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MG-115

CAS No.
133407-86-0
Chemical Name:
MG-115
Synonyms
MG-115;Z-LLnV;(S)-MG115;Z-LL-NVA-CHO;MG115, Z-LLnV;Z-LEU-LEU-NVA-H;Z-LEU-LEU-NVA-CHO;z-leu-leu-norvalinal;Z-LEU-LEU-NVA-ALDEHYDE;MG-115 (DMSO solution)
CBNumber:
CB0195607
Molecular Formula:
C25H39N3O5
Molecular Weight:
461.59
MDL Number:
MFCD00274411
MOL File:
133407-86-0.mol
MSDS File:
SDS
Last updated:2023-09-04 15:50:00

MG-115 Properties

Boiling point 678.8±55.0 °C(Predicted)
Density 1.082±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility DMSO: soluble
form powder
pka 11.14±0.46(Predicted)
color white

SAFETY

Risk and Safety Statements

WGK Germany  3

MG-115 price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 474780 MG-115 Potent reversible proteasome inhibitor (K 133407-86-0 5mg $259 2024-03-01 Buy
Sigma-Aldrich C6706 Z-Leu-Leu-Norvalinal ≥90% (HPLC), powder 133407-86-0 1mg $99.3 2023-06-20 Buy
Cayman Chemical 15413 (S)-MG115 ≥95% 133407-86-0 1mg $51 2024-03-01 Buy
Cayman Chemical 15413 (S)-MG115 ≥95% 133407-86-0 5mg $128 2024-03-01 Buy
Cayman Chemical 15413 (S)-MG115 ≥95% 133407-86-0 10mg $229 2024-03-01 Buy
Product number Packaging Price Buy
474780 5mg $259 Buy
C6706 1mg $99.3 Buy
15413 1mg $51 Buy
15413 5mg $128 Buy
15413 10mg $229 Buy

MG-115 Chemical Properties,Uses,Production

Description

(S)-MG115 is a potent and reversible proteasome inhibitor, targeting the chymotryptic site on the 20S particle (Ki = 21 nM). It reduces the degradation of ubiquitin-conjugated proteins in extracts. (S)-MG115 also blocks the degradation of long- and short-lived proteins in intact cells as well as the proteolytic generation of diverse proteins, including NF-κB, antigens, and p53. Proteasome inhibitors, including (S)-MG115, can induce a heat shock response and apoptosis, particularly in cancer cells.

Uses

(S)-MG115 is a potent and reversible proteasome inhibitor, targeting the chymotryptic site on the 20S particle (Ki = 21 nM). It reduces the degradation of ubiquitin-conjugated proteins in extracts. (S)-MG115 also blocks the degradation of long- and short-lived proteins in intact cells as well as the proteolytic generation of diverse proteins, including NF-κB, antigens, and p53. Proteasome inhibitors, including (S)-MG115, can induce a heat shock response and apoptosis, particularly in cancer cells.[Cayman Chemical]

Uses

MG-115 is a compound that inhibits the chymotrypsin-like activity of the proteasome.

Definition

ChEBI: 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 is a peptide.

General Description

Potent reversible proteasome inhibitor (Ki = 21 nM and 35 nM for 20S and 26S proteasome, respectively).

Biochem/physiol Actions

Product does not compete with ATP.

References

1. involvement of heat shock protein 90 in the degradation of mutant insulin receptors by the proteasome. imamura, t., haruta, t., takata, y., usui, i., iwata, m., ishihara, h., ishiki, m., ishibashi, o., ueno, e., sasaoka, t., kobayashi, m. j. biol. chem. (1998)

MG-115 Preparation Products And Raw materials

Raw materials

Preparation Products

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PROTEASOME INHIBITOR MG-115 N-CBZ-LEU-LEU-NORVALINAL MG-115 Z-LL-NVA-CHO Z-LEU-LEU-NVA-ALDEHYDE Z-LEU-LEU-NVA-CHO Z-LEU-LEU-NVA-H Z-LEU-LEU-NVA-H (ALDEHYDE) CARBOBENZOXY-L-LEUCYL-L-LEUCYL-L-NORVALINAL CARBOBENZOXY-L-LEUCYL-L-LEUCYL-NORVALINAL BENZYLOXYCARBONYL-L-LEUCYL-L-LEUCYL-L-NORVALINAL z-leu-leu-norvalinal N-carbobenzyloxy-Leu-Leu-norvalinal MG115, Z-LLnV Z-Leu-Leu-Norvalinal,MG115, Z-LLnV (S)-MG115 Z-LLnV L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[(1S)-1-formylbutyl]- MG-115 - CAS 133407-86-0 - Calbiochem MG-115 (DMSO solution) 133407-86-0 C25H39N3O5 Inhibitors BioChemical Biochemicals and Reagents Application Index Cell Signaling Enzymes Proteasome, Calpain and Lysosomal Proteases Proteasomes Enzymes, Inhibitors, and Substrates Calpain and Lysosomal Proteases Proteasome Inhibitors Aldehydes and Substrates Application Index Bioactive Small Molecules Biochemicals and Reagents Building Blocks C13-C60 Calpain and Proteasome Inhibitors Carbonyl Compounds Cell Biology Cell Signaling and Neuroscience Cell Signaling Enzymes Chemical Synthesis Endoplasmic Reticulum Stress Enzymes Inhibitors Intracellular Protein Degradation Nitric Oxide and Cell Stress Organic Building Blocks Proteasome Proteasomes Z ProteasomeInhibitors peptides