11460
8-Azaxanthine monohydrate
≥98.0% (HPLC)
Synonym(s):
2,6-Dihydroxy-8-azapurine
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About This Item
Empirical Formula (Hill Notation):
C4H3N5O2 · H2O
CAS Number:
Molecular Weight:
171.11
Beilstein:
10424
EC Number:
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.25
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Quality Level
Assay
≥98.0% (HPLC)
form
solid
SMILES string
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
InChI key
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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)
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)
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