
LYN-1604
CAS No. 2088939-99-3
LYN-1604( LYN1604 )
Catalog No. M13261 CAS No. 2088939-99-3
LYN-1604 is a potential ULK1 agonist (enzymatic activity=195.7% at 100 nM and IC50=1.66 uM against MDA-MB-231 cells).
Purity : >98% (HPLC)






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Biological Information
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Product NameLYN-1604
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NoteResearch use only, not for human use.
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Brief DescriptionLYN-1604 is a potential ULK1 agonist (enzymatic activity=195.7% at 100 nM and IC50=1.66 uM against MDA-MB-231 cells).
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DescriptionLYN-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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In VitroLYN-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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In VivoLYN-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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SynonymsLYN1604
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PathwayAutophagy
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TargetULK
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RecptorULK1
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number2088939-99-3
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Formula Weight584.626
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Molecular FormulaC33H43Cl2N3O2
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Purity>98% (HPLC)
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SolubilityDMSO: 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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Chemical NameEthanone, 2-[bis(2-methylpropyl)amino]-1-[4-[2-(2,4-dichlorophenyl)-2-(2-naphthalenylmethoxy)ethyl]-1-piperazinyl]-
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. 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.
molnova catalog



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