Comparison

Carfilzomib (PR-171) European Partner

Manufacturer Selleckchem
Category
Type Inhibitors
Specific against other
Amount 100 mg
Item no. S2853-100
CASRN 868540-17-4
eClass 6.1 30220300
eClass 9.0 32160605
Available
Administration
i.v.
Animal Models
Beige-nude-XID mice
Cell lines
WST-1, ANBL-6 cells
Chemical Name
L-Phenylalaninamide, (S)--[[2-(4-morpholinyl)acetyl]amino]benzenebutanoyl-L-leucyl-N-[(1S)-3-methyl-1-[[(2R)-2-methyl-2-oxiranyl]carbonyl]butyl]-
Clinical Trials
Carfilzomib has entered in a Phase II clinical trial in the treatment of multiple myeloma.
Concentrations
100 nM
Description
Carfilzomib (PR-171) is a proteasome inhibitor with IC50 less than 5 nM.
Dosages
2.0 mg/kg
Formulation
10% sulfobutylether beta-cyclodextrin in 10 mmol/L citrate buffer pH 3.5,
IC50
5 nM [1], 5 nM [1], 5 nM [1], 5 nM [1], 5 nM [1], 5 nM [1]
In vitro
Carfilzomib inhibits proliferation in a variety of cell lines and patient-derived neoplastic cells, including multiple myeloma, and induced intrinsic and extrinsic apoptotic signaling pathways and activation of c-Jun-N-terminal kinase (JNK). Carfilzomib reveals enhanced anti-MM activity compared with bortezomib, overcome resistance to bortezomib and other agents, and acts synergistically with dexamethasone (Dex). Carfilzomib shoes preferential in vitro inhibitory potency against the ChT-L activity in the beta5 subunit, with over 80% inhibition at doses of 10 nM. Short exposure to low-dose Carfilzomib leads to preferential binding specificity for the beta5 constitutive 20S proteasome and the beta5i immunoproteasome subunits. Measurement of caspase activity in ANBL-6 cells pulsed with Carfilzomib reveals substantial increases in caspase-8, caspase-9, and caspase-3 activity after 8 hours, giving a 3.2-, 3.9- and 6.9-fold increase, respectively, over control cells after 8 hours. In carfilzomib pulse-treated cells, the mitochondrial membrane integrity is decreased to 41% (Q1 + Q2), compared with 75% in vehicle-treated control cells. [1] In another study, Carfilzomib has also shown preclinical effectiveness against hematological and solid malignancies. [2] Carfilzomib directly inhibits osteoclasts formation and bone resorption. [3]
In vivo
Carfilzomib moderately reduces tumor growth in an in vivo xenograft model. Carfilzomib effectively decreases multiple myeloma cell viability following continual or transient treatment mimicking. Carfilzomib increases trabecular bone volume, decreases bone resorption and enhances bone formation in non-tumor bearing mice. [3]
Incubation Time
1 hour
Kinase Assay
Enzyme-linked immunosorbent assay for subunit profiling of carfilzomib, ANBL-6 cells (2, 106/well) are plated in 96-well plates and treated with Carfilzomib doses from 0.001 to 10 uM for 1 hour. Cells are then lysed (20 mM Tris-HCl, 0.5 mM EDTA), and cleared lysates are transferred to polymerase chain reaction (PCR) plates. A standard curve is generated using untreated ANBL-6 cell lysates starting at a concentration of 6 ug protein/uL. The active site probe [biotin-(CH2)4-Leu-Leu-Leu-epoxyketone, 20 uM] is added and incubated at room temperature for 1 hour. Cell lysates are then denatured by adding 1% sodium dodecyl sulfate (SDS) and heating to 100C, followed by mixing with 20 uL per well streptavidin-sepharose high-performance beads in a 96-well multiscreen DV plate and incubated for 1 hour. These beads are then washed with enzyme-linked immunosorbent assay (ELISA) buffer (PBS, 1% bovine serum albumin, and 0.1% Tween-20), and incubated overnight at 4C on a plate shaker with antibodies to proteasome subunits. Antibodies used included mouse monoclonal anti-beta1, anti-beta2, anti-beta1i, and anti-beta5i, goat polyclonal anti-beta2i, and rabbit polyclonal anti-beta5 (affinity-purified antiserum against KLH-CWIRVSSDNVADLHDKYS peptide). The beads are washed and incubated for 2 hours with horseradish peroxidase-conjugated secondary goat antirabbit, goat antimouse or rabbit antigoat antibodies. After washing, the beads are developed using the supersignal ELISA picochemiluminescence substrate. Luminescent detection is performed. Raw luminescence is converted to ug/mL by comparison with the standard curve and expressed as the % inhibition relative to vehicle control. Curve fits are generated using the following nonsigmoidal dose-response equation: Y = Bottom + (Top-Bottom)/(1 + 10 ((LogEC50 X), HillSlope)), where X is the logarithm of concentration, Y is the % inhibition, and EC50 is the dose showing 50% effect.
Method
WST-1 is used to determine the effects of proteasome inhibitor Carfilzomib on cell proliferation. The inhibition of proliferation is calculated in relation to parallel control cells that receives vehicle alone. A linear spline function is used to interpolate the median inhibitory concentration (IC50) using XLfit 4 software. The degree of resistance (DOR) is calculated using the formula: DOR = IC50(resistant cells)/IC50(sensitive cells). ANBL-6 cells pulsed with 100 nM carfilzomib are washed and suspended in PBS containing 5 ug/mL of JC-1, which exhibits potential-dependent accumulation in mitochondria. Analysis of the mitochondrial membrane potential-dependent color shift from 525 to 590 nm is carried out on a FacScan, and the data are analyzed with CellQuest software.
Molecular Weight (MW)
719, 91
Picture ChemicalStructure Description
Carfilzomib (PR-171) Chemical Structure
Solubility (25C)
DMSO 50 mg/mL, Water <1 mg/mL, Ethanol <1 mg/mL
Storage
2 years -20CPowder, 2 weeks4Cin DMSO, 2 months-80Cin DMSO

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 mg
Available: In stock
available

Delivery expected until 4/11/2024 

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