Spiramycin (hexanedioate)
Based on 1 publication(s) in Google Scholar
Spiramycin hexanedioate (Rovamycin) is a macrolide antibiotic produced by Streptomyces ambofaciens with against bacteria and Toxoplasma gondii activities, and also has antiparasitic effect. Spiramycin hexanedioate is composed of a 16-member lactone ring, on which three sugars (mycaminose, forosamine, and mycarose) are attached.
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- No. CAS: 11034-40-5
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Almacenamiento:
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Actividad biológica
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Chemical Information
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Publications Citing Use of MedChemExpress (MCE) Spiramycin (hexanedioate)
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Actividad biológica
Descripciòn
IC50 & Target
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Macrolide |
In Vitro
Spiramycin (24 hours; 1-1000 μM; T. gondii infected HeLa cells and HeLa cells) treatment reduces the cytotoxicity, and shows anti-Toxoplasma gondii activity, with IC50 values of 189 μM for HeLa cells; and 262 μM for T. gondii-infected HeLa cells[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:T. gondii infected HeLa cells and HeLa cells
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Concentration:1-1000 μM
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Incubation Time:24 hours
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Result:Reduced the cytotoxicity.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:36 female KM mice with T.gondii[3]
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Dosage:100 mg/kg
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Administration:Intraperitoneal injection; every day; for 4 days
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Result:The number of tachyzoites was significantly reduced. Reduced hepatotoxicity and significantly enhanced antioxidative effects. Granuloma and cyst formation were inhibitied.
Chemical Information
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No. CAS 11034-40-5
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SMILES
N/A
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Synonyms
Rovamycin (hexanedioate)
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
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Journal Impact Factor
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Most Recent
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Cell Prolif
Direct inhibitory effect on viral entry of influenza A and SARS-CoV-2 viruses by azithromycin. [Abstract]2021 Jan;54(1):e12953. PMID: 33211371
Pureza y Documentación
Referencias
[1]. Nguyen HC, et al. Post-PKS tailoring steps of the spiramycin macrolactone ring in Streptomyces ambofaciens. Antimicrob Agents Chemother. 2013 Aug;57(8):3836-42. [Content Brief]
[2]. Etewa SE, et al. Assessment of spiramycin-loaded chitosan nanoparticles treatment on acute and chronic toxoplasmosis in mice. J Parasit Dis. 2018 Mar;42(1):102-113. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Spiramycin (hexanedioate) Related Classifications
HY-100593A Related Classifications
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