D2022
5,6-Dihydrothymidine
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About This Item
Formula empirica (notazione di Hill):
C10H16N2O5
Numero CAS:
Peso molecolare:
244.24
Numero MDL:
Codice UNSPSC:
12352204
Prezzi e disponibilità al momento non sono disponibili
Temperatura di conservazione
−20°C
Stringa SMILE
CC1CN(C2CC(O)C(CO)O2)C(=O)NC1=O
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
Efficiency of incision of an AP site within clustered DNA damage by the major human AP endonuclease.
Marie-Hélène David-Cordonnier et al.
Biochemistry, 41(2), 634-642 (2002-01-10)
A major DNA lesion induced by ionizing radiation and formed on removal of oxidized base lesions by various glycosylases is an apurinic/apyrimidinic site (AP site). The presence of an AP site within clustered DNA damage, induced following exposure to ionizing
E A Furlong et al.
Biochemistry, 25(15), 4344-4349 (1986-07-29)
5,6-Dihydrothymidine (dDHT) is a derivative thymidine formed during gamma-irradiation. This paper demonstrates the conditions under which dDHT is formed in solutions of DNA and that dDHT is produced in the DNA of HeLa cells during gamma-irradiation. The product of dDHT
M A Chaudhry et al.
Journal of molecular biology, 249(5), 914-922 (1995-06-23)
Energy deposition by ionizing radiation can lead to the formation of clustered DNA damage, i.e. more than one lesion situated within a helical turn of DNA. Among the postulated lesions are those characterized by damaged bases and abasic sites on
K A Tallman et al.
Journal of the American Chemical Society, 123(22), 5181-5187 (2001-07-18)
5,6-Dihydrothymidin-5-yl (1) was independently generated in a dinucleotide from a phenyl selenide precursor (4). Under free radical chain propagation conditions, the products resulting from hydrogen atom donation and radical-pair reaction are the major observed products in the absence of O(2).
J Cadet et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 39(2), 119-133 (1981-02-01)
The steady-state gamma radiolysis of deaerated aqueous solutions of thymidine generated a complex mixture of pyrimidine and nucleoside derivatives. Twenty-two of these compounds have been isolated and unambiguously characterized by spectroscopic methods including proton nuclear magnetic resonance and mass spectrometry.
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