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Found 77 with Last Name = 'gallaschun' and Initial = 'rj'
TargetCorticotropin-releasing factor receptor 1(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50058163(Butyl-[2,5-dimethyl-7-(2,4,6-trimethyl-phenyl)-7H-...)
Affinity DataKi:  2.70nMAssay Description:Binding affinity of the compound against [125I]-Try0-o-Corticotropin-releasing Factor to Corticotropin releasing hormone receptor 1 from ovineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50058163(Butyl-[2,5-dimethyl-7-(2,4,6-trimethyl-phenyl)-7H-...)
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of binding of [125I]-Tyr0-sauvagine to Corticotropin releasing hormone receptor 2 (CRF2)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246465(US9447114, 26)
Affinity DataIC50: <1nMpH: 7.2Assay Description:TRPC5 cells were induced 20-48 hours, removed from growth plates, and replated at low density (to attain good single-cell physical separation) on gla...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246466(US9447114, 27)
Affinity DataIC50: <1nMpH: 7.2Assay Description:TRPC5 cells were induced 20-48 hours, removed from growth plates, and replated at low density (to attain good single-cell physical separation) on gla...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246446(US9447114, 2)
Affinity DataIC50: <1nMpH: 7.2Assay Description:TRPC5 cells were induced 20-48 hours, removed from growth plates, and replated at low density (to attain good single-cell physical separation) on gla...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246445(US9447114, 1)
Affinity DataIC50: <1nMpH: 7.2Assay Description:TRPC5 cells were induced 20-48 hours, removed from growth plates, and replated at low density (to attain good single-cell physical separation) on gla...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246463(US9447114, 24)
Affinity DataIC50:  1.84nMpH: 7.2Assay Description:TRPC5 cells were induced 20-48 hours, removed from growth plates, and replated at low density (to attain good single-cell physical separation) on gla...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246465(US9447114, 26)
Affinity DataIC50:  1.91nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20954(2-(4-methoxy-2,6-dimethylphenoxy)-3,6-dimethyl-4-(...)
Affinity DataIC50:  2nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20950(2-(4-bromo-2,6-dimethylphenoxy)-3,6-dimethyl-4-(pe...)
Affinity DataIC50:  2.60nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20959(2-Aryloxy-4-alkoxy-pyridine, 40 | 2-[4-(methoxymet...)
Affinity DataIC50:  3.20nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20971(2-Arylamino-4-alkyloxypyridine, 13 | 3,6-dimethyl-...)
Affinity DataIC50:  3.70nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20966(2-Aryloxy-4-alkylaminopyridine, 3a | 3,6-dimethyl-...)
Affinity DataIC50:  5.10nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM50058163(Butyl-[2,5-dimethyl-7-(2,4,6-trimethyl-phenyl)-7H-...)
Affinity DataIC50:  5.5nMAssay Description:Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20949(2-(4-chloro-2,6-dimethylphenoxy)-3,6-dimethyl-4-(p...)
Affinity DataIC50:  5.5nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20968(2-(4-bromo-2,6-dimethylphenoxy)-3,6-dimethyl-N-(pe...)
Affinity DataIC50:  5.60nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20969(2-Aryloxy-4-alkylaminopyridine, 5a | methyl 2-(4-c...)
Affinity DataIC50:  6.40nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20933(3,6-dimethyl-4-(pentan-3-yloxy)-2-(2,4,6-trimethyl...)
Affinity DataIC50:  6.80nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20933(3,6-dimethyl-4-(pentan-3-yloxy)-2-(2,4,6-trimethyl...)
Affinity DataIC50:  6.80nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20967(2-(4-chloro-2,6-dimethylphenoxy)-3,6-dimethyl-N-(p...)
Affinity DataIC50:  7.20nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM50058164(But-2-enyl-[2,5-dimethyl-7-(2,4,6-trimethyl-phenyl...)
Affinity DataIC50:  7.60nMAssay Description:Inhibition of binding of 70 pM [125I]-Try0-o-Corticotropin-releasing Factor (CFR) to Corticotropin releasing hormone receptor 1 in Rat brain membraneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20935(2-Aryloxy-4-alkoxy-pyridine, 16 | 3-ethyl-6-methyl...)
Affinity DataIC50:  9.10nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20947(2-(2,6-dimethyl-4-propylphenoxy)-3,6-dimethyl-4-(p...)
Affinity DataIC50:  9.80nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20941(2-Aryloxy-4-alkoxy-pyridine, 22 | 3-bromo-6-methyl...)
Affinity DataIC50:  9.80nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20965(2-pyridinoxy-4-alkoxy-pyridine, 14 | 3,6-dimethyl-...)
Affinity DataIC50:  10nMAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20962(2-Aryloxy-4-alkoxy-pyridine, 43 | 4-[(1-methoxybut...)
Affinity DataIC50:  11nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20946(2-(4-ethyl-2,6-dimethylphenoxy)-3,6-dimethyl-4-(pe...)
Affinity DataIC50:  11nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20951(2-(4-iodo-2,6-dimethylphenoxy)-3,6-dimethyl-4-(pen...)
Affinity DataIC50:  12nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20939(2-Aryloxy-4-alkoxy-pyridine, 20 | 6-methyl-4-(pent...)
Affinity DataIC50:  12nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20938(2-Aryloxy-4-alkoxy-pyridine, 19 | 6-methyl-3-nitro...)
Affinity DataIC50:  15nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246464(US9447114, 25)
Affinity DataIC50:  15.7nMpH: 7.2Assay Description:TRPC5 cells were induced 20-48 hours, removed from growth plates, and replated at low density (to attain good single-cell physical separation) on gla...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20964(2-Aryloxy-4-alkoxy-pyridine, 13 | 3,6-dimethyl-4-[...)
Affinity DataIC50:  16nMAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20952(2-Aryloxy-4-alkoxy-pyridine, 33 | 4-{[3,6-dimethyl...)
Affinity DataIC50:  18nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20955(2-(4-ethoxy-2,6-dimethylphenoxy)-3,6-dimethyl-4-(p...)
Affinity DataIC50:  20nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246453(US9447114, 13)
Affinity DataIC50: <21nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20940(2-Aryloxy-4-alkoxy-pyridine, 21 | N,N,6-trimethyl-...)
Affinity DataIC50:  25nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246462(US9447114, 23)
Affinity DataIC50:  27nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246458(US9447114, 18)
Affinity DataIC50:  27nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246450(US9447114, 6)
Affinity DataIC50: <27nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246456(US9447114, 16)
Affinity DataIC50:  27nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246449(US9447114, 5)
Affinity DataIC50: <27nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20961(2-Aryloxy-4-alkoxy-pyridine, 42 | 4-(butan-2-yloxy...)
Affinity DataIC50:  28nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20970(2-(4-chloro-2,6-dimethylphenoxy)-4-{[(2S)-1-hydrox...)
Affinity DataIC50:  31nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246457(US9447114, 17)
Affinity DataIC50:  31.6nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20948(2-(4-fluoro-2,6-dimethylphenoxy)-3,6-dimethyl-4-(p...)
Affinity DataIC50:  32nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246451(US9447114, 7)
Affinity DataIC50:  34.9nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20957(2-Aryloxy-4-alkoxy-pyridine, 38 | 4-{[3,6-dimethyl...)
Affinity DataIC50:  40nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20960(2-(4-{[3,6-dimethyl-4-(pentan-3-yloxy)pyridin-2-yl...)
Affinity DataIC50:  40nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetShort transient receptor potential channel 5(Homo sapiens (Human))
Hydra Biosciences

US Patent
LigandPNGBDBM246448(US9447114, 4)
Affinity DataIC50:  55nMpH: 7.4 T: 2°CAssay Description:The commercially available HEK293/TREx line (Invitrogen) was stably transfected with a TRPC5 construct and screened by conventional calcium imaging t...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetCorticotropin-releasing factor receptor 1(Rattus norvegicus (rat))
Pfizer

LigandPNGBDBM20958((4-{[3,6-dimethyl-4-(pentan-3-yloxy)pyridin-2-yl]o...)
Affinity DataIC50:  61nMpH: 7.0 T: 2°CAssay Description:The IC50 values were measured by monitoring the inhibition effects of test compounds on [125I]-o-CRF binding to rat cortex in vitro. More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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