2240-25-7 | 5-Bromocytosine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$9.00	$6.00
10g	95%	in stock	$30.00	$21.00
100g	95%	in stock	$297.00	$208.00

Description

• Catalog Number: AB44823
• Chemical Name: 5-Bromocytosine
• CAS Number: 2240-25-7
• Molecular Formula: C4H4BrN3O
• Molecular Weight: 189.9981
• MDL Number: MFCD00056025
• SMILES: Nc1nc(=O)[nH]cc1Br

Computed Properties

• Complexity: 208
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: -0.3

Literature

• DNA duplexes and triplex-forming oligodeoxynucleotides incorporating modified nucleosides forming stable and selective triplexes.

  Organic & biomolecular chemistry 20120207

• Epigenetics of chronic rhinosinusitis and the role of the eosinophil.

  International forum of allergy & rhinology 20120101

• Enzymatic synthesis of long double-stranded DNA labeled with haloderivatives of nucleobases in a precisely pre-determined sequence.

  BMC biochemistry 20110101

• Epigenomics in environmental health.

  Frontiers in genetics 20110101

• Xanthine oxidase-activated prodrugs of thymidine phosphorylase inhibitors.

  European journal of medicinal chemistry 20080601

• Electrophysiological characterization of nicotinic acetylcholine receptors in cat petrosal ganglion neurons in culture: effects of cytisine and its bromo derivatives.

  Brain research 20060209

• Formation of intrastrand cross-link products between cytosine and adenine from UV irradiation of d((Br)CA) and duplex DNA containing a 5-bromocytosine.

  Journal of the American Chemical Society 20051012

• Analysis of vibrational spectra of 5-fluoro, 5-chloro and 5-bromo-cytosines based on density functional theory calculations.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20050301

• Synthesis and enzymatic evaluation of xanthine oxidase-activated prodrugs based on inhibitors of thymidine phosphorylase.

  Bioorganic & medicinal chemistry letters 20041101

• Lifetime regulation of the charge-separated state in DNA by modulating the oxidation potential of guanine in DNA through hydrogen bonding.

  Journal of the American Chemical Society 20041013

• Facile formation of an intrastrand cross-link lesion between cytosine and guanine upon pyrex-filtered UV light irradiation of d((Br)CG) and duplex DNA containing 5-bromocytosine.

  Journal of the American Chemical Society 20040602

• Activity of cytisine and its brominated isosteres on recombinant human alpha7, alpha4beta2 and alpha4beta4 nicotinic acetylcholine receptors.

  Journal of neurochemistry 20010901