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Fig. 8 | Parasites & Vectors

Fig. 8

From: Contemporary exploitation of natural products for arthropod-borne pathogen transmission-blocking interventions

Fig. 8

Chemical structures of compounds 99–124. Juliprosopine (99), tazopsine (100), NCP-tazopsine (101), sinococuline (102), berberine (103), harringtonine (104), halofuginone (105), tomatidine (106), castanospermine (107), lycorine (108), 1-acetyllycorine analogue (109), cherylline (110), emetine (111), epigallocatechin gallate (112), lophirone e (113), caffeic acid phenethyl ester (114), naringenin (115), chartaceone c (116), chartaceone d (117), chartaceone e (118), chartaceone f (119), baicalein (120), sotetsflavone (121), coumarin a 34sk001 (122), coumarin b 34sk002 (123), cardol triene (124)

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