Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Antiprotozoal diterpenes from Perovskia abrotanoides
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4483010
Author(s) Tabefam, Marzieh; Moridi Farimani, Mahdi; Danton, Ombeline; Ramseyer, Justine; Kaiser, Marcel; Ebrahimi, Samad Nejad; Salehi, Peyman; Batooli, Hoosien; Potterat, Olivier; Hamburger, Matthias
Author(s) at UniBasel Hamburger, Matthias
Potterat, Olivier
Danton, Ombeline Réjane
Ramseyer, Justine
Kaiser, Marcel
Year 2018
Title Antiprotozoal diterpenes from Perovskia abrotanoides
Journal Planta Medica
Volume 84
Number 12-13
Pages / Article-Number 913-919
Mesh terms Animals; Antiprotozoal Agents, pharmacology; Diterpenes, pharmacology; Lamiaceae, chemistry; Leishmania donovani, drug effects; Myoblasts, drug effects; Plant Components, Aerial, chemistry; Plasmodium falciparum, drug effects; Rats; Trypanosoma cruzi, drug effects
Abstract As part of a screening for new antiparasitic natural products from Iranian plants, n-hexane and ethyl acetate extracts from the aerial parts of Perovskia abrotanoides were found to exhibit strong inhibitory activity against Trypanosoma brucei rhodesiense and Leishmania donovani. The activity was tracked by high-performance liquid chromatography (HPLC)-based activity profiling. Preparative isolation by a combination of silica gel column chromatography and HPLC afforded 17 diterpenoids (1: -17: ), including 14 abietane-, two icetexane-, and one isopimarane-type derivatives. Among these, (5R,10S)-11-hydroxy-12-methoxy-20-norabieta-8,11,13-triene (2: ), 12-hydroxy-norabieta-1(10),8,11,13-tetraene-1,11-furan (6: ), and 12-methoxybarbatusol (9: ) were new compounds, the structure of which was established by comprehensive spectroscopic data analysis (one- and two-dimensional nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, electronic circular dichroism). The antiprotozoal activity of the isolated compounds was evaluated against T. b. rhodesiense, Trypanosoma cruzi, L. donovani, and Plasmodium falciparum. Selectivity indexes (SI) were calculated in comparison to cytotoxicity on rat myoblast (L6) cells. Particularly active were 7α-ethoxyrosmanol (4: ) with an IC50 of 0.8 µM against T. b. rhodesiense (SI 14.9) and an IC50 of 1.8 µM (SI 6.9) against L. donovani, ferruginol (8: ) with an IC50 of 2.9 µM (SI 19.2) against P. falciparum, and miltiodiol (10: ) with an IC50 of 0.5 µM (SI 10.5) against T. b. rhodesiense. None of the compounds exhibited selective toxicity against T. cruzi (SI ≤ 1.6).
Publisher Georg Thieme
ISSN/ISBN 0032-0943 ; 1439-0221
edoc-URL https://edoc.unibas.ch/65130/
Full Text on edoc No
Digital Object Identifier DOI 10.1055/a-0608-4946
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/29698984
ISI-Number WOS:000440378900011
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.368 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
24/04/2024