11460
8-Azaxanthine monohydrate
≥98.0% (HPLC)
Synonyme(s) :
2,6-Dihydroxy-8-azapurine
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About This Item
Formule empirique (notation de Hill):
C4H3N5O2 · H2O
Numéro CAS:
Poids moléculaire :
171.11
Beilstein:
10424
Numéro CE :
Numéro MDL:
Code UNSPSC :
41106305
ID de substance PubChem :
Nomenclature NACRES :
NA.25
Produits recommandés
Niveau de qualité
Essai
≥98.0% (HPLC)
Forme
solid
Chaîne SMILES
O.O=C1NC(=O)c2[nH]nnc2N1
InChI
1S/C4H3N5O2.H2O/c10-3-1-2(8-9-7-1)5-4(11)6-3;/h(H3,5,6,7,8,9,10,11);1H2
Clé InChI
VKEGPGRANAWNIN-UHFFFAOYSA-N
Application
8-Azaxanthine monohydrate has been used to determine the crystal and molecular structure of 1,3-dimethyl-8-azaxanthine (HDAX) monohydrate by X-ray diffraction.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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5-Methylsulfanyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-7(6H)-one (2-methylthio-8-azaxanthine) monohydrate
Maldonado, C.R., et al.
Acta Crystallographica Section C, Crystal Structure Communications, 62, 489-491 (2006)
Laurent Fraisse et al.
Analytical biochemistry, 309(2), 173-179 (2002-11-05)
Urate oxidase (E.C.1.7.3.3; uricase, urate oxygen oxidoreductase) is an enzyme of the purine breakdown pathway that catalyzes the oxidation of uric acid in the presence of oxygen to allantoin and hydrogen peroxide. A 96-well plate assay measurement of urate oxidase
J Giełdanowski
Archivum immunologiae et therapiae experimentalis, 28(3), 469-474 (1980-01-01)
The influence of antibiotics and purine and pyrimidine analogues on cells forming rosettes EA and EAC was evaluated in vitro. At the same time pH of solutions of examined immunosuppressors was estimated and a series of experiments with a buffer
R Pérez-Vicente et al.
Biochimica et biophysica acta, 1117(2), 159-166 (1992-09-15)
Xanthine dehydrogenase (XDH) from the unicellular green alga Chlamydomonas reinhardtii has been purified to electrophoretic homogeneity by a procedure which includes several conventional steps (gel filtration, anion exchange chromatography and preparative gel electrophoresis). The purified protein exhibited a specific activity
P Franchetti et al.
Journal of medicinal chemistry, 37(18), 2970-2975 (1994-09-02)
A series of 1,3-dimethyl- and 1,3-dipropyl-8-azaxanthines, substituted at the N8 or N7 position with substituents which usually increase the affinity of the xanthines for the adenosine receptors, was synthesized and studied in radioligand binding experiments. The substitution of CH with
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