Skip to main content
Fig. 7 | Parasites & Vectors

Fig. 7

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

Fig. 7

Chemical structures of compounds 81–98. Photogedunin (81), analog compound 82, ursolic acid (83), labda-8(20),13-diene-15-oic acid (84), quinine (85), securinine (86), virosecurinine (87), allosecurinine (88), cryptolepine (89), 3-chloro-8-nitro-tryptanthrin, 3-chloro-8-nitro-indolo [2,1-b] quinazoline-6,12-dione (nt1) (90), 3-chloro-indolo [2,1-b] quinazoline-6,12-dione (t8) (91), dihydronitidine (92), jozimine a2 (93), dioncophylline c (94), ealapasamine c (95), dimer compound 96, compound 97, (−)-R,S-dehydroemetine (98)

Back to article page