Found 58 hits Enz. Inhib. hit(s) with all data for entry = 50013190 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM22904
((2R)-1-(1H-imidazol-5-yl)propan-2-amine | (R)-alph...)Show InChI InChI=1S/C6H11N3/c1-5(7)2-6-3-8-4-9-6/h3-5H,2,7H2,1H3,(H,8,9)/t5-/m1/s1 | PDB
Reactome pathway KEGG
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| Article PubMed
| 0.880 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of Histamine H3 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127610
((1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclo...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| CHEMBL PC cid PC sid UniChem
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| Article PubMed
| 1.30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127604
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m0/s1 | PDB
Reactome pathway KEGG
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| 2.5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)Show InChI InChI=1S/C15H24N4S/c20-15(18-13-4-2-1-3-5-13)19-8-6-12(7-9-19)14-10-16-11-17-14/h10-13H,1-9H2,(H,16,17)(H,18,20) | PDB
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| 2.70 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127605
((1S,2S)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m0/s1 | PDB
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| 4.30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127608
(2-[2-(1H-Imidazol-4-yl)-cyclopropyl]-ethylamine | ...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m0/s1 | PDB
Reactome pathway KEGG
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| CHEMBL PC cid PC sid UniChem
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| Article PubMed
| 4.80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127603
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m1/s1 | PDB
Reactome pathway KEGG
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| Article PubMed
| 10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127609
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m0/s1 | PDB
Reactome pathway KEGG
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| 23 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127607
((1R,2R)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m1/s1 | PDB
Reactome pathway KEGG
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| Article PubMed
| 42 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127602
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m1/s1 | PDB
Reactome pathway KEGG
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| Article PubMed
| 65 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127601
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL5938...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m0/s1 | PDB
Reactome pathway KEGG
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| Article PubMed
| 91 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Rattus norvegicus (rat)) | BDBM50127606
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL2940...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m1/s1 | PDB
Reactome pathway KEGG
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| 1.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127601
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL5938...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m0/s1 | PDB
Reactome pathway KEGG
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| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127609
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m0/s1 | PDB
Reactome pathway KEGG
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CHEMBL PC cid PC sid UniChem
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| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127608
(2-[2-(1H-Imidazol-4-yl)-cyclopropyl]-ethylamine | ...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127610
((1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclo...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127606
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL2940...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m1/s1 | PDB
Reactome pathway KEGG
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127602
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m1/s1 | PDB
Reactome pathway KEGG
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127609
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127603
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127610
((1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclo...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127604
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m0/s1 | PDB
Reactome pathway KEGG
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127607
((1R,2R)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127601
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL5938...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127606
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL2940...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127602
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127606
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL2940...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127604
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127603
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127601
(2-(1H-Imidazol-4-yl)-cyclopropylamine | CHEMBL5938...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
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CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2.33E+3 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human H3-receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127604
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 96 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM7966
(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)Show InChI InChI=1S/C5H9N3/c6-2-1-5-3-7-4-8-5/h3-4H,1-2,6H2,(H,7,8) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank Article PubMed
| n/a | n/a | n/a | n/a | 77 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127605
((1S,2S)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 42 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127607
((1R,2R)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 724 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM7966
(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)Show InChI InChI=1S/C5H9N3/c6-2-1-5-3-7-4-8-5/h3-4H,1-2,6H2,(H,7,8) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank Article PubMed
| n/a | n/a | n/a | n/a | 75 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127607
((1R,2R)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127608
(2-[2-(1H-Imidazol-4-yl)-cyclopropyl]-ethylamine | ...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 93 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM22911
(2-(3H-imidazol-4-yl)ethylsulfanylmethanimidamide |...)Show InChI InChI=1S/C6H10N4S/c7-6(8)11-2-1-5-3-9-4-10-5/h3-4H,1-2H2,(H3,7,8)(H,9,10) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.90 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM22911
(2-(3H-imidazol-4-yl)ethylsulfanylmethanimidamide |...)Show InChI InChI=1S/C6H10N4S/c7-6(8)11-2-1-5-3-9-4-10-5/h3-4H,1-2H2,(H3,7,8)(H,9,10) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid PDB UniChem
Patents
Similars
| PDB Article PubMed
| n/a | n/a | n/a | n/a | 51 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127608
(2-[2-(1H-Imidazol-4-yl)-cyclopropyl]-ethylamine | ...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 1.41E+3 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM7966
(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)Show InChI InChI=1S/C5H9N3/c6-2-1-5-3-7-4-8-5/h3-4H,1-2,6H2,(H,7,8) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank Article PubMed
| n/a | n/a | n/a | n/a | 13 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127605
((1S,2S)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 864 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H3 receptor
(Homo sapiens (Human)) | BDBM50127610
((1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclo...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 10 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127605
((1S,2S)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 696 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM7966
(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)Show InChI InChI=1S/C5H9N3/c6-2-1-5-3-7-4-8-5/h3-4H,1-2,6H2,(H,7,8) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank Article PubMed
| n/a | n/a | n/a | n/a | 463 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127602
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6-/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H1 receptor
(Homo sapiens (Human)) | BDBM50127603
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H1 receptor using [3H]-pyrilamine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127609
(C-[2-(1H-Imidazol-4-yl)-cyclopropyl]-methylamine |...)Show InChI InChI=1S/C7H11N3/c8-2-5-1-6(5)7-3-9-4-10-7/h3-6H,1-2,8H2,(H,9,10)/t5-,6+/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H2 receptor
(Homo sapiens (Human)) | BDBM50127610
((1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclo...)Show InChI InChI=1S/C8H13N3/c9-2-1-6-3-7(6)8-4-10-5-11-8/h4-7H,1-3,9H2,(H,10,11)/t6-,7+/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H2 receptor using [3H]-tiotidine |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |
Histamine H4 receptor
(Homo sapiens (Human)) | BDBM50127607
((1R,2R)-2-(1H-Imidazol-4-yl)-cyclopropylamine | (1...)Show InChI InChI=1S/C6H9N3/c7-5-1-4(5)6-2-8-3-9-6/h2-5H,1,7H2,(H,8,9)/t4-,5-/m1/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | >0.000100 | n/a | n/a | n/a | n/a |
Hokkaido University
Curated by ChEMBL
| Assay Description Inhibition of human Histamine H4 receptor |
J Med Chem 46: 1980-8 (2003)
Article DOI: 10.1021/jm020415q BindingDB Entry DOI: 10.7270/Q2XG9QG6 |
More data for this Ligand-Target Pair | |