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Found 127 with Last Name = 'finel' and Initial = 'm'
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258529(CHEMBL449158 | bryostatin 1)
Affinity DataKi:  0.440nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCdelta expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataKi:  18.4nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50015677((S)-1-hydroxymethyl-2-octanoyloxy-ethyl ester | 1,...)
Affinity DataKi:  40nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCalpha expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258472(CHEMBL466211 | bis(3-(trifluoromethyl)benzyl)5-(hy...)
Affinity DataKi:  205nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCalpha expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258322(CHEMBL494361 | diheptan-3-yl 5-(hydroxymethyl)isop...)
Affinity DataKi:  319nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCalpha expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258322(CHEMBL494361 | diheptan-3-yl 5-(hydroxymethyl)isop...)
Affinity DataKi:  529nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCdelta expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258472(CHEMBL466211 | bis(3-(trifluoromethyl)benzyl)5-(hy...)
Affinity DataKi:  590nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCdelta expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258321(CHEMBL523053 | dihexan-3-yl 5-(hydroxymethyl)isoph...)
Affinity DataKi:  661nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCalpha expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50258321(CHEMBL523053 | dihexan-3-yl 5-(hydroxymethyl)isoph...)
Affinity DataKi:  915nMAssay Description:Displacement of [3H]PDBu from human recombinant PKCdelta expressed in Sf9 cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataKi:  2.18E+4nMAssay Description:Inhibition of human recombinant UGT2B17 assessed as reduction of scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183611((rac)-5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-...)
Affinity DataKi:  5.78E+4nMAssay Description:Competitive inhibition of UGT2B17-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 1A10(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50088511(CHEBI:87620 | Epiestriol | Epioestriol)
Affinity DataKi:  9.81E+4nMAssay Description:Inhibition of recombinant human C-terminal His-tagged UGT1A10 after 15 to 60 mins by Michaelis-Menten equation analysis in presence of UDPGAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183611((rac)-5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-...)
Affinity DataKi:  1.01E+5nMAssay Description:Competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183598((rac)-6-methyl-3,4-dihydro-2H-chromen-4-ol | CHEMB...)
Affinity DataKi:  1.13E+5nMAssay Description:Competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50088511(CHEBI:87620 | Epiestriol | Epioestriol)
Affinity DataKi:  1.62E+5nMAssay Description:Inhibition of recombinant human C-terminal His-tagged UGT2B7 after 15 to 60 mins by Michaelis-Menten equation analysis in presence of UDPGAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183611((rac)-5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-...)
Affinity DataKi:  1.90E+5nMAssay Description:Non competitive inhibition of UGT2B17-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183611((rac)-5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-...)
Affinity DataKi:  1.92E+5nMAssay Description:Non competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183598((rac)-6-methyl-3,4-dihydro-2H-chromen-4-ol | CHEMB...)
Affinity DataKi:  2.01E+5nMAssay Description:Competitive inhibition of UGT2B17-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183598((rac)-6-methyl-3,4-dihydro-2H-chromen-4-ol | CHEMB...)
Affinity DataKi:  2.58E+5nMAssay Description:Non competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183609((rac)-6-methyl-2,3-dihydro-1H-inden-1-ol | CHEMBL2...)
Affinity DataKi:  3.01E+5nMAssay Description:Competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183609((rac)-6-methyl-2,3-dihydro-1H-inden-1-ol | CHEMBL2...)
Affinity DataKi:  4.27E+5nMAssay Description:Competitive inhibition of UGT2B17-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183598((rac)-6-methyl-3,4-dihydro-2H-chromen-4-ol | CHEMB...)
Affinity DataKi:  6.08E+5nMAssay Description:Non competitive inhibition of UGT2B17-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183609((rac)-6-methyl-2,3-dihydro-1H-inden-1-ol | CHEMBL2...)
Affinity DataKi:  6.24E+5nMAssay Description:Non competitive inhibition of UGT2B7-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 1A9(Homo sapiens (Human))
Gdansk University Of Technology

Curated by ChEMBL
LigandPNGBDBM50008347(5-(2-(diethylamino)ethylamino)-8-hydroxy-6H-imidaz...)
Affinity DataKi:  9.58E+5nMAssay Description:Inhibition of human recombinant UGT1A9 activity expressed in baculovirus-infected Sf9 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B17(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50183609((rac)-6-methyl-2,3-dihydro-1H-inden-1-ol | CHEMBL2...)
Affinity DataKi:  1.44E+6nMAssay Description:Non competitive inhibition of UGT2B17-catalyzed scopoletin glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 1A9(Homo sapiens (Human))
Gdansk University Of Technology

Curated by ChEMBL
LigandPNGBDBM50088499(CHEMBL329092)
Affinity DataKi:  1.65E+6nMAssay Description:Inhibition of human recombinant UGT1A9 activity expressed in baculovirus-infected Sf9 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataIC50:  47nMAssay Description:Inhibition of human UGT2B7 by substrate-independent inhibition assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211740((1R)-phenyl-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricy...)
Affinity DataIC50:  54nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211775(((1S,3aR,4S,8aR,9S)-4,8,8-trimethyl-decahydro-1,4-...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211777((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211763((1R)-2-chloro-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211762((1S)-2-chloro-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211780((1S)-2,2-dimethyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimet...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211764((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211765(CHEMBL226344 | ethyl (3S)-3-hydroxy-3-[(1R,2S,7S,8...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211778((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211782((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  300nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211749(CHEMBL390574 | ethyl (3R)-3-hydroxy-3-[(1R,2S,7S,8...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211753((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211739((1R)-2-methyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211741((1S)-2-methyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethylt...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211769((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211743(2-[(1R,2S,7R,8S,9R)-3,3,7-trimethyltricyclo[5.4.0....)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211750((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211773((1R)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211781((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  600nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211766((1S)-1-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  700nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211744((2Z)-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  700nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211752((2E)-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5...)
Affinity DataIC50:  800nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 2B7(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50211748((1R)-2,2-dimethyl-1-[(1R,2S,7S,8S,9S)-3,3,7-trimet...)
Affinity DataIC50:  800nMAssay Description:Inhibition of human UGT2B7 assessed as reduction of estriol glucuronidationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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