SCHEMBL215687

SCHEMBL215687 is a lipid of Polyketides (PK) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 221 references associated with SCHEMBL215687 in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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All references with SCHEMBL215687

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Authors Title Published Journal PubMed Link
pmid:
Duval RA et al. Heterocyclic analogues of squamocin as inhibitors of mitochondrial complex I. On the role of the terminal lactone of annonaceous acetogenins. 2006 Biochemistry pmid:16489765
Duval RA et al. Remarkable substituent effect: beta-aminosquamocin, a potent dual inhibitor of mitochondrial complexes I and III. 2005 Biochim. Biophys. Acta pmid:16139789
Lin YS et al. A spectral graph theoretic approach to quantification and calibration of collective morphological differences in cell images. 2010 Bioinformatics pmid:20529919
Hochbaum DS et al. Ranking of multidimensional drug profiling data by fractional-adjusted bi-partitional scores. 2012 Bioinformatics pmid:22689749
Xu ZF et al. Inhibitory activities of three annonaceous acetogenins on NADH oxidase of chicken liver mitochondria. 2003 Biol. Pharm. Bull. pmid:12736522
Duval R et al. Semisynthesis of heterocyclic analogues of squamocin, a cytotoxic annonaceous acetogenin, by an unusual oxidative decarboxylation reaction. 2003 Bioorg. Med. Chem. pmid:12878138
Duval RA et al. Semisynthesis and biological activity of aminoacyl triesters of squamocin, an annonaceous acetogenin. 2005 Bioorg. Med. Chem. pmid:15863004
Derbré S et al. Highly cytotoxic and neurotoxic acetogenins of the Annonaceae: new putative biological targets of squamocin detected by activity-based protein profiling. 2008 Bioorg. Med. Chem. Lett. pmid:18851912
Lee CC et al. Squamocin modulates histone H3 phosphorylation levels and induces G1 phase arrest and apoptosis in cancer cells. 2011 BMC Cancer pmid:21299907