
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)






Size | Price / USD | Stock | Quantity |
50MG | 46 | In Stock |
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100MG | 82 | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameLAT1-IN-1
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NoteResearch use only, not for human use.
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Brief DescriptionLAT1-IN-1 (BCH) ?significantly inhibit cellular uptake of amino acids and mTOR phosphorylation, which induces the suppression of cancer growth and apoptosis.?
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DescriptionLAT1-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).
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In VitroBCH (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.
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In VivoBCH (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.
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SynonymsBCH
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PathwayApoptosis
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TargetApoptosis
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RecptorLAT1|Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number20448-79-7
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Formula Weight155.19
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Molecular FormulaC8H13NO2
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Purity>98% (HPLC)
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SolubilityH2O:12.5 mg/mL (80.55 mM; Need ultrasonic);DMSO:< 1 mg/mL (insoluble or slightly soluble)
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SMILESC1CC2CC1CC2(C(=O)O)N
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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.
molnova catalog



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