CN
质量水平
检测方案
97%
形式
powder
mp
318 °C (dec.) (lit.)
SMILES string
CC1=CC(=O)NC(=O)N1
InChI
1S/C5H6N2O2/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)
InChI key
SHVCSCWHWMSGTE-UHFFFAOYSA-N
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示例
T1503
货号
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25G
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PL860-CGA/SHF-1EA
MMYOMAG-74K-13
1000309185
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[Current methods for local drug therapy of infected wounds].
A P Chadaev et al.
Khirurgiia, (1)(1), 54-56 (2003-03-21)
Konstantin A Petrov et al.
British journal of pharmacology, 163(4), 732-744 (2011-01-15)
The rat respiratory muscle diaphragm has markedly lower sensitivity than the locomotor muscle extensor digitorum longus (EDL) to the new acetylcholinesterase (AChE) inhibitors, alkylammonium derivatives of 6-methyluracil (ADEMS). This study evaluated several possible reasons for differing sensitivity between the diaphragm
Effect of tetraalkylammonium derivatives of 6-methyluracil on the endplate potentials of muscles of different functional types.
I V Kovyazina et al.
Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections, 399, 458-460 (2005-02-19)
H Eshtiagh-Hosseini et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(5), 1392-1396 (2011-02-18)
This paper reports the hydrothermal synthesis, experimental and theoretical studies of a novel cocrystal compound in the 2:1 stoichiometric ratio of 6-methyluracil (6mu) and dipicolinic acid (pydcH(2)) formulated as [6mu](2)[pydcH(2)] (1), for the first time. DFT calculations were performed to
Zhiqiang Guo et al.
Bioorganic & medicinal chemistry letters, 13(19), 3311-3315 (2003-09-03)
The novel synthesis and SAR studies of 6-methyluracils as human GnRH receptor antagonists are discussed. Introduction of a small methyl substituent at the beta-position from N3 of the uracil improved the GnRH binding potency by 5- to 10-fold. The best
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