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Table 2 Cytotoxicity studies by Haemolytic activity of synthetic compounds 2 and 3a-i

From: Regioselective synthesis of 2-(bromomethyl)-5-aryl-thiophene derivatives viapalladium (0) catalyzed suzuki cross-coupling reactions: as antithrombotic and haemolytically active molecules

Compounds % of haemolysis
2 3.06 ± 0.03
3a 1.63 ± 0.02
3b 6.31 ± 0.07
3c 3.88 ± 0.04
3d 4.43 ± 0.05
3e 5.13 ± 0.05
3f 69.7 ± 1.23
3 g 9.87 ± 0.08
3 h 3.59 ± 0.03
3i 33.6 ± 0.87
Phosphate-buffered saline (PBS) 0.00 ± 0.00
Triton X-100 100 ± 0.58
  1. The results are average ± S.D of triplicate experiments p < 0.05.