BDBM388651 6-(4-Fluorophenyl)-3-(1-(4-methoxyphenyl)cyclopropyl)imidazo[1,2-a]pyrimidine::US10738052, Example 5::US11261191, Example 5::US9944645, 5

SMILES COc1ccc(cc1)C1(CC1)c1cnc2ncc(cn12)-c1ccc(F)cc1

InChI Key InChIKey=GVXCNEIGNURNGQ-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 388651   

TargetHepatocyte growth factor receptor(Human)
Incyte

US Patent
LigandPNGBDBM388651(6-(4-Fluorophenyl)-3-(1-(4-methoxyphenyl)cycloprop...)
Affinity DataIC50: 500nMAssay Description:Compounds were screened in vitro for their ability to inhibit c-Met kinase activity. The IC50 values of compounds for the inhibition of c-Met kinase ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/12/2020
Entry Details
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TargetHepatocyte growth factor receptor(Human)
Incyte

US Patent
LigandPNGBDBM388651(6-(4-Fluorophenyl)-3-(1-(4-methoxyphenyl)cycloprop...)
Affinity DataIC50: 500nMAssay Description:Briefly, histidine-tagged c-Met catalytic domain fusion protein was used for the assay. IC50 measurements were based on the degree of phosphorylation...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/4/2021
Entry Details
Go to US Patent

TargetHepatocyte growth factor receptor(Human)
Incyte

US Patent
LigandPNGBDBM388651(6-(4-Fluorophenyl)-3-(1-(4-methoxyphenyl)cycloprop...)
Affinity DataIC50: 500nMAssay Description:Compounds were screened in vitro for their ability to inhibit c-Met kinase activity. The IC50 values of compounds for the inhibition of c-Met kinase ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/24/2022
Entry Details
Go to US Patent