Two new anti-plasmodial flavonoid glycosides from Duranta repens

Fozia IjazKohat Institute of Medical Sciences, Kohat University of Science and Technology, Kohat-26000, N.W.F.P., Pakistan

Nisar AhmadDepartment of Botany, Kohat University of Science and Technology, Kohat-26000, N.W.F.P., Pakistan

Ijaz AhmadDepartment of Chemistry, Kohat University of Science and Technology, Kohat-26000, N.W.F.P., PakistanCorrespondence[email protected]

Azhar ul HaqDepartment of Chemistry, Kohat University of Science and Technology, Kohat-26000, N.W.F.P., Pakistan

Fanghai WangDepartment of Biological Sciences, University of Zhongshan, Guangzhou-510275, China

Figures & data

Figure 1. Structures of flavonoids 1–7.

Table 1. ¹H (400 MHz) and ¹³C NMR (100 MHz) assignments (δ ppm) of flavonoids (1 and 2) in CD₃OD.

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Figure 2. Important HMBC correlations of 1.

Table 2. In vitro IC₅₀ values of flavonoids (1–7) against W2 and D6 strains of P. falciparum.

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Two new anti-plasmodial flavonoid glycosides from Duranta repens

Table 1. ¹H (400 MHz) and ¹³C NMR (100 MHz) assignments (δ ppm) of flavonoids (1 and 2) in CD₃OD.

Table 2. In vitro IC₅₀ values of flavonoids (1–7) against W2 and D6 strains of P. falciparum.

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Two new anti-plasmodial flavonoid glycosides from Duranta repens

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Table 1. 1H (400 MHz) and 13C NMR (100 MHz) assignments (δ ppm) of flavonoids (1 and 2) in CD3OD.

Table 2. In vitro IC50 values of flavonoids (1–7) against W2 and D6 strains of P. falciparum.

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Table 1. ¹H (400 MHz) and ¹³C NMR (100 MHz) assignments (δ ppm) of flavonoids (1 and 2) in CD₃OD.

Table 2. In vitro IC₅₀ values of flavonoids (1–7) against W2 and D6 strains of P. falciparum.