5-Amino-7-(4-fluorobenzyl)-9-hydroxy-6H-pyrrolo[3,4-g]quinoline-6,8(7H)-dione
95%
- Product Code: 48400
CAS:
915690-75-4
| Molecular Weight: | 337.3 g./mol | Molecular Formula: | C₁₈H₁₂FN₃O₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 611.9±55.0 °C(Predicted) | |
| Density: | 1.582±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its potential biological activity. It is studied for its role as an intermediate in the synthesis of more complex molecules, particularly those targeting specific enzymes or receptors in the body. Its structure suggests potential applications in the development of drugs for treating diseases such as cancer, inflammation, or neurological disorders. Researchers explore its efficacy in inhibiting certain pathways or mechanisms involved in disease progression. Additionally, it may be investigated for its antioxidant or antimicrobial properties, contributing to the development of novel therapeutic agents. Its fluorinated benzyl group enhances its stability and bioavailability, making it a valuable component in drug design and optimization studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿11,592.00 |
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| 0.005 | 10-20 days | ฿41,391.00 |
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5-Amino-7-(4-fluorobenzyl)-9-hydroxy-6H-pyrrolo[3,4-g]quinoline-6,8(7H)-dione
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its potential biological activity. It is studied for its role as an intermediate in the synthesis of more complex molecules, particularly those targeting specific enzymes or receptors in the body. Its structure suggests potential applications in the development of drugs for treating diseases such as cancer, inflammation, or neurological disorders. Researchers explore its efficacy in inhibiting certain pathways or mechanisms involved in disease progression. Additionally, it may be investigated for its antioxidant or antimicrobial properties, contributing to the development of novel therapeutic agents. Its fluorinated benzyl group enhances its stability and bioavailability, making it a valuable component in drug design and optimization studies.
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