Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5-hydroxytryptamine receptor 1A/1B/1D/1F/2A/2B/2C/3A/3B/4/5A/5B/6/7 (Rattus norvegicus-Rattus norvegicus (rat)-RAT-Ratt...) | BDBM50025223 (CHEMBL343529) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 220 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description In vitro inhibition of Angiotensin I converting enzyme | J Med Chem 27: 41-5 (1984) BindingDB Entry DOI: 10.7270/Q2F76BJN | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
5-hydroxytryptamine receptor 1A/1B/1D/1F/2A/2B/2C/3A/3B/4/5A/5B/6/7 (Rattus norvegicus-Rattus norvegicus (rat)-RAT-Ratt...) | BDBM50028124 (2-(6-Methoxy-1H-indol-3-yl)-ethylamine | 2-(6-meth...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid PDB UniChem Patents Similars | PubMed | n/a | n/a | 630 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description In vitro inhibition of Angiotensin I converting enzyme | J Med Chem 27: 41-5 (1984) BindingDB Entry DOI: 10.7270/Q2F76BJN | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
5-hydroxytryptamine receptor 1A/1B/1D/1F/2A/2B/2C/3A/3B/4/5A/5B/6/7 (Rattus norvegicus-Rattus norvegicus (rat)-RAT-Ratt...) | BDBM50001859 ((buspirone) 8-[4-(4-Pyrimidin-2-yl-piperazin-1-yl)...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Binding affinity at serotonin 5-HT1-type site receptor in rat cortex by displacing [3H]5-HT | J Med Chem 29: 1476-82 (1986) BindingDB Entry DOI: 10.7270/Q2319WGB | |||||||||||
More data for this Ligand-Target Pair |