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. Author manuscript; available in PMC: 2019 Jul 14.
Published in final edited form as: Biochem Biophys Res Commun. 2018 Apr 4;499(3):556–562. doi: 10.1016/j.bbrc.2018.03.189

Table 2.

Structure-activity relationship of pyrrole and thiazole constituents of 1H-pyrrole-2-carboxamide compounds. IC50 values and max % inhibition were determined as in Table 1. DYN1 = dynamin-1.

graphic file with name nihms-1026813-t0013.jpg IC50 (μM) Max % inhibition


R1   R2 DRP1 OPA1 DYN1

8 Cl graphic file with name nihms-1026813-t0014.jpg 2.3 >100 >100 77
9 Ph graphic file with name nihms-1026813-t0015.jpg 1.5 >100 >100 l9
10 Me graphic file with name nihms-1026813-t0016.jpg 2.1 >100 >100 80
11 Me graphic file with name nihms-1026813-t0017.jpg >100 >100 >100 6