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(10)
By Target- c-Met/HGFR
- VEGFR(2)
- c-Kit(2)
- EGFR(1)
- FLT(1)
- Phospholipase(1)
- ROR(1)
- Src(1)
- TAM Receptor(1)
- c-Fms(1)
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Results for "
cmet inhibitor 1
" in TargetMol Product Catalog- Inhibitors & Agonists10
c-Met inhibitor 1 
T106551357072-61-7
c-Met inhibitor 1 is a c-Met receptor signaling pathway inhibitor, used for the treatment of cancer including glioblastoma, gastric, and pancreatic cancer.
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RPI-1
T2282269730-03-2
RPI-1 is a competitive, potent ATP-dependent Ret kinase inhibitor.
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c-Kit-IN-1
PDGFR inhibitor 1, DCC-2618
T43321225278-16-9
c-Kit-IN-1 (DCC-2618) is an effective inhibitor of c-Met and c-Kit (IC50s<200 nM).
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SYN1143
RON-IN-1, AMG-1
T8409913376-84-8
SYN1143 (AMG-1) is a potent inhibitor of human RON and c-Met.In vitro kinase assays showed that compound I is a potent inhibitor of human RON and c-Met with IC50s of 9 and 4 nmol L, respectively.
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EGFR-IN-8
T111622407957-87-1
EGFR-IN-8, a dual inhibitor targeting both EGFR and c-Met, shows potential as a promising candidate for further development in treating EGFR TKI-resistant NSCLC.
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CSF1R-IN-2
T131942271119-26-5
CSF1R-IN-2 is an oral-active SRC, MET and c-FMS inhibitor (IC50s: 0.12 nM, 0.14 nM and 0.76 nM for SRC, MET and c-FMS respectively).
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JNJ-38877618
OMO-1
T15617943540-74-7
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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Cabozantinib hydrochloride
XL184, Cabozantinib hydrochloride (849217-68-1(free base)), BMS-907351
T51641817759-42-4
Cabozantinib hydrochloride (XL184) is a potent pan-tyrosine kinases inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt4 (IC50s: 0.035, 1.3, 4.6, 7 and 6 nM).
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SCR-1481B1
c-Met inhibitor 2
T53491174161-86-4
SCR-1481B1 (c-Met inhibitor 2) has activity against cancers dependent on Met activation and also has activity against cancers as a VEGFR inhibitor
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MK-8033
TQ02191001917-37-8
MK-8033 is a new and selective dual ATP competitive c-Met Ron inhibitor (IC50: 1 nM Wt c-Met).
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