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Table 1 Titanocene structures (see Scheme 1) and in vitro cytotoxic activities (a)

From: Titanocene / cyclodextrin supramolecular systems: a theoretical approach

No

Code

Structure

pA 1

pA 2

pA 3

1

01TC

M: Si; X: CH3; Y: CH=CH2; R: all H; R’: all CH3

4.10

4.20

3.87

2

02TC

M: Si; X: CH3; Y: H; R: all CH3; R’: all CH3

3.96

4.23

3.93

3

03TC

M: Si; X: CH3; Y: (CH2)2Si(CH3)2(CH=CH2); R: all H; R’: all CH3

3.72

3.81

3.70

4

08TC

M: Si; X: CH3; Y: CH3; R: all H; R’: all CH3

3.87

4.18

4.02

5

09TC

M: Ge; X: CH3; Y: CH3; R: all H; R’: all CH3

3.81

4.14

3.97

6

10TC

M: Si; X: CH3; Y: H; R: all CH3; R’: all CH3

3.96

4.23

3.94

7

11TC

M: Si; X: CH3; Y: CH3; R: 3-CH3, 2,4,5-H; R’: all CH3

3.93

4.06

4.00

8

18TC

M: Si; X: CH3; Y: (CH2)2Si(CH=CH2)3; R: all H; R’: all CH3

3.70

3.70

 

9

23TC

M,X,Y: none; R: 3-CH2(3-pyridinium); R’: all H

3.94

  

10

24TC

M,X,Y: none; R: 3-CH2(3-pyridinium); R’: 3-CH2(3-pyridinium)

4.25

  

11

26TC

M,X,Y: none; R: 3-CH2(4-pyridinium); R: 3-CH2(4-pyridinium);

4.97

  
  1. (a) cytotoxic activity was expressed as the logarithm of the inverse inhibitory concentration 50%, pIC 50 = log(1/IC 50 ); pA 1 , pA 2 , pA 3 were used for in vitro cytotoxic activity against HeLa, K562, and Fem-x cell lines, respectively.