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Table 1 Chemical structures and anti-cancer activities of substituted 5-(1H-indol-5-yl)-1,3,4-thiadiazol-2-amine derivatives

From: QSAR studies on PIM1 and PIM2 inhibitors using statistical methods: a rustic strategy to screen for 5-(1H-indol-5-yl)-1,3,4-thiadiazol analogues and predict their PIM inhibitory activity

  1. a, bAre the test sets for PIM1 and PIM2 inhibitory activities respectively