Drug intelligence / Profile preview

Southeast Univ. PARP-1 compound 19c

Development stage
Preclinical
Lead developer
Southeast University
01

Overview

Southeast Univ. PARP-1 compound 19c: sourced facts only. name: "Among all the target compounds, 19b and 19c were found to exhibit more potent inhibitory activity and higher selectivity against PARP-1 than Olaparib, especially the latter had an IC50 value of 0.026 μM against PARP-1 enzyme and a PARP-2/PARP-1 selectivity of 85.19-fold over Olapanib." [PMID:37544273]; target: "Among all the target compounds, 19b and 19c were found to exhibit more potent inhibitory activity and higher selectivity against PARP-1 than Olaparib, especially the latter had an IC50 value of 0.026 μM against PARP-1 enzyme and a PARP-2/PARP-1 selectivity of 85.19-fold over Olapanib." [PMID:37544273]; developer: "Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, PR China; Jiangsu Province Hi-Tech Key Laboratory for Biomedical Research, Southeast University, Nanjing 211189, PR China." [PMID:37544273]; stage: "Apart from strong cytotoxicity against the tested cancer cell lines, 19c was most sensitive to SK-OV-3 cells, with an IC50 value of 4.98 μM superior to Olaparib." [PMID:37544273]

02

Targets

PARP1 (Poly (adp-ribose) polymerase 1)

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