化合物UPF 1069 T6181
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
1 mL | 1048371-03-4 | ¥363.00 | 询底价 |
5 mg | 1048371-03-4 | ¥328.00 | 询底价 |
50 mg | 1048371-03-4 | ¥1,550.00 | 询底价 |
100 mg | 1048371-03-4 | ¥2,480.00 | 询底价 |
1 mg | 1048371-03-4 | ¥153.00 | 询底价 |
10 mg | 1048371-03-4 | ¥517.00 | 询底价 |
25 mg | 1048371-03-4 | ¥959.00 | 询底价 |
Product Introduction
Bioactivity
英文名: UPF 1069
描述: UPF 1069 是一种特异性PARP 抑制剂,对 PARP-1 和 PARP-2 的IC50值分别为 8 和 0.3 μM。
体外活性: UPF 1069 是一种选择性的 PARP2 抑制剂,其 IC50 值为0.3 μM,同时对 PARP1 的抑制作用较弱,IC50 值为8 μM。[1]
体内活性: In organotypic hippocampal slices, PARP-2 inhibition with UPF-1069 (0.01-1 mM) causes a concentration-dependent exacerbation (up to 155%) of oxygen-glucose deprivation (OGD)-induced CA1 pyramidal cell death. Higher concentrations, acting on both PARP-1 and PARP-2, have no effect on OGD injury. In mouse mixed cortical cells exposed to OGD, UPF-1069 (1-10 mM) significantly reduces post-ischaemic damage. [1]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 27.9 mg/mL (100 mM)
关键字: UPF1069 | inhibit | PARP | Inhibitor | poly ADP ribose polymerase | UPF-1069 | UPF 1069
相关产品: PARP1/2/TNKS1/2-IN-1 | RBN-2397 | G007-LK | PJ34 | TIQ-A | PARP1-IN-16 | 4-amino-1,8-Naphthalimide | PARP10-IN-3 | PARP/PI3K-IN-1 | PARP1-IN-5 dihydrochloride
相关库: Anti-Prostate Cancer Compound Library | Anti-Breast Cancer Compound Library | Anti-Cancer Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Epigenetics Compound Library | DNA Damage & Repair Compound Library | Anti-Cardiovascular Disease Compound Library | NO PAINS Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途