Gly-Met-Ala-Ser-Lys-Ala-Gly-Ala-Ile-Ala-Gly-Lys-Ile-Ala-Lys-Val-Ala-Leu-Lys-Ala-Leu-NH2 trifluoroacetate
98%
- Product Code: 190943
CAS:
402950-23-6
| Molecular Weight: | 2082.48 g./mol | Molecular Formula: | C₉₀H₁₆₃F₃N₂₆O₂₄S |
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| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Dry, Lightproof, Inert Gas |
Product Description:
Used in research and development of bioactive peptides, this compound supports studies on antimicrobial activity and membrane interactions due to its amphipathic helical structure. It is applied in designing synthetic peptides that mimic natural host defense mechanisms, particularly in exploring new antimicrobial agents with selective toxicity against pathogens. Its sequence promotes cell penetration and stability, making it valuable in drug delivery investigations and peptide engineering. Commonly utilized in in vitro assays to evaluate cytotoxicity, hemolysis, and microbial growth inhibition.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 G | 10-20 days | ฿38,740.00 |
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Gly-Met-Ala-Ser-Lys-Ala-Gly-Ala-Ile-Ala-Gly-Lys-Ile-Ala-Lys-Val-Ala-Leu-Lys-Ala-Leu-NH2 trifluoroacetate
Used in research and development of bioactive peptides, this compound supports studies on antimicrobial activity and membrane interactions due to its amphipathic helical structure. It is applied in designing synthetic peptides that mimic natural host defense mechanisms, particularly in exploring new antimicrobial agents with selective toxicity against pathogens. Its sequence promotes cell penetration and stability, making it valuable in drug delivery investigations and peptide engineering. Commonly utilized in in vitro assays to evaluate cytotoxicity, hemolysis, and microbial growth inhibition.
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