LAT1-IN-1

CAS No. 20448-79-7

LAT1-IN-1( BCH )

Catalog No. M23915 CAS No. 20448-79-7

LAT1-IN-1 (BCH) ?significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis.?

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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50MG 46 In Stock
100MG 82 In Stock
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Biological Information

  • Product Name
    LAT1-IN-1
  • Note
    Research use only, not for human use.
  • Brief Description
    LAT1-IN-1 (BCH) ?significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis.?
  • Description
    LAT1-IN-1 (BCH) ?significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis.?is a selective and competitive inhibitor of large neutral amino acid transporter 1 (LAT1).
  • In Vitro
    BCH (1-100 mM; 3 days; KYSE30 and KYSE150 esophageal cancer cells) treatment suppresses cell proliferation in a dose-dependent manner.BCH (30 mM; 24 and 48 hours; KYSE30 and KYSE150 cells) treatment significantly increases cell population in the G0/G1 phase in both KYSE30 and KYSE150 cells, indicating that BCH induces cell cycle arrest at G1 phase. BCH (30 mM; 0-24 hours; KYSE30 and KYSE150 cells) treatment decreases phosphorylation of 4E-BP1 and p70S6K at 30 minutes and the decrease is continued for 24 hours. The amount of mTOR, 4E-BP1, and p70S6K proteins is slightly decreased. Cell Proliferation Assay Cell Line: KYSE30 and KYSE150 esophageal cancer cells Concentration:1 mM, 3 mM, 5 mM, 10 mM, 20 mM, 30 mM, 40 mM, 50 mM, or 100 mM Incubation Time:3 daysResult:Cell proliferation was suppressed in a dose-dependent manner. Cell Cycle Analysis Cell Line:KYSE30 and KYSE150 cells Concentration:30 mM Incubation Time:24 and 48 hours Result:Cell cycle arrest.Western Blot Analysis Cell Line:KYSE30 and KYSE150 cells Concentration:30 mM Incubation Time:0 hour, 0.5 hour, 1 hour, 3 hours, 6 hours, 24 hours Result: Phosphorylation of 4E-BP1 and p70S6K was decreased. The amount of mTOR, 4E-BP1, and p70S6K proteins was slightly decreased.
  • In Vivo
    BCH (200 mg/kg; intravenous injection; daily; for 14 days; male BALB/c nude mice) treatment significantly delays tumor growth and decreases glucose metabolism, indicating that LAT1 inhibition potentially suppresses esophageal cancer growth in vivo. Animal Model:Male BALB/c nude mice (5-week-old) with KYSE150 cells Dosage:200 mg/kg Administration:Intravenous injection; daily; for 14 days Result:Significantly delayed tumor growth and decreased glucose metabolism.
  • Synonyms
    BCH
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    LAT1|Apoptosis
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    20448-79-7
  • Formula Weight
    155.19
  • Molecular Formula
    C8H13NO2
  • Purity
    >98% (HPLC)
  • Solubility
    H2O:12.5 mg/mL (80.55 mM; Need ultrasonic);DMSO:< 1 mg/mL (insoluble or slightly soluble)
  • SMILES
    C1CC2CC1CC2(C(=O)O)N
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ohshima Y, et al. Efficacy of system l amino acid transporter 1 inhibition as a therapeutic target in esophageal squamous cell carcinoma. Cancer Sci. 2016 Oct;107(10):1499-1505.
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