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

Download all related citations
Per page 10 20 50 | Total 45
Authors Title Published Journal PubMed Link
Pomper KW et al. Identification of annonaceous acetogenins in the ripe fruit of the North American pawpaw ( Asimina triloba ). 2009 J. Agric. Food Chem. pmid:19711911
Tinsley JM and Roush WR Total synthesis of asimicin via highly stereoselective [3 + 2] annulation reactions of substituted allylsilanes. 2005 J. Am. Chem. Soc. pmid:16076173
Keum G et al. Stereoselective syntheses of rolliniastatin 1, rollimembrin, and membranacin. 2005 J. Am. Chem. Soc. pmid:16028952
Ghelli A et al. Measurement of the membrane potential generated by complex I in submitochondrial particles. 1997 J. Biochem. pmid:9163527
Nakamaru-Ogiso E et al. The membrane subunit NuoL(ND5) is involved in the indirect proton pumping mechanism of Escherichia coli complex I. 2010 J. Biol. Chem. pmid:20826797
Okun JG et al. Three classes of inhibitors share a common binding domain in mitochondrial complex I (NADH:ubiquinone oxidoreductase). 1999 J. Biol. Chem. pmid:9915790
Liang YJ et al. Bullatacin triggered ABCB1-overexpressing cell apoptosis via the mitochondrial-dependent pathway. 2009 J. Biomed. Biotechnol. pmid:19639048
Chen Y et al. Determination of bullatacin in rat plasma by liquid chromatography-mass spectrometry. 2012 J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. pmid:22534655
Sinha SC et al. Alteration of the bis-tetrahydrofuran core stereochemistries in asimicin can affect the cytotoxicity. 2008 J. Med. Chem. pmid:18975929
Ye Q et al. Longimicins A-D: novel bioactive acetogenins from Asimina longifolia (annonaceae) and structure-activity relationships of asimicin type of annonaceous acetogenins. 1996 J. Med. Chem. pmid:8627602
Oberlies NH et al. Structure-activity relationships of diverse Annonaceous acetogenins against multidrug resistant human mammary adenocarcinoma (MCF-7/Adr) cells. 1997 J. Med. Chem. pmid:9207950
Jiang S et al. Mimicry of annonaceous acetogenins: enantioselective synthesis of a (4R)-hydroxy analogue having potent antitumor activity. 2002 J. Org. Chem. pmid:12003552
Marshall JA et al. A modular synthesis of annonaceous acetogenins. 2003 J. Org. Chem. pmid:12608790
Avedissian H et al. Total synthesis of asimicin and bullatacin. 2000 J. Org. Chem. pmid:10987938
Chih HW et al. Bullatacin, a potent antitumor annonaceous acetogenin, inhibits proliferation of human hepatocarcinoma cell line 2.2.15 by apoptosis induction. 2001 Life Sci. pmid:11521756
Morré DJ et al. Mode of action of bullatacin, a potent antitumor acetogenin: inhibition of NADH oxidase activity of HeLa and HL-60, but not liver, plasma membranes. 1995 Life Sci. pmid:7837933
Ahammadsahib KI et al. Mode of action of bullatacin: a potent antitumor and pesticidal annonaceous acetogenin. 1993 Life Sci. pmid:8371627
Luna-Cazares LM and Gonzalez-Esquinca AR Susceptibility of complete bacteria and spheroplasts of Escherichia coli, Pseudomonas aeruginosa and Salmonella typhi to rolliniastatin-2. 2010 Nat. Prod. Res. pmid:20582808
Carelli V et al. Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype. 1997 Neurology pmid:9191778
Zhao H et al. Advances in Lewis acid controlled carbon-carbon bond-forming reactions enable a concise and convergent total synthesis of bullatacin. 2006 Org. Lett. pmid:16956231