BAP1-IN-1
CAS No. 353495-21-3
BAP1-IN-1 ( —— )
产品货号. M36516 CAS No. 353495-21-3
BAP1-IN-1 (Compound 8) 是一种 BRCA1 相关蛋白 1 (BAP1) 催化活性抑制剂,其 IC50 为 0.1-1μM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥282 | 有现货 |
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| 10MG | ¥464 | 有现货 |
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| 25MG | ¥734 | 有现货 |
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| 50MG | ¥1097 | 有现货 |
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| 100MG | ¥1584 | 有现货 |
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| 200MG | ¥2331 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥319 | 有现货 |
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生物学信息
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产品名称BAP1-IN-1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述BAP1-IN-1 (Compound 8) 是一种 BRCA1 相关蛋白 1 (BAP1) 催化活性抑制剂,其 IC50 为 0.1-1μM。
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产品描述BAP1-IN-1 (Compound 8) is a BRCA1 associated protein 1 (BAP1) catalytic activity inhibitor with an IC50 of 0.1-1 μM.
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体外实验BAP1-IN-1 (Compound 8) (1 μM; 30 min) specifically inhibits BAP1 not just in vitro but also within the cellular context.BAP1-IN-1 (0.1 μM; 24 h) significantly alters 240 genes in BAP1-WT cells, whereas only 33 transcripts are changed in BAP1-KO cells, demonstrating that the gene expression changes mainly depend on the presence of BAP1 protein.BAP1-IN-1 (0-10 μM; 72 h) selectively inhibits cells with ASXL1 GOF mutations.Western Blot Analysis Cell Line:CAL51 cells Concentration:1 μM Incubation Time:30 min Result:Remarkably inhibited BAP1 catalytic activity.Cell Viability Assay Cell Line:THP1, MOML13, K562, THP1-ASXL1-WT and THP1-ASXL1-Y591fs cells Concentration:0, 0.1, 0.3, 1, 3 and 10 μM Incubation Time:72?h Result:K562 cells (ASXL1-Y591*) were significantly more sensitive to the treatment. Cells with ASXL1fs mutations were ten times more sensitive to the treatment.
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体内实验BAP1-IN-1 (Compound 8) (50 mg/kg/d; i.p.; 4 weeks) delays the progression of ASXL1-mutant leukemia and improves survival in mice.Animal Model:NSGS mice, K562 (ASXL1-WT/Y591*) xenograft model and patient-derived tumor cells (ASXL1-WT/Q588*) modelDosage:50 mg/kg/d Administration:Intraperitoneal injection, drug treatments were started at day 28 after transplantation Result:Significantly delayed progression of disease in both models.
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同义词——
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通路Others
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靶点Other Targets
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受体Others
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研究领域——
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适应症——
化学信息
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CAS Number353495-21-3
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分子量292.33
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分子式C18H16N2O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 50 mg/mL (171.04 mM; 超声助溶 )
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SMILESO=[N+]([O-])C1=CC=C2NC(C3CC=CC3C2=C1)C4=CC=CC=C4
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Wang L, et al. Epigenetic targeted therapy of stabilized BAP1 in ASXL1 gain-of-function mutated leukemia. Nat Cancer. 2021 May;2(5):515-526.?
产品手册
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