LAT1-IN-1
CAS No. 20448-79-7
LAT1-IN-1 ( BCH )
产品货号. M23915 CAS No. 20448-79-7
LAT1-IN-1 (BCH) 显着抑制细胞对氨基酸的摄取和 mTOR 磷酸化,从而抑制癌症生长和细胞凋亡。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 50MG | ¥413 | 有现货 |
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| 100MG | ¥737 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称LAT1-IN-1
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述LAT1-IN-1 (BCH) 显着抑制细胞对氨基酸的摄取和 mTOR 磷酸化,从而抑制癌症生长和细胞凋亡。
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产品描述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).
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体外实验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.
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体内实验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.
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同义词BCH
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通路Apoptosis
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靶点Apoptosis
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受体LAT1|Apoptosis
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研究领域——
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适应症——
化学信息
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CAS Number20448-79-7
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分子量155.19
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分子式C8H13NO2
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纯度>98% (HPLC)
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溶解度H2O: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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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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.
产品手册
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