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. 2021 Jul 23;9:657599. doi: 10.3389/fchem.2021.657599

TABLE 1.

Half-maximal inhibitory concentrations (IC50 values) of organotin(IV) derivatives.

No Compounds IC50 (μM) References
HeLa A549 HCT-116 HepG2 MCF-7 K562 HL-60 Jurkat E6.1
1 Et2SnL1 82.4 79.7 Devi et al. (2020)
2 Bu2SnL1 77.5 74.2 Devi et al. (2020)
3 Ph2SnL1 86.4 95.7 Devi et al. (2020)
4 Me2SnL2 94.1 91.2 Devi et al. (2020)
5 Et2SnL2 13.4 15.2 Devi et al. (2020)
6 Bu2SnL2 84.6 83.2 Devi et al. (2020)
7 Ph2SnL2 73.1 71.2 Devi et al. (2020)
8 Me2SnL3 85.7 82.5 Devi et al. (2020)
9 Et2SnL3 29.6 27.8 Devi et al. (2020)
10 Ph2SnL3 80.5 77.1 Devi et al. (2020)
11 Me2SnL4 107.9 103.2 Devi et al. (2020)
12 Et2SnL4 23.8 20.5 Devi et al. (2020)
13 Bu2SnL4 33.6 31.2 Devi et al. (2020)
14 Ph2SnL4 106.7 104.2 Devi et al. (2020)
15 n-Bu3Sn(5tpO) 0.07 0.07 0.23 Attanzio et al. (2020)
16 n-Bu3Sn(mtpO) 0.034 0.053 0.118 Attanzio et al. (2020)
17 n-Bu3Sn(HtpO2) 0.1 0.117 0.487 Attanzio et al. (2020)
18 Ph3Sn(HtpO2) 0.06 0.063 0.102 Attanzio et al. (2020)
19 (C6H5)2Sn[S2CN(C3H7O) (CH3)]2 4.0 Kamaludin et al. (2019)
20 (C6H5)3Sn[S2CN(C3H7O) (CH3)] 8.0 Kamaludin et al. (2019)
21 (C4H9)ClSnL2 758 Adeyemi et al. (2019)
22 (CH3)2SnL2 56 Adeyemi et al. (2019)
23 (C4H9)2SnL2 288 Adeyemi et al. (2019)
24 (C6H5)2SnL2 2 Adeyemi et al. (2019)
25 Me2SnL1 14.4 9.9 Liu et al. (2017)
26 Ph2SnL1 0.62 1.2 Liu et al. (2017)
27 Me2SnL2 34.69 19.50 Liu et al. (2017)
28 Ph2SnL2 1.25 3.4 Liu et al. (2017)
29 (C4H9)2SnL 0.40 Awang et al. (2016)
30 (C6H5)2SL 0.35 Awang et al. (2016)
31 n-Bu3SnCl 0.0027 Fickova et al. (2015)
32 Ph3SnCl 0.609 Fickova et al. (2015)
33 {[Ph3SnL]·0.5C6H6}n 1.76 Liang et al. (2014)
34 [Bu2LSnOSnLBu2]2 6.6 Liang et al. (2014)
35 Ph2Sn(mstsc) 0.3 Khandani et al. (2013)
36 Me2Sn(mstsc) 0.7 Khandani et al. (2013)
37 Bu2Sn(mstsc) 0.1 Khandani et al. (2013)