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Corynoxeine is an alkaloid that has been found in Uncaria and has diverse biological activities.1,2,3,4 It inhibits LPS-induced production of nitric oxide (NO) in primary rat microglia (IC50 = 15.7 µM).1 Corynoxeine (5-50 µM) inhibits PDGF-BB-induced ERK1/2 activation in, and proliferation of, rat aortic vascular smooth muscle cells (VSMCs).2 It inhibits histamine release from LAD 2 mast cells induced by compound 48/80 (Item No. 22173) when used at concentrations ranging from 25 to 200 µM.3 In vivo, corynoxeine (0.5, 2.5, and 5 mg/kg) reduces compound 48/80-induced local anaphylaxis and mast cell degranulation in mouse hind paws. Corynoxeine (30 and 100 mg/kg) also reduces methamphetamine-induced hyperlocomotion in mice.4
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1. Alkaloids from the leaves of Uncaria rhynchophylla and their inhibitory activity on NO production in lipopolysaccharide-
2. Corynoxeine isolated from the hook of Uncaria rhynchophylla inhibits rat aortic vascular smooth muscle cell proliferation through the blocking of extracellular signal regulated kinase ½ phosphorylation. Biol. Pharm. Bull. 31(11), 2073-2078 (2008).
3. Anti-
4. Effect on locomotion of indole alkaloids from the hooks of Uncaria plants. Phytomedicine 6(3), 163-168 (1999).
Identification of PXR activators from Uncaria rhynchophylla (Gou Teng) and Uncaria tomentosa (cat’s claw). Drug Metab. Dispos. 51(5), 629-636 (2023).