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Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae).
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2020 Jun 21; Vol. 25 (12). Date of Electronic Publication: 2020 Jun 21. - Publication Year :
- 2020
-
Abstract
- The MeOH/CH <subscript>2</subscript> Cl <subscript>2</subscript> (1:1) extracts of the roots and leaves of Beilschmiedia louisii and B. obscura showed potent antitrypanosomal activity during preliminary screening on Trypanosoma brucei brucei . Phytochemical investigation of these extracts led to the isolation of a mixture of two new endiandric acid derivatives beilschmiedol B ( 1 ) and beilschmiedol C ( 2 ), and one new phenylalkene obscurene A ( 3 ) together with twelve known compounds ( 4 - 15 ). In addition, four new derivatives ( 11a - 11d ) were synthesized from compound 11 . Their structures were elucidated based on their NMR and MS data. Compounds 5 , 6 , and 7 were isolated for the first time from the Beilschmiedia genus. Additionally, the NMR data of compound 4 are given here for the first time. The isolates were evaluated for their antitrypanosomal and antimalarial activities against Tb brucei and the Plasmodium falciparum chloroquine-resistant strain Pf3D7 in vitro, respectively. From the tested compounds, the mixture of new compounds 1 and 2 exhibited the most potent antitrypanosomal activity in vitro with IC <subscript>50</subscript> value of 4.91 μM.
- Subjects :
- Cell Survival drug effects
Chloroquine pharmacology
Inhibitory Concentration 50
Magnetic Resonance Spectroscopy
Mass Spectrometry
Microbial Sensitivity Tests
Molecular Structure
Plant Leaves chemistry
Plant Roots chemistry
Plasmodium falciparum drug effects
Trypanosoma brucei brucei drug effects
Anti-Infective Agents analysis
Antimalarials pharmacology
Antiparasitic Agents pharmacology
Carboxylic Acids chemistry
Lauraceae chemistry
Plant Extracts chemistry
Plant Extracts pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 25
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 32575860
- Full Text :
- https://doi.org/10.3390/molecules25122862