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. Author manuscript; available in PMC: 2015 Jan 15.
Published in final edited form as: Bioorg Med Chem Lett. 2013 Dec 4;24(2):630–635. doi: 10.1016/j.bmcl.2013.11.081

Table 2.

SAR of ML148 and related analogues.

graphic file with name nihms551976u3.jpg graphic file with name nihms551976u4.jpg

Compound R1 IC50 (nM)a Compound R2 IC50 (nM)a
ML148 graphic file with name nihms551976t5.jpg 19 14a phenyl 22
11a graphic file with name nihms551976t6.jpg 22 14b 2-OMe-phenyl 27
11b graphic file with name nihms551976t7.jpg 271 14c 3-Cl-phenyl 12
11c graphic file with name nihms551976t8.jpg 48 14d 3-OMe-phenyl 19
11d graphic file with name nihms551976t9.jpg 68 14e 3-CF3-phenyl 48
11e graphic file with name nihms551976t10.jpg 68 14f 3-iPr-phenyl 68
11f graphic file with name nihms551976t11.jpg 76 14g 3-tBu-phenyl 171
11g graphic file with name nihms551976t12.jpg 1524 14h 4-Me-phenyl 19
11h graphic file with name nihms551976t13.jpg 383 14i 4-Cl-phenyl 22
11i graphic file with name nihms551976t14.jpg 383 14j 4-OMe-phenyl 19
11j graphic file with name nihms551976t15.jpg 429 14k 4-CF3-phenyl 86
11k graphic file with name nihms551976t16.jpg 961 14l 4-tBu-phenyl 54
11l graphic file with name nihms551976t17.jpg 1358 14m tBu 34
11m graphic file with name nihms551976t18.jpg 2710 14n nBu 68
11n graphic file with name nihms551976t19.jpg 3040
a

determined using the HTS enzymatic assay and tested in triplicate.