89310
胸腺嘧啶
≥97.0% (UV)
别名:
2,4-二羟基-5-甲基嘧啶, 5-甲基尿嘧啶
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关于此项目
经验公式（希尔记法）:
C5H6N2O2
化学文摘社编号:
分子量:
126.11
EC Number:
200-616-1
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
117880
MDL number:
assay
≥97.0% (UV)
mp
~320 °C (dec.) (lit.)
SMILES string
CC1=CNC(=O)NC1=O
InChI
1S/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9)
InChI key
RWQNBRDOKXIBIV-UHFFFAOYSA-N
Gene Information
mouse ... Tymp(72962)
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存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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Andrew Thompson et al.
Current protocols in nucleic acid chemistry, Chapter 1, Unit1-Unit1 (2012-12-21)
A detailed protocol for the synthesis of North-methanocarba-thymidine (N-MCT), a potent antiviral nucleoside with a restricted bicyclo[3.1.0]hexane pseudosugar conformation, is presented. The process is described in two parts. The first basic protocol deals with the synthesis of the carbobicyclic pseudosugar
Robert N Barnett et al.
Journal of the American Chemical Society, 135(10), 3904-3914 (2013-02-21)
One-electron oxidation of A/T-rich DNA leads to mutations at thymine. Experimental investigation of DNA containing methyl-deuterated thymine reveals a large isotope effect establishing that cleavage of this carbon-hydrogen bond is involved in the rate-determining step of the reaction. First-principles quantum
Diogo Almeida et al.
Physical review letters, 110(2), 023201-023201 (2013-02-07)
Electron transfer in alkali-molecule collisions to gas phase thymine and uracil yielding H- formation is selectively controlled in the energy range between 5.3 and 66.1 eV. By tuning the collision energy, electron transfer from the alkali to partly deuterated thymine
Ganglong Cui et al.
The Journal of chemical physics, 138(4), 044315-044315 (2013-02-08)
Thiothymidine has a potential application as a photosensitizer in cancer photodynamic therapy (PDT). As the chromophore of thiothymidine, 2-thiothymine exhibits ultrahigh quantum yield of intersystem crossing to the lowest triplet state T(1) (ca. 100%), which contrasts with the excited-state behavior
Yusuke Sato et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 29(1), 15-19 (2013-01-11)
We describe a competitive binding assay for the analysis of single-base mutation by using abasic site (AP site)-specific binding fluorescent ligands and masking ligands bound to the AP site in DNA duplexes. 2-Amino-5,6,7-trimethyl-1,8-naphthyridine (ATMND) can strongly bind to not only
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