Spautin-1 (b)

CAS No. 1262888-28-7

Spautin-1 (b)( Spautin1 )

Catalog No. M11101 CAS No. 1262888-28-7

Spautin-1 is a potent, small molecule inhibitor of autophagy with IC50 of 0.74 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 30 In Stock
5MG 43 In Stock
10MG 55 In Stock
25MG 103 In Stock
50MG 186 In Stock
100MG 332 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Spautin-1 (b)
  • Note
    Research use only, not for human use.
  • Brief Description
    Spautin-1 is a potent, small molecule inhibitor of autophagy with IC50 of 0.74 uM.
  • Description
    Spautin-1 is a potent, small molecule inhibitor of autophagy with IC50 of 0.74 uM, inhibits USP10 and USP13 with IC50 of 0.6-0.7 uM, but not USP14; promotes cell death under starvation condition and inhibits autophagic cell death, selectively promotes the degradation of Vps34 complexes, reduces the levels of PtdIns3P in cells, but is not a direct inhibitor of class III PI3 kinase activity; promotes the degradation of p53 via inhibition of USP10, which can be inhibited in the presence of MG132; sensitizes ovarian cancer cells to cisplatin and PARP inhibitor (olaparib).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Spautin1
  • Pathway
    Proteasome/Ubiquitin
  • Target
    DUB
  • Recptor
    USP10|USP13
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1262888-28-7
  • Formula Weight
    271.271
  • Molecular Formula
    C15H11F2N3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 27.1 mg/mL (100 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    FC1=CC=C(CNC2=C3C=C(F)C=CC3=NC=N2)C=C1
  • Chemical Name
    6-fluoro-N-[(4-fluorophenyl)methyl]-4-quinazolinamine

Shipping & Storage Information

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

Reference

1. Liu J, et al. Cell. 2011 Sep 30;147(1):223-34. 2. Li Y, et al. Nat Commun. 2017 Jun 1;8:15752. doi: 10.1038/ncomms15752. 3. Mateo R, et al. J Virol. 2013 Feb;87(3):1312-21. 4. Vakifahmetoglu-Norberg H, et al. Genes Dev. 2013 Aug 1;27(15):1718-30.
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