| Weight | 80.09 g/mol |
|---|---|
| Formula | C4H4N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
PYRIMIDINE (289-95-2, 25247-63-6)
Score:
#1342 in Biochemistry
,
#3259 in Biology
,
#4070 in Chemistry
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- DNA repair in an active gene: Removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall (Cell, 1985)
- The purine and pyrimidine composition of deoxypentose nucleic acids. (Biochemical Journal, 1951)
- High and Selective CO2 Uptake in a Cobalt Adeninate MetalOrganic Framework Exhibiting Pyrimidine- and Amino-Decorated Pores (Journal of the American Chemical Society, 2010)
- Purine and pyrimidine receptors (Cellular and Molecular Life Sciences, 2007)
- Synthesis of activated pyrimidine ribonucleotides in prebiotically plausible conditions (Nature, 2009)
- Pyrimidine Nucleotide Biosynthesis in Animals: Genes, Enzymes, and Regulation of UMP Biosynthesis (Annual Review of Biochemistry, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CN=CN=C1
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InChIKeyCZPWVGJYEJSRLH-UHFFFAOYSA-N
- Pubchem - PYRIMIDINE
- Wikipedia - pyrimidine
Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogen atoms at positions 1 and 3 in the ring. The other diazines are pyrazine (nitrogen atoms at the 1 and 4 positions) and pyridazine (nitrogen atoms at the 1 and 2 positions).
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PYRIMIDINE
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