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TAK-715

Catalog No. T6150   CAS 303162-79-0

TAK-715 is a p38 MAPK inhibitor for p38α.

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TAK-715 Chemical Structure
TAK-715, CAS 303162-79-0
Pack Size Availability Price/USD Quantity
1 mg In stock $ 34.00
2 mg In stock $ 48.00
5 mg In stock $ 79.00
10 mg In stock $ 100.00
25 mg In stock $ 178.00
50 mg In stock $ 340.00
100 mg In stock $ 533.00
1 mL * 10 mM (in DMSO) In stock $ 88.00
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Purity: 99.69%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description TAK-715 is a p38 MAPK inhibitor for p38α.
Targets&IC50 p38α:7.1 nM, p38β:0.20 μM
In vitro TAK 715 inhibits LPS-stimulated release of TNF-alpha from THP-1 with IC50 of 48 nM. [1] TAK 715 (10 μM) inhibits Wnt-3a-induced hDvl2 phosphorylation and the hDvl2 shift in U2OS-EFC cells. [2] The amide NH of TAK 715 is hydrogen bonded to the main-chain carbonyl of Met109 of p38 alpha. TAK 715 binds relatively high in the ATP pocket, occupying the hydrophobic back pocket, the adenine region and the front pocket of p38 as well as extending to most of the length of the Gly-rich loop. [3]
In vivo TAK 715 (10 mg/kg, po) inhibits LPS-induced TNF-alpha production in mice with 87.6% inhibition. TAK 715 has a modest mouse bioavailability of 18.4% and a slightly improved rat bioavailability of 21.1%. TAK 715 has a modest mouse bioavailability of 18.4% and a slightly improved rat bioavailability of 21.1%. TAK 715 results in Cmax of 0.19 μg/mL and AUC(0-24 hours) of 1.16 μg·h/mL in rats. TAK 715 (30 mg/kg, po) significantly reduces the secondary paw volume with 25 % inhibition in a rat adjuvant-induced arthritis (AA) model. [1]
Kinase Assay Assay of PI3K enzyme inhibition: The inhibition of PI3Kβ, PI3Kα, PI3Kγ, and PI3Kδ is evaluated in an AlphaScreen based enzyme activity assay using human recombinant enzymes. The assay measures PI3K-mediated conversion of PIP2 to PIP3. Biotinylated PIP3, a GST-tagged pleckstrin homology (PH) domain and the two AlphaScreen beads form a complex that elicits a signal upon laser excitation at 680 nm. The PIP3 formed in the enzyme reaction competes with the biotinylated PIP3 for binding to the PH domain thus reducing the signal with increasing enzyme product. The AZD6482 is dissolved in DMSO and added to 384 well plates. PBKβ, PBKα, PBKγ, or PBKδ is added in a Tris buffer (50 mM Tris pH 7.6, 0.05% CHAPS, 5 mM DTT, and 24 mM MgCl2) and allowed to preincubate with AZD6482 for 20 minutes prior to the addition of substrate solution containing PIP2 and ATP. The enzyme reaction is stopped after 20 minutes by addition of stop solution containing EDTA and biotin-PIP3, followed by addition of detection solution containing GST-grpl PH and AlphaScreen beads. Plates are left for a minimum of 5 hours in the dark prior to analysis. The final concentration of DMSO, ATP and PIP2 in the assay are, 0.8%, 4 μM, and 40 μM, respectively. IC50 values are calculated according to the equation, y = {a+[(b-a)/(l+(x/IC50)s)]}, where y = % inhibition; a = 0%; b = 100%; s = the slope of the concentration-response curve; x = AZD6482 concentration.
Molecular Weight 399.51
Formula C24H21N3OS
CAS No. 303162-79-0

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

Ethanol: 20 mg/mL (50 mM)

DMSO: 40 mg/mL (100 mM)

TargetMolReferences and Literature

1. Miwatashi S, et al. J Med Chem, 2005, 48(19), 5966-5979. 2. Verkaar F, et al. Chem Biol, 2011, 18(4), 485-494. 3. Azevedo R, et al. Acta Crystallogr D Biol Crystallogr. 2012 Aug;68(Pt 8):1041-50.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Drug Library Kinase Inhibitor Library Drug Repurposing Compound Library Inhibitor Library Anti-Cancer Clinical Compound Library Anti-Neurodegenerative Disease Compound Library Reprogramming Compound Library Anti-Diabetic Compound Library HIF-1 Signaling Pathway Compound Library Anti-Prostate Cancer Compound Library

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Keywords

TAK-715 303162-79-0 Stem Cells MAPK Metabolism p38 MAPK Casein Kinase JNK CYP3A4 MEKK1 orally ERK1 TAK715 IKKβ TNF-α CTGF Snai1 Inhibitor JNK1 Wnt/β-catenin TAK1 arthritis inhibit hDvl2 TAK 715 inhibitor

 

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