Compile Data Set for Download or QSAR
Found 18 of ki data for polymerid = 49001070
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320472((3S,6S,9S,15S)-3-((4R,7S,10S,13S,16S,19R)-13-((1H-...)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50302273((4R,7S,10S,13S,16S,19R)-13-((1H-indol-3-yl)methyl)...)copy SMILEScopy InChI
Affinity DataKi:  0.120nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50302273((4R,7S,10S,13S,16S,19R)-13-((1H-indol-3-yl)methyl)...)copy SMILEScopy InChI
Affinity DataKi:  0.120nMAssay Description:Displacement of [125I]urotensin 2 from rat urotensin 2 receptor expressed in CHOK1 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75GD7PubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320454(AGTAD[CFWKYC]V | CHEMBL1163463)copy SMILEScopy InChI
Affinity DataKi:  0.190nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50240963((S)-3,4-dichloro-N-(1-(4-(3-(dimethylamino)propoxy...)copy SMILEScopy InChI
Affinity DataKi:  3.20nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320471((4R,7S,10S,13S,16S,19R)-13-((1H-indol-3-yl)methyl)...)copy SMILEScopy InChI
Affinity DataKi:  4.10nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50302274((4R,10bR)-4-(3,4-dimethoxyphenyl)-10-(4-ethylpiper...)copy SMILEScopy InChI
Affinity DataKi:  6.30nMAssay Description:Agonist activity at rat urotensin 2 receptor expressed in CHO cells assessed as calcium mobilization by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM86516(ETPDCFWKYCV | Human U-II | L-Ala-Gly-L-Thr-L-Ala-L...)copy SMILEScopy InChI
Affinity DataKi:  6.70nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H993RWPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320466(Ac-[CFWKYC]-NH2 | CHEMBL1165794)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320469(Ac-[CFWKFC]-NH2 | CHEMBL1163471)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320474((7R)-7-(3,4-dimethoxyphenyl)-1-(4-ethylpiperazin-1...)copy SMILEScopy InChI
Affinity DataKi:  34nMAssay Description:Agonist activity at rat urotensin 2 receptor expressed in CHO cells assessed as calcium mobilization by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320470((4R,7S,10S,13S,16S,19R)-19-acetamido-10-(4-aminobu...)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320478(CHEMBL1164523 | N-((S)-1-((S)-1-(4-(3-(dimethylami...)copy SMILEScopy InChI
Affinity DataKi:  600nMAssay Description:Agonist activity at rat urotensin 2 receptor expressed in CHO cells assessed as calcium mobilization at 1000 nM by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320467(Ac-[CFwKYC]-NH2 | CHEMBL1163477)copy SMILEScopy InChI
Affinity DataKi:  610nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50302272(1-(2-(4-benzyl-4-hydroxypiperidin-1-yl)ethyl)-3-(2...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at rat urotensin 2 receptor expressed in CHO cells assessed as calcium mobilization by FLIPRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320468(Ac-[CFWKyC]-NH2 | CHEMBL1163479)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50302272(1-(2-(4-benzyl-4-hydroxypiperidin-1-yl)ethyl)-3-(2...)copy SMILEScopy InChI
Affinity DataKi:  1.48E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H993RWPubMed
TargetUrotensin-2 receptor(RAT)
Johnson& Johnson Pharmaceutical Research& Development

Curated by ChEMBL
LigandPNGBDBM50320473(Ac-[CFWKAC]-NH2 | CHEMBL1165765)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [125I]U2 from rat urotensin 2 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3K9NPubMed