Table 8.
Sl. No. | Structure | Supplied by | % purity |
Ki/EC50/IC50 (Reported) |
Cellular toxicity |
Antiviral activity |
Reason for no antiviral activity |
Permeability (P) (10-6 cmS-1) |
---|---|---|---|---|---|---|---|---|
1 | Ac-RTSKKR-CONH2 | GL Biochem (China) |
>95% | Ki = 12.14 µM | X | X | Inability to permeate & disadvantage of Peptide nature of the drug | 0 Not detectible |
2 | Maybridge (UK) | >95% | Ki = 44 ± 5 µM | X | X | Positive charge on guanidine and basic moiety limitations | 0 Not detectible |
|
3 | BZ-Ala-Lys-Arg-Arg-H | Mimotopes (Australia) |
62% | Ki = 5.3 µM | X | X | Very high charge On compound |
0 Not detectible |
4 | Otava (Ukraine) |
>95% | Ki = 17.0 ± 4.3 µM IC50 = 67.0 ± 7 µM |
X | X | High IC50 value | 4.12 ± 0.45 | |
5 |
ARDP0006 |
Sigma-Aldrich (USA) |
>95% |
EC50 = 4.2 ± 1.9 µM |
X | Highly permeable | 4.45 ± 0.6 | |
6 | In-house | >95% | Ki = 2.0 µM | X | X | Poor permeability owing to high polarity | 0 Not detectible |
|
7 | Cambridge Screening Library (USA) |
>95% | NR | X | X | Lacked membrane permeability | 0 Not detectible |
|
8 | Maybridge (UK) | >95% | Ki = 35.7 µM | X | X | Unknown reason |
8.40 ± 0.15 | |
9 | Cambridge Screening Library (USA) |
>95% | Ki = 15 ± 3 µM | X | X | Lacked membrane permeability | 0 Not detectible |
|
10 | Cambridge Screening Library (USA) |
>95% | IC50 = 27.0 ± 1.3 µM | X | X | Positively charged nature of compound | 0 Not detectible |
|
11 | GL Biochem (China) |
>95% | Ki = 15.6 ± 1.1 µM | X | X | Highly cationic nature of compound | 0 Not detectible |
|
12 | GL Biochem (China) |
>95% | Ki = 1.4 ± 0.1 µM | X | X | Highly cationic nature of compound | 0 Not detectible |
|
13 | Alexidine hydrochloride | Sigma-Aldrich (USA) |
>95% | Ki = 41 ± 3 µM | X | X | Cationic guanidine moieties | 0 Not detectible |
14 | Ivermectin | Sigma-Aldrich (USA) |
>95% | Ki = 79 ± 21 µM | --- | --- | --- | |
15 | Selamectin | Sigma-Aldrich (USA) |
>95% | Ki = 63 ± 18 µM | ‘ --- | --- | --- |