7540-51-4

7540-51-4 is a lipid of Prenol Lipids (PR) class.

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

Current reference collection contains 68 references associated with 7540-51-4 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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Authors Title Published Journal PubMed Link
Gao P et al. Expeditious construction of (+)-mintlactone via intramolecular hetero-Pauson-Khand reaction. 2009 J. Org. Chem. pmid:19228032
Liang B and Negishi E Highly efficient asymmetric synthesis of fluvirucinine A1 via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-lipase-catalyzed acetylation tandem process. 2008 Org. Lett. pmid:18076181
Belani JD and Rychnovsky SD A concise synthesis of ent-Cholesterol. 2008 J. Org. Chem. pmid:18336043
Yoshida N et al. Inhibitory effects of terpenoids on multidrug resistance-associated protein 2- and breast cancer resistance protein-mediated transport. 2008 Drug Metab. Dispos. pmid:18436619
Majumder AB et al. Enantioselective transacetylation of (R,S)-beta-citronellol by propanol rinsed immobilized Rhizomucor miehei lipase. 2007 Chem Cent J pmid:17880741
Varseev GN and Maier ME Enantioselective total synthesis of (+)-neosymbioimine. 2007 Org. Lett. pmid:17378570
Dyer BS et al. Synthesis and structure of phosphatidylinositol dimannoside. 2007 J. Org. Chem. pmid:17385918
Schmiedeberg K et al. Structural determinants of odorant recognition by the human olfactory receptors OR1A1 and OR1A2. 2007 J. Struct. Biol. pmid:17601748
Yamauchi N and Endoh S Improved isotopic deuterium labeling at the diastereotopic methyl group of leucine: a synthetic route to (4S)- and (4R)-[5-2H1]leucine. 2006 Biosci. Biotechnol. Biochem. pmid:16428849
Yoshida N et al. Inhibition of P-glycoprotein-mediated transport by extracts of and monoterpenoids contained in Zanthoxyli fructus. 2005 Toxicol. Appl. Pharmacol. pmid:15890377