LACTACYSTIN CAS 133343-34-7

Introduction:Basic information about LACTACYSTIN CAS 133343-34-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

LACTACYSTIN Basic information

Product Name:LACTACYSTIN
Synonyms:(2R,3S,4R)-3-HYDROXY-2-[(1S)-1-HYDROXY-2-METHYLPROPYL]-4-METHYL-5-OXO-2-PYRROLIDINECARBOXY-N-ACETYL-L-CYSTEINE THIOESTER;3S-HYDROXY-2R-(1-HYDROXY-2-METHYLPROPYL)-4R-METHYL-5-OXO-2-PYRROLIDINECARBOXYLATE-N-ACETYL-L-CYSTEINE;(+)-LACTACYSTIN;LACTACYSTIN;LACTACYSTIN (NATIVE);LACTACYSTIN, STREPTOMYCES SP;LACTACYSTIN, SYNTHETIC;N-ACETYL-S-[(2R,3S,4R)-3-HYDROXY-2-[(1S)-1-HYDROXY-2-METHYLPROPYL]-4-METHYL-5-OXO-2-PYRROLIDINECARBONYL]-L-CYSTEINE
CAS:133343-34-7
MF:C15H24N2O7S
MW:376.43
EINECS:200-258-5
Product Categories:All Inhibitors;Inhibitors;Metabolites;Calpain and Proteasome InhibitorsProteasome, Calpain and Lysosomal Proteases;InhibitorsProtease Inhibitors;Intracellular Protein Degradation;Nitric Oxide and Cell Stress;P to;Protease Inhibitor Specificity Index;Proteasome inhibitor;Proteasome inhibitorEnzyme Inhibitors by Enzyme;Proteasomes;Protease;ProteaseInhibitors
Mol File:133343-34-7.mol

LACTACYSTIN Chemical Properties

Melting point 233-235°C dec.
Boiling point 714.9±60.0 °C(Predicted)
density 1.367±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Soluble in DMSO (up to 20 mg/ml), in Water (up to 10 mg/ml), or in Ethanol (up to 1 mg/ml).
pka3.11±0.10(Predicted)
form powder
color White to off-white
Water Solubility Soluble to 10 mM in water
Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month. Solutions in water are not stable and must be used with one working day. Aqueous solutions should not be stored.
InChIKeyDAQAKHDKYAWHCG-RWTHQLGUSA-N
SMILESCC(C)[C@H](O)[C@]1(NC(=O)[C@H](C)[C@@H]1O)C(=O)SC[C@H](NC(C)=O)C(O)=O

Safety Information

WGK Germany 3
Storage Class11 - Combustible Solids

LACTACYSTIN Usage And Synthesis

DescriptionLactacystin is a microbial metabolite isolated from Streptomyces that is now widely used as a selective inhibitor of the 20S proteasome. Lactacystin was first characterized by its ability to induce differentiation and inhibit cell cycle progression in several tumor cell lines. At concentrations from 2 to 10 μM, lactacystin induces the outgrowth of neurites in the neuroblastoma cell line Neuro2a. Lactacystin irreversibly alkylates subunit X of the 20S proteasome. The concomitant inhibition of proteasome peptidase activity results in the accumulation of a variety of ubiquitinated proteins which would normally undergo rapid degradation. Thus, the effects of lactacystin are pleiotropic and depend substantially on the expression pattern of signalling proteins within the treated cell.
Chemical PropertiesWhite Powder
UsesA selective and potent inhibitor of proteasome-mediated degradation of ubiquitin-tagged proteins. A Streptomyces metabolite that acts as a highly specific inhibitor of the 20S proteasome (MCP: multicatalytic proteinase complex)
UsesLactacystin has been used:
  • as a proteasome inhibitor to inhibit protein degradation
  • to inhibit proteasomal activity of cells for live cell imaging
  • to block proteasomal proteolysis in human monocyte-derived dendritic cells (MoDCs) for 24 h
  • to provide unilateral injection to animals to induce nigrostriatal lesions

DefinitionChEBI: L-Cysteine substituted at nitrogen by an acetyl group and at sulfur by a substituted-lactam carbonyl group.
General DescriptionLactacystin is an antibiotic?and a metabolite of Streptomyces?spp.
Biochem/physiol ActionsLactacystin can block the development of cell cycle and stimulate differentiation in a murine neuroblastoma cell line. It can serve as a precursor for?clasto-lactacystin β-lactone. Cell-permeable and irreversible proteasome inhibitor (Ki = 4nM). Inhibits NF-kB activation (IC50 = 10mM). Induces neurite outgrowth in neuro2A mouse neuroblastoma cells.
targetGABA Receptor | HDAC | NF-kB | p65 | Caspase
storage+4°C
References[1] S OMURA. Lactacystin, a novel microbial metabolite, induces neuritogenesis of neuroblastoma cells.[J]. Journal of Antibiotics, 1991, 44 1: 113-116. DOI:10.7164/antibiotics.44.113
[2] GABRIEL FENTEANY. Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin[J]. Science, 1995, 268 5211. DOI:10.1126/science.7732382

LACTACYSTIN Preparation Products And Raw materials

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