NVS-CECR2-1

CAS No. 1992047-61-6

NVS-CECR2-1( —— )

Catalog No. M34918 CAS No. 1992047-61-6

NVS-CECR2-1 is a selective cat eye syndrome chromosome region candidate 2 (CECR2) inhibitor with antitumor activity and inhibits chromatin binding of CECR2 BRD. NVS-CECR2-1 is cytotoxic and can induce apoptosis.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    NVS-CECR2-1
  • Note
    Research use only, not for human use.
  • Brief Description
    NVS-CECR2-1 is a selective cat eye syndrome chromosome region candidate 2 (CECR2) inhibitor with antitumor activity and inhibits chromatin binding of CECR2 BRD. NVS-CECR2-1 is cytotoxic and can induce apoptosis.
  • Description
    NVS-CECR2-1, a non-BET family Bromodomain (BRD) inhibitor, is a potent and selective cat eye syndrome chromosome region, candidate 2 (CECR2) inhibitor. NVS-CECR2-1 binds to CECR2 BRD with high affinity (IC50=47 nM; KD=80 nM). NVS-CECR2-1 exhibits cytotoxic activity and induces apoptosis against various cancer cells by targeting CECR2 as well as via CECR2-independent mechanism.
  • In Vitro
    Cell Viability AssayCell Line:Colon (SW48, HT29 and HCT116), lung (H460), uroepithelium (SV-HUC-1), cervix (HeLa) and bone (U2OS), human embryonic kidney (HEK) 293 T cells Concentration:1, 1.5, 2, 2.5, 3, 4 μM Incubation Time:72 hours Result: Decreased the viability of all cancer cells analyzed in a dose dependent manner. Showed a dose-dependent cytotoxicity on HEK 293 T cells.Apoptosis Analysis Cell Line:SW48 cells Concentration:0.5, 1, 1.5, 2, 4, 6 μM Incubation Time:72 hours Result:Increased apoptosis in a dose-dependent manner, with more than 80% cells undergoing apoptosis at 6 μM, and had virtually no effect on necrosis.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    Apoptosis | CDK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1992047-61-6
  • Formula Weight
    495.68
  • Molecular Formula
    C27H37N5O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 66.67 mg/mL (134.50 mM; Ultrasonic )
  • SMILES
    O=S(=O)(C1=NC(=CC(=N1)C2=CC=C3C(C=CN3C4CC(NC(C)(C)C4)(C)C)=C2)NC5CC5)CCC
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Seul Gi Park, et al. Cytotoxic activity of bromodomain inhibitor NVS-CECR2-1 on human cancer cells. Sci Rep. 2020 Oct 1;10(1):16330.?
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