BDBM50566497 2,2-DIMETHYLBUTYRATE::2,2-Dimethyl-Butyric Acid::CHEBI:38649
SMILES CCC(C)(C)C(O)=O
InChI Key InChIKey=VUAXHMVRKOTJKP-UHFFFAOYSA-N
Data 22 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 22 hits for monomerid = 50566497
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP1A2 in human liver microsomes using Phenacetin as substrateMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 8(Homo sapiens (Human))
HemoShear Therapeutics Inc.
Curated by ChEMBL
HemoShear Therapeutics Inc.
Curated by ChEMBL
Affinity DataIC50: 3.51E+6nMAssay Description:Inhibition of human OAT3 assessed as reduction in OAT3-mediated tenofovir transportMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP2C8 in human liver microsomes using amodiaquine as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP2C9 in human liver microsomes using diclofenac as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP2C19 in human liver microsomes using S-mephenytoin as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP2D6 in human liver microsomes using bufuralol as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP3A4 in human liver microsomes using midazolam as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP3A5 in human liver microsomes using midazolam as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP3A4 in human liver microsomes using testosterone as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP3A5 in human liver microsomes using testosterone as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP1A2 in human liver microsomes using Phenacetin as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP2B6 in human liver microsomes using bupropion as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP2C8 in human liver microsomes using amodiaquine as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP2C9 in human liver microsomes using diclofenac as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP2C19 in human liver microsomes using S-mephenytoin as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP2D6 in human liver microsomes using bufuralol as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP3A4 in human liver microsomes using midazolam as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP3A5 in human liver microsomes using midazolam as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP3A4 in human liver microsomes using testosterone as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Time-dependent inhibition of CYP3A5 in human liver microsomes using testosterone as substrate preincubated for 30 minsMore data for this Ligand-Target Pair
TargetSolute carrier family 22 member 6(Homo sapiens (Human))
HemoShear Therapeutics Inc.
Curated by ChEMBL
HemoShear Therapeutics Inc.
Curated by ChEMBL
Affinity DataIC50: 3.86E+6nMAssay Description:Inhibition of human OAT1 assessed as reduction in OAT1-mediated tenofovir transportMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:Direct inhibition of CYP2B6 in human liver microsomes using bupropion as substrateMore data for this Ligand-Target Pair