Bromosporine 是一种有效的BET抑制剂,对 PCAF 的IC50为 2.1 μM。Bromosporine 能阻滞癌细胞的细胞周期,诱导细胞凋亡 (apoptosis)。Bromosporine 与 5-FU (HY-90006) 联合使用时,在移植瘤小鼠模型中表现出良好的抗肿瘤活性。在HIV-1潜伏期模型中,Bromosporine 可增加CDK9T-loop 磷酸化,从而保护 HIV-1 复制免受潜伏期的影响。Bromosporine 可用于大肠癌、急性髓系白血病 (AML) 和艾滋病 (AIDS) 的研究。
生物活性 | Bromosporine is a potentBETinhibitor with anIC50value of 2.1 μM for PCAF. Bromosporine can arrest cell cycle and induceapoptosisincancercells. Bromosporine exhibits excellent antitumor activity in xenograft mice model when combined with5-FU(HY-90006). Bromosporine can increaseCDK9T-loop phosphorylation inHIV-1latency models, resulting the protection of reactivateHIV-1replication from latency. Bromosporine can be used to research colorectalcancer, acute myeloid leukemia (AML) and AIDS[1][2][3][4]. |
IC50& Target | IC50: 2.1 μM (PCAF)[2] Apoptosis, BET, CDK9, HIV-1[1][3][4] |
体外研究 (In Vitro) | Bromosporine (0-1000 nM; 72 h) synergistically inhibits cell growth in CRC cells with5-FU(HY-90006)[1]. Bromosporine (various concentration; 48 h) causes a distinct increase in the cells arrested at G1 phase when combined with5-FU[1]. Bromosporine (various concentration; 48 h) decreases the expressions of PARP, caspase 3, and 9[1]. Bromosporine (0.1, 0.5 and 1 μM; 6-10 days) inhibits AML cells in a dose-dependent manner[3]. Bromosporine (2.5 μM; 72 h) activates HIV-1 replication in vitro in latent HIV-1 J-Lat clone C11 cells[4]. Bromosporine (1-50 μM; 48 h) does not induce marked toxicity in primary CD4+ T cells[4].
Cell Proliferation Assay[1] Cell Line: | HCT116 and HT29 | Concentration: | 0, 30, 60, 120, 240, 480 and 1000 nM | Incubation Time: | 72 h | Result: | Synergistically inhibited cell growth in CRC cells with5-FU(HY-90006) (0-16 μg/mL) and exhibited a dose-dependent manner. |
Cell Cycle Analysis[1] Cell Line: | HCT116 and HT29 | Concentration: | Various concentration | Incubation Time: | 48 h | Result: | Caused a distinct increase in the cells arrested at G1 phase when combined with5-FU(HY-90006). |
Western Blot Analysis[1] Cell Line: | HCT116 and HT29 | Concentration: | Various concentration | Incubation Time: | 48 h | Result: | Elevated the level of apoptosis in both cell lines through cleavage of PARP, caspase 3, and 9. |
Cell Proliferation Assay[3] Cell Line: | MV4;11, KASUMI-1, OCI-AML3 and K562 | Concentration: | 0.1, 0.5 and 1 μM | Incubation Time: | 6-10 days | Result: | Inhibited these AML cells in a dose-dependent manner. |
Cell Cytotoxicity Assay[4] Cell Line: | PBMCs | Concentration: | 1 μM, 2.5 μM, 5 μM, 10 μM, 25 μM and 50 μM | Incubation Time: | 48 h | Result: | Did not induce marked toxicity in primary CD4+ T cells with CC50over 10 μM. |
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体内研究 (In Vivo) | Bromosporine (100 mg/kg; i.p.; daily for 10 days) shows better antitumor activity than individual when co-treated with5-FU(HY-90006)[1].
Animal Model: | Female BALB/c nude mice (5-6 weeks; injected with 1 × 106 cells/100 μL of HT116 cells)[1] | Dosage: | 100 mg/kg | Administration: | i.p.; daily for 10 days | Result: | Exhibited better antitumor activity than individual Bromosporine or5-FU(HY-90006) when co-treated with the two agent. |
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运输条件 | Room temperature in continental US; may vary elsewhere. |
储存方式 | Powder | -20°C | 3 years | | 4°C | 2 years | In solvent | -80°C | 6 months | | -20°C | 1 month |
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溶解性数据 | In Vitro: DMSO : ≥ 51.7 mg/mL(127.83 mM) *"≥" means soluble, but saturation unknown. 配制储备液 1 mM | 2.4726 mL | 12.3628 mL | 24.7255 mL | 5 mM | 0.4945 mL | 2.4726 mL | 4.9451 mL | 10 mM | 0.2473 mL | 1.2363 mL | 2.4726 mL |
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