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| Product | Description | |
|---|---|---|
| Rifamycin SV Sodium | Semi-synthetic antibiotic derived from Rifamycin S. Antibacterial. Potency >900 units (dry basis). Group: Biochemicals. Alternative Names: 5,6,9,17,19,21-Hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-. Grades: Highly Purified. CAS No. 14897-39-3. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| Rifamycin SV sodium salt | Rifamycin SV sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Nsc133100. Product Category: Heterocyclic Organic Compound. CAS No. 15105-92-7. Product ID: ACM15105927. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Rifamycin sodium | Rifamycin sodium (Rifamycin SV monosodium) belongs to the family of ansamycin antibiotics and has been isolated from the fermentation of A. mediterranei or its mutants. Rifamycin sodium displays a broad spectrum of antibiotic activity against Gram-positive and, to a lesser extent, Gram-negative bacteria [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Rifamycin SV sodium. CAS No. 14897-39-3. Pack Sizes: 10 mM * 1 mL; 50 mg. Product ID: HY-B1907. |  |
| Rifamycin Sodium | Rifamycin SV is a derivative of rifamycin, an antibiotic that inhibits bacterial DNA-dependent RNA polymerase. It is effective against Gram-positive bacteria. Uses: Antirheumatic agents. Synonyms: sodium;(7S, 9E, 11S, 12R, 13S, 14R, 15R, 16R, 17S, 18S, 19E, 21Z)-13-acetyloxy-2, 15, 17, 29-tetrahydroxy-11-methoxy-3, 7, 12, 14, 16, 18, 22-heptamethyl-6, 23-dioxo-8, 30-dioxa-24-azatetracyclo[23.3.1.1^{4, 7}.0^{5, 28}]triaconta-1(29), 2, 4, 9, 19, 21, 25, 27-octaen-27-olate; sodium;(7S, 9E, 11S, 12R, 13S, 14R, 15R, 16R, 17S, 18S, 19E, 21Z)-13-acetyloxy-2, 15, 17, 29-tetrahydroxy-11-methoxy-3, 7, 12, 14, 16, 18, 22-heptamethyl-6, 23-dioxo-8, 30-dioxa-24-azatetracyclo[23.3.1.1^{4, 7}.0^{5, 28}]triaconta-1(29), 2, 4, 9, 19, 21, 25, 27-octaen-27-olate. Grades: 99 %. CAS No. 14897-39-3. Molecular formula: C37H46NO12Na. Mole weight: 719.75. |  |
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