5,8-Dihydroxy-[6,7]-N-(4-fluorobenzyl)-succinimido-quinoline
95%
- Product Code: 50270
CAS:
684284-29-5
| Molecular Weight: | 338.3 g./mol | Molecular Formula: | C₁₈H₁₁FN₂O₄ |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core and a fluorobenzyl group, makes it suitable for developing compounds with potential therapeutic applications, particularly in targeting enzymes or receptors involved in disease pathways. Researchers often explore its use in designing inhibitors for specific proteins, which could be relevant in treating conditions like cancer or inflammatory diseases. Additionally, the presence of the fluorobenzyl group enhances its ability to interact with biological targets, improving binding affinity and selectivity. Its application extends to drug discovery programs, where it is employed to optimize lead compounds for better efficacy and pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,046.53 |
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| 0.250 | 10-20 days | $2,126.70 |
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5,8-Dihydroxy-[6,7]-N-(4-fluorobenzyl)-succinimido-quinoline
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core and a fluorobenzyl group, makes it suitable for developing compounds with potential therapeutic applications, particularly in targeting enzymes or receptors involved in disease pathways. Researchers often explore its use in designing inhibitors for specific proteins, which could be relevant in treating conditions like cancer or inflammatory diseases. Additionally, the presence of the fluorobenzyl group enhances its ability to interact with biological targets, improving binding affinity and selectivity. Its application extends to drug discovery programs, where it is employed to optimize lead compounds for better efficacy and pharmacokinetic properties.
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