Table 2 In-silico predicted physiochemical parameters of the test compounds Compound code Mol.
Table 3 In vitro cytotoxicity of compounds 1 5 Compound Codes HeLa (Cervical cancer) (IC50± S.D).
Table 1 gives an example of the distance spectrum of the compound code.
Lemma 1 and Lemma 2 provide an important information about the output weights of the compound code: d weights of the compound code always experience at least two independent channels.
Compound-linked information includes bioactivity, therapeutic classification, detailed patent information, literature references, company names, compound codes, generic names, trade names and development phase.
Recalling that in NCC, the destination applies the BCJR algorithm on the compound code G, which is described in Section 2.1.
The compound code G is formed from the individual code g as follows: begin{array}{*{20}l} mathbf{G} = left[begin{array}{ccc} mathbf{g} & mathbf{0} & mathbf{g} mathbf{0} & mathbf{g} & mathbf{g} end{array} right], end{array} (4).
The compound code G has the compound input X= [ x 1,x 2,x NC ] and the channel output (mathbf {Y} =,[!mathbf {y}_{S_{1}D}, mathbf {y}_{S_{2}D}, mathbf {y}_{R_{NC}D}]).
To decode the source data, the destination applies the joint network/channel decoding algorithm to a "compound code" G [21] which sees the relayed signal as additional parity bits (redundancy).
As the contribution of these factors are comparable and equal to the input weights of the compound code (shown in Table 1 as an example), the diversity order of NCC is dominated by the diversity order 2 factor.
To derive (10), it requires the knowledge of the minimum distance F of the compound code, the input weight w i (d), and how d output wrights in the compound codeword X are distributed among the three channels S1→D, S2→D and R NC →D.
