(+)-aristolochene

(+)-aristolochene is a lipid of Prenol Lipids (PR) class.

Cross Reference

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

Current reference collection contains 147 references associated with (+)-aristolochene 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 (+)-aristolochene

PubChem Biomolecular Interactions and Pathways

NCBI Entrez Crosslinks

All references with (+)-aristolochene

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Authors Title Published Journal PubMed Link
Harris DM et al. Exploring and dissecting genome-wide gene expression responses of Penicillium chrysogenum to phenylacetic acid consumption and penicillinG production. 2009 BMC Genomics pmid:19203396
Shishova EY et al. X-ray crystallographic studies of substrate binding to aristolochene synthase suggest a metal ion binding sequence for catalysis. 2008 J. Biol. Chem. pmid:18385128
Allemann RK et al. Synthetic efficiency in enzyme mechanisms involving carbocations: aristolochene synthase. 2007 J. Am. Chem. Soc. pmid:17918834
Faraldos JA et al. Interception of the enzymatic conversion of farnesyl diphosphate to 5-epi-aristolochene by using a fluoro substrate analogue: 1-fluorogermacrene A from (2E,6Z)-6-fluorofarnesyl diphosphate. 2007 Chembiochem pmid:17886322
Miller DJ et al. Aristolochene synthase-catalyzed cyclization of 2-fluorofarnesyl-diphosphate to 2-fluorogermacrene A. 2007 Chembiochem pmid:17683054
Shishova EY et al. X-ray crystal structure of aristolochene synthase from Aspergillus terreus and evolution of templates for the cyclization of farnesyl diphosphate. 2007 Biochemistry pmid:17261032
Blay G et al. Rearrangement of 4,5-epoxy-9-trimethylsilyldecalines. Application to the synthesis of the natural eremophilane (-)-aristolochene. 2006 J. Org. Chem. pmid:16776523
Karlshøj K and Larsen TO Differentiation of species from the Penicillium roqueforti group by volatile metabolite profiling. 2005 J. Agric. Food Chem. pmid:15686424
Zhao Y et al. Eremophilane sesquiterpenes from capsidiol. 2004 J. Org. Chem. pmid:15497966
Felicetti B and Cane DE Aristolochene synthase: mechanistic analysis of active site residues by site-directed mutagenesis. 2004 J. Am. Chem. Soc. pmid:15186158