Details
Stereochemistry | ACHIRAL |
Molecular Formula | C4H5N3O2 |
Molecular Weight | 127.1014 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CNC(=O)NC1=O
InChI
InChIKey=BISHACNKZIBDFM-UHFFFAOYSA-N
InChI=1S/C4H5N3O2/c5-2-1-6-4(9)7-3(2)8/h1H,5H2,(H2,6,7,8,9)
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: map04110 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25926388 |
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Target ID: CHEMBL2311221 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25926388 |
PubMed
Title | Date | PubMed |
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Synthesis and spectroscopic studies on the new Schiff base derived from the 1:2 condensation of 2,6-diformyl-4-methylphenol with 5-aminouracil (BDF5AU) and its transition metal complexes. Influence on biologically active peptides-regulating aminopeptidases. | 2003 Apr 1 |
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G2 checkpoint targets late replicating DNA. | 2003 Nov |
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DNA injury induced by 5-aminouracil and caffeine in G2 checkpoints path of higher plant cells. | 2005 Aug |
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Facile synthesis and detailed characterization of a new ferrocenyl uracil peptide nucleic acid monomer. | 2006 Sep 29 |
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FTIR and raman spectra compared with ab initio calculated frequency modes for 5-aminouracil. | 2008 Dec |
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Effect of amino substitution on the excited state dynamics of uracil. | 2008 Jul |
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R2O7EKY9G9
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DB03792
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213-252-3
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DTXSID1061312
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SUBSTANCE RECORD