Synthesis, Characterization, Semiempirical and Biological Activities of Organotin(IV) Carboxylates with 4-Piperidinecarboxylic Acid

Table 11

Antifungal activity data^{a, b} of organotin complexes 1–5.

Comp. number	Fungal inhibition zone (mm)
	A. alternata	G. lucidum	P. notatum	T. harzianum	A. niger
HL	—	—	—	—	—
1	14^c  ±  0.15	21^c  ±  0.20	14^c  ±  0.11	13^c  ±  0.07	25^c  ±  0.23
2	20^bc  ±  0.19	22^bc  ±  0.13	19^bc  ±  0.08	18^c  ±  0.15	26^bc  ±  0.23
3	22^bc  ±  0.20	24^bc  ±  0.14	28^bc  ±  0.14	21^ab  ±  0.18	26^bc  ±  0.21
4	18^bc  ±  0.11	23^bc  ±  0.19	17^bc  ±  0.07	17^bc  ±  0.12	26^bc  ±  0.15
5	25^bc  ±  0.23	25^bc  ±  0.21	28^bc  ±  0.12	23^a  ±  0.20	28^bc  ±  0.23
Fluconazole	38^a  ±  0.29	41^a  ±  0.21	45^a  ±  0.31	—	37^a  ±  0.23

Data are expressed as the mean ± standard deviation of samples analyzed individually in triplicate at .
^bIt refers that how does fungal inhibition zones are being calculated.