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KMH-233
本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。
KMH-233图片
CAS NO:1941174-13-5
包装与价格：
包装价格(元)
5mg电议
10mg电议
25mg电议

产品介绍
KMH-233 是一种有效，可逆的且选择性的 l 型氨基酸转运蛋白 1 (LAT1) 抑制剂，可抑制LAT1底物，l-leucin 的摄取 (IC50=18 µM) 以及细胞生长。即使在低浓度 (25 µM) 下，KMH-233 仍可显着增强 Bestatin 和顺铂的疗效。
Cas No.1941174-13-5
Canonical SMILESO=C([C@H](CC1=CC=CC(C(NC2=C(C(C3=CC=C(C=C3)OCC(NC)=O)=C(C4=NC5=CC=CC=C5N24)C#N)C#N)=O)=C1)N)O
分子式C32H25N7O5
分子量587.58
溶解度DMSO : 100 mg/mL (170.19 mM)
储存条件Store at -20℃
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

KMH-233, a potent, reversible and selective l-type amino acid transporter 1 (LAT1) inhibitor, inhibits the uptake of LAT1 substrate, l-leucin (IC50=18 µM) as well as cell growth. KMH-233 significantly potentiates the efficacy of Bestatin and Cisplatin even at low concentrations (25 µM)[1].

KMH-233 is able to inhibit binding and transport of essential neutral amino acids and thus, inhibit the cell growth of cancer cells[1].KMH-233 shows a significant reduction of cell growth with an IC50 of 124 µM[1].KMH-233 is effective and able to potentiate the anti-proliferative efficacy of Bestatin (100 µM) and Cisplatin (100 µM) at a lower concentration of 25 µM, inhibiting cell growth 53% and 50%, respectively[1].

References:
[1]. Huttunen KM, et al. A Selective and Slowly Reversible Inhibitor of l-Type Amino Acid Transporter 1 (LAT1) Potentiates Antiproliferative Drug Efficacy in Cancer Cells. J Med Chem. 2016;59(12):5740-5751.