MeSH term | MeSH ID | Detail |
---|---|---|
Adenocarcinoma | D000230 | 166 associated lipids |
Total
1
Rolliniastatin-1 is a lipid of Polyketides (PK) class.
We collected disease MeSH terms mapped to the references associated with Rolliniastatin-1
MeSH term | MeSH ID | Detail |
---|---|---|
Adenocarcinoma | D000230 | 166 associated lipids |
Authors | Title | Published | Journal | PubMed Link |
---|---|---|---|---|
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 |
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 |
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 |
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 |
Marshall JA et al. | A modular synthesis of annonaceous acetogenins. | 2003 | J. Org. Chem. | pmid:12608790 |
Hamada T et al. | Synthesis and inhibitory action of novel acetogenin mimics with bovine heart mitochondrial complex I. | 2004 | Biochemistry | pmid:15035635 |
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 |
Tinsley JM et al. | Synthesis of (+)-bullatacin via the highly diastereoselective [3+2] annulation reaction of a racemic aldehyde and a nonracemic allylsilane. | 2005 | Org. Lett. | pmid:16146398 |
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 |