BOS-318
CAS No. 2387633-15-8
BOS-318( —— )
Catalog No. M28989 CAS No. 2387633-15-8
BOS-318 is a Furin inhibitor with slowly dissociating, highly selective, and cell-pemeable characteristcs.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 87 | Get Quote |
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10MG | 143 | Get Quote |
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25MG | 290 | Get Quote |
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50MG | 462 | Get Quote |
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100MG | 672 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameBOS-318
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NoteResearch use only, not for human use.
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Brief DescriptionBOS-318 is a Furin inhibitor with slowly dissociating, highly selective, and cell-pemeable characteristcs.
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DescriptionBOS-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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In VitroBOS-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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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number2387633-15-8
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Formula Weight423.38
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Molecular FormulaC17H31NO7P2
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Purity>98% (HPLC)
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SolubilityIn 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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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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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