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. 2017 Jun 1;12(6):e0178381. doi: 10.1371/journal.pone.0178381

Fig 4. Structure-activity relationship study of fragment derivatives.

Fig 4

(a) Chemical structures of the hit fragment 1 and four rationally designed fragment derivatives (2 to 5). (b) Calorimetric titration of compound 5 with mTEAD4 protein. The data shows weak binding of the compound to the protein.