| Weight | 152.113 g/mol |
|---|---|
| Formula | C5H4N4O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
xanthine (69-89-6)
Score:
#1192 in Biochemistry
,
#3010 in Biology
,
#3761 in Chemistry
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- The reduction of cytochrome c by milk xanthine oxidase. (Journal of Biological Chemistry, 1968)
- Superoxide, hydrogen peroxide, and singlet oxygen in lipid peroxidation by a xanthine oxidase system. (Journal of Biological Chemistry, 1975)
- Quantitative Aspects of the Production of Superoxide Anion Radical by Milk Xanthine Oxidase (Journal of Biological Chemistry, 1970)
- Role of xanthine oxidase and granulocytes in ischemia-reperfusion injury (American Journal of Physiology-heart and Circulatory Physiology, 1988)
- Selection for animal cells that express the Escherichia coli gene coding for xanthine-guanine phosphoribosyltransferase (Proceedings of the National Academy of Sciences of the United States of America, 1981)
- StructureActivity Relationship and Classification of Flavonoids as Inhibitors of Xanthine Oxidase and Superoxide Scavengers (Journal of Natural Products, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC2=C(N1)C(=O)NC(=O)N2
-
InChIKeyLRFVTYWOQMYALW-UHFFFAOYSA-N
- Pubchem - xanthine
- Wikipedia - xanthine
Xanthine ( or ; archaically xanthic acid) (3,7-dihydropurine-2,6-dione), is a purine base found in most human body tissues and fluids and in other organisms. A number of stimulants are derived from xanthine, including caffeine and theobromine. Xanthine is a product on the pathway of purine degradation.
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Similar Compounds
hypoxanthine
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(17801-69-3)
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2-aminopurine
(452-06-2)
1 alternate name
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98550-19-7
(98550-19-7)
1 alternate name
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xanthine
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