BDBM50128218 CHEMBL302593::Sulfamic acid 5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester

SMILES: CC1(C)OCC(O1)C1OC2OC(C)(C)OC2[C@H]1OS(N)(=O)=O

InChI Key: InChIKey=NEFHIYCLJNJIDP-DVOJEQBISA-N

Data: 3 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 3 hits for monomerid = 50128218   

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))	BDBM50128218 (CHEMBL302593 | Sulfamic acid 5-(2,2-dimethyl-[1,3]...) Show SMILES CC1(C)OCC(O1)C1OC2OC(C)(C)OC2[C@H]1OS(N)(=O)=O Show InChI InChI=1S/C12H21NO8S/c1-11(2)16-5-6(18-11)7-8(21-22(13,14)15)9-10(17-7)20-12(3,4)19-9/h6-10H,5H2,1-4H3,(H2,13,14,15)/t6?,7?,8-,9?,10?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	15	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Montpellier II Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase II				J Med Chem 46: 2197-204 (2003) Article DOI: 10.1021/jm021124k BindingDB Entry DOI: 10.7270/Q28P617T
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50128218 (CHEMBL302593 | Sulfamic acid 5-(2,2-dimethyl-[1,3]...) Show SMILES CC1(C)OCC(O1)C1OC2OC(C)(C)OC2[C@H]1OS(N)(=O)=O Show InChI InChI=1S/C12H21NO8S/c1-11(2)16-5-6(18-11)7-8(21-22(13,14)15)9-10(17-7)20-12(3,4)19-9/h6-10H,5H2,1-4H3,(H2,13,14,15)/t6?,7?,8-,9?,10?/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 Similars	Article PubMed	39	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Montpellier II Curated by ChEMBL					Assay Description Inhibitory concentration against catalytic domain of human cloned carbonic anhydrase IX.				J Med Chem 46: 2197-204 (2003) Article DOI: 10.1021/jm021124k BindingDB Entry DOI: 10.7270/Q28P617T
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50128218 (CHEMBL302593 | Sulfamic acid 5-(2,2-dimethyl-[1,3]...) Show SMILES CC1(C)OCC(O1)C1OC2OC(C)(C)OC2[C@H]1OS(N)(=O)=O Show InChI InChI=1S/C12H21NO8S/c1-11(2)16-5-6(18-11)7-8(21-22(13,14)15)9-10(17-7)20-12(3,4)19-9/h6-10H,5H2,1-4H3,(H2,13,14,15)/t6?,7?,8-,9?,10?/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 Similars	Article PubMed	278	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Montpellier II Curated by ChEMBL					Assay Description Inhibition of human recombinant carbonic anhydrase I				J Med Chem 46: 2197-204 (2003) Article DOI: 10.1021/jm021124k BindingDB Entry DOI: 10.7270/Q28P617T
					More data for this Ligand-Target Pair