Farnesyltransferase inhibitor with antitumor properties. Inhibits the efflux of anticancer drugs from multidrug-resistant cancer cells. Secondary fungal metabolite from Penicillium and Aspergillus.
Product Specification
| Formula: | C28H38O7 |
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| MW: | 486.6 |
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| Purity: | ≥95% (HPLC) |
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| Appearance: | White to off-white powder. |
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| CAS: | 174232-42-9 |
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| Source/Host: | Isolated from Aspergillus fumigatus. |
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| Solubility: | Soluble in DMSO, methanol, chloroform or ethyl acetate; insoluble in hexane or water. |
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| Long Term Storage: | -20°C |
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| Hazard: | HARMFUL. |
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Product Literature References
Mycotoxins and other secondary metabolites produced in vitro by Penicillium paneum Frisvad and Penicillium roqueforti Thom isolated from baled grass silage in Ireland: M. O'Brien, et al.; J. Agric. Food Chem.
54, 9268 (2006),
Abstract;
Andrastin A and barceloneic acid metabolites, protein farnesyl transferase inhibitors from Penicillium albocoremium: chemotaxonomic significance and pathological implications: D.P. Overy, et al.; Mycol. Res.
109, 1243 (2005),
Abstract;
Andrastins A-D, Penicillium roqueforti Metabolites consistently produced in blue-mold-ripened cheese: K.F. Nielsen, et al.; J. Agric. Food Chem.
53, 2908 (2005),
Abstract;
Modeling of binding modes and inhibition mechanism of some natural ligands of farnesyl transferase using molecular docking: A. Pedretti, et al.; J. Med. Chem.
45, 1460 (2002),
Abstract;
Enhancement of drug accumulation by andrastin A produced by Penicillium sp. FO-3929 in vincristine-resistant KB cells: M.C. Rho, et al.; J. Antibiot. (Tokyo)
51, 68 (1998),
Abstract;
Full Text
Andrastins A-C, new protein farnesyltransferase inhibitors produced by Penicillium sp. FO-3929. II. Structure elucidation and biosynthesis: R. Uchida, et al.; J. Antibiot. (Tokyo)
49, 418 (1996),
Abstract;