Compile Data Set for Download or QSAR
Found 93 with Last Name = 'peschke' and Initial = 'b'
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159110(1-(3-(4-(piperidin-1-ylmethyl)phenoxy)propyl)piper...)copy SMILEScopy InChI
Affinity DataKi:  0.200nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50146832(1-(3,4-Dimethoxy-phenyl)-4-[4-(1-ethyl-propyl)-pip...)copy SMILEScopy InChI
Affinity DataKi:  0.380nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM22541(Clobenpropit | N''-[(4-chlorophenyl)methyl]{[3-(1H...)copy SMILEScopy InChI
Affinity DataKi:  0.600nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159113(2-(4-Cyclopropyl-piperazin-1-yl)-6-pyrazol-1-yl-qu...)copy SMILEScopy InChI
Affinity DataKi:  1.10nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159114(CHEMBL179234 | Cyclopropyl-[2-(4-cyclopropyl-piper...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50120543(7-Methyl-2-[4-(3-piperidin-1-yl-propoxy)-phenyl]-i...)copy SMILEScopy InChI
Affinity DataKi:  2nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159116(2-[4-(1-Ethyl-propyl)-piperazin-1-yl]-quinoline | ...)copy SMILEScopy InChI
Affinity DataKi:  2.90nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159122(2-(4-Cyclopropyl-piperazin-1-yl)-6-methoxy-quinoli...)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185376((S)-benzo[b]thiophen-2-yl(2-(pyrrolidin-1-ylmethyl...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185383((S)-(2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl)(5-(...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159121(2-(4-Cyclopropyl-piperazin-1-yl)-quinoline-6-carbo...)copy SMILEScopy InChI
Affinity DataKi:  4.80nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185371((S)-(5-chlorobenzofuran-2-yl)(2-(pyrrolidin-1-ylme...)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185378((S)-2-(2-(pyrrolidin-1-ylmethyl)pyrrolidine-1-carb...)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159120(2-(4-Propyl-piperazin-1-yl)-quinoline | CHEMBL1804...)copy SMILEScopy InChI
Affinity DataKi:  6nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159108(2-(4-Isopropyl-piperazin-1-yl)-quinoline | CHEMBL3...)copy SMILEScopy InChI
Affinity DataKi:  6.80nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185382((S)-(7-ethoxybenzofuran-2-yl)(2-(pyrrolidin-1-ylme...)copy SMILEScopy InChI
Affinity DataKi:  7nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185370((S)-(2-(piperidin-1-ylmethyl)pyrrolidin-1-yl)(5-(t...)copy SMILEScopy InChI
Affinity DataKi:  7nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185377((S)-(2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl)(5-(...)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185381((S)-(3-chlorobenzo[b]thiophen-2-yl)(2-(pyrrolidin-...)copy SMILEScopy InChI
Affinity DataKi:  12nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159109(2-(4-Cyclopropyl-piperazin-1-yl)-quinoline | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185372((S)-(2-((diethylamino)methyl)pyrrolidin-1-yl)(5-(t...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185380((S)-(2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl)(6-(...)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159111((R)-2-Quinolin-2-yl-octahydro-pyrido[1,2-a]pyrazin...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185375((S)-(2-(piperidin-1-ylmethyl)pyrrolidin-1-yl)(6-(t...)copy SMILEScopy InChI
Affinity DataKi:  22nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159118(6-Chloro-2-(4-cyclopropyl-piperazin-1-yl)-quinolin...)copy SMILEScopy InChI
Affinity DataKi:  24nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159117(2-(4-Cyclopentyl-piperazin-1-yl)-quinoline | CHEMB...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159123(6-Cyclohexyl-2-(4-cyclopropyl-piperazin-1-yl)-quin...)copy SMILEScopy InChI
Affinity DataKi:  33nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185374((S)-(2-((diethylamino)methyl)pyrrolidin-1-yl)(6-(t...)copy SMILEScopy InChI
Affinity DataKi:  46nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159112(2-(4-Cyclopropyl-piperazin-1-yl)-6-trifluoromethyl...)copy SMILEScopy InChI
Affinity DataKi:  52nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM27213(4-[3-(4-cyclopropanecarbonylphenoxy)propyl]-1H-imi...)copy SMILEScopy InChI
Affinity DataKi:  94nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159115(CHEMBL179306 | [2-(4-Cyclopropyl-piperazin-1-yl)-q...)copy SMILEScopy InChI
Affinity DataKi:  110nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185373((S)-(2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl)(qui...)copy SMILEScopy InChI
Affinity DataKi: >150nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50185379((S)-(2-(piperidin-1-ylmethyl)pyrrolidin-1-yl)(quin...)copy SMILEScopy InChI
Affinity DataKi: >150nMAssay Description:Antagonist activity at human histamine H3 receptor by [35S]GTPgammaS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T1537PPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159124(5,7-Dichloro-2-(4-cyclopropyl-piperazin-1-yl)-quin...)copy SMILEScopy InChI
Affinity DataKi:  300nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159119(7-Chloro-2-(4-cyclopropyl-piperazin-1-yl)-quinolin...)copy SMILEScopy InChI
Affinity DataKi:  323nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50053631(2-(4-Methyl-piperazin-1-yl)-quinoline | 2-(4-methy...)copy SMILEScopy InChI
Affinity DataKi:  410nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50001884(2-[4-(4-Methyl-benzyl)-piperazin-1-yl]-1-(2-methyl...)copy SMILEScopy InChI
Affinity DataKi:  631nMAssay Description:Antagonist potency against human H3 receptor in GTPgamma[S]-AssayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347173(CHEMBL1797527)copy SMILEScopy InChI
Affinity DataKi:  8.00E+3nMAssay Description:Inhibition of recombinant F7a using S-2288 as substrate after 15 mins by linear fitting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347170(CHEMBL1797524)copy SMILEScopy InChI
Affinity DataKi:  4.30E+4nMAssay Description:Inhibition of recombinant F7a using S-2288 as substrate after 15 mins by linear fitting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347172(CHEMBL1797526)copy SMILEScopy InChI
Affinity DataKi:  8.90E+4nMAssay Description:Inhibition of recombinant F7a using S-2288 as substrate after 15 mins by linear fitting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159109(2-(4-Cyclopropyl-piperazin-1-yl)-quinoline | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibiton of [3H]-ketanserin binding to human 5-HT2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159114(CHEMBL179234 | Cyclopropyl-[2-(4-cyclopropyl-piper...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of [125I]-aminopotentidine binding to human H2 histamine receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
Target5-hydroxytryptamine receptor 2A(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159114(CHEMBL179234 | Cyclopropyl-[2-(4-cyclopropyl-piper...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibiton of [3H]-ketanserin binding to human 5-HT2 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159114(CHEMBL179234 | Cyclopropyl-[2-(4-cyclopropyl-piper...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of [3H]-pyrilamine binding to human H1 histamine receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Novo Nordisk A/S

Curated by ChEMBL
LigandPNGBDBM50159114(CHEMBL179234 | Cyclopropyl-[2-(4-cyclopropyl-piper...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibiton of [3H]-histamine binding to human H4 histamine receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N0161TPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347173(CHEMBL1797527)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of recombinant F7a using S-2288 as substrate after 15 mins by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347170(CHEMBL1797524)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of recombinant F7a using S-2288 as substrate after 15 mins by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
TargetCoagulation factor VII(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347172(CHEMBL1797526)copy SMILEScopy InChI
Affinity DataIC50: 1.09E+5nMAssay Description:Inhibition of recombinant F7a using S-2288 as substrate after 15 mins by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Technical University of Denmark

Curated by ChEMBL
LigandPNGBDBM50347169(CHEMBL1797523)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibition of F10a using S-2288 as substrate after 15 mins by competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8M1VPubMed
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