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. 2017 Apr 10;8(3):135–142. doi: 10.1007/s12672-017-0294-5

Fig. 2.

Fig. 2

Hybrid drug co-targeting strategy and chemical structures are indicated. a Schematic representation of a hybrid drug capable of targeting simultaneously both ER and NFκB and its potential benefit in breast cancer. b Chemical structures of the parent drugs, raloxifene and dimethyl fumarate (DMF), along with the co-targeting drugs are shown. The fumarate moiety of Ral-Fum hybrids is highlighted