| Weight | 135.13 g/mol |
|---|---|
| Formula | C5H5N5 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1H-Pyrazolo[3,4-d]pyrimidin-4-amine (2380-63-4, 20289-44-5)
4-aminopyrazolo(3,4-d)pyrimidine · aminopurinol · 4APP-4
Score:
#80 in Molecular and cellular biology
,
#2213 in Biochemistry
,
#5680 in Chemistry
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- Metabolism of pyrazolo(3,4-d)pyrimidines in Leishmania braziliensis and Leishmania donovani. Allopurinol, oxipurinol, and 4-aminopyrazolo(3,4-d)pyrimidine. (Journal of Biological Chemistry, 1979)
- 4-aminopyrazolo(3-,4-D)pyrimidine and 4-aminopyrazolo-(3,4-D)pyridine tyrosine kinase inhibitors (1995)
- Cholesterogenesis: derepression in extrahepatic tissues with 4-aminopyrazolo (3,4-d) pyrimidine. (Science, 1976)
- Distribution of 3-hydroxy-3-methylglutaryl coenzyme A reductase and alkaline phosphatase activities in isolated ileal epithelial cells of fed, fasted, cholestyramine-fed, and 4-aminopyrazolo[3,4-d]pyrimidine-treated rats. (Journal of Lipid Research, 1979)
- Inhibition of Experimental Neoplasms by 4-Aminopyrazolo(3,4-d)Pyrimidine. (Experimental Biology and Medicine, 1955)
- 4-Aminopyrazolo(3,4-d)pyrimidine: an Inhibitor of the Synthesis of Purines and Proteins in Ehrlich Ascites Cells (Journal of Biological Chemistry, 1961)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-aminopyrazolo(3,4-d)pyrimidine
- aminopurinol
- 4APP-4
-
SMILESC1=NNC2=C1C(=NC=N2)N
-
InChIKeyLHCPRYRLDOSKHK-UHFFFAOYSA-N
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