Compile Data Set for Download or QSAR
Report error Found 108 Enz. Inhib. hit(s) with all data for entry = 50012508
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119704BDBM50119704(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  1.60nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119707BDBM50119707(4-[3-(4-Hexanoyl-phenoxy)-propyl]-piperazine-1-car...)
Affinity DataKi:  2nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119710BDBM50119710(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  2.70nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119721BDBM50119721(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  2.70nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119735BDBM50119735(3-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  2.80nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119722BDBM50119722(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  2.90nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119712BDBM50119712(3-Chloro-N-{(S)-1-[3-(4-cyclopropanecarbonyl-pheno...)
Affinity DataKi:  3nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119705BDBM50119705(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  3nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119701BDBM50119701(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  3.5nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119711BDBM50119711(2-Chloro-N-{(S)-1-[3-(4-cyclopropanecarbonyl-pheno...)
Affinity DataKi:  3.70nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119728BDBM50119728(4-Chloro-N-{(S)-1-[3-(4-cyclopropanecarbonyl-pheno...)
Affinity DataKi:  3.80nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50404001BDBM50404001(CHEMBL2112451)
Affinity DataKi:  4nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119720BDBM50119720(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  4.20nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119702BDBM50119702(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  4.60nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119736BDBM50119736(4-Bromo-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  5nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119725BDBM50119725(4-tert-Butyl-N-{(S)-1-[3-(4-cyclopropanecarbonyl-p...)
Affinity DataKi:  5.20nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119733BDBM50119733(N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-...)
Affinity DataKi:  6nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119698BDBM50119698(1-Methyl-1H-imidazole-4-sulfonic acid {(S)-1-[3-(4...)
Affinity DataKi:  10nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119708BDBM50119708(2-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  11nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119730BDBM50119730(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  11nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50404002BDBM50404002(CHEMBL2112452)
Affinity DataKi:  17nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119739BDBM50119739({4-[3-((1S,4S)-5-Benzenesulfonyl-2,5-diaza-bicyclo...)
Affinity DataKi:  19nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119703BDBM50119703(N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-...)
Affinity DataKi:  37nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119723BDBM50119723(N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-...)
Affinity DataKi:  40nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119719BDBM50119719(2-Pyridin-3-yl-thiazole-4-carboxylic acid {(S)-1-[...)
Affinity DataKi:  50nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119706BDBM50119706(2-Pyridin-3-yl-thiazole-4-carboxylic acid {(S)-1-[...)
Affinity DataKi:  55nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119724BDBM50119724((3-{(1S,4S)-5-[3-(4-Cyclopropanecarbonyl-phenoxy)-...)
Affinity DataKi:  71nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119734BDBM50119734(Cyclopropyl-{4-[3-((1S,4S)-5-ethanesulfonyl-2,5-di...)
Affinity DataKi:  120nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119740BDBM50119740({4-[3-((1S,4S)-5-Cyclohexanecarbonyl-2,5-diaza-bic...)
Affinity DataKi:  134nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119713BDBM50119713((S)-N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrroli...)
Affinity DataKi:  151nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119697BDBM50119697(Cyclopropyl-(4-{3-[(1S,4S)-5-(pyridine-2-carbonyl)...)
Affinity DataKi:  191nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119709BDBM50119709(Pyrazine-2-carboxylic acid {(S)-1-[3-(4-acetyl-phe...)
Affinity DataKi:  202nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119729BDBM50119729(Cyclopropyl-(4-{3-[(1S,4S)-5-(furan-2-carbonyl)-2,...)
Affinity DataKi:  208nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119727BDBM50119727((S)-2-({(2S,7S)-5-[3-(4-Cyclopropanecarbonyl-pheno...)
Affinity DataKi:  232nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119717BDBM50119717(Cyclopropyl-(4-{3-[(1S,4S)-5-(4-fluoro-benzoyl)-2,...)
Affinity DataKi:  258nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119728BDBM50119728(4-Chloro-N-{(S)-1-[3-(4-cyclopropanecarbonyl-pheno...)
Affinity DataKi:  290nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119736BDBM50119736(4-Bromo-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  290nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119726BDBM50119726((1-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin...)
Affinity DataKi:  307nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119700BDBM50119700((1-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin...)
Affinity DataKi:  310nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119731BDBM50119731(2-(tert-Butoxycarbonyl-{(3S,6S)-5-[3-(4-cyclopropa...)
Affinity DataKi:  311nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119702BDBM50119702(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  330nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119732BDBM50119732({4-[3-((1S,4S)-5-Benzoyl-2,5-diaza-bicyclo[2.2.1]h...)
Affinity DataKi:  344nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119720BDBM50119720(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  380nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119714BDBM50119714(2-({(2S,7S)-5-[3-(4-Cyclopropanecarbonyl-phenoxy)-...)
Affinity DataKi:  413nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119701BDBM50119701(N-{(S)-1-[3-(4-Cyclopropanecarbonyl-phenoxy)-propy...)
Affinity DataKi:  500nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119715BDBM50119715(((S)-1-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrol...)
Affinity DataKi:  587nMAssay Description:Binding affinity towards rats Histamine type 3 (H3) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119696BDBM50119696(1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...)
Affinity DataKi:  676nMAssay Description:Binding affinity towards rat Histamine H3 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119712BDBM50119712(3-Chloro-N-{(S)-1-[3-(4-cyclopropanecarbonyl-pheno...)
Affinity DataKi:  700nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119708BDBM50119708(2-Cyano-N-{(S)-1-[3-(4-cyclopropanecarbonyl-phenox...)
Affinity DataKi:  710nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50119725BDBM50119725(4-tert-Butyl-N-{(S)-1-[3-(4-cyclopropanecarbonyl-p...)
Affinity DataKi:  730nMAssay Description:Binding affinity towards human Histamine H2 receptor (For compound 11)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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