932-52-5 | 5-Aminouracil

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$15.00	$10.00
1g	97%	in stock	$16.00	$11.00
5g	97%	in stock	$25.00	$18.00
25g	97%	in stock	$67.00	$47.00
100g	97%	in stock	$200.00	$140.00

Description

• Catalog Number: AB68812
• Chemical Name: 5-Aminouracil
• CAS Number: 932-52-5
• Molecular Formula: C4H5N3O2
• Molecular Weight: 127.1014
• MDL Number: MFCD00006025
• SMILES: NC1C=NC(=O)NC1=O
• NSC Number: 22474

Computed Properties

• Complexity: 196
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• XLogP3: -1.5

Literature

• Compound instability in dimethyl sulphoxide, case studies with 5-aminopyrimidines and the implications for compound storage and screening.

  Bioorganic & medicinal chemistry letters 20121015

• [Antidepressant effect and mechanism of action of a novel aminouracil derivative].

  Eksperimental'naia i klinicheskaia farmakologiia 20110101

• Pyrimidine based highly sensitive fluorescent receptor for Al3+ showing dual signalling mechanism.

  Organic & biomolecular chemistry 20101107

• The peculiar spectral properties of amino-substituted uracils: a combined theoretical and experimental study.

  The journal of physical chemistry. B 20101007

• Al3+ selective an efficient colorimetric receptor derived from 5-aminouracil.

  Talanta 20100715

• Novel acyclic amide-conjugated nucleosides and their analogues.

  Nucleosides, nucleotides & nucleic acids 20090201

• FTIR and raman spectra compared with ab initio calculated frequency modes for 5-aminouracil.

  Journal of biological physics 20081201

• Effect of amino substitution on the excited state dynamics of uracil.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20080701

• Facile synthesis and detailed characterization of a new ferrocenyl uracil peptide nucleic acid monomer.

  The Journal of organic chemistry 20060929

• DNA injury induced by 5-aminouracil and caffeine in G2 checkpoints path of higher plant cells.

  Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al 20050801

• G2 checkpoint targets late replicating DNA.

  Biology of the cell 20031101

• 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.

  Journal of inorganic biochemistry 20030401

• Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.

  Biochemical pharmacology 19940817