The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Editor

Share

Personal info

View

Links

Table of contents

About

Terms

 

Chemical Compound Review: 

Dillapiol     4,5-dimethoxy-6-prop-2-enyl- benzo[1,3]dioxole

Synonyms: Dillapiole, Dill apiole, CHEMBL470874, SureCN310992, Dill apiol, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

High impact information on Dill apiole

  • The resolution of dillapiole and dihydrodillapiole has been achieved on RP-18 column using methanol-water (90:10, v/v) as mobile phase and a photodiode array detector at 207 nm [1].
  • In vivo activity was improved by (1) incorporation into an easy to absorb suspension, (2) preparation of a more stable compound, 7-methoxygedunin; and (3) synergism with dillapiol, a cytochrome P450 3A4 inhibitor [2].
 

Analytical, diagnostic and therapeutic context of Dill apiole

  • Preparative HPLC with 5-micrometer silica allowed isolation of gram quantities of parsleyapiole and dillapiole from extracts of plain parsley seeds and dill seeds, respectively [3].

References

  1. Liquid chromatographic method for the analysis of two plant based insecticide synergists dillapiole and dihydrodillapiole. Walia, S., Saha, S., Parmar, B.S. Journal of chromatography. A. (2004) [Pubmed]
  2. Traditionally-used antimalarials from the Meliaceae. Omar, S., Zhang, J., MacKinnon, S., Leaman, D., Durst, T., Philogene, B.J., Arnason, J.T., Sanchez-Vindas, P.E., Poveda, L., Tamez, P.A., Pezzuto, J.M. Current topics in medicinal chemistry. (2003) [Pubmed]
  3. High-pressure liquid chromatographic separation of the naturally occurring toxicants myristicin, related aromatic ethers and falcarinol. Wulf, L.W., Nagel, C.W., Branen, A.L. J. Chromatogr. (1978) [Pubmed]
Contributions to this collaborative article are from individual authors of WikiGenes or mined by the WikiGenes Data Mining Engine from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.About WikiGenesOpen Access LicencePrivacy PolicyTerms of Useapsburg
 
WikiGenes - Universities