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Wang J, Yi Y, Xiao Y, Dong L, Liang L, Teng L, Ying JM, Lu T, Liu Y, Guan Y, Pang J, Zhou L, Lu J, Zhang Z, Liu X, Liang X, Zeng X, Yi X, Zhou W, Xia X, Yang L, Zhang J, Kopetz S , Futreal PA, Wu H, Liang Z

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J Exp Med (2006) 203(11):241924.10.1084/jem.20061254 79 SuanDSundlingCBrinkR

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445 nm = 12,600 M 1 cm 1 , SmTGR U597S

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(59) used molecular docking and revealed that kaempferol-3-rutinoside was one of the most active inhibitors of Bcl-2

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