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About This Item
经验公式(希尔记法):
C10H14N5O7P · xNa+
CAS号:
分子量:
347.22 (free acid basis)
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
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方案
≥90%
储存温度
−20°C
SMILES字符串
[Na].NC1=NC(=O)c2ncn(C3CC(OP(O)(O)=O)C(CO)O3)c2N1
应用
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.
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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
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
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
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
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