BDBM50215224 12-(3-hydroxy-5-pentyl-phenoxy)-dodecanoic acid(2-hydroxy-ethyl)-amide::CHEMBL228404
SMILES: CCCCCc1cc(O)cc(OCCCCCCCCCCCC(=O)NCCO)c1
InChI Key: InChIKey=QUDVCWZKXYUWQP-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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cannabinoid receptor 2 (Homo sapiens (Human)) | BDBM50215224 (12-(3-hydroxy-5-pentyl-phenoxy)-dodecanoic acid(2-...) | PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Similars | Article PubMed | 39 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Siena Curated by ChEMBL | Assay Description Displacement of [3H]CP-55940 from human CB2 receptor expressed in HEK cells | Bioorg Med Chem 15: 5406-16 (2007) Article DOI: 10.1016/j.bmc.2007.05.060 BindingDB Entry DOI: 10.7270/Q2T154G7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cannabinoid receptor 1 (Homo sapiens (Human)) | BDBM50215224 (12-(3-hydroxy-5-pentyl-phenoxy)-dodecanoic acid(2-...) | PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Similars | Article PubMed | 60 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ degli Studi di Siena Curated by ChEMBL | Assay Description Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK cells | Bioorg Med Chem 15: 5406-16 (2007) Article DOI: 10.1016/j.bmc.2007.05.060 BindingDB Entry DOI: 10.7270/Q2T154G7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat)) | BDBM50215224 (12-(3-hydroxy-5-pentyl-phenoxy)-dodecanoic acid(2-...) | PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL KEGG 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 |
Universit£ degli Studi di Siena Curated by ChEMBL | Assay Description Inhibition of rat brain FAAH assessed as inhibition of [14C]anandamide hydrolysis | Bioorg Med Chem 15: 5406-16 (2007) Article DOI: 10.1016/j.bmc.2007.05.060 BindingDB Entry DOI: 10.7270/Q2T154G7 | |||||||||||
More data for this Ligand-Target Pair |