| Weight | 94.117 g/mol |
|---|---|
| Formula | C5H6N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Methylpyrimidine (2036-41-1)
Score:
#2964 in Biochemistry
,
#5419 in Biology
,
#7255 in Chemistry
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- Crystal structure of 4-amino-5-hydroxymethyl-2-methylpyrimidine phosphate kinase from Salmonella typhimurium at 2.3 A resolution. (Structure, 2002)
- ThiC is an [Fe-S] cluster protein that requires AdoMet to generate the 4-amino-5-hydroxymethyl-2-methylpyrimidine moiety in thiamin synthesis. (Biochemistry, 2008)
- Characterization of Two Kinases Involved in Thiamine Pyrophosphate and Pyridoxal Phosphate Biosynthesis in Bacillus subtilis: 4-Amino-5-Hydroxymethyl-2-Methylpyrimidine Kinase and Pyridoxal Kinase (Journal of Bacteriology, 2004)
- Vitamin B1 de novo synthesis in the human malaria parasite Plasmodium falciparum depends on external provision of 4-amino-5-hydroxymethyl-2-methylpyrimidine. (Biological Chemistry, 2006)
- ChemInform Abstract: Overexpression, Purification and Characterization of Two Pyrimidine Kinases Involved in the Biosynthesis of Thiamin: 4-Amino-5-hydroxymethyl-2-methylpyrimidine Kinase and 4-Amino-5-hydroxymethyl-2-methylpyrimidine Phosphate Kinase. (Tetrahedron, 1998)
- Molecular characterization of the thi3 gene involved in thiamine biosynthesis in Zea mays: cDNA sequence and enzymatic and structural properties of the recombinant bifunctional protein with 4-amino-5-hydroxymethyl-2-methylpyrimidine (phosphate) kinase and thiamine monophosphate synthase activities (Biochemical Journal, 2007)
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SMILESCC1=CN=CN=C1
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InChIKeyTWGNOYAGHYUFFR-UHFFFAOYSA-N
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5-Methylpyrimidine
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