NVP 231

CAS No. 362003-83-6

NVP 231( NVP231 | NVP 231 | NVP-231 )

Catalog No. M14241 CAS No. 362003-83-6

NVP-231 is a potent, specific, and reversible CerK inhibitor(IC50=12±2 nM) that competitively inhibits binding of ceramide to CerK.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 50 In Stock
5MG 29 In Stock
10MG 46 In Stock
25MG 82 In Stock
50MG 126 In Stock
100MG 210 In Stock
200MG 386 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    NVP 231
  • Note
    Research use only, not for human use.
  • Brief Description
    NVP-231 is a potent, specific, and reversible CerK inhibitor(IC50=12±2 nM) that competitively inhibits binding of ceramide to CerK.
  • Description
    NVP-231 is a potent, specific, and reversible CerK inhibitor(IC50=12±2 nM) that competitively inhibits binding of ceramide to CerK.
  • In Vitro
    Cell Viability Assay Cell Line:MCF-7 cells; NCI-H358 cells Concentration:0 nM, 10 nM, 100 nM, 300 nM, 500 nM, 1000 nM Incubation Time:48 hours Result:Reduced MCF-7 cells and NCI-H358 cells in a concentration manner. Apoptosis Analysis Cell Line:MCF-7 cells; NCI-H358 cells Concentration:1000 nM Incubation Time:24-72 hours Result:Increases caspase-3 and caspase-9 cleavage in MCF-7?and NCI-H358 cells.Western Blot Analysis Cell Line:MCF-7 cells; NCI-H358 cells Concentration:0 nM, 100 nM, 300 nM, 500 nM Incubation Time:24 hours Result:Decreased p-cyclin B1, p-CDK1 as a concentration manner.
  • In Vivo
    ——
  • Synonyms
    NVP231 | NVP 231 | NVP-231
  • Pathway
    MAPK/ERK Signaling
  • Target
    ERK
  • Recptor
    CERK
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    362003-83-6
  • Formula Weight
    431.55
  • Molecular Formula
    C25H25N3O2S
  • Purity
    >98% (HPLC)
  • Solubility
    Soluble in DMSO
  • SMILES
    O=C(C1(C2)C[C@H]3C[C@@H]2C[C@H](C3)C1)NC4=CC=C5N=C(NC(C6=CC=CC=C6)=O)SC5=C4
  • Chemical Name
    N -[2-(Benzoylamino)-6-benzothiazolyl]tricyclo[3.3.1.13,7]decane-1-carboxamide

Shipping & Storage Information

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

Reference

1.Graf C, et al.Mol Pharmacol. 2008 Oct;74(4):925-32.
molnova catalog
related products
  • SCH-772984

    A novel potent and selective inhibitor of ERK1/ERK2 with IC50 of 4 nM/1 nM, respectively.

  • Ulixertinib hydrochl...

    Ulixertinib hydrochloride (Ulixertinib HCl) is an orally available, selective and potent ERK1/2 inhibitor with anticancer and antitumor activity that inhibits the NB cell cycle and promotes apoptosis, and may be used in the study of solid tumors.

  • SMI-4a

    TCS-PIM-1-4a, a Pim inhibitor, blocks mTORC1 activity through activation of AMPK and kills a wide range of both myeloid and lymphoid cell lines (IC50=0.8-40 μM).