Compile Data Set for Download or QSAR
Found 67 with Last Name = 'nellans' and Initial = 'hn'
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230127(CHEMBL407606)copy SMILEScopy InChI
Affinity DataKi:  0.0245nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230129(CHEMBL407123)copy SMILEScopy InChI
Affinity DataKi:  0.0427nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230120(CHEMBL405737)copy SMILEScopy InChI
Affinity DataKi:  0.0776nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230123(CHEMBL385042)copy SMILEScopy InChI
Affinity DataKi:  0.0933nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230122(CHEMBL415571)copy SMILEScopy InChI
Affinity DataKi:  0.155nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230126(CHEMBL385468)copy SMILEScopy InChI
Affinity DataKi:  0.186nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230124(CHEMBL429240)copy SMILEScopy InChI
Affinity DataKi:  0.209nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230128(CHEMBL437798)copy SMILEScopy InChI
Affinity DataKi:  0.380nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230130(CHEMBL266205)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230121(CHEMBL217405)copy SMILEScopy InChI
Affinity DataKi:  2.20nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230125(CHEMBL274682)copy SMILEScopy InChI
Affinity DataKi:  2.60nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetLutropin-choriogonadotropic hormone receptor(Rattus norvegicus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50230119(CHEMBL414071)copy SMILEScopy InChI
Affinity DataKi:  9.30nMAssay Description:Negative logarithm of equilibrium dissociation constant in the rat pituitary luteinizing releasing hormone receptor binding assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24Q7X6MPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017780(CHEMBL284451 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017780(CHEMBL284451 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMpH: 6.0Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017783(CHEMBL440779 | N-{1-[1-(4-Azido-1-cyclohexylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.550nMpH: 6.0Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017783(CHEMBL440779 | N-{1-[1-(4-Azido-1-cyclohexylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.550nMpH: 6.0Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017782(CHEMBL280744 | Tetrahydro-pyran-4-carboxylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 0.700nMpH: 6.0Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050056(2-[(R)-1-[(S)-2-(3-Cyclohexyl-3-methyl-ureido)-4-m...)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017777(CHEMBL281436 | N-[1-[1-(4-Azido-1-cyclohexylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 2nMpH: 6.0Assay Description:Inhibitory activity against human plasma renin at pH 7.4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017778(CHEMBL282757 | Morpholine-4-carboxylic acid {1-[1-...)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMpH: 7.4Assay Description:Inhibitory activity against human plasma renin at pH 7.4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017778(CHEMBL282757 | Morpholine-4-carboxylic acid {1-[1-...)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMpH: 7.4Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017773(CHEMBL280503 | Morpholine-4-carboxylic acid [1-[1-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMpH: 6.0Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050063(2-[(R)-1-[(S)-2-(Cyclohexyl-methyl-carbamoyloxy)-4...)copy SMILEScopy InChI
Affinity DataIC50: 4.60nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017774(CHEMBL29004 | {1-[1-(4-Azido-1-cyclohexylmethyl-2,...)copy SMILEScopy InChI
Affinity DataIC50: 4.80nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017779(CHEMBL28679 | {1-[1-(4-Azido-1-cyclohexylmethyl-2-...)copy SMILEScopy InChI
Affinity DataIC50: 5.40nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017775(CHEMBL29315 | {1-[1-(3-Azido-1-cyclohexylmethyl-2-...)copy SMILEScopy InChI
Affinity DataIC50: 7.5nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017782(CHEMBL280744 | Tetrahydro-pyran-4-carboxylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 7.60nMpH: 7.4Assay Description:Inhibitory activity against purified human plasma renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017780(CHEMBL284451 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 9nMpH: 7.4Assay Description:Inhibitory activity against human plasma renin at pH 7.4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050058(2-[(R)-1-((S)-2-Cyclohexylcarbamoyloxy-4-methyl-pe...)copy SMILEScopy InChI
Affinity DataIC50: 9.30nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017786(CHEMBL408084 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 10nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017777(CHEMBL281436 | N-[1-[1-(4-Azido-1-cyclohexylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 10nMpH: 7.4Assay Description:Inhibitory activity against human plasma renin at pH 7.4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050047(2-[(R)-1-[(S)-2-(3-Cyclohexyl-ureido)-4-methyl-pen...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050064(2-[(R)-1-((S)-2-Cyclohexyloxycarbonyloxy-4-methyl-...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017773(CHEMBL280503 | Morpholine-4-carboxylic acid [1-[1-...)copy SMILEScopy InChI
Affinity DataIC50: 20nMpH: 7.4Assay Description:Inhibitory activity against human plasma renin at pH 7.4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017776(CHEMBL28701 | {1-[1-(4-Azido-1-cyclohexylmethyl-2-...)copy SMILEScopy InChI
Affinity DataIC50: 20nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050051(2-[(R)-1-((S)-2-Cyclohexylcarbamoyloxy-4-methyl-pe...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050055(2-[(R)-1-[(S)-2-(3-Cyclohexyl-1-methyl-ureido)-4-m...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050059(2-[(R)-1-[(S)-2-(3-Cyclohexyl-3-methyl-ureido)-4-m...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017781(CHEMBL432280 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 26nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050061(2-[(R)-1-((R)-2-Cyclohexylcarbamoylmethyl-4-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050060(2-[(R)-1-((S)-2-Cyclohexyloxycarbonylamino-4-methy...)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017785(CHEMBL284891 | {1-[1-(3-Azidomethyl-1-cyclohexylme...)copy SMILEScopy InChI
Affinity DataIC50: 55nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050062(2-[(R)-1-((S)-2-Cyclohexyloxycarbonylamino-4-methy...)copy SMILEScopy InChI
Affinity DataIC50: 76nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050042(2-[(R)-1-[(S)-2-(3-Cyclohexyl-ureido)-4-methyl-pen...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050054(2-[(R)-1-((R)-2-Cyclohexylcarbamoylmethyl-4-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50017784(CHEMBL265319 | {1-[1-(4-Azido-1-cyclohexylmethyl-2...)copy SMILEScopy InChI
Affinity DataIC50: 370nMpH: 6.0Assay Description:Inhibitory activity against purified human renal renin at pH 6.0More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050052(2-[(R)-1-[(S)-2-(3-Cyclohexyl-1-methyl-ureido)-4-m...)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050057(2-[(R)-1-[(S)-2-(2-Cyclohexyl-acetylamino)-4-methy...)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetEndothelin-1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50050053(2-[(R)-1-[(S)-2-(2-Cyclohexyl-acetylamino)-4-methy...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibitory activity was evaluated against human Endothelin A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DB80WGPubMed
TargetRenin(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM912((3S,4S)-3-hydroxy-4-[(2S)-2-[(3S,4S)-3-hydroxy-6-m...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+3nMpH: 6.0Assay Description:Inhibitory activity against human plasma renin at pH 7.4More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2474BFRPubMed
Displayed 1 to 50 (of 67 total ) | Next | Last >>
Jump to: