Research Article

Synthesis of Novel Thiazolyl Hydrazine Derivatives and Their Antifungal Activity

Table 2

EC50 values of compounds 3a–3o against tested fungi in vitro.

Comp.PathogensRegression equationEC50 (µg/mL)Comp.PathogensRegression equationEC50 (µg/mL)

3aB. d.y = 0.493x + 4.9871.05±0.173hV. d.y = 0.541x + 4.6963.63±0.18
G. s.y = 1.104x + 4.2205.08±0.20T. c.y = 1.186x + 3.62614.4 ± 0.33
S. s.y = 1.491x + 3.36112.6 ± 0.63iB. d.y = 1.028x + 4.9921.01±0.09
T. c.y = 0.759x + 4.11014.9 ± 1.33jB. d.y = 0.562x + 4.4831.75±0.16
3bB. d.y = 0.460x + 4.9371.36±0.53S. s.y = 0.508x + 4.5477.77 ± 0.70
G. s.y = 0.476x + 4.9771.11±0.13V. d.y = 0.672x + 4.5434.78±0.32
S. s.y = 1.545x + 3.6517.45 ± 0.29T. c.y = 1.726x + 4.2692.64±0.06
V. d.y = 0.677x + 4.9391.22±0.253kB. d.y = 0.476x + 5.0300.86±0.12
T. c.y = 0.905x + 4.4444.10±0.27G. s.y = 0.596x + 4.7722.41±0.15
F. o.y = 1.162x + 3.9847.47 ± 0.21S. s.y = 1.352x + 3.55911.6 ± 0.38
3cB. d.y = 0.351x + 4.9391.48±0.22T. c.y = 1.578x + 4.6361.70±0.02
G. s.y = 0.281x + 4.8064.89±0.523lB. d.y = 0.547x + 5.1230.59±0.04
T. c.y = 0.827x + 4.2198.77 ± 0.85G. s.y = 1.163x + 5.1860.69±0.04
F. o.y = 0.528x + 4.31819.6 ± 3.5S. s.y = 1.352x + 3.5595.57±0.30
3dB. d.y = 0.585x + 4.8831.58±0.06V. d.y = 1.208x + 4.8201.40±0.06
G. s.y = 1.048x + 4.7211.84±0.12T. c.y = 1.150x + 4.3303.82±0.17
S. s.y = 2.100x + 2.9139.48 ± 0.243mB. d.y = 0.695x + 4.3737.97 ± 0.91
V. d.y = 1.171x + 4.3463.61±0.153oB. d.y = 0.690x + 4.3927.60 ± 0.51
T. c.y = 0.967x + 4.4783.46±0.23CBB. d.y = 1.131x + 5.9960.13 ± 0.01
3eB. d.y = 0.695x + 4.3737.97 ± 0.91G. s.y = 4.016x + 5.6290.70 ± 0.01
3fB. d.y = 0.507x + 5.0150.93±0.03S. s.y = 3.322x + 7.3260.20 ± 0.01
G. s.y = 0.524x + 4.6824.05±0.12T. c.y = 2.322x + 4.7721.25 ± 0.05
3gB. d.y = 0.520x + 5.1330.55±0.02F. o.y = 4.116x + 6.0580.55 ± 0.01
G. s.y = 0.558x + 4.8152.14±0.21