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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.