(1H-Pyrazolo[4,3-b]pyridin-6-yl)methanol
97%
- Product Code: 36184
CAS:
1934501-30-0
| Molecular Weight: | 149.1500 g./mol | Molecular Formula: | C₇H₇N₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22396183 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
(1H-Pyrazolo[4,3-b]pyridin-6-yl)methanol is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting kinase enzymes. Kinase inhibitors are crucial in the development of drugs for treating cancers, inflammatory diseases, and other conditions where abnormal kinase activity plays a role. The pyrazolopyridine core of this compound is known for its ability to interact with ATP-binding sites of kinases, making it a valuable scaffold for designing potent and selective inhibitors. Additionally, its methanol group provides a versatile handle for further chemical modifications, enabling the creation of diverse derivatives with tailored pharmacological properties. This compound is also explored in the development of small-molecule probes for studying biological pathways and identifying new therapeutic targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,532.00 |
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(1H-Pyrazolo[4,3-b]pyridin-6-yl)methanol
(1H-Pyrazolo[4,3-b]pyridin-6-yl)methanol is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting kinase enzymes. Kinase inhibitors are crucial in the development of drugs for treating cancers, inflammatory diseases, and other conditions where abnormal kinase activity plays a role. The pyrazolopyridine core of this compound is known for its ability to interact with ATP-binding sites of kinases, making it a valuable scaffold for designing potent and selective inhibitors. Additionally, its methanol group provides a versatile handle for further chemical modifications, enabling the creation of diverse derivatives with tailored pharmacological properties. This compound is also explored in the development of small-molecule probes for studying biological pathways and identifying new therapeutic targets.
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