Scientific publications
Pierre Yemback
Other affiliations: University of Buea · University of Jos · Paderborn University · University of Johannesburg · Centre Pasteur du Cameroun
Eyong Kenneth Oben
Other affiliations: University of Buea · University of Jos · Paderborn University · University of Johannesburg · Centre Pasteur du Cameroun
Dereck T Ndinteh
Other affiliations: University of Buea · University of Jos · Paderborn University · University of Johannesburg · Centre Pasteur du Cameroun
Patricia Odumosu
Other affiliations: University of Buea · University of Jos · Paderborn University · University of Johannesburg · Centre Pasteur du Cameroun
Other affiliations: University of Buea · University of Jos · Paderborn University · University of Johannesburg · Centre Pasteur du Cameroun
Thomas Werner
Other affiliations: University of Buea · University of Jos · Paderborn University · University of Johannesburg · Centre Pasteur du Cameroun
Noella Molisa Efange
Michael H. K. Kamdem
Lawrence Ayong
Research Square
Abstract To search for leads against malaria, compounds from the Cameroon Natural Product Library (CANAPL), were screened by molecular docking studies against the enzyme target Glyceraldehyde-3-phosphate dehydrogenase (P f GAPDH) for Plasmodium falciparum . Amongst these docking hits were the lupeol cinnamate (1) and oleanane cinnamate (2). Triterpenoids with structural similarities to (1) and (2) were isolated from Baillonella toxisperma (Pierre); olean-12-en-3β-hexadecanoate (3), 3-β-trans cinnamoyloxylup-20(29)-ene (4), oleanoic acid benzoate (5), 3β-amyrin (6), taraxerol (7), betulonic acid (8), β-sitosterol (9), betulinic acid (10), 3β-(trans-p-Coumaroyl)oxylup-20(29)-en-28-oïc acid (11), and screened alongside Betuline (12) and oleanolic acid (13). The favorable compounds 8 and 11 with 100% growth inhibition on Plasmodium falciparum 3D7 strains together with compounds 4, 10 and 12 were structurally optimized to afford new lupane derivatives with the privilege α-β unsaturated carbonyl medicinal scaffolds; betulonic acid acryl aldehyde (14 ) , betulin acryl aldehyde (15), 3β-( trans-p -Coumaroyl)oxylup-20(29)-en-28-oïc acid acryl aldehyde (16), betulinic acid acryl aldehyde (18) and 3-β- trans cinnamoyloxylup-20(29)-ene acryl aldehyde (19) exhibiting more potent anti-malarial activities with IC 50 values of 0.703 µM, 2.15 µM, 1.28 µM, and 3.79 µM for compounds 14, 15, 16 and 18 respectively. The modified compounds with the privilege α, β-unsaturated carbonyl medicinal scaffolds could be further optimized into potent antimalarial agents.
