2'-Deoxyinosine - CAS 890-38-0
Category:
Nucleosides
Product Name:
2'-Deoxyinosine
Catalog Number:
890-38-0
CAS Number:
890-38-0
Molecular Weight:
252.23
Molecular Formula:
C10H12N4O4
COA:
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MSDS:
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Structure\Application:
2'-Deoxy-Nucleosides
Chemical Structure
CAS 890-38-0 2'-Deoxyinosine

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Reference Reading


1.Biodistribution, tumor uptake and efficacy of 5-FU-loaded liposomes: why size matters.
Fanciullino R1, Mollard S, Correard F, Giacometti S, Serdjebi C, Iliadis A, Ciccolini J. Pharm Res. 2014 Oct;31(10):2677-84. doi: 10.1007/s11095-014-1364-9. Epub 2014 Apr 22.
PURPOSE: We have investigated the impact of particle size on the biodistribution, tumor uptake and antiproliferative efficacy of 5-FU-loaded liposomes.
2.In vitro and in vivo evaluation of lipofufol, a new triple stealth liposomal formulation of modulated 5-fu: impact on efficacy and toxicity.
Fanciullino R1, Mollard S, Giacometti S, Berda-Haddad Y, Chefrour M, Aubert C, Iliadis A, Ciccolini J. Pharm Res. 2013 May;30(5):1281-90. doi: 10.1007/s11095-012-0967-2. Epub 2013 Feb 6.
PURPOSE: Drug resistance and severe toxicities are limitations when handling 5-FU. We have developed a triple liposomal formulation of 5-FU combined to 2'-deoxyinosine and folinic acid to improve its efficacy-toxicity balance.
3.Simultaneous quantification of purine and pyrimidine bases, nucleosides and their degradation products in bovine blood plasma by high performance liquid chromatography tandem mass spectrometry.
Stentoft C1, Vestergaard M2, Løvendahl P3, Kristensen NB4, Moorby JM5, Jensen SK6. J Chromatogr A. 2014 Aug 22;1356:197-210. doi: 10.1016/j.chroma.2014.06.065. Epub 2014 Jun 27.
Improved nitrogen utilization in cattle is important in order to secure a sustainable cattle production. As purines and pyrimidines (PP) constitute an appreciable part of rumen nitrogen, an improved understanding of the absorption and intermediary metabolism of PP is essential. The present work describes the development and validation of a sensitive and specific method for simultaneous determination of 20 purines (adenine, guanine, guanosine, inosine, 2'-deoxyguanosine, 2'-deoxyinosine, xanthine, hypoxanthine), pyrimidines (cytosine, thymine, uracil, cytidine, uridine, thymidine, 2'-deoxyuridine), and their degradation products (uric acid, allantoin, β-alanine, β-ureidopropionic acid, β-aminoisobutyric acid) in blood plasma of dairy cows. The high performance liquid chromatography-based technique coupled to electrospray ionization tandem mass spectrometry (LC-MS/MS) was combined with individual matrix-matched calibration standards and stable isotopically labelled reference compounds.
4.DNA Adduct Formation from Metabolic 5'-Hydroxylation of the Tobacco-Specific Carcinogen N'-Nitrosonornicotine in Human Enzyme Systems and in Rats.
Zarth AT1,2, Upadhyaya P1, Yang J1, Hecht SS1,2. Chem Res Toxicol. 2016 Mar 21;29(3):380-9. doi: 10.1021/acs.chemrestox.5b00520. Epub 2016 Feb 9.
N'-Nitrosonornicotine (NNN) is carcinogenic in multiple animal models and has been evaluated as a human carcinogen. NNN can be metabolized by cytochrome P450s through two activation pathways: 2'-hydroxylation and 5'-hydroxylation. While most previous studies have focused on 2'-hydroxylation in target tissues of rats, available evidence suggests that 5'-hydroxylation is a major activation pathway in human enzyme systems, in nonhuman primates, and in target tissues of some other rodent carcinogenicity models. In the study reported here, we investigated DNA damage resulting from NNN 5'-hydroxylation by quantifying the adduct 2-(2-(3-pyridyl)-N-pyrrolidinyl)-2'-deoxyinosine (py-py-dI). In rats treated with NNN in the drinking water (7-500 ppm), py-py-dI was the major DNA adduct resulting from 5'-hydroxylation of NNN in vivo. Levels of py-py-dI in the lung and nasal cavity were the highest, consistent with the tissue distribution of CYP2A3. In rats treated with (S)-NNN or (R)-NNN, the ratios of formation of (R)-py-py-dI to (S)-py-py-dI were not the expected mirror image, suggesting that there may be a carrier for one of the unstable intermediates formed upon 5'-hydroxylation of NNN.