MG115 chemical structure
Chemical structureResearch use only
CAT. NO. DC34242Featured

MG115

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Product overview

Description & Application

MG-115(MG 115) is an inhibitor of NFκB in the cytoplasm by acting on IKK or the proteasome.

ParameterValue
Chemical NameMG-115
CAS No.133407-86-0
SynonymsL-Leucinamide,N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[(1S)-1-formylbutyl]-;(S)-MG115;MG-115;MG-115 (Z-LL-Nva-CHO);Z-Leu-Leu-Norvalinal;benzyl N-[(2S)-4-methyl-1-[[(2S)-4-methyl-1-oxo-1-[[(2S)-1-oxopentan-2-yl]amino]pentan-2-yl]amino]-1-oxopentan-2-yl]carbamate;MG115 Z-LLnV;MG115;Z-LLnV;Z-LL-NVA-CHO;Z-LEU-LEU-NVA-H;Z-LEU-LEU-NVA-CHO;Z-LEU-LEU-NVA-ALDEHYDE;N-CBZ-LEU-LEU-NORVALINAL;MG115, Z-LLnV;N-[(2S)-4-methyl-1-[[(2S)-4-methyl-1-oxo-1-[[(2S)-1-oxopentan-2-yl]amino]pentan-2-yl]amino]-1-oxopentan-2-yl]carbamic acid (phenylmethyl) ester;CHEBI:95100;GTPL11639;Cbz-Leu-Leu-norvalinal;CS-0029136;Q27166869;carbobenzoxy-leucyl-leucyl-norvalinal;Curator_000004;EX-A1500B;Carbobenzoxy-L-leucyl-L-leucyl-L-norvalinal;DTXSID00432100;J-006370;AKOS040744889;HY-108552;CHEMBL4518490;SCHEMBL2140161;n-benzyloxycarbonyl-l-leucyl-l-leucyl-l-norvalinal;133407-86-0;NCGC00345815-01;Z-Leu-Leu-Norvalinal, >=90% (HPLC), powder;BDBM476985;QEJRGURBLQWEOU-FKBYEOEOSA-N;DA-55451;DTXCID50382929;benzyl N-((2S)-4-methyl-1-(((2S)-4-methyl-1-oxo-1-(((2S)-1-oxopentan-2-yl)amino)pentan-2-yl)amino)-1-oxopentan-2-yl)carbamate;G12577
FormulaC25H39N3O5
M.Wt461.594267129898
SMILESO=C([C@H](CC(C)C)NC(=O)OCC1C=CC=CC=1)N[C@H](C(N[C@H](C=O)CCC)=O)CC(C)C
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

MG-115(MG 115) is an inhibitor of NFκB in the cytoplasm by acting on IKK or the proteasome.

In Vitro

MG-115 (0.1-10 μM; 24 h) dose-dependently decreases the viability of HepG2 cells[3]. MG-115 (0.1-10 μM; 24 h) amplifies the reporter gene expression mediated by CWK18 DNA condensates[3]. Cell Viability Assay[3] Cell Line: HepG2 cells Concentration: 0.1, 1, 2, 5, 10 μM Incubation Time: 24 hours Result: Dose-dependently decreased cell viability. Inhibited the proteasomal activity, with an IC50 of 2 μM.

In Vivo

No in vivo data are provided in the current product source. Contact us for further information.

Target

Ki: 21 nM (20S proteasome); 35 nM (26 Sproteasome)[1]

References & source

[1]. Rock KL, et, al. Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules. Cell. 1994 Sep 9;78(5):761-71.

[2]. Lopes UG, et, al. p53-dependent induction of apoptosis by proteasome inhibitors. J Biol Chem. 1997 May 16;272(20):12893-6.

[3]. Kim J, et, al. The proteasome metabolizes peptide-mediated nonviral gene delivery systems. Gene Ther. 2005 Nov;12(21):1581-90.

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

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