Fmoc-3-chloro-L-homophenylalanine
95%
- Product Code: 113682
CAS:
1260587-49-2
| Molecular Weight: | 435.90 g./mol | Molecular Formula: | C₂₅H₂₂ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07372175 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Fmoc-3-chloro-L-homophenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild basic conditions, making it valuable for constructing complex peptides. The presence of the chloro group on the homophenylalanine side chain introduces unique steric and electronic properties, which can be leveraged to modify peptide interactions with biological targets. This makes it useful in the development of peptide-based drugs, enzyme inhibitors, and bioactive molecules. Additionally, it is employed in research to study structure-activity relationships (SAR) in peptides, aiding in the optimization of therapeutic compounds. Its application extends to the synthesis of peptidomimetics, where it helps mimic natural peptide structures for enhanced stability and efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿3,906.00 |
+
-
|
| 0.250 | 10-20 days | ฿11,880.00 |
+
-
|
| 1.000 | 10-20 days | ฿29,790.00 |
+
-
|
Fmoc-3-chloro-L-homophenylalanine
Fmoc-3-chloro-L-homophenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild basic conditions, making it valuable for constructing complex peptides. The presence of the chloro group on the homophenylalanine side chain introduces unique steric and electronic properties, which can be leveraged to modify peptide interactions with biological targets. This makes it useful in the development of peptide-based drugs, enzyme inhibitors, and bioactive molecules. Additionally, it is employed in research to study structure-activity relationships (SAR) in peptides, aiding in the optimization of therapeutic compounds. Its application extends to the synthesis of peptidomimetics, where it helps mimic natural peptide structures for enhanced stability and efficacy.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :