[CAS NO. 1228591-30-7]  TAK-632

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PRODUCTS SPECIFICATIONS [1228591-30-7]

Store
Catalog
SLK-S7291
Brand
Selleck
CAS
1228591-30-7

DESCRIPTION [1228591-30-7]

Overview

MDLMFCD26960965
Molecular Weight554.52
Molecular FormulaC27H18F4N4O3S
SMILESO=C(C1CC1)NC2=NC3=CC=C(OC4=CC=C(F)C(NC(CC5=CC=CC(C(F)(F)F)=C5)=O)=C4)C(C#N)=C3S2

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Description

TAK-632 is a potent pan- inhibitor with of 8.3 nM and 1.4 nM for B-Raf(wt) and C-Raf in cell-free assays, respectively, showing less or no inhibition against other tested kinases.

Features

Orally bioavailable, pan-raf inhibitor that targets both wild-type and mutant forms.

Targets


In vitro

TAK-632 inhibits phosphorylation of MEK and ERK in melanoma A375 cells (BRAFV600E) with IC50 of 12 nM and 16 nM, respectively. In human melanoma HMVII cells (NRASQ61K/BRAFG469V), TAK-632 also shows strong inhibition of pMEK and pERK with IC50 of 49 nM and 50 nM, respectively. Moreover, TAK-632 also exhibits antiproliferative activity in both A375 and HMVII cells with GI50 of 66 nM and 200 nM, respectively. TAK-632 induces RAF dimerization but inhibits the kinase activity of the RAF dimer because of its slow dissociation from RAF. The combination of TAK-632 and TAK-733 exhibits synergistic antiproliferative effects in BRAF- and NRAS-mutated melanoma cells.

In vivo

TAK-632 shows superior oral bioavailability in both rats and dogs. TAK-632 (3.9–24.1 mg/kg, p.o.) exhibits dose-dependent antitumor efficacy without severe body weight reduction in a melanoma A375 (BRAFV600E) xenograft model and a human melanoma HMVII (NRASQ61K/BRAFG469V) xenograft in rats. In NRAS-mutant melanoma SK-MEL-2 xenograft model, TAK-632 (60 or 120 mg/kg, p.o.) also exhibits potent antitumor efficacy without severe toxicity.