence the "deoxy-" part of the name). It is used as a monomer in DNA.
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