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V349004-100mgViramidine Hydrochloride is a liver-targeting antiviral nucleoside analog. A 3-carboxamidine prodrug of Ribavirin.Product descriptionTaribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin
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V349004-10mgViramidine Hydrochloride is a liver-targeting antiviral nucleoside analog. A 3-carboxamidine prodrug of Ribavirin.Product descriptionTaribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin
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V349004-25mgViramidine Hydrochloride is a liver-targeting antiviral nucleoside analog. A 3-carboxamidine prodrug of Ribavirin.Product descriptionTaribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin
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V349004-50mgViramidine Hydrochloride is a liver-targeting antiviral nucleoside analog. A 3-carboxamidine prodrug of Ribavirin.Product descriptionTaribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin
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V349004-5mgViramidine Hydrochloride is a liver-targeting antiviral nucleoside analog. A 3-carboxamidine prodrug of Ribavirin.Product descriptionTaribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin
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V329421-5mgVirginiamycin Complex is a solid powder mixture of 75% virginiamycin M1 (Ostreogrycin A, sc-202269) and 25% virginiamycin S1, two streptogramin antibiotics which present a synergistic bacteriocidal action. Virginiamycin M1 inhibits the function of
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V102390-5mgOstreogrycin A, also known as Virginiamycin M1, is a streptogramin macrolide antibiotic. Ostreogrycin A interacts with the bacterial 50S ribosome, inhibiting its function in a reversible manner. Activity of Ostreogrycin A at the ribosome blocks
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V465591-5mgDescriptionChemical structure: macrolideThe antibiotic virginiamycin is produced byStreptomyces virginiaeand is a member of the virginiamycin family. Each member is produced as a mixture of two structurally different compounds that exhibit
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V329621-1mgViridicatin is a 3-hydroxy-4-arylquinolin-2(1H)-one fungal metabolite isolated from several|Penicillium|species. The mechanism of action of Viridicatin remains unexplored in literature reports. Viridicatin demonstrates efficacy against|Mycobacterium
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V329441-1mgViridicatumtoxin is a tetracycline-like metabolite produced by several species of|Penicillium|, first isolated as a mycotoxin. It is a potent antibacterial, with activity against|S. aureus|including MRSA and QRSA strains.
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V329625-1mgA 18-membered macrolide. Active against trichomonads and various RNA and DNA viruses.
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V329625-5mgA 18-membered macrolide. Active against trichomonads and various RNA and DNA viruses.