Fmoc-S-3-amino-4-(4-methoxyphenyl)-butyric acid
98%
- Product Code: 105148
CAS:
1352435-52-9
Molecular Weight: | 431.48 g./mol | Molecular Formula: | C₂₆H₂₅NO₅ |
---|---|---|---|
EC Number: | MDL Number: | MFCD22887414 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The presence of the 4-methoxyphenyl group in its structure makes it valuable for introducing specific aromatic and hydrophobic properties into peptide sequences, which can be crucial for studying peptide-protein interactions or designing bioactive peptides. Its application is prominent in pharmaceutical research, where it aids in the development of peptide-based drugs, enzyme inhibitors, and probes for biochemical studies. Additionally, it is utilized in the synthesis of modified peptides for exploring structure-activity relationships (SAR) in drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
0.100 | 10-20 days | Ft21,623.63 |
+
-
|
0.250 | 10-20 days | Ft36,847.45 |
+
-
|
1.000 | 10-20 days | Ft77,864.48 |
+
-
|
5.000 | 10-20 days | Ft373,613.74 |
+
-
|
Fmoc-S-3-amino-4-(4-methoxyphenyl)-butyric acid
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The presence of the 4-methoxyphenyl group in its structure makes it valuable for introducing specific aromatic and hydrophobic properties into peptide sequences, which can be crucial for studying peptide-protein interactions or designing bioactive peptides. Its application is prominent in pharmaceutical research, where it aids in the development of peptide-based drugs, enzyme inhibitors, and probes for biochemical studies. Additionally, it is utilized in the synthesis of modified peptides for exploring structure-activity relationships (SAR) in drug discovery.
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:
Ft0.00
Ft0.00
Total :