BDBM50266966 CHEMBL1662::di(2,6-di-t-butylphenol)
SMILES: CC(C)(C)c1cc(cc(c1O)C(C)(C)C)-c1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C
InChI Key: InChIKey=GSOYMOAPJZYXTB-UHFFFAOYSA-N
Data: 2 KI
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Carbonic anhydrase 2 (Homo sapiens (Human)) | BDBM50266966 (CHEMBL1662 | di(2,6-di-t-butylphenol)) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 290 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Ataturk University Curated by ChEMBL | Assay Description Inhibition of human erythrocyte CA2 esterase activity using 4-nitrophenyl acetate substrate | Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Carbonic anhydrase 1 (Homo sapiens (Human)) | BDBM50266966 (CHEMBL1662 | di(2,6-di-t-butylphenol)) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 3.75E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Ataturk University Curated by ChEMBL | Assay Description Inhibition of human erythrocyte CA1 esterase activity using 4-nitrophenyl acetate substrate | Bioorg Med Chem 17: 3207-11 (2009) Article DOI: 10.1016/j.bmc.2009.01.067 BindingDB Entry DOI: 10.7270/Q2N58M7V | |||||||||||
More data for this Ligand-Target Pair |