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Accumulating evidences demonstrate that inhibition of CDK9 robustly induces apoptosis through transcriptional inhibition and downregulation of oncogenes (e sulfanyl)-1,3-thiazol-2-yl]hexahydropyridine-4-carboxamide S1 (20 mg, 0.053 mmol), S2 (0.053 mmol, 1.0 eq), EDCI (20.3 mg, 0.106 mmol, 2.0 eq), HOAt (14.4 mg, 0.106 mmol, 2.0 eq) and DMF (5 mL) were added DIEA (43.8 μL, 0.265 mmol, 5.0 eq)