BDBM589988 (R)-1-(4-(6-amino-5-(trifluoromethoxy)pyridin-3-yl)-1-(3-fluorobicyclo[1.1.1]pentan-1-yl)-1H-imidazol-2-yl)-2,2,2-trifluoroethanol::US11560366, Example 1a::US11560366, Example 1b

SMILES Nc1ncc(cc1OC(F)(F)F)-c1cn(c(n1)[C@@H](O)C(F)(F)F)C12CC(F)(C1)C2

InChI Key InChIKey=XUOJHVFYSAMHNK-UHFFFAOYSA-N

Data  6 IC50  2 Kd

  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 8 hits for monomerid = 589988   

TargetMitogen-activated protein kinase kinase kinase 12(Human)
Board of Regents, The University of Texas System

US Patent
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataKd:  2.20nMAssay Description:A fusion protein of full length of human DLK (amino acids 1-859) and the DNA binding domain of NFkB was expressed in transiently transfected HEK293 c...More data for this Ligand-Target Pair
In DepthDetails
US Patent

TargetMitogen-activated protein kinase kinase kinase 12(Human)
Board of Regents, The University of Texas System

US Patent
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataKd:  120nMAssay Description:A fusion protein of full length of human DLK (amino acids 1-859) and the DNA binding domain of NFkB was expressed in transiently transfected HEK293 c...More data for this Ligand-Target Pair
In DepthDetails
US Patent

TargetMitogen-activated protein kinase kinase kinase 12(Human)
Board of Regents, The University of Texas System

US Patent
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataIC50: 107nMAssay Description:Inhibition of doxycycline-inducible human DLK transfected in HEK293 cells assessed as reduction in c-Jun phosphorylation at Ser63 residue incubated f...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
The University of Texas Md Anderson Cancer Center

Curated by ChEMBL
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of hERG expressed in CHO cells at -80 mV holding potential by QPatch automated electrophysiology assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCytochrome P450 2C9(Human)
The University of Texas Md Anderson Cancer Center

Curated by ChEMBL
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C9 in human liver microsomes using diclofenac as substrate incubated for 10 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCytochrome P450 2D6(Human)
The University of Texas Md Anderson Cancer Center

Curated by ChEMBL
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2D6 in human liver microsomes using bufuralol as substrate incubated for 10 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCytochrome P450 3A4(Human)
The University of Texas Md Anderson Cancer Center

Curated by ChEMBL
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using testosterone as substrate incubated for 5 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCytochrome P450 2C19(Human)
The University of Texas Md Anderson Cancer Center

Curated by ChEMBL
LigandPNGBDBM589988(US11560366, Example 1a | (R)-1-(4-(6-amino-5-(trif...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CYP2C19 in human liver microsomes using S-mephenytoin as substrate incubated for 45 mins in presence of NADPH by LC-MS/MS analysisMore data for this Ligand-Target Pair
In DepthDetails
PubMed