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thiopyrimidine

National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

Sulfur Compoundspyrimidine analog

Narrower (1)

Thiouracil

Papers overview

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Highly Cited
2012
Highly Cited
2012
Synthesis and Kinetic Testing of Tetrahydropyrimidine‐2‐thione and Pyrrole Derivatives as Inhibitors of the Metallo‐β‐lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa
Metallo‐β‐lactamases (MBLs), produced by an increasing number of bacterial pathogens, facilitate the hydrolysis of many commonly… 
2008
2008
Preferential protonation and methylation site of thiopyrimidine derivatives in solution: NMR data.
Protonation (alkylation) sites of several thiopyrimidine derivatives were directly determined by 1H-15N (1H-13C) heteronuclear… 
2003
2003
Synthesis of Theophylline and 6-Thiotheophylline 7-Ribosyl Nucleosides
The syntheses of theophylline and thiotheophylline 7-ribopyranose and 7-ribofuranose nucleosides, both by direct coupling of the… 
2002
2002
Ambiguous coding is required for the lethal interaction between methylated DNA bases and DNA mismatch repair.
1983
1983
The experimental herbicide UKJ72J is an inhibitor of succinate oxidation in plant mitochondria
1977
1977
Pseudouridine-deficient transfer RNAs from Escherichia coli B and their use as substrates for pseudouridine synthetase.
1972
1972
Specific inhibition of poliovirus induced blockade of cell protein synthesis by a thiopyrimidine derivative.
Summary A thiopyrimidine derivative, i.e. ethyl-2-methylthio-4-methyl-5-pyrimidine carboxylate (S-7) is capable of preventing… 
1971
1971
Cytotoxic effects of thiopyrimidines
The cytotoxic action of 2‐thiouracil, 2‐thiocytosine, 2‐thiouridine and 4‐thiouridine was studied in cultures of a clone of… 
1969
1969
Optical properties of thiopyrimidine nucleosides.
The ORD, CD and UV of various 2-thiopyrimidine nucleosides have been measured and a tentative rule pertaining to the sign of ORD… 
1968
1968
Radiolysis of 4-thiouracil and of the 4-thiouracil moieties of 4-thiouridine and transfer ribonucleic acid from Escherichia coli in aqueous solutions.
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