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 H1 receptor (RAT) | BDBM22868![]() (11-(1-methylpiperidin-4-ylidene)-6,11-dihydro-5H-b...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | Purchase CHEBI CHEMBL DrugBank KEGG PC cid PC sid UniChem Patents Similars | Article PubMed | 3.90 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM35938![]() (1-(p-chlorophenyl)-1-(2-pyridyl)-3-N,N-dimethylpro...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | Purchase CHEBI CHEMBL DrugBank KEGG PC cid PC sid UniChem Patents Similars | Article PubMed | 5.5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007464![]() (4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,2-b...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 21 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007461![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 48 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007465![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 51 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007454![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 81 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007466![]() (CHEMBL140924 | [4-(8-Chloro-5,6-dihydro-benzo[5,6]...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 190 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007470![]() (1-[4-(8-Methyl-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 190 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007463![]() (CHEMBL124466 | N-[3-(8-Chloro-5,6-dihydro-benzo[5,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 290 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007473![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 320 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM22876![]() (CHEMBL998 | Claritin | Loratadine | Sch 29851 | US...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | Purchase CHEMBL DrugBank PC cid PC sid UniChem Patents Similars | Article PubMed | 350 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007462![]() (1-[4-(8-Fluoro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 720 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007474![]() (CHEMBL141432 | N-[3-(8-Chloro-5,6-dihydro-benzo[5,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 850 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007472![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007460![]() (1-[4-(9-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007456![]() (1-[4-(8-Methoxy-5,6-dihydro-benzo[5,6]cyclohepta[1...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007467![]() (1-[4-(5,6-Dihydro-benzo[5,6]cyclohepta[1,2-b]pyrid...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007458![]() (1-[4-(9-Fluoro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 2.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007459![]() (1-[4-(8,9-Dichloro-5,6-dihydro-benzo[5,6]cyclohept...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50406423![]() (CHEMBL334318) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007469![]() (1-{4-[(4-Chloro-phenyl)-pyridin-2-yl-methylene]-pi...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | >6.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007475![]() (1-[4-(8-Hydroxy-5,6-dihydro-benzo[5,6]cyclohepta[1...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | >6.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine H1 receptor (RAT) | BDBM50007457![]() (1-[4-(8,9-Difluoro-5,6-dihydro-benzo[5,6]cyclohept...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Binding affinity to histamine H1 receptor in rat brain membranes was evaluated using [3H]-pyrilamine as radioligand | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50000714![]() (3-[4-(2-Chloro-phenyl)-9-methyl-6H-1-thia-5,7,8,9a...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007473![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 610 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007462![]() (1-[4-(8-Fluoro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 670 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007455![]() (1-[4-(8-Bromo-5,6-dihydro-benzo[5,6]cyclohepta[1,2...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 810 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007458![]() (1-[4-(9-Fluoro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 820 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007457![]() (1-[4-(8,9-Difluoro-5,6-dihydro-benzo[5,6]cyclohept...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007470![]() (1-[4-(8-Methyl-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007467![]() (1-[4-(5,6-Dihydro-benzo[5,6]cyclohepta[1,2-b]pyrid...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50002831![]() ((2R,5R)-2,5-Bis-(3,4,5-trimethoxy-phenyl)-tetrahyd...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007459![]() (1-[4-(8,9-Dichloro-5,6-dihydro-benzo[5,6]cyclohept...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007461![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007456![]() (1-[4-(8-Methoxy-5,6-dihydro-benzo[5,6]cyclohepta[1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007460![]() (1-[4-(9-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007475![]() (1-[4-(8-Hydroxy-5,6-dihydro-benzo[5,6]cyclohepta[1...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 8.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007464![]() (4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,2-b...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 1.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007469![]() (1-{4-[(4-Chloro-phenyl)-pyridin-2-yl-methylene]-pi...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 2.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007465![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 3.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50406423![]() (CHEMBL334318) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 4.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM35938![]() (1-(p-chlorophenyl)-1-(2-pyridyl)-3-N,N-dimethylpro...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | Purchase CHEBI CHEMBL DrugBank KEGG PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007466![]() (CHEMBL140924 | [4-(8-Chloro-5,6-dihydro-benzo[5,6]...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007474![]() (CHEMBL141432 | N-[3-(8-Chloro-5,6-dihydro-benzo[5,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM22876![]() (CHEMBL998 | Claritin | Loratadine | Sch 29851 | US...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | Purchase CHEMBL DrugBank PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007463![]() (CHEMBL124466 | N-[3-(8-Chloro-5,6-dihydro-benzo[5,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007472![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM22868![]() (11-(1-methylpiperidin-4-ylidene)-6,11-dihydro-5H-b...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | Purchase CHEBI CHEMBL DrugBank KEGG PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Platelet activating factor receptor (Homo sapiens (Human)) | BDBM50007454![]() (1-[4-(8-Chloro-5,6-dihydro-benzo[5,6]cyclohepta[1,...) | PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Schering-Plough Corporation Curated by ChEMBL | Assay Description Concentration required to cause 50% inhibition of platelet activating factor (PAF)-induced platelet aggregation of human platelet rich plasma when ch... | J Med Chem 34: 457-61 (1991) Article DOI: 10.1021/jm00105a069 BindingDB Entry DOI: 10.7270/Q2BV7FK0 | |||||||||||
More data for this Ligand-Target Pair |