Magnolia officinalis magnolol from

Dean JR, Liu B, Price R. Extraction of magnolol from Magnolia officinalis using supercritical fluid extraction and phytosol solvent extraction. Ph5dochem Anal 1998 9 248-252. 

Lo YC, Teng CM, Chen CF, Magnolol and honokiol from Magnolia officinalis protect tat heatt mitochondria against lipid petoxidation, Biochem Pharmacol... 

Magnolol is a bioactivator extracted from Magnolia officinalis with protective effects on cholinergic neurons. Magnolol restores the impaired abilities of learning and memory induced by scopolamine, and AChE, NOS, and SOD activities in mice [277]. 

Wang, J.P., Ho,T.F., Chang, L.C., and Chen, C.C. (1995) Anti-Inflammatory Effect of Magnolol, Isolated from Magnolia officinalis, on A23187-Induced Pleurisy in Mice, J. Pharm. Pharmacol. 47, 857-860. 

Magnolol and Honokiol Isolated from Magnolia officinalis Protect Rat Heart Mitochondria Against Lipid Peroxidation, Biochem. Pharmacol. 47, 549-553. 

Chen, Y.L., Lin, K.F., Shiao, M.S., Chen, Y.T., Hong, C.Y., and Lin, S.J. (2001) Magnolol, a Potent Antioxidant from Magnolia officinalis. Attenuates Intimal Thickening and MCP-1 Expression After Balloon Injury of the Aorta in Cholesterol-Fed Rabbits, Basic Res. Cardiol. 96, 353-363. 

Watanabe K, Watanabe H, Goto Y, Yamaguchi M, Yamamoto N, Hagino K 1983 Pharmacological properties of magnolol and hinokiol extracted from Magnolia officinalis Central depressant effects. Planta Med 103-108... 

Xu, Q., Yi, L. T., Pan, Y., Wang, X., Li, Y. C., et al. (2008) Antidepressant-like effects of the mixture of honokiol and magnolol from the barks of Magnolia officinalis in stressed rodents. Prog Neuropsychopharmacol Biol Psychiatry 32, 715-725. 

Teng, C.M., Yu, S.M., Chen, C.C., Huang, Y.L., and Huang, T.F. (1990) EDRF-Release and Ca " -Channel Blockade by Magnolol, an Antiplatelet Agent Isolated from Chinese Herb Magnolia officinalis, in Rat Thoracic Aorta, Life. Sci. 47, 1153-1161. 

Magnolol 217 (Scheme 14.42), a simple antiviral BIPOL isolated from the bark of Magnolia officinalis, is readily constructed by the Negishi cross-coupling of 214 with its corresponding iodide 215, both readily obtained by DoM-transmetallation or DoM-iodination reaction, to yield 216, which, upon simple hydrolysis, affords the natural product 217 [158]. 

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