BDBM50382558 CHEMBL2022997
SMILES Cc1cccc(c1)C(CCCN)(c1ccccc1)c1ccccc1
InChI Key InChIKey=CYKPIMPUPKXTNO-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 10 hits for monomerid = 50382558
TargetKinesin-like protein KIF11(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataKi: 8.80nMAssay Description:Inhibition of N-terminal hexa-histidine tagged human cloned Eg5 (1 to 368 amino acids) expressed in Escherichia coli BL21 (DE3) assessed as reduction...More data for this Ligand-Target Pair
TargetKinesin-like protein KIF11(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataKi: 8.80nMAssay Description:Inhibition of human N-terminal His6-tagged Eg5 (1 to 368 amino acid residues) motor domain basal ATPase activity expressed in Escherichia coli BL21 (...More data for this Ligand-Target Pair
TargetKinesin-like protein KIF11(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataKi: 10.8nMAssay Description:Inhibition of N-terminal hexa-histidine tagged human cloned Eg5 (1 to 368 amino acids) expressed in Escherichia coli BL21 (DE3) assessed as reduction...More data for this Ligand-Target Pair
TargetKinesin-like protein KIF11(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataKi: 14nMAssay Description:Inhibition of MT-stimulated human N-terminal His6-tagged Eg5 (1 to 368 amino acid residues) motor domain ATPase activity expressed in Escherichia col...More data for this Ligand-Target Pair
TargetCytochrome P450 3A4(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
TargetCytochrome P450 2D6(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataIC50: 8.50E+3nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
TargetCytochrome P450 2C19(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
TargetCytochrome P450 1A2(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataIC50: >2.50E+4nMAssay Description:Inhibition of CYP1A2More data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataIC50: 6.48E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
TargetCytochrome P450 2C9(Homo sapiens (Human))
The Beatson Institute For Cancer Research
Curated by ChEMBL
The Beatson Institute For Cancer Research
Curated by ChEMBL
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of CYP2C9More data for this Ligand-Target Pair