X0626

Xanthine

≥99.5% (HPLC), purified by recrystallization

• Sinónimos: 2,6-Dioxopurine, 3,7-Dihydropurine-2,6-dione, Xanthin, 2,6-Dihydroxypurine
• Fórmula empírica (notación de Hill): C₅H₄N₄O₂
• Número de CAS: 69-89-6
• Peso molecular: 152.11
• Beilstein: 8733
• Número CE: 200-718-6
• Número MDL: MFCD00078453
• Código UNSPSC: 41106305
• ID de la sustancia en PubChem: 24902122
• NACRES: NA.51

Propiedades

• Análisis: ≥99.5% (HPLC)
• formulario: powder
• purificado por: recrystallization
• solubilidad: 1 M NaOH: soluble 50 mg/mL, clear, colorless to faintly yellow
• cadena SMILES: O=C1NC(=O)c2nc[nH]c2N1
• InChI: 1S/C5H4N4O2/c10-4-2-3(7-1-6-2)8-5(11)9-4/h1H,(H3,6,7,8,9,10,11)
• Clave InChI: LRFVTYWOQMYALW-UHFFFAOYSA-N

Descripción

Descripción general

Xanthine is an important component of the various natural and synthetic medicinal active compounds. Various forms of xanthine such as caffeine, theobromine, and theophylline are found in chocolate, cocoa, tea, yeast, potatoes, animal organs, and coffee. Xanthine is a purine-based natural heterocyclic alkaloid composed of a central nitrogen atom and a pyrimidine ring that is fused with an imidazole ring. Xanthine is produced from several different precursors in the purine metabolic pathway: deamination of guanine-by-guanine deaminase and conversion of hypoxanthine by xanthine oxidoreductase.

Acciones bioquímicas o fisiológicas

Xanthine participates in the catabolism of nucleic acids and nucleotides and is a precursor of uric acid. It is a versatile compound that shows therapeutic effects in several pharmacological conditions related to respiratory tract, central nervous system (CNS), kidney, stomach, smooth muscle cells, and heart. Xanthine acts as a biomarker for detecting gout.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Equipo de protección personal: dust mask type N95 (US), Eyeshields, Faceshields, Gloves