BDBM50215509 6-methoxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-carboxylic acid::CHEMBL245503

SMILES: COc1ccc2[nH]c3C(OCCc3c2c1)C(O)=O

InChI Key: InChIKey=ZENNAQZPBNWPLL-UHFFFAOYSA-N

Data: 1 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 1 hit for monomerid = 50215509   

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
MAP kinase-activated protein kinase 2 (Homo sapiens (Human))	BDBM50215509 (6-methoxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-...) Show SMILES COc1ccc2[nH]c3C(OCCc3c2c1)C(O)=O |w:8.17| Show InChI InChI=1S/C13H13NO4/c1-17-7-2-3-10-9(6-7)8-4-5-18-12(13(15)16)11(8)14-10/h2-3,6,12,14H,4-5H2,1H3,(H,15,16)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of MK2				Bioorg Med Chem Lett 17: 4657-63 (2007) Article DOI: 10.1016/j.bmcl.2007.05.070 BindingDB Entry DOI: 10.7270/Q2PR7VPC
					More data for this Ligand-Target Pair