Compile Data Set for Download or QSAR
maximum 50k data
Found 216 with Last Name = 'yli-kauhaluoma' and Initial = 'j'
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
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50000092((-)-(etorphine) | (-)-morphine | (1S,5R,13R,14S)-1...)
Affinity DataKi:  4nMAssay Description:Displacement of [3H]diprenorphine from human MOR expressed in African green monkey COS1 cell membranes incubated for 1 hr by scintillation counting m...More data for this Ligand-Target Pair
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
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50000092((-)-(etorphine) | (-)-morphine | (1S,5R,13R,14S)-1...)
Affinity DataKi:  340nMAssay Description:Displacement of [3H]diprenorphine from human DOR expressed in African green monkey COS1 cell membranes incubated for 1 hr by scintillation counting m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

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
TargetBotulinum neurotoxin type A(Clostridium botulinum)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50340404(28-Hemisuccinylbetulin | CHEMBL1761333)
Affinity DataKi:  800nMAssay Description:Inhibition of Clostridium BoNT/A protease light chainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50370401(CHEMBL4168822)
Affinity DataKi:  814nMAssay Description:Displacement of [3H]diprenorphine from human MOR expressed in African green monkey COS1 cell membranes incubated for 1 hr by scintillation counting m...More 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
TargetMu-type opioid receptor(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50370393(CHEMBL4168247)
Affinity DataKi:  1.08E+3nMAssay Description:Displacement of [3H]diprenorphine from human MOR expressed in African green monkey COS1 cell membranes incubated for 1 hr by scintillation counting m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50370393(CHEMBL4168247)
Affinity DataKi:  1.13E+3nMAssay Description:Displacement of [3H]diprenorphine from human DOR expressed in African green monkey COS1 cell membranes incubated for 1 hr by scintillation counting m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50370401(CHEMBL4168822)
Affinity DataKi:  1.69E+3nMAssay Description:Displacement of [3H]diprenorphine from human DOR expressed in African green monkey COS1 cell membranes incubated for 1 hr by scintillation counting m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetOrexin/Hypocretin receptor type 1(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50468969(CHEMBL4295121)
Affinity DataKi:  3.10E+3nMAssay Description:Antagonist activity at human OX1 receptor expressed in CHOK1 cells assessed as inhibition of orexin-A-induced calcium accumulation preincubated for 3...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetOrexin receptor type 2(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50468969(CHEMBL4295121)
Affinity DataKi:  3.20E+3nMAssay Description:Antagonist activity at human OX2 receptor expressed in CHOK1 cells assessed as inhibition of orexin-A-induced calcium accumulation preincubated for 3...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetOrexin receptor type 2(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50468970(CHEMBL4281212)
Affinity DataKi:  3.60E+3nMAssay Description:Antagonist activity at human OX2 receptor expressed in CHOK1 cells assessed as inhibition of orexin-A-induced calcium accumulation preincubated for 3...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetOrexin receptor type 2(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50468971(CHEMBL4291497)
Affinity DataKi:  4.30E+3nMAssay Description:Antagonist activity at human OX2 receptor expressed in CHOK1 cells assessed as inhibition of orexin-A-induced calcium accumulation preincubated for 3...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetOrexin/Hypocretin receptor type 1(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50468970(CHEMBL4281212)
Affinity DataKi:  4.80E+3nMAssay Description:Antagonist activity at human OX1 receptor expressed in CHOK1 cells assessed as inhibition of orexin-A-induced calcium accumulation preincubated for 3...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetOrexin/Hypocretin receptor type 1(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50468971(CHEMBL4291497)
Affinity DataKi:  5.40E+3nMAssay Description:Antagonist activity at human OX1 receptor expressed in CHOK1 cells assessed as inhibition of orexin-A-induced calcium accumulation preincubated for 3...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBotulinum neurotoxin type A(Clostridium botulinum)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50340405(Betulinyl 28-carboxymethoxycarvacrolate | CHEMBL10...)
Affinity DataKi:  1.33E+4nMAssay Description:Inhibition of Clostridium BoNT/A protease light chainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBotulinum neurotoxin type A(Clostridium botulinum)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM23208((1R,2R,5S,8R,9R,10R,13R,14R,17S,19R)-17-hydroxy-1,...)
Affinity DataKi:  1.43E+4nMAssay Description:Inhibition of Clostridium BoNT/A protease light chainMore 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 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 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 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
TargetPhosphatidylserine lipase ABHD16A(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50507489(CHEMBL4564841)
Affinity DataIC50:  32nMAssay Description:Inhibition of ABHD16A (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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
TargetPhosphatidylserine lipase ABHD16A(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50336546(CHEMBL1673415 | Palmostatin B)
Affinity DataIC50:  57nMAssay Description:Reversible inhibition of human ABHD16A expressed in HEK293 cells preincubated for 30 mins followed by 40 fold compound dilution and subsequent 1-LG s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylserine lipase ABHD16A(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM195603(KC01)
Affinity DataIC50:  90nMAssay Description:Inhibition of ABHD16A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylserine lipase ABHD16A(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50336546(CHEMBL1673415 | Palmostatin B)
Affinity DataIC50:  99nMAssay Description:Inhibition of human ABHD16A expressed in HEK293 cells preincubated for 30 mins followed by 1-LG substrate addition and measured after 90 to 120 mins ...More 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
TargetPhosphatidylserine lipase ABHD16A(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM50336546(CHEMBL1673415 | Palmostatin B)
Affinity DataIC50:  100nMAssay Description:Inhibition of ABHD16A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylserine lipase ABHD16A(Homo sapiens (Human))
University Of Helsinki

Curated by ChEMBL
LigandPNGBDBM24567((2S)-1-[(2S,3S)-3-hexyl-4-oxooxetan-2-yl]tridecan-...)
Affinity DataIC50:  170nMAssay Description:Inhibition of ABHD16A (unknown origin)More 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
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
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
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
Displayed 1 to 50 (of 216 total ) | Next | Last >>
Jump to: