
LYN-1604
CAS No. 2088939-99-3
LYN-1604 ( LYN1604 )
产品货号. M13261 CAS No. 2088939-99-3
LYN-1604 是一种潜在的 ULK1 激动剂(100 nM 时酶活性 = 195.7%,针对 MDA-MB-231 细胞的 IC50 = 1.66 uM)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥996 | 有现货 |
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5MG | ¥1806 | 有现货 |
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10MG | ¥2778 | 有现货 |
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25MG | ¥4690 | 有现货 |
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50MG | ¥6715 | 有现货 |
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100MG | ¥9315 | 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LYN-1604
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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LYN-1604 是一种潜在的 ULK1 激动剂(100 nM 时酶活性 = 195.7%,针对 MDA-MB-231 细胞的 IC50 = 1.66 uM)。
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产品描述LYN-1604 is a potential ULK1 agonist (enzymatic activity=195.7% at 100 nM and IC50=1.66 uM against MDA-MB-231 cells), displays a good effect on ULK1 activation with an EC50 of 18.94 nM; induces cell death, associated with autophagy by the ULK complex (ULK1-mATG13-FIP200-ATG101) in MDA-MB-231 cells; induces cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis; inhibits the growth of xenograft TNBC.
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体外实验LYN-1604 is a potential ULK1 agonist (enzymatic activity=195.7% at 100 nM and IC50=1.66 μM against MDA-MB-231 cells) . LYN-1604 binds to wild-type ULK1 with a binding affinity in the nanomole range (KD=291.4 nM) .LYN-1604 (0.5, 1.0 and 2.0 μM) induces cell death via the ULK complex in MDA-MB-231 cells.LYN-1604 (0.5-2 μM, 24 hours) induces remarkable up-regulation of Beclin-1 and degradation of p62, as well as transformation of LC3-I to LC3-II in MDA-MB-231 cells.LYN-1604 induces ATG5-dependent autophagy via the ULK complex.LYN-1604 can also increase cleavage of caspase3 and induce apoptosis.Cell Viability AssayCell Line:MDA-MB-231 cells Concentration:0.5, 1.0 and 2.0 μM Incubation Time:Result:Induced cell death.Autophagy ratio was increased in a dose-dependent manner.Western Blot AnalysisCell Line:MDA-MB-231 cells Concentration:0, 0.5, 1, and 2 μM Incubation Time:24 hours Result:Induced remarkable up-regulation of Beclin-1 and degradation of p62, as well as transformation of LC3-I to LC3-II.
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体内实验LYN-1604 (low dose, 25 mg/kg; median dose, 50 mg/kg; high dose, 100 mg/kg; intragastric administration once a day for 14 days) inhibits the growth of xenograft TNBC by targeting ULK1-modulated cell death. Animal Model:24 female nude mice (BALB/c, 6-8 weeks, 20-22 g)Dosage:Low dose, 25 mg/kg; median dose, 50 mg/kg; high dose, 100 mg/kg Administration:Intragastric administration; once a day for 14 days Result:Significantly inhibited the growth of xenograft MDA-MB-231 cells. The body weights of mice were stable. By the end of the experiment, the liver and spleen weight indexes of mice were slightly increased in parts of the groups, while the kidney weight index was not affected in all dose groups.
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同义词LYN1604
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通路Autophagy
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靶点ULK
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受体ULK1
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研究领域Other Indications
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适应症——
化学信息
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CAS Number2088939-99-3
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分子量584.626
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分子式C33H43Cl2N3O2
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纯度>98% (HPLC)
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溶解度DMSO: 46 mg/mL (78.7 mM); Water: 90 mg/mL (153.9 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESCC(C)CN(CC(C)C)CC(=O)N1CCN(CC1)CC(C2=C(C=C(C=C2)Cl)Cl)OCC3=CC4=CC=CC=C4C=C3
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化学全称Ethanone, 2-[bis(2-methylpropyl)amino]-1-[4-[2-(2,4-dichlorophenyl)-2-(2-naphthalenylmethoxy)ethyl]-1-piperazinyl]-
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. Zhang L, et al. Chem Sci. 2017 Apr 1;8(4):2687-2701.
2. Ouyang L, et al. Autophagy. 2017 Apr 3;13(4):777-778.