Antimycobacterial cycloartane derivatives from the roots of Trichilia welwistchii C. DC (Meliaceae)

Author:

Tsamo Armelle Tontsa1ORCID,Fodja Saah Edwige P.2,Langat Moses K.34,Mkounga Pierre2,Kamdem Waffo Alain François5,Nkengfack Augustin Ephrem2

Affiliation:

1. Department of Organic Chemistry , University of Yaoundé I , P. O. Box 812 , Yaoundé , Cameroon

2. Department of Organic Chemistry , Faculty of Science, University of Yaoundé I , P. O. Box 812 , Yaoundé , Cameroon

3. Jodrell Laboratory , Natural Capital and Plant Health , Royal Botanic Gardens, Kew , Richmond , TW9 3DS , UK

4. Department of Chemistry , Faculty of Engineering and Physical Sciences, University of Surrey , Guildford , Surrey GU2 7XH , UK

5. Department of Chemistry , Faculty of Science, University of Douala , P. O. Box 24157 , Douala , Cameroon

Abstract

Abstract Chemical investigation of the roots of Trichilia welwitschii yielded a cycloartane type terpenoid 28,29-bis-norcycloart-24-en-3β,4α,6α-triol (1), isolated as pure compound for the first time, three coumarins and three sterols. New cycloartane derivatives (1a) and (1b+1c) were obtained by hemi-synthetic reaction of compound 1. The structures of 1ac were established by spectroscopic methods including 1D and 2D-NMR analysis, HR-EIMS, chemical transformations and by comparison of these data with those of related compounds. Evaluated for their antimycobacterial potential, compound 1 and 1b+1c were determined to show significant activities against Mycobacterium tuberculosis MIC values of 6.25 μg mL−1 while compound 1a displayed weak activity showing MIC > 100 μg mL−1. Compounds 24 displayed moderate activity with MIC values range from 12.5 to 50 μg mL−1.

Publisher

Walter de Gruyter GmbH

Subject

General Chemistry

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