275514
6-氮杂-2-硫代胸腺嘧啶
99%
别名:
2-硫代-6-氮胸腺嘧啶, 3,4-二氢-6-甲基-3-巯基-1,2,4-三嗪-5(2H)-酮
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关于此项目
经验公式（希尔记法）:
C4H5N3OS
化学文摘社编号:
分子量:
143.17
EC Number:
210-445-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
4861
MDL number:
InChI key
NKOPQOSBROLOFP-UHFFFAOYSA-N
InChI
1S/C4H5N3OS/c1-2-3(8)5-4(9)7-6-2/h1H3,(H2,5,7,8,9)
SMILES string
CC1=NNC(=S)NC1=O
assay
99%
mp
218-221 °C (lit.)
solubility
formic acid: soluble 5%, clear, colorless to light yellow-green
Application
6-Aza-2-thiothymine was used in the preparation of a matrix that was utilized for ionizing small molecules.
存储类别
13 - Non 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
新产品
此项目有
Alba Hykollari et al.
Electrophoresis, 38(17), 2175-2183 (2017-05-31)
The unusual nature of the N-glycans of the cellular slime mould Dictyostelium discoideum has been revealed by a number of studies, primarily based on examination of radiolabeled glycopeptides but more recently also by MS. The complexity of the N-glycomes of
David Weigt et al.
Scientific reports, 8(1), 11260-11260 (2018-07-28)
Recent advances in matrix-assisted laser desorption/ionization (MALDI) mass spectrometry have enabled whole cell-MALDI mass spectrometry biotyping of drug-treated cultured cells for rapid monitoring of known abundant pharmacodynamic protein markers such as polyacetylated histones. In contrast, generic and automated analytical workflows
Selina Rahman Shanta et al.
The Analyst, 137(24), 5757-5762 (2012-10-23)
Since the development of matrix-assisted laser desorption/ionization (MALDI) mass spectrometry, this procedure has been specifically used for analyzing proteins or high molecular weight compounds because of the interference of matrix signals in the regions of the low mass range. Recently
Shi Yan et al.
Analytical chemistry, 90(1), 928-935 (2017-11-29)
Despite years of research, the glycome of the model nematode Caenorhabditis elegans is still not fully understood. Certainly, data over the years have indicated that this organism synthesizes unusual N-glycans with a range of galactose and fucose modifications on the
Rui-Rui Guo et al.
Frontiers in bioengineering and biotechnology, 8, 741-741 (2020-07-29)
Peptide-N4-(N-acetyl-β-glucosaminyl) asparagine amidases (PNGases, N-glycanases, EC 3.5.1.52) are indispensable tools in releasing N-glycans from glycoproteins. So far, only a limited number of PNGase candidates are available for the structural analysis of glycoproteins and their glycan moieties. Herein, a panel of
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