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JNJ-38877618

JNJ-38877618
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Purity:99.52%
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JNJ-38877618

Catalog No. T15617Cas No. 943540-74-7
JNJ-38877618 (OMO-1) is an effective and highly selective inhibitor of Met kinase (IC50s: 2 and 3 nM for wild type and mutant Met, respectively).
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Pack SizePriceAvailabilityQuantity
1 mg$57In Stock
2 mg$82In Stock
5 mg$139In Stock
10 mg$222In Stock
25 mg$447In Stock
50 mg$659In Stock
100 mg$939In Stock
500 mg$1,880In Stock
1 mL x 10 mM (in DMSO)$155In Stock
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Product Introduction

Bioactivity
Description
JNJ-38877618 (OMO-1) is an effective and highly selective inhibitor of Met kinase (IC50s: 2 and 3 nM for wild type and mutant Met, respectively).
Targets&IC50
MET (mutant):2 nM, MET (WT):2 nM
In vitro
JNJ-38877618 shows nM potency against Met Ampl/mutant and therapy-resistant models. JNJ-38877618 has nM binding affinity (Kd=1.4 nM) and enzyme inhibitory activity against wt and M1268T mutant Met (2 and 3 nM IC50). Met inhibitory effects are assessed in proliferation, colony formation, and motility assays.
In vivo
JNJ-38877618 effectively induces regression in substantial Met-amplified EBC-1 SqNSCLC by dose- and time-dependently inhibiting Met kinase activation, with the inhibition lasting significantly longer than its plasma presence. It entirely halts tumor growth in three distinct models: SNU5 Met amp gastric, U87-MG HGF autocrine glioblastoma, and Hs746T Met exon 14 skipping mutant gastric cancer. Additionally, combination therapies are well tolerated and enhance EGFR-targeted treatments[1].
AliasOMO-1
Chemical Properties
Molecular Weight374.35
FormulaC20H12F2N6
Cas No.943540-74-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 4.5 mg/mL (12.02 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6713 mL13.3565 mL26.7130 mL133.5648 mL
5 mM0.5343 mL2.6713 mL5.3426 mL26.7130 mL
10 mM0.2671 mL1.3356 mL2.6713 mL13.3565 mL

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