(R)-N-(5-(5-Ethyl-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-yl)-1-methyl-1H-pyrazole-4-carboxamide
98%
- Product Code: 228770
CAS:
2364554-48-1
| Molecular Weight: | 337.38 g./mol | Molecular Formula: | C₁₈H₁₉N₅O₂ |
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| EC Number: | MDL Number: | MFCD34602690 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.40±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used in pharmaceutical research as a potent and selective inhibitor of soluble epoxide hydrolase (sEH), this compound is investigated for its anti-inflammatory and analgesic properties. It shows potential in treating neuropathic pain and inflammatory conditions by stabilizing endogenous epoxy fatty acids, which have natural anti-inflammatory effects. Due to its ability to cross the blood-brain barrier, it is also explored for central nervous system disorders. Preclinical studies suggest benefits in models of chronic pain, diabetes-related complications, and cardiovascular diseases. Its role in modulating pain pathways without opioid mechanisms makes it a candidate for non-addictive pain therapies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.001 | 10-20 days | $237.70 |
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| 0.005 | 10-20 days | $594.25 |
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| 0.010 | 10-20 days | $927.95 |
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(R)-N-(5-(5-Ethyl-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-inden-1-yl)-1-methyl-1H-pyrazole-4-carboxamide
Used in pharmaceutical research as a potent and selective inhibitor of soluble epoxide hydrolase (sEH), this compound is investigated for its anti-inflammatory and analgesic properties. It shows potential in treating neuropathic pain and inflammatory conditions by stabilizing endogenous epoxy fatty acids, which have natural anti-inflammatory effects. Due to its ability to cross the blood-brain barrier, it is also explored for central nervous system disorders. Preclinical studies suggest benefits in models of chronic pain, diabetes-related complications, and cardiovascular diseases. Its role in modulating pain pathways without opioid mechanisms makes it a candidate for non-addictive pain therapies.
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