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Key Documents

D3264

Sigma-Aldrich

2′-Deoxyguanosine 3′-monophosphate sodium salt

≥90%

Synonym(s):

3′-dGMP

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About This Item

Empirical Formula (Hill Notation):
C10H14N5O7P · xNa+
CAS Number:
Molecular Weight:
347.22 (free acid basis)
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
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Assay

≥90%

storage temp.

−20°C

SMILES string

[Na].NC1=NC(=O)c2ncn(C3CC(OP(O)(O)=O)C(CO)O3)c2N1

Application

2′-Deoxyguanosine 3-monophosphate (3′-dGMP) may be used to study the physical nature of mesophases of guanosine gels. 3′-dGMP is also used as a model compound to study mechanisms of nucleotide oxidation and of DNA adduct formation.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Sunhee Choi et al.
Journal of the American Chemical Society, 127(6), 1773-1781 (2005-02-11)
Many transition-metal complexes mediate DNA oxidation in the presence of oxidizing radiation, photosensitizers, or oxidants. The DNA oxidation products depend on the nature of the metal complex and the structure of the DNA. Earlier we reported trans-d,l-1,2-diaminocyclohexanetetrachloroplatinum (trans-Pt(d,l)(1,2-(NH(2))(2)C(6)H(10))Cl(4), [Pt(IV)Cl(4)(dach)]; dach
Laura Rudd et al.
Physical chemistry chemical physics : PCCP, 8(37), 4347-4358 (2006-09-21)
The unusual columnar aqueous mesophases of self-assembled guanosine stacks, such as 2'-deoxyguanosine 5'-monophosphate and 2'-deoxyguanosine 3'-monophosphate, are analyzed in terms of a general theory of azimuthal correlations between the charged helices. This theory considers forces, specific to the helical structure
Yukari Totsuka et al.
Chemical research in toxicology, 15(10), 1288-1294 (2002-10-22)
A mutagenic heterocyclic amine (HCA), 9-(4'-aminophenyl)-9H-pyrido[3,4-b]indole (aminophenylnorharman, APNH), is produced in the presence of S9 mix by the reaction of norharman and aniline, both of which are nonmutagenic and abundantly present in our environment. It has been previously reported that
Sunhee Choi et al.
Inorganic chemistry, 45(25), 10108-10114 (2006-12-05)
The kinetics of redox reactions of the PtIV complexes trans-Pt(d,l)(1,2-(NH2)2C6H10)Cl4 ([PtIVCl4(dach)]) and Pt(NH2CH2CH2NH2)Cl4 ([PtIVCl4(en)]) with 5'- and 3'-dGMP (G) have been studied. These redox reactions involve substitution followed by an inner-sphere electron transfer. The substitution is catalyzed by PtII and

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