146877-98-7
Chemical Structure
2'-Deoxyguanosine 5'-monophosphate disodium hydrate
Synonym(s): 5'-Deoxyguanylic acid disodium hydrate
- CAS No.: 146877-98-7
- Formula:C10H14N5O7.H2O.2Na
- Molecular Weight:N/A
SMILES: O[C@H]1C[C@H](N2C=NC3=C2NC(N)=NC3=O)O[C@@H]1COP(O[Na])(O[Na])=O.[x].O
Biological Activity: 2'-Deoxyguanosine 5'-monophosphate (5'-Deoxyguanylic acid; dGMP) disodium hydrate is an oxidizable target of the photosensitizer pterin (PT) and can be used to evaluate the photosensitizing properties of biopterins (such as Bip, Fop and Cap) . Pterin causes a photosensitive reaction of dGMP under UV-A radiation, causing damage to DNA molecules. There are two main mechanisms for the photosensitive oxidation of purine nucleotides by pterin in vitro: one is the hydrogen abstraction reaction of electron transfer from dGMP to the triplet excited state of pterin (type I mechanism), and the other is the interaction between dGMP and pterin. The reaction produces singlet molecular oxygen (1O2) (Type II mechanism)[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2'-Deoxyguanosine 5'-monophosphate disodium hydrate | 99.0% | 2'-Deoxyguanosine 5'-monophosphate (5'-Deoxyguanylic acid; dGMP) disodium hydrate is an oxidizable target of the photosensitizer pterin (PT) and can be used to evaluate the photosensitizing properties of biopterins (such as Bip, Fop and Cap) . Pterin causes a photosensitive reaction of dGMP under UV-A radiation, causing damage to DNA molecules. There are two main mechanisms for the photosensitive oxidation of purine nucleotides by pterin in vitro: one is the hydrogen abstraction reaction of electron transfer from dGMP to the triplet excited state of pterin (type I mechanism), and the other is the interaction between dGMP and pterin. The reaction produces singlet molecular oxygen (1O2) (Type II mechanism). | ||||||||||||||||||||
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References
- [1]. Petroselli G, Dántola M L, Cabrerizo F M, et al. Oxidation of 2 ‘-Deoxyguanosine 5 ‘-Monophosphate Photoinduced by Pterin: Type I versus Type II Mechanism[J]. Journal of the American Chemical Society, 2008, 130(10): 3001-3011.
- [2]. Song B, Sigel H. Metal Ion-Coordinating Properties of 2 ‘-Deoxyguanosine 5 ‘-Monophosphate (dGMP2-) 1 in Aqueous Solution. Quantification of Macrochelate Formation[J]. Inorganic Chemistry, 1998, 37(8): 2066-2069.
