Turraea heterophylla Smith (Meliaceae) is a species used in Ivorian's traditional medicine for its various properties, such as antimalarial and aphrodisiac. This study aims to determine the chemical composition of the leaves from T. heterophylla and their content in polyphenols, in addition the antibacterial activity of the methanolic extract. Chemical test and spectrophotometry methods were used for phyotchemical study. The antibacterial activity was assessed using the agar well diffusion method against Staphylococcus aureus (ATCC 25923), Escherichia coli (CIP 54127AF) and Pseudomonas aeruginosa (CIP 103467). Phytochemical study revealed the presence of polyterpenes, steroids, alkaloids, saponins, polyphenols and flavonoids. A very high content of flavonoids and polyphenols were observed in the ethyl acetate and aqueous extracts. The antibacterial tests indicated that the methanol extract of the leaves from T. heterophylla had bacteriostatic properties against the germs tested with MIC values greater than 3000 µg / mL.

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Four compounds were isolated from the leaves of Monodora brevipes Benth. (Annonaceae). Among them, one new natural indole named 5-formylindole (1) and three known aporphine alkaloids: (+)-roemeroline (2); (+)-corydine (3) and (+)-menispermine (4). They were isolated for the first time from this species. The structures of these compounds were established according to their spectral data (NMR, SM, IR and UV).Eric et al., International Current Pharmaceutical Journal, June 2017, 6(7): 40-43http://www.icpjonline.com/documents/Vol6Issue7/01.pdf

Two sterols namely β-sitosterol (1) and stigmasterol (2) were isolated from methanolic extract of the fruit barks of Coelocaryon klainei Pierre ex Heckel (Myristicaceae). They were isolated for the first time from this species. It is the first isolation of compounds in this genus Coelocaryon. The structures were elucidated on the basis of one and two-dimensional NMR, SM, IR and UV.Akoubet et al., International Current Pharmaceutical Journal, August 2017, 6(9): 49-52http://www.icpjonline.com/documents/Vol6Issue9/01.pdf

From (2,3-dihydro-1H-perimidin-2-yl)-phenyl, the substitution of OH group in ortho or para position on the phenyl ring, allows us to synthesize the studied compounds. These three compounds have been characterized by conventional spectroscopic methods (NMR and MS). The interest of this work is to review the antioxidant activity of our compounds. The antioxidant activity screening carried out according to FRAP and DPPH methods revealed significant anti-free radical properties for compounds 1 and 2 even at low concentrations. In contrast to the compound 2, compound 3 for which the OH group is substituted in para position has the lowest activity in both cases. Therefore the para position seems to be the least sensitive position to increase the antioxidant activity of this pharmacophore.