Fig. 3. (A) Each scatters plot column represents different sets of samples from different time points and treatments. A 100 μL 3^rd, 4^th and 5^th-day gametocyte rich culture was seeded in microtiter plates in triplicates for each treatment (0.5 μM) and control and three wells each was fixed and stained by the Giemsa staining. Both compounds had an apparent reduction of intact gametocytes compared to control; (B) the most representative morphologies were documented. Both compounds had an evident detrimental effect on the normal morphology to the extent that none of the treated samples had any mature gametocytes even though with 50% viability in SYBR green screenings.