BDBM50110302 Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxalic acid::CHEMBL277988
SMILES: C(CNc1c2ccccc2nc2ccccc12)CN1CCCCC1
InChI Key: InChIKey=NXTOUTQSWQTEPN-UHFFFAOYSA-N
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 |
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Histamine H3 receptor (Homo sapiens (Human)) | BDBM50110302 (Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxal...) | Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 188 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Freie Universität Berlin Curated by ChEMBL | Assay Description Affinity for displacement of [125I]-iodoproxyfan from human histamine H3 receptors stably expressed in CHO cells | J Med Chem 45: 1128-41 (2002) BindingDB Entry DOI: 10.7270/Q2H70F4V | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Histamine N-methyltransferase (Rattus norvegicus) | BDBM50110302 (Acridin-9-yl-(3-piperidin-1-yl-propyl)-amine; Oxal...) | KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Freie Universität Berlin Curated by ChEMBL | Assay Description Inhibition of rat kidney Histamine N-Methyltransferase (HMT) activity determined by the formation of N-methylhistamine | J Med Chem 45: 1128-41 (2002) BindingDB Entry DOI: 10.7270/Q2H70F4V | |||||||||||
More data for this Ligand-Target Pair |