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Similarly, less potent compounds are grouped together.
SAR studies led to a series of potent compounds.
Representative potent compounds were effective inhibitors of cancer cell migration.
Potent compounds evolved inhibiting the protein-protein interaction p53-MDM2.
Specific cancer cell cytotoxicity was confirmed for the most potent compounds.
Notably, among the eight (very) highly potent compounds are six antiandrogens like linuron and cypermethrin.
The results of potent compounds are accessible in Table 24 (Ma et al. [28]).
FragFCA also identifies fragment combinations that are characteristic of highly potent compounds against defined targets.
The results of potent compounds are presented in Table 27 (Kumar et al. [35]).
The results of potent compounds are presented in Table 26 (Anh et al. [34]).
The significant results of potent compounds are given in Table 28 (Hossain et al. [37]).
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