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Found 174 with Last Name = 'mahon' and Initial = 'mf'
TargetCholecystokinin receptor type A(RAT)
TBA

Curated by ChEMBL
LigandPNGBDBM50281617(Asp Tyr (OSO3H) Met Gly Trp Met Asp Phe | CHEMBL26...)
Affinity DataIC50:  0.100nMAssay Description:Compound was tested for the inhibition of specific binding of [125I]-Bolton Hunter CCK-8 to Cholecystokinin type A receptor in the rat pancreasMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24341(4-{[(4-chloro-3-hydroxyphenyl)methyl](4H-1,2,4-tri...)
Affinity DataIC50:  0.180nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50281617(Asp Tyr (OSO3H) Met Gly Trp Met Asp Phe | CHEMBL26...)
Affinity DataIC50:  0.300nMAssay Description:Compound was tested for the inhibition of specific binding of [125I]-Bolton Hunter CCK-8 to Cholecystokinin type B receptor in mouse cerebral cortexMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24328(4-{[(4-hydroxy-3-iodophenyl)methyl](4H-1,2,4-triaz...)
Affinity DataIC50:  0.330nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24344(4-({[3-hydroxy-4-(trifluoromethyl)phenyl]methyl}(4...)
Affinity DataIC50:  0.400nMAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10016(4-{[(4-bromophenyl)methyl](4H-1,2,4-triazol-4-yl)a...)
Affinity DataIC50:  0.5nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24342(4-{[(4-bromo-3-hydroxyphenyl)methyl](4H-1,2,4-tria...)
Affinity DataIC50:  0.5nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24332(4-{[(3-chloro-4-hydroxy-5-methoxyphenyl)methyl](4H...)
Affinity DataIC50:  0.510nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24340(4-{[(4-fluoro-3-hydroxyphenyl)methyl](4H-1,2,4-tri...)
Affinity DataIC50:  0.600nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24335((5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  0.770nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10020((2-bromo-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)
Affinity DataIC50:  0.820nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24331(4-({[4-hydroxy-3-(trifluoromethyl)phenyl]methyl}(4...)
Affinity DataIC50:  0.880nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24336((2-chloro-5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)
Affinity DataIC50:  0.920nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24327(4-{[(3-bromo-4-hydroxyphenyl)methyl](4H-1,2,4-tria...)
Affinity DataIC50:  1.10nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24343(4-{[(3-hydroxy-4-methoxyphenyl)methyl](4H-1,2,4-tr...)
Affinity DataIC50:  1.20nMAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24320((4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  1.5nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM13058(6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-...)
Affinity DataIC50:  1.5nMAssay Description:The extent of in vitro inhibition of sulfatase activities was assessed using intact monolayers of JEG-3 cells. Sulfatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10019((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)
Affinity DataIC50:  2.30nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24326(4-{[(3-chloro-4-hydroxyphenyl)methyl](4H-1,2,4-tri...)
Affinity DataIC50:  2.5nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24329(4-{[(4-hydroxy-3-methoxyphenyl)methyl](4H-1,2,4-tr...)
Affinity DataIC50:  2.80nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24339(4-{[(3-hydroxyphenyl)methyl](4H-1,2,4-triazol-4-yl...)
Affinity DataIC50:  2.80nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24323((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)
Affinity DataIC50:  2.90nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24325(4-{[(3-fluoro-4-hydroxyphenyl)methyl](4H-1,2,4-tri...)
Affinity DataIC50:  2.90nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50281619((1R,2S)-1-[(R)-2-(Adamantan-2-yloxycarbonylamino)-...)
Affinity DataIC50:  3.90nMAssay Description:Compound was tested for the inhibition of specific binding of [125I]-Bolton Hunter CCK-8 to Cholecystokinin type B receptor in mouse cerebral cortexMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24337((2-bromo-5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)
Affinity DataIC50:  3.90nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24333(4-{[(3,5-dichloro-4-hydroxyphenyl)methyl](4H-1,2,4...)
Affinity DataIC50:  7.60nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10018((4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  12nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24338((5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  12nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50341860(8-chloro-2-(4-(4-(4-fluorophenyl)-5,6-dihydropyrid...)
Affinity DataIC50:  13nMAssay Description:Inhibition of full length human PARP-1 after 10 mins by FlashPlate scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM50171448((9BETA,14BETA,17BETA)-17-HYDROXY-2-METHOXYESTRA-1,...)
Affinity DataIC50:  16nMAssay Description:Inhibition of steroid sulfatase-mediated coversion of [3H]E1S to E1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10019((2-chloro-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-y...)
Affinity DataIC50:  20nMAssay Description:The extent of in vitro inhibition of sulfatase activities was assessed using intact monolayers of JEG-3 cells. Sulfatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM50134329(CHEMBL122708 | Sulfamic acid (11R,12S,15S,16S)-13-...)
Affinity DataIC50:  22nMAssay Description:Inhibitory concentration against steroid sulfatase in placental microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24324(4-{[(4-hydroxyphenyl)methyl](4H-1,2,4-triazol-4-yl...)
Affinity DataIC50:  23nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24330(5-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]me...)
Affinity DataIC50:  24nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholecystokinin receptor type A(RAT)
TBA

Curated by ChEMBL
LigandPNGBDBM50281619((1R,2S)-1-[(R)-2-(Adamantan-2-yloxycarbonylamino)-...)
Affinity DataIC50:  26nMAssay Description:Compound was tested for the inhibition of specific binding of [125I]-Bolton Hunter CCK-8 to Cholecystokinin type A receptor in the rat pancreasMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24322((2-cyano-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)
Affinity DataIC50:  27nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50237104(2-((8R,9S,13S,14S,16R)-2-ethyl-3-hydroxy-13-methyl...)
Affinity DataIC50:  27nMAssay Description:Inhibitory activity against 17 beta hydroxysteroid dehydrogenase type 1 in T47D cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50341859(2-(4-chlorophenyl)quinoxaline-5-carboxamide | CHEM...)
Affinity DataIC50:  30nMAssay Description:Inhibition of full length human PARP-1 after 10 mins by FlashPlate scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM50171448((9BETA,14BETA,17BETA)-17-HYDROXY-2-METHOXYESTRA-1,...)
Affinity DataIC50:  34nMAssay Description:Inhibitory concentration against steroid sulfatase in placental microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50370656(CHEMBL1627749)
Affinity DataIC50:  37nMAssay Description:Inhibitory activity against 17 beta hydroxysteroid dehydrogenase type 1 in T47D cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
University Of Bath

Curated by ChEMBL
LigandPNGBDBM50370656(CHEMBL1627749)
Affinity DataIC50:  37nMAssay Description:Inhibition of 17-beta HSD1 in T47D cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10020((2-bromo-4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl...)
Affinity DataIC50:  39nMAssay Description:The extent of in vitro inhibition of sulfatase activities was assessed using intact monolayers of JEG-3 cells. Sulfatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM50200936((9BETA,13ALPHA,14BETA,17ALPHA)-2-METHOXYESTRA-1,3,...)
Affinity DataIC50:  39nMAssay Description:Inhibition of steroid sulfatase-mediated coversion of [3H]E1S to E1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10021((3-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  39nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM10018((4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  40nMAssay Description:The extent of in vitro inhibition of sulfatase activities was assessed using intact monolayers of JEG-3 cells. Sulfatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM50219531(17beta-carbamoyloxy-3-sulfamoyloxyestra-1,3,5(10)-...)
Affinity DataIC50:  40nMAssay Description:Inhibition of steroid sulfatase in placental microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAromatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM24321((4-{[(4-cyanophenyl)(4H-1,2,4-triazol-4-yl)amino]m...)
Affinity DataIC50:  42nMpH: 7.5 T: 2°CAssay Description:The extent of in vitro inhibition of aromatase activities was assessed using intact monolayers of JEG-3 cells. Aromatase activity was measured using ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
University Of Bath

LigandPNGBDBM50171450((8R,9S,13S,14S)-2-Methoxy-13-methyl-17-oxo-7,8,9,1...)
Affinity DataIC50:  42nMAssay Description:Inhibitory concentration against steroid sulfatase in placental microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50281620((Z)-2-[(R)-2-(Adamantan-2-yloxycarbonylamino)-3-(1...)
Affinity DataIC50:  54nMAssay Description:Compound was tested for the inhibition of specific binding of [125I]-Bolton Hunter CCK-8 to Cholecystokinin type B receptor in mouse cerebral cortexMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCholecystokinin receptor type A(RAT)
TBA

Curated by ChEMBL
LigandPNGBDBM50281620((Z)-2-[(R)-2-(Adamantan-2-yloxycarbonylamino)-3-(1...)
Affinity DataIC50:  60nMAssay Description:Compound was tested for the inhibition of specific binding of [125I]-Bolton Hunter CCK-8 to Cholecystokinin type A receptor in the rat pancreasMore data for this Ligand-Target Pair
In DepthDetails Article
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