BDBM50049386 1,3-Dioxa-cyclopenta[b]fluoren-9-one::CHEMBL348920

SMILES: O=C1c2ccccc2-c2cc3OCOc3cc12

InChI Key: InChIKey=DHARSBAXFUGPFO-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50049386   

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
Adenosine receptor A1 (Rattus norvegicus (rat))	BDBM50049386 (1,3-Dioxa-cyclopenta[b]fluoren-9-one | CHEMBL34892...) Show SMILES O=C1c2ccccc2-c2cc3OCOc3cc12 Show InChI InChI=1S/C14H8O3/c15-14-9-4-2-1-3-8(9)10-5-12-13(6-11(10)14)17-7-16-12/h1-6H,7H2	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	8.89E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Displacement of specific [3H]-PIA binding from adenosine A1 receptor in rat brain membranes.				J Med Chem 39: 781-8 (1996) Article DOI: 10.1021/jm950661k BindingDB Entry DOI: 10.7270/Q2M32TV4
					More data for this Ligand-Target Pair
Adenosine Receptors A2a (A2a) (Rattus norvegicus (rat))	BDBM50049386 (1,3-Dioxa-cyclopenta[b]fluoren-9-one | CHEMBL34892...) Show SMILES O=C1c2ccccc2-c2cc3OCOc3cc12 Show InChI InChI=1S/C14H8O3/c15-14-9-4-2-1-3-8(9)10-5-12-13(6-11(10)14)17-7-16-12/h1-6H,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	8.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Affinity at Adenosine A2A receptor in rat striatal membranes by [3H]- CGS 21680 displacement.				J Med Chem 39: 781-8 (1996) Article DOI: 10.1021/jm950661k BindingDB Entry DOI: 10.7270/Q2M32TV4
					More data for this Ligand-Target Pair