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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391288![]() (CHEMBL5288438) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391281![]() (CHEMBL5286642) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | 1.39E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM325598![]() (3-[5-(1-Cyclopropylmethyl-piperidin-4-yl)-[1,3,4]o...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | n/a | n/a | 3.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM325596![]() (3-[5-(1-Cyclobutyl-piperidin-4-yl)-[1,3,4]oxadiazo...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | n/a | n/a | 3.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50403292![]() (CHEMBL5285364) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL KEGG PC cid PC sid UniChem Similars | n/a | n/a | 3.77E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-2 adrenergic receptor from guinea pig trachea. | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM325597![]() (1-Isopropyl-3-[5-(1-isopropyl-piperidin-4-yl)-[1,3...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM325594![]() (3-[5-(1-Cyclobutylmethyl-piperidin-4-yl)-[1,3,4]ox...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391283![]() (CHEMBL5268064) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM325561![]() (1-Isopropyl-3-{5-[1-(3-methoxy propyl) piperidin-4...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | Purchase MCE PC cid PC sid UniChem | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM325602![]() (1-Isopropyl-3-{5-[1-(tetrahydro-pyran-4-ylmethyl)-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig left atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391298![]() (CHEMBL5275605) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for alpha-adrenergic activity against Alpha-1 adrenergic receptor from rat aorta. | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391278![]() (CHEMBL5274204) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description The compound was tested for beta-adrenergic activity against Beta-1 adrenergic receptor from guinea pig right atria | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391267![]() (CHEMBL5289747) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | Purchase CHEMBL MCE PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description Antagonistic activity against Thromboxane A2 receptor in guinea pig trachea in the presence of 11,9-epoxymethano-PGH2 | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391266![]() (CHEMBL5271080) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | Purchase CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391265![]() (CHEMBL5276171) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391246![]() (CHEMBL5275895) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description Inhibition of rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate | Citation and Details | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cytochrome P450 2D6 (Homo sapiens (Human)) | BDBM50391248![]() (CHEMBL5284140) | PDB UniProtKB/SwissProt GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | n/a | n/a | >4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | |
TBA | Assay Description Evaluated for inhibitory activity against rabbit lung angiotensin I converting enzyme (ACE) using hippuryl-histidyl-leucine as substrate | Citation and Details | |||||||||||
More data for this Ligand-Target Pair |