UC-112

CAS No. 383392-66-3

UC-112( UC112 )

Catalog No. M14330 CAS No. 383392-66-3

UC-112 is a novel IAP inhibitor that potently inhibits human melanoma (A375 and M14) and human prostate (PC-3 and DU145) cancer cell lines with IC50 of 0.7-3.4 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 61 Get Quote
5MG 102 Get Quote
10MG 160 Get Quote
25MG 338 Get Quote
50MG 519 Get Quote
100MG 743 Get Quote
500MG 1512 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    UC-112
  • Note
    Research use only, not for human use.
  • Brief Description
    UC-112 is a novel IAP inhibitor that potently inhibits human melanoma (A375 and M14) and human prostate (PC-3 and DU145) cancer cell lines with IC50 of 0.7-3.4 uM.
  • Description
    UC-112 is a novel IAP inhibitor that potently inhibits human melanoma (A375 and M14) and human prostate (PC-3 and DU145) cancer cell lines with IC50 of 0.7-3.4 uM; also potently inhibits the growth of P-gp-overexpressed multidrug-resistant cancer cells, strongly activates caspase-3/7 and caspase-9 activities, and selectively downregulates survivin level at 1 uM; strongly inhibits tumor growth and reduces both X chromosome-linked IAP and survivin levels in an A375 human melanoma xenograft model in vivo.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    UC112
  • Pathway
    Apoptosis
  • Target
    IAP
  • Recptor
    IAP
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    383392-66-3
  • Formula Weight
    348.4382
  • Molecular Formula
    C22H24N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    OC1=C2N=CC=CC2=C(COCC3=CC=CC=C3)C=C1CN4CCCC4
  • Chemical Name
    8-Quinolinol, 5-[(phenylmethoxy)methyl]-7-(1-pyrrolidinylmethyl)-

Shipping & Storage Information

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

Reference

1. Wang J, et al. J Pharmacol Exp Ther. 2014 May;349(2):319-29. 2. Xiao M, et al. PLoS One. 2015 Jun 12;10(6):e0129807.
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