BDBM50105181 4-(4-Chloro-phenoxy)-thieno[2,3-c]pyridine-2-carboxylic acid amide::CHEMBL118518
SMILES: NC(=O)c1cc2c(Oc3ccc(Cl)cc3)cncc2s1
InChI Key: InChIKey=ONVYPVVYNXLFQK-UHFFFAOYSA-N
Data: 5 IC50
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Selectin E (Homo sapiens (Human)) | BDBM50105181 (4-(4-Chloro-phenoxy)-thieno[2,3-c]pyridine-2-carbo...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description Inhibition of selectin E in human endothelial cells | J Med Chem 44: 3469-87 (2001) BindingDB Entry DOI: 10.7270/Q2KW5FBM | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Intercellular adhesion molecule (ICAM-1), Integrin alpha-L/beta-2 (Homo sapiens (Human)) | BDBM50105181 (4-(4-Chloro-phenoxy)-thieno[2,3-c]pyridine-2-carbo...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 9 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description Inhibition of intercellular adhesion molecule-1 (ICAM1) in human endothelial cells | J Med Chem 44: 3469-87 (2001) BindingDB Entry DOI: 10.7270/Q2KW5FBM | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cyclin-Dependent Kinase 9 (CDK9) (Homo sapiens (Human)) | BDBM50105181 (4-(4-Chloro-phenoxy)-thieno[2,3-c]pyridine-2-carbo...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 2.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Genentech, Inc Curated by ChEMBL | Assay Description Inhibition of full length human recombinant His-tagged CDK9/Cyclin T expressed in baculovirus expression system using Cdk7/9tide as substrate by adap... | ACS Med Chem Lett 7: 223-8 (2016) BindingDB Entry DOI: 10.7270/Q29G5PPC | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Cyclin-C (Homo sapiens (Human)) | BDBM50105181 (4-(4-Chloro-phenoxy)-thieno[2,3-c]pyridine-2-carbo...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 6.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Genentech, Inc Curated by ChEMBL | Assay Description Inhibition of full length human recombinant His-tagged CDK8/Cyclin C expressed in baculovirus expression system by fluorescence polarization assay | ACS Med Chem Lett 7: 223-8 (2016) BindingDB Entry DOI: 10.7270/Q29G5PPC | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
VCAM-1 (Homo sapiens (Human)) | BDBM50105181 (4-(4-Chloro-phenoxy)-thieno[2,3-c]pyridine-2-carbo...) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 3.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories Curated by ChEMBL | Assay Description Inhibition of VCAM-1 in human endothelial cells | J Med Chem 44: 3469-87 (2001) BindingDB Entry DOI: 10.7270/Q2KW5FBM | |||||||||||
More data for this Ligand-Target Pair |