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| Product | Description | |
|---|---|---|
| Valinomycin | A hydrophobic cyclodepsipeptide with potent antitumour activity; a highly selective potassium ionophore; a biosensor to detect potassium efflux. Synonyms: Potassium ionophore I; valino; Valinomicin; NSC122023; Antibiotic N-329 B; cyclo[-D-O-Val-D-Val-L-O-Ala-L-Val]3; BRN 0078657; (3R, 6R, 9S, 12S, 15R, 18R, 21S, 24S, 27R, 30R, 33S, 36S)-3, 6, 9, 15, 18, 21, 27, 30, 33-Nonaisopropyl-12, 24, 36-trimethyl-1, 7, 13, 19, 25, 31-hexaoxa-4, 10, 16, 22, 28, 34-hexaazacyclohexatriacontane-2, 5, 8, 11, 14, 17, 20, 23, 26, 29, 32,35-dodecone. Grades: >95% by HPLC. CAS No. 2001-95-8. Molecular formula: C54H90N6O18. Mole weight: 1111.32. |  |
| Valinomycin | Valinomycin is a hydrophobic cyclodepsipeptide with potent antitumor activity. Valinomycin is a highly selective potassium ionophore and this action leads to a diverse range of profound cell membrane effects. More recently, Valinomycin has found application in biosensors. Group: Biochemicals. Grades: Highly Purified. CAS No. 2001-95-8. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| Valinomycin | Valinomycin is a potassium-specific ionophore, the valinomycin-K + complex can be incorporated into biological bilayer membranes with the hydrophobic surface of valinomycin, destroys the normal K + gradient across the membrane, and as a result kills the cells, incorporating into liposomes can significantly reduces the cytotoxicity and enhances the targeting effect. Valinomycin exhibits antibiotic , antifungal, antiviral, antitumor and insecticidal efficacy, thus can be used for relevant research [1] [2]. Uses: Scientific research. Group: Peptides. Alternative Names: NSC 122023. CAS No. 2001-95-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N6693. |  |
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