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TPCA-1 Europäischer Partner

ArtNr S2824-10
Hersteller Selleckchem
CAS-Nr. 507475-17-4
Menge 10 mg
Quantity options 10 mg 1 g 10 g 10 mM/1 mL 50 mg 5 g
Kategorie
Typ Inhibitors
Specific against other
Smiles C1=CC(=CC=C1C2=CC(=C(S2)NC(=O)N)C(=O)N)F
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias GW683965
Similar products TPCA-1
Lieferbar
Storage Conditions
2 years -80 in solvent
Molecular Weight
279, 29
Administration
Administered via i.p. or b.i.d.
Animal Models
Murine collagen-induced arthritis
Cell lines
U87, MT330, SJ-G2, and GBM6 human glioma lines
Concentrations
0-50 uM
Dosages
3, 10, or 20 mg/kg
Formulation
0.9% DMSO, 7% dimethylacetoacetamide (DMA), and 10% Cremophor El
IC50
17.9 nM [1], 17.9 nM [1], 17.9 nM [1], 17.9 nM [1], 17.9 nM [1], 17.9 nM [1]
In vitro
In a time-resolved fluorescence resonance energy transfer assay, TPCA-1 inhibits human IKK-2 activity with an IC50 of 17.9 nM. In addition, TPCA-1 is demonstrated to be ATP-competitive. Besides, TPCA-1 exhibits IC50 values of 400 nM and 3600 nM against IKK-1 and JNK3, respectively. TPCA-1 inhibits the production of TNF-alpha, IL-6, and IL-8 in a concentration-dependent manner, exhibiting IC50 values of 170, 290, and 320 nM, respectively. [1] TPCA-1 inhibits glioma cell proliferation, as well as TNF-induced RelA (p65) nuclear translocation and NFkappaB-dependent IL8 gene expression. Importantly, TPCA-1 inhibits IFN-induced gene expression, completely suppressing MX1 and GBP1 gene expression, while having only a minor effect on ISG15 expression. [2]
In vivo
Prophylactic administration of TPCA-1 at 3, 10, or 20 mg/kg, i.p., b.i.d., results in a dose-dependent reduction in the severity of murine collagen-induced arthritis (CIA). The significantly reduced disease severity and delay of disease onset resulting from administration of TPCA-1 at 10 mg/kg, i.p., b.i.d. are comparable to the effects of the antirheumatic drug, etanercept, when administered prophylactically at 4 mg/kg, i.p., every other day. Nuclear localization of p65, as well as levels of IL-1beta, IL-6, TNF-alpha, and interferon-gamma, is significantly reduced in the paw tissue of TPCA-1- and etanercept-treated mice. In addition, administration of TPCA-1 in vivo results in significantly decreased collagen-induced T cell proliferation ex vivo. Therapeutic administration of TPCA-1 at 20 mg/kg, but not at 3 or 10 mg/kg, i.p., b.i.d., significantly reduces the severity of CIA, as does etanercept administration at 12.5 mg/kg, i.p., every other day. [1]
Incubation Time
3 days
Kinase Assay
IKK-2 Assay, Recombinant human IKK-2 (residues 1-756) is expressed in baculovirus as an N-terminal GST-tagged fusion protein, and its activity is assessed using a time-resolved fluorescence resonance energy transfer assay. In brief, IKK-2 (5 nM final) diluted in assay buffer (50 mM HEPES, 10 mM MgCl2, 1 mM CHAPS, pH 7.4, with 1 mM DTT and 0.01% w/v BSA) is added to wells containing various concentrations of compound or dimethyl sulfoxide (DMSO) vehicle (3% final). The reaction is initiated by the addition of GST-IkappaBalpha substrate (25 nM final)/ATP (1 uM final), in a total volume of 30 uL. The reaction is incubated for 30 min at room temperature, then terminated by the addition of 15 uL of 50 mM EDTA. Detection reagent (15 uL) in buffer (100 mM HEPES, pH 7.4, 150 mM NaCl, and 0.1% w/v BSA) containing antiphosphoserine- IkappaBalpha-32/36 monoclonal antibody 12C2, labeled with W-1024 europium chelate, and an allophycocyanin-labeled anti-GST antibody is added, and the reaction is further incubated for 60 min at room temperature. The degree of phosphorylation of GST- IkappaBalphais measured as a ratio of specific 665-nm energy transfer signal to reference europium 620-nm signal, using a Packard Discovery plate reader.
Method
Ten microliters of 3-(4, 5-Dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) from stock solution (10 mg/mL) is added to each well of 96-well plates containing glioma cells and incubated at 37 C for 2–4 h. Oxidized MTT is solubilized by adding 100 uL of 10% sodium dodecyl sulfate (SDS) in 0.01 N HCL, and plates were incubated at 37 C for 4 h in a humidified chamber. Plates were read at 570 nm on a plate reader.
Solubility (25C)
DMSO 56 mg/mL, Water <1 mg/mL, Ethanol <1 mg/mL
Information
TPCA-1 (GW683965) is an inhibitor of IKK-2 with IC50 of 17.9 nM in a cell-free assay, inhibits NF-κB pathway, exhibits 22-fold selectivity over IKK-1. TPCA-1 is also an inhibitor of STAT3 and enhances apoptosis.
Chemical Name
3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-(4-fluorophenyl)-

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Menge: 10 mg
Lieferbar: In stock
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