null

SMILES Cc1nn2c(O)cc(nc2c1-c1ccc(F)cc1)C1CCN(CC1)C(=O)c1ccc(Br)nc1

InChI Key InChIKey=ZPEBUNDBUIAHKC-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50239166   

TargetShort transient receptor potential channel 6(Mus musculus)
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (MOE) and Hubei Provinc

Curated by ChEMBL
LigandPNGBDBM50239166(CHEMBL4083411)copy SMILEScopy InChI
Affinity DataEC50:  1.23E+4nMAssay Description:Agonist activity at mouse TRPC6 expressed in HEK293 cells co-expressing Gq11-PLCbeta fused M5 receptor assessed as increase in intracellular calcium ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D220RNPubMed
TargetShort transient receptor potential channel 4(Mus musculus)
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (MOE) and Hubei Provinc

Curated by ChEMBL
LigandPNGBDBM50239166(CHEMBL4083411)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat Angiotensin I converting enzyme (ACE), using Hip-Gly-Gly as synthetic substrate.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D220RNPubMed