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Merck

X0626

Sigma-Aldrich

Xanthin

≥99.5% (HPLC), purified by recrystallization

Synonym(e):

2,6-Dihydroxy-purin

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About This Item

Empirische Formel (Hill-System):
C5H4N4O2
CAS-Nummer:
Molekulargewicht:
152.11
Beilstein:
8733
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41106305
PubChem Substanz-ID:
NACRES:
NA.51

Assay

≥99.5% (HPLC)

Form

powder

Aufgereinigt durch

recrystallization

Löslichkeit

1 M NaOH: soluble 50 mg/mL, clear, colorless to faintly yellow

SMILES String

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)

InChIKey

LRFVTYWOQMYALW-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

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.

Biochem./physiol. Wirkung

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.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Protokolle

Enzymatic Assay of Superoxide Dismutase

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