(+)-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
Zhao Y et al. Eremophilane sesquiterpenes from capsidiol. 2004 J. Org. Chem. pmid:15497966
Karlshøj K and Larsen TO Differentiation of species from the Penicillium roqueforti group by volatile metabolite profiling. 2005 J. Agric. Food Chem. pmid:15686424
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
pmid:16791319
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
Miller DJ et al. Aristolochene synthase-catalyzed cyclization of 2-fluorofarnesyl-diphosphate to 2-fluorogermacrene A. 2007 Chembiochem pmid:17683054
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
Allemann RK et al. Synthetic efficiency in enzyme mechanisms involving carbocations: aristolochene synthase. 2007 J. Am. Chem. Soc. pmid:17918834
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
pmid:18843388