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LK-44: sourced facts only. name: "Following screening of the in-house library, the lead compound 01 was identified with potent inhibition on hCES2A, which was further optimized to obtain LK-44 with potent inhibitory activity (IC50 = 5.02 ± 0.67 μM) and high selectivity on hCES2A." [PMID:37300962]; target: "Following screening of the in-house library, the lead compound 01 was identified with potent inhibition on hCES2A, which was further optimized to obtain LK-44 with potent inhibitory activity (IC50 = 5.02 ± 0.67 μM) and high selectivity on hCES2A." [PMID:37300962]; developer: "School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, PR China." [PMID:37300962]; stage: "Importantly, in vivo studies showed that LK-44 significantly reduced the side effects of irinotecan-induced diarrhea." [PMID:37300962]
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