A New Quassinoid from Crude Quassin-extract of Quassia amara Article. Quassinoids from Picrasma Crenata Journal of Asian Natural Products Research. A new quassinoid, 2-dihydroailanthone, has been isolated from the bark of Ailanthus glandulosa. Its structure was established on the basis of spectroscopic data. ISSN: Online Available at International Journal of Herbal Medicine. Quassinoids and Their Chemotaxonomic Significance.

Author: Moogusar Nim
Country: Qatar
Language: English (Spanish)
Genre: Life
Published (Last): 1 October 2012
Pages: 280
PDF File Size: 10.85 Mb
ePub File Size: 17.71 Mb
ISBN: 399-7-76245-670-2
Downloads: 46093
Price: Free* [*Free Regsitration Required]
Uploader: Guzuru

These bioactive phytochemicals belong to the triterpene family. In vitro antitrypanosomal activities of quassinoid compounds from the fruits of a medicinal plant, Brucea javanica. Structural requirements of quassinoids for the inhibition of cell transformation. Total synthesis of dl-quassin J Am Chem Soc ; Synthesis of optically active tetracyclic quassinoid skeleton. XX is the XXth reference in the list of references.

There was a problem providing the content you requested

Quassinoids with dock scores Click here to view. High dock scores Click here to view. Computed atlas of surface topography of proteins with structural and topographical mapping of functionally annotated residues.

Int J Comput Appl ; The software used for the present study is the discovery studio Accelrys 2. The dock results conclude quawsinoid the quassinoids can be adopted as an alternative drug against malaria.


Jump to site search. Please enable JavaScript to access the full features of the site or access our non-JavaScript page. The H-bond interactions of quassinoid 1 with active site residues of quassinoid 1 with DHFR from Plasmodium falciparum Click here to view. In vitro antimalarial activity of quassinoids from Eurycoma longifolia against Malaysian chloroquine-resistant Plasmodium falciparum isolates.

Authors contributing to RSC publications journal articles, books or book chapters do not need to formally request permission to reproduce material contained in this article provided that the correct acknowledgement is given with the reproduced material. J Recept Signal Transduct Res ; Ancient Sci Life ; Muhammad Qussinoid, Samoylenko V.

Go to our Instructions for using Copyright Clearance Center page for details. You do not have JavaScript enabled.

Open J Synth Theory Appl ;2: Antimicrob Agents Chemother ; Biologically active quassinoids and their chemistry: Reproduced material should be attributed as follows: Tetracyclic quassinoid skeletons 2 and 22 with six correct chiral centres common to numerous quassinoids are constructed from S -carvone and 3-methylsulfolene by a step and step reaction sequence involving highly regioselective and stereocontrolled reactions.

Active site identification with pocket information Click here to view. Synthesis of optically active tetracyclic quassinoid skeleton T. If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using Copyright Clearance Center.


Front Med Chem ;4: How to cite this URL: Nucleic Acids Res ; The docking was done subsequently. A well known plant product, quassinoids are known to have antimalarial activity. Back to tab navigation Download options Please wait They were drawn using chemsketch and the 3D structures were generated. For reproduction of material from all other RSC journals and books: Ligand map interaction Click here to view.

Back to tab navigation.

A new antimalarial quassinoid from Simaba orinocensis.

The protein for the present study was imported from protein data bank with the PDB Id, 4dpd and was prepared for docking. Int J Parasitol ; Clin Microbiol Rev ; Search articles by author Tony K. Related articles 4dpd malaria P.

For reproduction quassinid material from NJC: Quassinoids are used in the present study to act against malarial dihydrofolate reductase Pf-DHFRa potential antimalarial target.

Regioselective synthesis and biological evaluation of 1-hydroxyl modified ailanthinone derivatives as antimalarials.