BDBM50438500 CHEMBL2414822

SMILES: CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O

InChI Key: InChIKey=ORWGLTVVJUYBTM-OEAFFKCNSA-N

Data: 2 KI  3 IC50

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 5 hits for monomerid = 50438500   

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
Acidic alpha-glucosidase (Rattus norvegicus)	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Competitive inhibition of rat intestinal maltase using maltose as substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
alpha-Glucosidase (α-Glucosidase) (Rattus norvegicus (Rat))	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.71E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Competitive inhibition of rat intestinal sucrase using sucrose as substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
alpha-Glucosidase (α-Glucosidase) (Rattus norvegicus (Rat))	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal sucrase using sucrose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
Acidic alpha-glucosidase (Rattus norvegicus)	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of rat intestinal maltase using maltose as substrate assessed as D-glucose release from substrate preincubated for 15 mins measured after ...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair
α-glucosidase (Saccharomyces cerevisiae S288c (Baker's yeast))	BDBM50438500 (CHEMBL2414822) Show SMILES CC(=O)Oc1ccc(\C=C\C(=O)NC[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1OC(C)=O |r| Show InChI InChI=1S/C20H25NO10/c1-10(23)29-13-5-3-12(7-14(13)30-11(2)24)4-6-17(25)21-8-15-18(26)20(28)19(27)16(9-22)31-15/h3-7,15-16,18-20,22,26-28H,8-9H2,1-2H3,(H,21,25)/b6-4+/t15-,16+,18-,19+,20+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.55E+5	n/a	n/a	n/a	n/a	n/a	n/a
Xi'an Jiaotong University Curated by ChEMBL					Assay Description Inhibition of Saccharomyces cerevisiae alpha-glucosidase assessed as 4-nitrophenol release from 4-nitrophenyl alpha-D-glucopyranoside preincubated fo...				Bioorg Med Chem 21: 5442-50 (2013) Article DOI: 10.1016/j.bmc.2013.06.002 BindingDB Entry DOI: 10.7270/Q2HD7X24
					More data for this Ligand-Target Pair