2-Bromohexadecanoic acid

CAS No. 18263-25-7

2-Bromohexadecanoic acid( 2-BP | 2-bromopalmitate )

Catalog No. M28032 CAS No. 18263-25-7

2-bromohexadecanoic acid (2-BP, 2-bromopalmitate) is a non-metabolizable palmitate analogue, which can be used as palmitoylation inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 33 In Stock
10MG 53 In Stock
25MG 81 In Stock
50MG 104 In Stock
100MG 155 In Stock
500MG 390 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    2-Bromohexadecanoic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    2-bromohexadecanoic acid (2-BP, 2-bromopalmitate) is a non-metabolizable palmitate analogue, which can be used as palmitoylation inhibitor.
  • Description
    2-bromohexadecanoic acid (2-BP, 2-bromopalmitate) is a non-metabolizable palmitate analogue, which can be used as palmitoylation inhibitor. 2-BP directly and irreversibly inhibits the palmitoyltransferase activity of all DHHC (Asp-His-His-Cys) proteins.(In Vitro):2-Bromohexadecanoic acid induces the interactions between GSDME-N and GSDME-C, and inhibits the GSDME-C palmitoylation, exhibiting chemotherapyinduced pyroptosis.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    2-BP | 2-bromopalmitate
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Antioxidant|DPPH
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    18263-25-7
  • Formula Weight
    335.326
  • Molecular Formula
    C16H31BrO2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (298.22 mM)
  • SMILES
    CCCCCCCCCCCCCCC(Br)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Tjahjandarie Tjitjik, Tanjung, Mulyadi. Phenolic compounds from the stem bark of Erythrina orientalis and their cytotoxic and antioxidant activities. Der Pharma Chemica, 2015 , 7 (1) :206-211.
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