MK-2461Catalog No. A11753

Quick Overview

MK-2461, a novel multitargeted kinase inhibitor, preferentially inhibits the activated c-Met receptor.
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Product Information
Catalog Num A11753
M. Wt 495.6
Formula C24H25N5O5S
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 917879-39-1
Synonyms MK2461
Chemical Name N-((2R)-1,4-Dioxan-2-ylmethyl)-N-methyl-N'-[3-(1-methyl-1H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]sulfamide
SMILES Code CN1C=C(C=N1)C2=CN=C3C=CC4=C(C=C(C=C4)NS(=O)(=O)N(C)C[[email protected]@H]5COCCO5)C(=O)C3=C2

Biological activity
MK-2461, a novel multitargeted kinase inhibitor, preferentially inhibits the activated c-Met receptor.
Target Value
c-Met(M1250T)IC50: 0.4nM
c-Met(Y1235D)IC50: 0.5nM
c-Met(Y1230H)IC50: 1.0nM
c-Met(N1100)IC50: 1.5nM
c-Met(Y1230C)IC50: 1.5nM
c-MetIC50: 2.5nM
RONIC50: 7nM
FLT1IC50: 10nM
FLT3IC50: 22nM
PDGFRβIC50: 22nM
MerIC50: 24nM
FGFR2IC50: 39nM
KDRIC50: 44nM
TrkAIC50: 46nM
FGFR3IC50: 50nM
TrkBIC50: 61nM
FGFR1IC50: 65nM
FLT4IC50: 78nM
DRAK1IC50: 199nM
JAK2IC50: 225nM
IRAK4IC50: 298nM
MELKIC50: 606nM
RETIC50: 635nM
DYRK2IC50: 1.143μM
MLK1IC50: 4.303μM
IRAK1IC50: 5.459μM
AblIC50: 7.747μM
Solubility (25C) * In vitro DMSO 99 mg/mL (199.77 mM)
Water <1 mg/mL (<1 mM)
Ethanol <1 mg/mL (<1 mM)
In vivo 1% DMSO/30% polyethylene glycol/1% Tween 80, pH 4 15 mg/mL
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
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High Purity Kinase Inhibitors on Signaling Pathways

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