Ceranib1

CAS No. 328076-61-5

Ceranib1( —— )

Catalog No. M26103 CAS No. 328076-61-5

Ceranib1 is an inhibitor of ceramidase. It inhibits the proliferation of ovarian cancer cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 55 In Stock
5MG 83 In Stock
10MG 101 In Stock
25MG 223 In Stock
50MG 326 In Stock
100MG 458 In Stock
200MG Get Quote In Stock
500MG 918 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Ceranib1
  • Note
    Research use only, not for human use.
  • Brief Description
    Ceranib1 is an inhibitor of ceramidase. It inhibits the proliferation of ovarian cancer cells.
  • Description
    Ceranib1 is an inhibitor of ceramidase. It inhibits the proliferation of ovarian cancer cells. Ceranib1 inhibits ceramidase activity toward an exogenous ceramide analog, induces the accumulation of multiple ceramide species, decreases levels of S1P and sphingosine.(In Vitro):Ceranib1 produces a dose-dependent decrease in ceramidase activity, with 50% inhibition at 55 and 28 μM in SKOV3 cells. Ceranib1 prevents the hydrolysis of endogenous ceramide species and reduces intracellular sphingosine and S1P. Ceranib1 (10 nM-10 μM; 72 hours) exhibits antiproliferative activity for SKOV3 cells. Ceranib1 (24 hours) does not cause significant acute cytotoxicity at concentrations up to at least those used in the ceramidase assay in SKOV3 cells.
  • In Vitro
    Ceranib1 produces a dose-dependent decrease in ceramidase activity, with 50% inhibition at 55 and 28 μM in SKOV3 cells.Ceranib1 (24 hours) does not cause significant acute cytotoxicity at concentrations up to at least those used in the ceramidase assay in SKOV3 cells.Ceranib1 prevents the hydrolysis of endogenous ceramide species and reduces intracellular sphingosine and S1P.Ceranib1 (10 nM-10 μM; 72 hours) exhibits antiproliferative activity for SKOV3 cells. Cell Proliferation Assay Cell Line:SKOV3 cellsConcentration:10 nM-10 μM (varying concentrations)Incubation Time:72 hours Result:Inhibited cell proliferation with IC50 values of 3.9 ± 0.3 μM.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    PROTAC Linker
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    328076-61-5
  • Formula Weight
    395.458
  • Molecular Formula
    C26H21NO3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    COc1ccc(\C=C\C(=O)c2c(-c3ccccc3)c3cc(C)ccc3[nH]c2=O)cc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Khan S, et al. A selective BCL-XL PROTAC degrader achieves safe and potent antitumor activity. Nat Med. 2019 Dec;25(12):1938-1947.
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