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About This Item
Empirical Formula (Hill Notation):
C5H6N2O2
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-949-4
Beilstein/REAXYS Number:
115647
MDL number:
Assay:
97%
Form:
powder
InChI key
SHVCSCWHWMSGTE-UHFFFAOYSA-N
InChI
1S/C5H6N2O2/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)
SMILES string
CC1=CC(=O)NC(=O)N1
assay
97%
form
powder
mp
318 °C (dec.) (lit.)
Quality Level
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Lucie Brulíková et al.
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A number of 5-alkoxymethyluracil analogues were synthesized to evaluate their cytotoxic activity. 5-Alkoxymethyluracil derivatives 1 were prepared via known nucleophilic substitution of 5-chloromethyluracil 5 and subsequently transformed to their corresponding nucleosides 2. All prepared compounds were submitted to cytotoxic activity
Xiao Lu et al.
Bioorganic & medicinal chemistry, 15(23), 7399-7407 (2007-09-18)
Novel compounds 1a-u, which can be considered as hybrid analogues of MKC-442 and pyridinon, have been synthesized and evaluated as inhibitors of HIV-1 reverse transcriptase (HIV-1 RT). Starting from 6-methyluracil 2, 1-alkylated-5-bromomethyl-6-methyluracils 8 was prepared in four steps by hydroxymethylation
Fabio C Tucci et al.
Chirality, 17(9), 559-564 (2005-10-01)
1-(2,6-Difluorobenzyl)-3-[(2R)-amino-2-phenethyl]-5-(2-fluoro-3-methoxyphenyl)-6-methyluracil (6), a potent and orally active antagonist of the human gonadotropin-releasing hormone receptor, exists as a pair of atropisomers in solution, which was detected by NMR spectroscopy, and separable by HPLC. In addition to a (R)-configured benzylamine, there is
M Iu Gerasimenko et al.
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Clinical, biochemical, experimental, heat physical studies and mathematical calculations have shown that combined effect of drug-laser can be differentiated into the following effects: photophoresis, light pressure and photodynamic effect.
[Surgical infected wound treatment in patients with severe gastrointestinal ulcer hemorrhage].
V V Ganzhiĭ
Klinichna khirurhiia, (11-12)(11-12), 18-19 (2003-01-29)
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