| Weight | 136.114 g/mol |
|---|---|
| Formula | C5H4N4O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
hypoxanthine (68-94-0)
Score:
#1124 in Biochemistry
,
#2868 in Biology
,
#3591 in Chemistry
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- Extracellular Adenosine, Inosine, Hypoxanthine, and Xanthine in Relation to Tissue Nucleotides and Purines in Rat Striatum During Transient Ischemia (Journal of Neurochemistry, 1987)
- Structure of a natural guanine-responsive riboswitch complexed with the metabolite hypoxanthine. (Nature, 2004)
- Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in Gout (Annals of Internal Medicine, 1969)
- Insertional Tagging, Cloning, and Expression of the Toxoplasma gondii Hypoxanthine-Xanthine-Guanine Phosphoribosyltransferase Gene USE AS A SELECTABLE MARKER FOR STABLE TRANSFORMATION (Journal of Biological Chemistry, 1996)
- Iron ion-dependent modification of bases in DNA by the superoxide radical-generating system hypoxanthine/xanthine oxidase. (Journal of Biological Chemistry, 1989)
- Hypoxanthine as an indicator of hypoxia: its role in health and disease through free radical production (Pediatric Research, 1988)
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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)N=CN2
-
InChIKeyFDGQSTZJBFJUBT-UHFFFAOYSA-N
- Pubchem - hypoxanthine
- Wikipedia - hypoxanthine
Hypoxanthine is a naturally occurring purine derivative. It is occasionally found as a constituent of nucleic acids, where it is present in the anticodon of tRNA in the form of its nucleoside inosine. It has a tautomer known as 6-hydroxypurine.
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hypoxanthine
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