Rolliniastatin-1

Rolliniastatin-1 is a lipid of Polyketides (PK) class.

Cross Reference

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

Current reference collection contains 351 references associated with Rolliniastatin-1 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.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.


Here are additional resources we collected from PubChem and MeSH for Rolliniastatin-1

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Rolliniastatin-1

MeSH term MeSH ID Detail
Adenocarcinoma D000230 166 associated lipids
Total 1

NCBI Entrez Crosslinks

All references with Rolliniastatin-1

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Authors Title Published Journal PubMed Link
pmid:
Carelli V et al. Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy. 1999 Ann. Neurol. pmid:10072046
Tormo JR et al. Kinetic characterization of mitochondrial complex I inhibitors using annonaceous acetogenins. 1999 Arch. Biochem. Biophys. pmid:10462447
Estornell E et al. Cherimolin-1, new selective inhibitor of the first energy-coupling site of the NADH: ubiquinone oxidoreductase (complex I). 1997 Biochem. Biophys. Res. Commun. pmid:9367916
Degli Esposti M et al. Natural substances (acetogenins) from the family Annonaceae are powerful inhibitors of mitochondrial NADH dehydrogenase (Complex I). 1994 Biochem. J. pmid:8037664
Chiu HF et al. Bullatacin, a potent antitumor Annonaceous acetogenin, induces apoptosis through a reduction of intracellular cAMP and cGMP levels in human hepatoma 2.2.15 cells. 2003 Biochem. Pharmacol. pmid:12527325
Shimada H et al. Membrane conformations and their relation to cytotoxicity of asimicin and its analogues. 1998 Biochemistry pmid:9454575
Kakutani N et al. Exploring the binding site of delta(lac)-acetogenin in bovine heart mitochondrial NADH-ubiquinone oxidoreductase. 2010 Biochemistry pmid:20459120
Hamada T et al. Synthesis and inhibitory action of novel acetogenin mimics with bovine heart mitochondrial complex I. 2004 Biochemistry pmid:15035635
Masuya T et al. Pinpoint chemical modification of Asp160 in the 49 kDa subunit of bovine mitochondrial complex I via a combination of ligand-directed tosyl chemistry and click chemistry. 2014 Biochemistry pmid:25419630
Takada M et al. Definition of crucial structural factors of acetogenins, potent inhibitors of mitochondrial complex I. 2000 Biochim. Biophys. Acta pmid:11106771
Fato R et al. Differential effects of mitochondrial Complex I inhibitors on production of reactive oxygen species. 2009 Biochim. Biophys. Acta pmid:19059197
Darrouzet E and Dupuis A Genetic evidence for the existence of two quinone related inhibitor binding sites in NADH-CoQ reductase. 1997 Biochim. Biophys. Acta pmid:9107311
Zhao GX et al. The absolute configuration of adjacent bis-THF acetogenins and asiminocin, a novel highly potent asimicin isomer from Asimina triloba. 1996 Bioorg. Med. Chem. pmid:8689234
Tormo JR et al. Gamma-lactone-Functionalized antitumoral acetogenins are the most potent inhibitors of mitochondrial complex I. 2001 Bioorg. Med. Chem. Lett. pmid:11266168
Oberlies NH et al. The Annonaceous acetogenin bullatacin is cytotoxic against multidrug-resistant human mammary adenocarcinoma cells. 1997 Cancer Lett. pmid:9097981
Shi JF et al. Synthesis and tumor cell growth inhibitory activity of biotinylated annonaceous acetogenins. 2014 Eur J Med Chem pmid:24308999
Nakamaru-Ogiso E et al. The ND2 subunit is labeled by a photoaffinity analogue of asimicin, a potent complex I inhibitor. 2010 FEBS Lett. pmid:20074573
López-Gallardo E et al. Food derived respiratory complex I inhibitors modify the effect of Leber hereditary optic neuropathy mutations. 2018 Food Chem. Toxicol. pmid:29991444
Chen Y et al. Anti-tumor activity of Annona squamosa seeds extract containing annonaceous acetogenin compounds. 2012 J Ethnopharmacol pmid:22609808