Compile Data Set for Download or QSAR
Found 134 with Last Name = 'rossetti' and Initial = 't'
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326858(CHEMBL1254556 | N-((3R,4R,5S,6R)-2,4-bis(4-chlorob...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326859(CHEMBL1254630 | N-((3R,4R,5S,6R)-4-(4-chlorobenzyl...)copy SMILEScopy InChI
Affinity DataKi:  1.80E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326860(CHEMBL1254711 | N-((3R,4R,5S,6R)-2-(4-chlorobenzyl...)copy SMILEScopy InChI
Affinity DataKi:  2.60E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326861(CHEMBL1254796 | N-((3R,4R,5S,6R)-4-(4-chlorobenzyl...)copy SMILEScopy InChI
Affinity DataKi:  3.50E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326862(4-(diaminomethyleneamino)-N-((3R,4R,5S,6R)-5-hydro...)copy SMILEScopy InChI
Affinity DataKi:  5.10E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326863(3-(diaminomethyleneamino)-N-((3R,4R,5S,6R)-5-hydro...)copy SMILEScopy InChI
Affinity DataKi:  6.30E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326864(CHEMBL1254883 | N-((3R,4R,5S,6R)-4-(4-chlorobenzyl...)copy SMILEScopy InChI
Affinity DataKi:  6.60E+3nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607682(CHEMBL5220685)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607676(CHEMBL5218698)copy SMILES
Affinity DataIC50: 1.90nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607678(CHEMBL5218878)copy SMILES
Affinity DataIC50: 2.10nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607681(CHEMBL5218552)copy SMILES
Affinity DataIC50: 2.20nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607679(CHEMBL5218615)copy SMILES
Affinity DataIC50: 2.40nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607682(CHEMBL5220685)copy SMILES
Affinity DataIC50: 2.5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607683(CHEMBL5219579)copy SMILES
Affinity DataIC50: 3.30nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607676(CHEMBL5218698)copy SMILES
Affinity DataIC50: 3.90nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607680(CHEMBL5218702)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607685(CHEMBL5220647)copy SMILES
Affinity DataIC50: 4.60nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607686(CHEMBL5219830)copy SMILES
Affinity DataIC50: 5.5nMMore data for this Ligand-Target Pair
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607678(CHEMBL5218878)copy SMILES
Affinity DataIC50: 5.5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607684(CHEMBL5219443)copy SMILES
Affinity DataIC50: 5.5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607673(CHEMBL5220895)copy SMILES
Affinity DataIC50: 6.70nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607674(CHEMBL5220347)copy SMILES
Affinity DataIC50: 7.80nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607685(CHEMBL5220647)copy SMILES
Affinity DataIC50: 11nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607672(CHEMBL5220723)copy SMILES
Affinity DataIC50: 12nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607679(CHEMBL5218615)copy SMILES
Affinity DataIC50: 15nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607675(CHEMBL5219922)copy SMILES
Affinity DataIC50: 17nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607680(CHEMBL5218702)copy SMILES
Affinity DataIC50: 17nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607681(CHEMBL5218552)copy SMILES
Affinity DataIC50: 20nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607667(CHEMBL5219530)copy SMILES
Affinity DataIC50: 21nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607684(CHEMBL5219443)copy SMILES
Affinity DataIC50: 23nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607677(CHEMBL5220632)copy SMILES
Affinity DataIC50: 24nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577248(CHEMBL4878379)copy SMILES
Affinity DataIC50: 28nMAssay Description:Inhibition of human soluble adenylyl cyclase assessed as reduction in cAMP levels in the presence of alpha-32p labeled ATP by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1VWQPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607683(CHEMBL5219579)copy SMILES
Affinity DataIC50: 35nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Rattus norvegicus)TBA
LigandPNGBDBM50607677(CHEMBL5220632)copy SMILES
Affinity DataIC50: 38nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326854((Naphth-2-yl)methyl-2-(4'-Aminobutyrylamido)-3-O-(...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Displacement of [125I]iodotyrosyl from human SST5 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607660(CHEMBL5221008)copy SMILES
Affinity DataIC50: 64nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607666(CHEMBL5220075)copy SMILES
Affinity DataIC50: 67nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326878((2R,3S,5R)-5-(3-aminopropylamino)-4-(4-chlorobenzy...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Displacement of [125I]iodotyrosyl from human SST5 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326872(CHEMBL1254140 | Naphth-2-yl)methyl-2-(4'-Aminobuty...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Displacement of [125I]iodotyrosyl from human SST5 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577241(CHEMBL4848035)copy SMILES
Affinity DataIC50: 74nMAssay Description:Inhibition of human soluble adenylyl cyclase assessed as reduction in cAMP levels in the presence of alpha-32p labeled ATP by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1VWQPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607671(CHEMBL5221093)copy SMILES
Affinity DataIC50: 87nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577242(CHEMBL4854762)copy SMILES
Affinity DataIC50: 92nMAssay Description:Inhibition of human soluble adenylyl cyclase transfected (4-4 clones)in human HEK293 cells assessed as reduction in cAMP levels preincubated for 5 mi...More data for this Ligand-Target Pair
TargetSomatostatin receptor type 5(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326879((2R,3S,5R)-5-(2-aminoethylamino)-2-(methoxymethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Displacement of [125I]iodotyrosyl from human SST5 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577241(CHEMBL4848035)copy SMILES
Affinity DataIC50: 102nMAssay Description:Inhibition of human soluble adenylyl cyclase transfected (4-4 clones)in human HEK293 cells assessed as reduction in cAMP levels preincubated for 5 mi...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1VWQPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577243(CHEMBL4868801)copy SMILES
Affinity DataIC50: 107nMAssay Description:Inhibition of human soluble adenylyl cyclase assessed as reduction in cAMP levels in the presence of alpha-32p labeled ATP by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1VWQPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50607662(CHEMBL5219193)copy SMILES
Affinity DataIC50: 112nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057M2BPubMed
TargetMelanin-concentrating hormone receptor 1(Homo sapiens (Human))
Alchemia Ltd

Curated by ChEMBL
LigandPNGBDBM50326865((4'-Chlorobenzyl)3-O-(4'-Chlorobenzyl)-2-deoxy-2-(...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Displacement of [I125I]MCH from human MCH1 receptor expressed in CHO cells by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QC03QKPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577244(CHEMBL4864668)copy SMILES
Affinity DataIC50: 126nMAssay Description:Inhibition of human soluble adenylyl cyclase assessed as reduction in cAMP levels in the presence of alpha-32p labeled ATP by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1VWQPubMed
TargetAdenylate cyclase type 10(Homo sapiens (Human))TBA
LigandPNGBDBM50577236(CHEMBL4857305)copy SMILES
Affinity DataIC50: 132nMAssay Description:Inhibition of human soluble adenylyl cyclase assessed as reduction in cAMP levels in the presence of alpha-32p labeled ATP by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1VWQPubMed
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