“…In addition, the other pharmacological effects of biflavonoids are: morelloflavone has 63% preventive inhibition of PLA2-induced myotoxic activity, its 38% cure rate inhibits myotoxicity, and it can inhibit edema formation and anticoagulation in a concentration-dependent manner, proving that morelloflavone can be developed as an inhibitor of secretory PLA2 such as in snake venom [ 309 ]; GB1 can inhibit α-glucosidase (IC 50 = 0.90 ± 0.01 mM) and aromatase (IC 50 = 0.28 ± 0.02 mM), and produce anti-plasmodium activity [ 310 ]; robustaflavone-4′-dimethyl ether can inhibit the accumulation of inflammatory cells by inhibiting the AKT and APK pathways, improve lung tissue damage, and reduce pulmonary edema [ 311 ]; rhusflavone, from Rhus parviflora, has a sedative and hypnotic effect, significantly binds to the GABAA-BZD receptor (IC 50 = 0.045 mM), and induces sleep [ 178 ]; II-3, I-5, II-5, II-7, I-4′,II-4′-hexahydroxy-(I-3,II-8)-flavonylflavanonol, from G arcinia nervosa var. pubescens King can produce 73.9% in 18.2 μg/mL Platelet-Activating-Factor Inhibition (IC 50 = 20.4 μM) [ 312 ]; and GB-2a-II-4′-OMe has a certain analgesic effect on the pain sensation induced by Marfrine, and its mechanism from analgesic effect is different of morphine [ 64 ]; amentoflavone can reduce the influence of gamma rays [ 313 ], and six biflavonoids of Araucaria angustifolia can improve DNA damage caused by ultraviolet radiation, including: amentoflavone, mono- O -methylamentoflavone, di- O -methylamentoflavone, ginkgetin, tri- O -methylamentoflavone, and tetra- O -methylamentoflavone [ 314 ]; GB-2a can inhibit the formation of melanin [ 315 ]; studies have shown that isoginkgetin is an inhibitor of mRNA splicing [ 316 ]; and chamaejasmine and ginkgetin can improve chronic dermatitis through anti-inflammatory effects [ 317 , 318 , 319 ].…”