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Kendomycin (CAS 183202-73-5)

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Solicitud:A broadly efficacious polyketide macrocycle antibiotic
Número CAS:183202-73-5
Pureza:>95%
Peso Molecular:486.64
Fórmula Molecular:C29H42O6
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Nombre del productoNúmero de catálogoUnidadPrecioCantidadAñadir 
Kendomycin sc-202196 100 µg $162
Kendomycin sc-202196A 500 µg $592
Descripción
Kendomycin is a polyketide macrolide antibiotic isolated from various Streptomyces strains, with demonstrated cytotoxic and antiosteoporotic properties. Structurally intriguing to synthetic chemists, the macrocycle of Kendomycin contains a rare quinone methide chromophore. The antibiotic activity of Kendomycin shows efficacy against a range of bacteria including Methicillin- and Vancomycin-resistant Staphylococcus aureus. Studies correlate the demonstrated cytotoxicity of Kendomycin against multiple tumor cell lines to an inhibition of chymotrypsin-like proteasome activity. Kendomycin is also described to disable the antiapoptotic protein Bcl-xl by blocking protein-protein interaction with Bak, though this finding showed no direct correlation to cytotoxicity. Early reports described Kendomycin as an endothelin receptor antagonist, and the antiosteoporotic effects were correlated to calcitonin receptor agonism.
Información Técnica
Apariencia:Yellow
Estado Físico:Solid
Derivado de:Streptomyces sp.
Solubilidad:Soluble in ethanol, methanol, DMF or DMSO. Limited water solubility
Almacenamiento:Store at -20° C
Seguridad e Información de Referencia
ID en PubChem:5472093
Número MDL:MFCD00076711
SMILES:CC1CCC2C(C(C(C(O2)C3=C(C(=O)C(=C4C3=CC(O4)(C(CC(CC(=C1)C)C)C)O)C)O)C)O)C
Para Uso Exclusivo en Investigación. No está diseñado para uso en diagnosis o terapia.
References
1. Yuan, Y., et al. 2004. J. Am. Chem. Soc. 126: 14720-14721. PMID: 15535687
2. Mulzer, J., et al. 2004. Proc. Natl. Acad. Sci. U.S.A. 101: 11980-11985. PMID: 15277689
3. Elnakady, Y.A., et al. 2007. Chembiochem. 8: 1261-1272. PMID: 17592829
4. Janssen, C.O., et al. 2008. Bioorg. Med. Chem. Lett. 18: 5771-5773. PMID: 18845435
5. Bahnck, K.B., et al. 2008. J. Am. Chem. Soc. 130: 13177-13181. PMID: 18767844
6. Martin, H.J., et al. 2010. Angew. Chem. Int. Ed. Engl. 49: 5614-5626. PMID: 20818753
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