BI 01383298

CAS No. 2227549-00-8

BI 01383298( —— )

Catalog No. M20075 CAS No. 2227549-00-8

BI 01383298 is a selective inhibitor of the sodium-citrate co-transporter (SLC13A5).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 29 In Stock
10MG 44 In Stock
25MG 95 In Stock
50MG 152 In Stock
100MG 242 In Stock
200MG 344 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    BI 01383298
  • Note
    Research use only, not for human use.
  • Brief Description
    BI 01383298 is a selective inhibitor of the sodium-citrate co-transporter (SLC13A5).
  • Description
    BI 01383298 is a selective inhibitor of the sodium-citrate co-transporter (SLC13A5).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Sodium Channel
  • Recptor
    SLC13A5
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2227549-00-8
  • Formula Weight
    445.34
  • Molecular Formula
    C19H19Cl2FN2O3S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 22 mg/mL (49.4 mM);Water: Insoluble
  • SMILES
    Fc1ccc(CNC(=O)C2CCN(CC2)S(=O)(=O)c2cc(Cl)cc(Cl)c2)cc1
  • Chemical Name
    1-((35-Dichlorophenyl)sulfonyl)-N-(4-fluorobenzyl)piperidine-4-carboxamide

Shipping & Storage Information

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

Reference

1.Peters JM. Flipping a citrate switch on liver cancer cells. J Biol Chem. 2017 Aug 18;292(33):13902-13903.
molnova catalog
related products
  • XEN-402

    XEN-402 (Funapide;TV-45070) is a potent and selective, orally available sodium channel Nav1.7 and Nav1.8 blocker for treatment of pain.

  • ProTx II

    Selective NaV1.7 channel blocker. Shifts activation gating positively and decreases current magnitude. Displays 100-fold selectivity over other sodium channel subtypes.

  • PF-06305591

    PF-06305591 (PF06305591) is a potent, highly selective selective NaV1.8 blocker with IC50 of 15 nM, displays no significant activity against other sodium channel subtypes, K+ channels and Ca2+ channels.