BDBM50233543 CHEMBL4089410

SMILES: COc1ccc(C[C@H]2C[C@H]2CO)cc1OC

InChI Key: InChIKey=KNGUIYRTJMUWSR-QWRGUYRKSA-N

Data: 4 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50233543   

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 1 (Homo sapiens (Human))	BDBM50233543 (CHEMBL4089410) Show SMILES COc1ccc(C[C@H]2C[C@H]2CO)cc1OC |r| Show InChI InChI=1S/C13H18O3/c1-15-12-4-3-9(6-13(12)16-2)5-10-7-11(10)8-14/h3-4,6,10-11,14H,5,7-8H2,1-2H3/t10-,11-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	2.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Atat£rk University Curated by ChEMBL					Assay Description Inhibition of human CA1 using para-nitrophenylacetate as substrate measured over 3 mins by UV-vis spectrophotometric method				J Med Chem 58: 640-50 (2015) BindingDB Entry DOI: 10.7270/Q2PR7Z6B
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50233543 (CHEMBL4089410) Show SMILES COc1ccc(C[C@H]2C[C@H]2CO)cc1OC |r| Show InChI InChI=1S/C13H18O3/c1-15-12-4-3-9(6-13(12)16-2)5-10-7-11(10)8-14/h3-4,6,10-11,14H,5,7-8H2,1-2H3/t10-,11-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Atat£rk University Curated by ChEMBL					Assay Description Inhibition of human CA2 using para-nitrophenylacetate as substrate measured over 3 mins by UV-vis spectrophotometric method				J Med Chem 58: 640-50 (2015) BindingDB Entry DOI: 10.7270/Q2PR7Z6B
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50233543 (CHEMBL4089410) Show SMILES COc1ccc(C[C@H]2C[C@H]2CO)cc1OC |r| Show InChI InChI=1S/C13H18O3/c1-15-12-4-3-9(6-13(12)16-2)5-10-7-11(10)8-14/h3-4,6,10-11,14H,5,7-8H2,1-2H3/t10-,11-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Atat£rk University Curated by ChEMBL					Assay Description Inhibition of human CA9 by stopped-flow CO2 hydration method				J Med Chem 58: 640-50 (2015) BindingDB Entry DOI: 10.7270/Q2PR7Z6B
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50233543 (CHEMBL4089410) Show SMILES COc1ccc(C[C@H]2C[C@H]2CO)cc1OC |r| Show InChI InChI=1S/C13H18O3/c1-15-12-4-3-9(6-13(12)16-2)5-10-7-11(10)8-14/h3-4,6,10-11,14H,5,7-8H2,1-2H3/t10-,11-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Atat£rk University Curated by ChEMBL					Assay Description Inhibition of human CA12 by stopped-flow CO2 hydration method				J Med Chem 58: 640-50 (2015) BindingDB Entry DOI: 10.7270/Q2PR7Z6B
					More data for this Ligand-Target Pair