(6-ammonio-N-[(2S)-2-ammonio-3-(1H-imidazol-5-yl)propanoyl]-L-norleucylamino)acetate
95%
- Product Code: 76470
CAS:
62024-09-3
| Molecular Weight: | 340.38 g./mol | Molecular Formula: | C₁₄H₂₅N₆O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192197 | |
| Melting Point: | Boiling Point: | 829.7 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in biochemical research and pharmaceutical development due to its structural similarity to peptides and amino acids. It serves as a key intermediate in the synthesis of complex peptides, particularly those involved in enzyme inhibition and receptor binding studies. Its imidazole and amino groups make it valuable in designing molecules that mimic natural substrates, aiding in the study of enzymatic mechanisms and drug interactions. Additionally, it is employed in the development of therapeutic agents targeting conditions related to amino acid metabolism or signaling pathways. Its role in creating bioactive peptides also extends to applications in cancer research, where it helps in designing inhibitors for specific protein targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿16,830.00 |
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| 1.000 | 10-20 days | ฿47,232.00 |
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(6-ammonio-N-[(2S)-2-ammonio-3-(1H-imidazol-5-yl)propanoyl]-L-norleucylamino)acetate
This compound is primarily utilized in biochemical research and pharmaceutical development due to its structural similarity to peptides and amino acids. It serves as a key intermediate in the synthesis of complex peptides, particularly those involved in enzyme inhibition and receptor binding studies. Its imidazole and amino groups make it valuable in designing molecules that mimic natural substrates, aiding in the study of enzymatic mechanisms and drug interactions. Additionally, it is employed in the development of therapeutic agents targeting conditions related to amino acid metabolism or signaling pathways. Its role in creating bioactive peptides also extends to applications in cancer research, where it helps in designing inhibitors for specific protein targets.
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