Compile Data Set for Download or QSAR
Report error Found 113 Enz. Inhib. hit(s) with all data for entry = 6176
TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113660BDBM113660(US8637501, 64)
Affinity DataKi:  4.60nM ΔG°:  -47.6kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113617BDBM113617(US8637501, 21)
Affinity DataKi:  4.70nM ΔG°:  -47.5kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113619BDBM113619(US8637501, 23)
Affinity DataKi:  4.70nM ΔG°:  -47.5kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113628BDBM113628(US8637501, 32)
Affinity DataKi:  4.90nM ΔG°:  -47.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113625BDBM113625(US8637501, 29)
Affinity DataKi:  5nM ΔG°:  -47.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113659BDBM113659(US8637501, 63)
Affinity DataKi:  5nM ΔG°:  -47.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113626BDBM113626(US8637501, 30)
Affinity DataKi:  5nM ΔG°:  -47.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113623BDBM113623(US8637501, 27)
Affinity DataKi:  5.30nM ΔG°:  -47.2kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113631BDBM113631(US8637501, 35)
Affinity DataKi:  5.80nM ΔG°:  -47.0kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113709BDBM113709(US8637501, 113)
Affinity DataKi:  5.90nM ΔG°:  -47.0kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113699BDBM113699(US8637501, 103)
Affinity DataKi:  6nM ΔG°:  -46.9kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113603BDBM113603(US8637501, 7)
Affinity DataKi:  6nM ΔG°:  -46.9kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113622BDBM113622(US8637501, 26)
Affinity DataKi:  6.10nM ΔG°:  -46.9kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113686BDBM113686(US8637501, 90)
Affinity DataKi:  6.40nM ΔG°:  -46.8kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113620BDBM113620(US8637501, 24)
Affinity DataKi:  6.40nM ΔG°:  -46.8kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113683BDBM113683(US8637501, 87)
Affinity DataKi:  6.90nM ΔG°:  -46.6kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113600BDBM113600(US8637501, 4)
Affinity DataKi:  7.10nM ΔG°:  -46.5kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113613BDBM113613(US8637501, 17)
Affinity DataKi:  7.20nM ΔG°:  -46.5kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113636BDBM113636(US8637501, 40)
Affinity DataKi:  7.20nM ΔG°:  -46.5kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113662BDBM113662(US8637501, 66)
Affinity DataKi:  7.30nM ΔG°:  -46.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113653BDBM113653(US8637501, 57)
Affinity DataKi:  7.30nM ΔG°:  -46.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113646BDBM113646(US8637501, 50)
Affinity DataKi:  7.40nM ΔG°:  -46.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113668BDBM113668(US8637501, 72)
Affinity DataKi:  7.5nM ΔG°:  -46.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113701BDBM113701(US8637501, 105)
Affinity DataKi:  7.60nM ΔG°:  -46.3kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113691BDBM113691(US8637501, 95)
Affinity DataKi:  7.80nM ΔG°:  -46.3kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113648BDBM113648(US8637501, 52)
Affinity DataKi:  7.80nM ΔG°:  -46.3kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113664BDBM113664(US8637501, 68)
Affinity DataKi:  8.20nM ΔG°:  -46.2kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113667BDBM113667(US8637501, 71)
Affinity DataKi:  8.5nM ΔG°:  -46.1kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113684BDBM113684(US8637501, 88)
Affinity DataKi:  8.70nM ΔG°:  -46.0kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113666BDBM113666(US8637501, 70)
Affinity DataKi:  8.80nM ΔG°:  -46.0kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113639BDBM113639(US8637501, 43)
Affinity DataKi:  8.90nM ΔG°:  -46.0kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113708BDBM113708(US8637501, 112)
Affinity DataKi:  8.90nM ΔG°:  -46.0kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113692BDBM113692(US8637501, 96)
Affinity DataKi:  9.20nM ΔG°:  -45.9kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113627BDBM113627(US8637501, 31)
Affinity DataKi:  9.40nM ΔG°:  -45.8kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113669BDBM113669(US8637501, 73)
Affinity DataKi:  9.40nM ΔG°:  -45.8kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113705BDBM113705(US8637501, 109)
Affinity DataKi:  9.60nM ΔG°:  -45.8kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113610BDBM113610(US8637501, 14)
Affinity DataKi:  9.60nM ΔG°:  -45.8kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113703BDBM113703(US8637501, 107)
Affinity DataKi:  9.70nM ΔG°:  -45.7kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113672BDBM113672(US8637501, 76)
Affinity DataKi:  9.80nM ΔG°:  -45.7kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113697BDBM113697(US8637501, 101)
Affinity DataKi:  9.90nM ΔG°:  -45.7kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113670BDBM113670(US8637501, 74)
Affinity DataKi:  10nM ΔG°:  -45.7kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113696BDBM113696(US8637501, 100)
Affinity DataKi:  10nM ΔG°:  -45.7kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113637BDBM113637(US8637501, 41)
Affinity DataKi:  10nM ΔG°:  -45.7kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113599BDBM113599(US8637501, 3)
Affinity DataKi:  10.1nM ΔG°:  -45.6kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113609BDBM113609(US8637501, 13)
Affinity DataKi:  10.3nM ΔG°:  -45.6kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113611BDBM113611(US8637501, 15)
Affinity DataKi:  10.4nM ΔG°:  -45.6kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113630BDBM113630(US8637501, 34)
Affinity DataKi:  10.6nM ΔG°:  -45.5kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113624BDBM113624(US8637501, 28)
Affinity DataKi:  10.9nM ΔG°:  -45.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113673BDBM113673(US8637501, 77)
Affinity DataKi:  11nM ΔG°:  -45.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1(Human)
Albany Molecular Research

US Patent
LigandChemical structure of BindingDB Monomer ID 113661BDBM113661(US8637501, 65)
Affinity DataKi:  11nM ΔG°:  -45.4kJ/molepH: 7.4 T: 2°CAssay Description:Evaluation of the affinity of compounds for the human MCH-1 receptor was accomplished using 4-(3,4,5-tritritiumbenzyloxy)-1-(1-(2-(pyrrolidin-1-yl)et...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/6/2014
Entry Details
US Patent

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