Compile Data Set for Download or QSAR
Found 89 with Last Name = 'nisato' and Initial = 'd'
TargetVasopressin V1b receptor(RAT)
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  1.30nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V1b receptor(Homo sapiens (Human))
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  1.5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V1b receptor(BOVINE)
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  2.70nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V1b receptor(RAT)
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  3.70nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V1b receptor(Homo sapiens (Human))
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  4.20nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V1a receptor(Homo sapiens (Human))
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  91nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetOxytocin receptor(RAT)
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  270nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V1a receptor(RAT)
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  1.05E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V2 receptor(Homo sapiens (Human))
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  1.41E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
TargetVasopressin V2 receptor(Rattus norvegicus (Rat))
Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database
LigandPNGBDBM50299343((2S,4R)-1-((R)-5-chloro-1-(2,4-dimethoxyphenylsulf...)copy SMILEScopy InChI
Affinity DataKi:  2.90E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8BBWPubMed
LigandPNGBDBM50282260(7-Butyl-8-[2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmeth...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibition of specific binding of [125I]-AII to Angiotensin II receptor, type 1 from rat liver membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66QV
LigandPNGBDBM50042235(2-butyl-3-{[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:In vitro inhibition of specific binding of [125I]-AII to Angiotensin II receptor, type 1 from rat liver membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66QV
LigandPNGBDBM50282261(7-Butyl-10,10-dimethyl-8-[2'-(2H-tetrazol-5-yl)-bi...)copy SMILEScopy InChI
Affinity DataIC50: 2.20nMAssay Description:In vitro inhibition of specific binding of [125I]-AII to Angiotensin II receptor, type 1 from rat liver membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66QV
LigandPNGBDBM50282270(4'-(2-Butyl-4-cyclopentyl-4-methyl-5-oxo-4,5-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 3.30nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282264(2-Butyl-5-cyclohexyl-5-methyl-3-[2'-(1H-tetrazol-5...)copy SMILEScopy InChI
Affinity DataIC50: 5.20nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282264(2-Butyl-5-cyclohexyl-5-methyl-3-[2'-(1H-tetrazol-5...)copy SMILEScopy InChI
Affinity DataIC50: 5.20nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282267(4'-(2-Butyl-4-isopropyl-4-methyl-5-oxo-4,5-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 7.30nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282263(2-Butyl-5-cyclopentyl-5-methyl-3-[2'-(2H-tetrazol-...)copy SMILEScopy InChI
Affinity DataIC50: 7.60nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282262(4'-(2-Butyl-4-cyclohexyl-4-methyl-5-oxo-4,5-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282268(4'-(2-Butyl-4-cyclopropyl-4-methyl-5-oxo-4,5-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282265(4'-(2-Butyl-4-methyl-5-oxo-4-phenyl-4,5-dihydro-im...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50025903(4-(2-{4-[2-(2-tert-Butoxycarbonylamino-3-phenyl-pr...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50024167(3-Hydroxy-4-[2-(3-hydroxy-6-methyl-4-{2-[2-(3-meth...)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50024187(4-(2-{4-[2-(2-tert-Butoxycarbonylamino-3-phenyl-pr...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
LigandPNGBDBM50042244(4'-(2-Butyl-4,4-dimethyl-5-oxo-4,5-dihydro-imidazo...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421779(CHEMBL308300 | CHEMBL3142338)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421775(CHEMBL3142326 | CHEMBL73556)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50226299(CHEMBL3142798)copy SMILEScopy InChI
Affinity DataIC50: 51nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
LigandPNGBDBM50282269(4'-(2-Butyl-4-cyclohexyl-4-ethyl-5-oxo-4,5-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 52nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
LigandPNGBDBM50282257(4'-(7-Butyl-9-oxo-6,8-diaza-spiro[4.5]dec-6-en-8-y...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:In vitro inhibition of specific binding of [125I]-AII to Angiotensin II receptor, type 1 from rat liver membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66QV
LigandPNGBDBM50042240(4'-(2-Butyl-4,4-diethyl-5-oxo-4,5-dihydro-imidazol...)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421770(CHEMBL2311099)copy SMILEScopy InChI
Affinity DataIC50: 65nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
LigandPNGBDBM50282258(4'-(8-Butyl-6-oxo-7,9-diaza-spiro[4.5]dec-8-en-7-y...)copy SMILEScopy InChI
Affinity DataIC50: 71nMAssay Description:In vitro inhibition of specific binding of [125I]-AII to Angiotensin II receptor, type 1 from rat liver membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66QV
LigandPNGBDBM50042239(4'-(2-Butyl-4,4-dicyclopropyl-5-oxo-4,5-dihydro-im...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421783(CHEMBL3142339 | CHEMBL74979)copy SMILEScopy InChI
Affinity DataIC50: 93nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421778(CHEMBL3142325 | CHEMBL75458)copy SMILEScopy InChI
Affinity DataIC50: 112nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421769(CHEMBL3142320 | CHEMBL75210)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421776(CHEMBL310597 | CHEMBL3142315)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50024181(4-(2-{4-[2-[2-tert-Butoxycarbonylamino-3-(1H-indol...)copy SMILEScopy InChI
Affinity DataIC50: 141nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
LigandPNGBDBM50282266(4'-(2-Butyl-4-cyclohexylmethyl-4-methyl-5-oxo-4,5-...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50022516(Boc-Trp-Trp-Sta-Ala-Sta-OMe | CHEMBL3142766)copy SMILEScopy InChI
Affinity DataIC50: 151nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421767(CHEMBL312075 | CHEMBL3142324)copy SMILEScopy InChI
Affinity DataIC50: 151nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50024163(4-[2-(4-{2-[2-Benzyloxycarbonylamino-3-(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 151nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421771(CHEMBL307703 | CHEMBL3142321)copy SMILEScopy InChI
Affinity DataIC50: 174nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421761(CHEMBL2311113)copy SMILEScopy InChI
Affinity DataIC50: 178nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50024174(4-(2-{4-[2-(2-tert-Butoxycarbonylamino-3-phenyl-pr...)copy SMILEScopy InChI
Affinity DataIC50: 191nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
LigandPNGBDBM50282271(4'-[2-Butyl-4-(2,4-dimethyl-pentyl)-4-methyl-5-oxo...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:In vitro binding affinity at Angiotensin II receptor, type 1 from rat liver membrane by [125I]- A II displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M045CQ
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421772(CHEMBL3142323 | CHEMBL75470)copy SMILEScopy InChI
Affinity DataIC50: 251nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421768(CHEMBL3142319 | CHEMBL75987)copy SMILEScopy InChI
Affinity DataIC50: 257nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
TargetRenin(Homo sapiens (Human))
SANOFI Recherche

Curated by ChEMBL
LigandPNGBDBM50421766(CHEMBL3142335 | CHEMBL74682)copy SMILEScopy InChI
Affinity DataIC50: 316nMAssay Description:Inhibition of human plasma reninMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50P7GPubMed
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