BOS-318
CAS No. 2387633-15-8
BOS-318 ( —— )
产品货号. M28989 CAS No. 2387633-15-8
BOS-318 是一种 Furin 抑制剂,具有缓慢解离、高选择性和细胞渗透性的特点。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥786 | 有现货 |
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| 10MG | ¥1288 | 有现货 |
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| 25MG | ¥2608 | 有现货 |
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| 50MG | ¥4155 | 有现货 |
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| 100MG | ¥6051 | 有现货 |
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| 200MG | 获取报价 | 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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生物学信息
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产品名称BOS-318
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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BOS-318 是一种 Furin 抑制剂,具有缓慢解离、高选择性和细胞渗透性的特点。
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产品描述BOS-318 is a Furin inhibitor with slowly dissociating, highly selective, and cell-pemeable characteristcs.(In Vitro):BOS-318 (0.001-1 μM) provides cytoprotection against toxicity in CuFi-1 cells induced by P aeruginosa exotoxin A (PEA). BOS-318 (U2OS cells) to be approximately 13 times more potent against furin than PCSK5 (IC50 = 25.3 nM), 24 times more potent that PCSK7 (IC50 = 45.8 nM), and 110 times more potent than PCSK6 (IC50 = 209.4 nM). BOS-318 (0.3 μM, 2h or 48 h)reduces ENaC-mediated Na+ absorption in CF HBECs and protects aganist NE- and CF sputum-sol-mediated activation of ENaC.
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体外实验BOS-318 (0.001-1 μM, 72 hours) provides cytoprotection against toxicity in CuFi-1 cells induced by P aeruginosa exotoxin A (PEA).BOS-318 (U2OS cells) to be approximately 13 times more potent against furin than PCSK5 (IC50 = 25.3 nM), 24 times more potent than PCSK7 (IC50 = 45.8 nM), and 110 times more potent than PCSK6 (IC50 = 209.4 nM) .BOS-318 (0.3 μM, 2 hours or 48 hours) reduces ENaC-mediated Na+ absorption in CF HBECs and protects against NE- and CF sputum-sol-mediated activation of the ENaC.Cell Viability AssayCell Line:CuFi-1 cells Concentration:17.4 and 263.0 nM Incubation Time:2 and 48 hours Result:Significantly inhibited ENaC-mediated Na+ transport as measured in differentiated human bronchial epithelial cells under both short- (IC50= 263.0 nM) and long-term (IC50= 17.4 nM) treatment conditions.Cell Viability Assay Cell Line:CuFi-1 cells Concentration:0.3 μM Incubation Time:72 hours Result:Significantly increased cell viability in PEA-treated cells to approximately 88% of control levels.Cell Cytotoxicity Assay Cell Line:CuFi-1 cells Concentration:0.001, 0.01, 0.03, 0.1, 0.3 and 1 μM Incubation Time:72 hours Result:Provided protection against PEA-mediated cytotoxicity in a dose-dependent manner, over a period of 72 h, with an EC50 of 47.8 nM.
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体内实验——
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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——
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研究领域——
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适应症——
化学信息
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CAS Number2387633-15-8
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分子量423.38
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分子式C17H31NO7P2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 50 mg/mL (87.49 mM)
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SMILESCCCCCCCCCCOc1ccc[n+](CC(P([O-])(O)=O)P(O)(O)=O)c1
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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.Tsuburaya N, et al. A small-molecule inhibitor of SOD1-Derlin-1 interaction ameliorates pathology in an ALS mouse model. Nat Commun. 2018 Jul 10;9(1):2668.
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