11460
8-Azaxanthine monohydrate
≥98.0% (HPLC)
Sinonimo/i:
2,6-Dihydroxy-8-azapurine
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About This Item
Formula empirica (notazione di Hill):
C4H3N5O2 · H2O
Numero CAS:
Peso molecolare:
171.11
Beilstein:
10424
Numero CE:
Numero MDL:
Codice UNSPSC:
41106305
ID PubChem:
NACRES:
NA.25
Prodotti consigliati
Livello qualitativo
Saggio
≥98.0% (HPLC)
Stato
solid
Stringa SMILE
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
VKEGPGRANAWNIN-UHFFFAOYSA-N
Applicazioni
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.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
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
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
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
Molecular orbital study of 8-azaxanthine derivatives and crystal structure of 1,3-dimethyl-8-azaxanthine monohydrate
Purificacion Sanchez, M., et al.
Journal of Molecular Structure, 344, 257-264 (1995)
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)
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