Comparison

Dalcetrapib (JTT-705) European Partner

Item no. S2772-10
Manufacturer Selleckchem
CASRN 211513-37-0
Amount 10 mg
Quantity options 10 mg 100 mg 1 g 10 g 10 mM/1 ml 5 mg 50 mg 5 g
Category
Type Inhibitors
Specific against other
Smiles CCC(CC)CC1(CCCCC1)C(=O)NC2=CC=CC=C2SC(=O)C(C)C
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias RO4607381
Similar products Dalcetrapib
Available
Storage Conditions
2 years -80 in solvent
Molecular Weight
389, 59
Administration
Oral gavage
Animal Models
Syrian hamsters
Cell lines
HepG2 cells
Clinical Trials
Dalcetrapib has enered in a Phase III clinical trial in the treatment of cardiovascular disease, dyslipidemia, peripheral arterial disease (PAD).
Concentrations
0-30 uM
Dosages
100 mg/kg
Formulation
0.5% methylcellulose
IC50
0.2 uM [1], 0.2 uM [1], 0.2 uM [1], 0.2 uM [1], 0.2 uM [1], 0.2 uM [1]
In vitro
Dalcetrapib modulates CETP activity. Dalcetrapib induces a conformational change in CETP, when added to human plasma. CETP-induced pre-beta-HDL formation in human plasma is unchanged by Dalcetrapib <=3 uM and increased at 10 uM. Dalcetrapib statistically and significantly increases pre-beta-HDL formation. [1] Dalcetrapib achieves 50% inhibition of CETP activity in human plasma at a concentration of 9 uM. [2] Dalcetrapib inhibits the CETP activity of media in HepG2 in a dose-dependent manner. [3]
In vivo
Treatment with Dalcetrapib leads to significant increases in HDL-C levels. In hamsters injected with [3H]cholesterol-labeled autologous macrophages Dalcetrapib significantly increases fecal elimination of both [3H]neutral sterols and [3H]bile acids. Dalcetrapib increases plasma HDL-[3H]cholesterol. [1] Dalcetrapib has 95% inhibition of CETP activity in male Japanese white rabbits at an oral dose of 30 mg/kg. Dalcetrapib increases the plasma HDL cholesterol level by 27% and 54%, respectively, when given at oral doses of 30 mg/kg or 100 mg/kg once a day for 3 days to male Japanese white rabbits. [2] Treatment with Dalcetrapib markedly increases serum levels of HDL-C. The ratio of HDL2-C to HDL3-C is significantly higher in Dalcetrapib–treated rabbits than in control rabbits at 5 and 7 months, indicating that the inhibition of CETP activity by Dalcetrapib changes the distribution of HDL subfractions and preferentially increases HDL2-C levels. Dalcetrapib treatment increases serum paraoxonase activity and HDL-sociated platelet-activating factor acetylhydrolase activity, but decreases the plasma lysophosphatidylcholine concentration. [4]
Incubation Time
24 hours
Kinase Assay
Inhibition of rhCETP and C13S CETP-mediated transfer of CE from HDL to LDL, The inhibitory potency (IC50) of Dalcetrapib to decrease CE transfer from HDL to LDL by rhCETP and C13S CETP is measured using a scintillation proximity assay kit. Briefly, [3H]CE-labeled HDL donor particles are incubated in the presence of purified CETP proteins (final concentration 0.5 ug/mL) and biotinylated LDL acceptor particles for 3 hours at 37 C. Subsequently, streptavidin-coupled polyvinyltoluene beads containing liquid scintillation cocktail binding selectively to biotinylated LDL are added, and the amount of [3H]CE molecules transferred to LDL is measured by beta counting.
Method
The HepG2 cells are seeded in 6-well plates and cultured to 70–80% confluence. After being washed with PBS, the cells are incubated with growth medium and a different concentration (0 uM–30 uM) of chemical inhibitor Dalcetrapib and dissolved in 2% DMSO for 24 hours. Total RNA is used for RT-PCR.
Solubility (25C)
DMSO 78 mg/mL, Water <1 mg/mL, Ethanol 78 mg/mL
Information
Dalcetrapib (JTT-705) is a rhCETP inhibitor with IC50 of 0.2 μM that increases the plasma HDL cholesterol. Phase 3.
Chemical Name
S-2-(1-(2-ethylbutyl)cyclohexanecarboxamido)phenyl 2-methylpropanethioate

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: 10 mg
Available: In stock
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