PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34526906-0 2021 Corrigendum: 7-Ethyl-10-Hydroxycamptothecin, A DNA Topoisomerase I Inhibitor, Performs BRD4 Inhibitory Activity and Inhibits Human Leukemic Cell Growth. Irinotecan 13-43 bromodomain containing 4 Homo sapiens 87-91 33995089-0 2021 Case Report: 7-Ethyl-10-Hydroxycamptothecin, a DNA Topoisomerase I Inhibitor, Performs BRD4 Inhibitory Activity and Inhibits Human Leukemic Cell Growth. Irinotecan 13-43 bromodomain containing 4 Homo sapiens 87-91 33995089-2 2021 In our study, SN-38 was characterized as a potent and reversible BRD4 inhibitor [IC50 = 660.2 nM against BRD4 (BD1) and IC50 = 547.7 nM against BRD4 (BD2)] in biochemical assay using drug repurposing strategy. Irinotecan 14-19 bromodomain containing 4 Homo sapiens 65-69 33995089-2 2021 In our study, SN-38 was characterized as a potent and reversible BRD4 inhibitor [IC50 = 660.2 nM against BRD4 (BD1) and IC50 = 547.7 nM against BRD4 (BD2)] in biochemical assay using drug repurposing strategy. Irinotecan 14-19 bromodomain containing 4 Homo sapiens 105-109 33995089-2 2021 In our study, SN-38 was characterized as a potent and reversible BRD4 inhibitor [IC50 = 660.2 nM against BRD4 (BD1) and IC50 = 547.7 nM against BRD4 (BD2)] in biochemical assay using drug repurposing strategy. Irinotecan 14-19 bromodomain containing 4 Homo sapiens 105-109 33995089-3 2021 Additional cellular assay suggested that SN-38 can bind BRD4 in human leukemic cell K562 and inhibit cell growth with IC50 = 0.2798 muM in a BRD4 dependent manner partially. Irinotecan 41-46 bromodomain containing 4 Homo sapiens 56-60 33995089-3 2021 Additional cellular assay suggested that SN-38 can bind BRD4 in human leukemic cell K562 and inhibit cell growth with IC50 = 0.2798 muM in a BRD4 dependent manner partially. Irinotecan 41-46 bromodomain containing 4 Homo sapiens 141-145 33995089-4 2021 Additionally, mechanism study indicated that SN-38 can induce the accumulation of BRD4 substrate c-Myc and cleavage of caspase 3. Irinotecan 45-50 bromodomain containing 4 Homo sapiens 82-86 33995089-5 2021 In sum, our findings identified BRD4 as a new target of SN-38 and reveals SN-38 as a modifier of histone acetylation reader for the first time, which may provide a new insight for further optimization of dual target inhibitor. Irinotecan 56-61 bromodomain containing 4 Homo sapiens 32-36