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
10MG 143 Get Quote
25MG 290 Get Quote
50MG 462 Get Quote
100MG 672 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    BOS-318
  • Note
    Research use only, not for human use.
  • Brief Description
    BOS-318 is a Furin inhibitor with slowly dissociating, highly selective, and cell-pemeable characteristcs.
  • Description
    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.
  • In Vitro
    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.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2387633-15-8
  • Formula Weight
    423.38
  • Molecular Formula
    C17H31NO7P2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (87.49 mM)
  • SMILES
    CCCCCCCCCCOc1ccc[n+](CC(P([O-])(O)=O)P(O)(O)=O)c1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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