| Weight | 298.324 g/mol |
|---|---|
| Formula | C11H14N4O4S |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
6-Methylmercaptopurine riboside (342-69-8)
Methylthioinosine · 6 Methylthiopurine Riboside · 6 Methylmercaptopurine Riboside
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- Purine Analogue 6-Methylmercaptopurine Riboside Inhibits Early and Late Phases of the Angiogenesis Process (Cancer Research, 1999)
- Metabolism to methionine and growth stimulation by 5-methylthioadenosine and 5-methylthioinosine in mammalian cells (Biochemical and Biophysical Research Communications, 1983)
- Effect of Methylthioinosine on Nucleotide Concentrations in L5178Y Cells (Cancer Research, 1973)
- Conversion of 5-Deoxy-5-methylthioadenosine and 5-Deoxy-5-methylthioinosine to Methionine in Cultured Human Leukemic Cells (Cancer Research, 1983)
- 6Methylmercaptopurine Riboside Is a Potent and Selective Inhibitor of Nerve Growth FactorActivated Protein Kinase N (Journal of Neurochemistry, 1992)
- Interference of 6-mercaptopurine riboside, 6-methylmercaptopurine riboside and azathioprine with the morphogenetic differentiation of mouse extremities in vivo and in organ culture (Naunyn-schmiedebergs Archives of Pharmacology, 1977)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Methylthioinosine
- 6 Methylthiopurine Riboside
- 6 Methylmercaptopurine Riboside
- 6-Methylthiopurine Riboside
-
SMILESCSC1=NC=NC2=C1N=CN2C3C(C(C(O3)CO)O)O
-
InChIKeyZDRFDHHANOYUTE-UHFFFAOYSA-N
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