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1 Supporting information Effective Antimalarial Activities of α-Hydroxy Diynes Isolated from Ongokea gore Joséphine Kankolongo Ntumba1, Christian Muamba Tshiongo1, Michel Ngoma Mifundu1, Raphäel Robiette2, Kalulu Muzele Taba1 Affiliation 1 Department of Chemistry, Faculty of Sciences, University of Kinshasa, Democratic Republic of Congo 2 Institute of Condensed Matter and Nanosciences, Université Catholique de Louvain, Belgium Correspondence Prof. Dr. Joséphine Kankolongo Ntumba Department of Chemistry Faculty of Sciences University of Kinshasa B.P. 190 Kinshasa IX Democratic Republic of Congo Phone: +243 811779393 josephine.ntumba@unikin.ac.cd © Georg Thieme Verlag KG · 10.1055/s-0043-124974 · Planta Med · Ntumba JK et al. 2 Compound 1 © Georg Thieme Verlag KG · 10.1055/s-0043-124974 · Planta Med · Ntumba JK et al. 3 Compound 2 Linear regression gives a more precise correlation. 𝑦 = 25.05𝑋 + 46.888. And at 50 %: 50 = 25.05𝑋 + 46.888 𝑋= 3.1115 = 0.124 → 𝐶 = 1.331 25.05 © Georg Thieme Verlag KG · 10.1055/s-0043-124974 · Planta Med · Ntumba JK et al. 4 Compound 3 The same applies to compound 3. 𝑦 = 18.206𝑋 + 55.335. And at 50%: 50 = 18.206𝑋 + 55.335 𝑋= −5.335 = −0.293 → 𝐶 = 0.509 18.206 © Georg Thieme Verlag KG · 10.1055/s-0043-124974 · Planta Med · Ntumba JK et al. 5 Standard compound (quinine) For quinine, a non-linear regression gave the following: 𝑦 = 58.5501 + 38.6526𝑋 − 8.7969𝑋 2 . At 50%: 50 = 58.5501 + 38.6526𝑋 − 8.7969𝑋 2 −8.7969𝑋 2 + 38.6526𝑋 + 8.5501 = 0 √∆ = ±42.366 𝑋1 = 4.605 → 𝐶1 = 40267 (rejected value) 𝑋2 = −0.211 → 𝐶2 = 0.615 (retained value) Fig. 1S. IC50 determinations as dose-response curves as well as the mathematical method of determination of the values for respectively compounds 1, 2, and 3 and the standard compound quinine. © Georg Thieme Verlag KG · 10.1055/s-0043-124974 · Planta Med · Ntumba JK et al.