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Merck
CN

331902

5′-Deoxythymidine

98%

别名:

2′,5′-Dideoxythymidine

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关于此项目

经验公式(希尔记法):
C10H14N2O4
化学文摘社编号:
分子量:
226.23
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
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assay

98%

optical activity

[α]28/D +8.9°, c = 0.6 in H2O

mp

192-193 °C (lit.)

SMILES string

C[C@H]1O[C@H](C[C@@H]1O)N2C=C(C)C(=O)NC2=O

InChI

1S/C10H14N2O4/c1-5-4-12(10(15)11-9(5)14)8-3-7(13)6(2)16-8/h4,6-8,13H,3H2,1-2H3,(H,11,14,15)/t6-,7+,8-/m1/s1

InChI key

UGUILUGCFSCUKR-GJMOJQLCSA-N



存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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B A Domin et al.
Molecular pharmacology, 41(5), 950-956 (1992-05-01)
The membrane permeation characteristics of 5'-deoxythymidine (5'-ddThd) and 5'-azido-5'-deoxythymidine (5'-N3-5'-ddThd) were investigated in human erythrocytes, with an inhibitor-stop assay, at 20 degrees. Uptake of both nucleoside analogs occurred without metabolism, was nonconcentrative, and was partially inhibited by nucleosides or inhibitors
Ayşegül Akbay et al.
Arzneimittel-Forschung, 53(4), 266-271 (2003-06-06)
In this study, the synthesis of some benzoxazoles and their analogues were described and their antiviral activities were studied together with the previously synthesized 2,5,6-trisubstituted benzoxazole, benzothiazole, benzimidazole and oxazolo(4,5-b)pyridine derivatives. The reverse transcriptase (RT) inhibitory activity of these compounds
Amitava Adhikary et al.
The journal of physical chemistry. B, 114(28), 9289-9299 (2010-06-26)
Employing electron spin resonance (ESR) spectroscopy, we have characterized the radicals formed in 3'-azido-3'-deoxythymidine (3'-AZT) and in its 5'-analog 5'-azido-5'-deoxythymidine (5'-AZT) after electron attachment in gamma-irradiated aqueous (H(2)O or D(2)O) glassy (7.5 M LiCl) systems. ESR spectral studies and theoretical