Compile Data Set for Download or QSAR
Report error Found 247 Enz. Inhib. hit(s) with all data for entry = 8563
TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258794BDBM258794(US9499482, 213)
Affinity DataKi:  0.300nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258758BDBM258758(US9499482, 157)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258817BDBM258817(US9499482, 252)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258754BDBM258754(US9499482, 153)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258767BDBM258767(US9499482, 167)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258797BDBM258797(US9499482, 216)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258766BDBM258766(US9499482, 166)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258763BDBM258763(US9499482, 163)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258795BDBM258795(US9499482, 214)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258778BDBM258778(US9499482, 184)
Affinity DataKi:  0.400nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258709BDBM258709(US9499482, 108)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258755BDBM258755(US9499482, 154)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258756BDBM258756(US9499482, 155)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258769BDBM258769(US9499482, 169)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258752BDBM258752(US9499482, 151)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258715BDBM258715(US9499482, 114)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258764BDBM258764(US9499482, 164)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258713BDBM258713(US9499482, 112)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258793BDBM258793(US9499482, 212)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258762BDBM258762(US9499482, 161)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258711BDBM258711(US9499482, 110)
Affinity DataKi:  0.5nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258771BDBM258771(US9499482, 171)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258787BDBM258787(US9499482, 205)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258786BDBM258786(US9499482, 193)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258783BDBM258783(US9499482, 189)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258784BDBM258784(US9499482, 190)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258747BDBM258747(US9499482, 146)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258779BDBM258779(US9499482, 185)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258825BDBM258825(US9499482, 260)
Affinity DataKi:  0.600nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258757BDBM258757(US9499482, 156)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258831BDBM258831(US9499482, 266)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258751BDBM258751(US9499482, 150)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258799BDBM258799(US9499482, 218)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258800BDBM258800(US9499482, 219)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258765BDBM258765(US9499482, 165)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258798BDBM258798(US9499482, 217)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258743BDBM258743(US9499482, 142)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258776BDBM258776(US9499482, 176)
Affinity DataKi:  0.700nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258693BDBM258693(US9499482, 92)
Affinity DataKi:  0.75nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258822BDBM258822(US9499482, 257)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258673BDBM258673(US9499482, 72)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258658BDBM258658(US9499482, 57)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258749BDBM258749(US9499482, 148)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258829BDBM258829(US9499482, 264)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258750BDBM258750(US9499482, 149)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258666BDBM258666(US9499482, 65)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258746BDBM258746(US9499482, 145)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258744BDBM258744(US9499482, 143)
Affinity DataKi:  0.800nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258773BDBM258773(US9499482, 173)
Affinity DataKi:  0.900nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

TargetMelanin-concentrating hormone receptor 1 [E4Q,A5T](Human)
Bristol-Myers Squibb

US Patent
LigandChemical structure of BindingDB Monomer ID 258789BDBM258789(US9499482, 207)
Affinity DataKi:  0.900nMpH: 7.4Assay Description:An in vitro binding assay was used to determine the compound Ki value or ability to antagonize binding of a peptide agonist to the human melanin conc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2017
Entry Details
US Patent

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