BDBM50269635 CHEMBL463571::leucanthin B

SMILES: C[C@H]1O[C@@]1(C)C(=O)O[C@H]1[C@@H]2[C@H](OC(=O)C2=C)[C@H]2O[C@@]2(C)[C@@H]2O[C@@H]2\C=C(/[C@@H]1OC(C)=O)C(O)=O

InChI Key: InChIKey=YOARICMECKZMHY-XIMYPQPTSA-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 = 50269635   

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
Cyclooxygenase (Homo sapiens (Human))	BDBM50269635 (CHEMBL463571 | leucanthin B) Show SMILES C[C@H]1O[C@@]1(C)C(=O)O[C@H]1[C@@H]2[C@H](OC(=O)C2=C)[C@H]2O[C@@]2(C)[C@@H]2O[C@@H]2\C=C(/[C@@H]1OC(C)=O)C(O)=O |r,c:27| Show InChI InChI=1S/C22H24O11/c1-7-12-14(31-20(27)21(4)8(2)32-21)13(28-9(3)23)10(18(24)25)6-11-16(29-11)22(5)17(33-22)15(12)30-19(7)26/h6,8,11-17H,1H2,2-5H3,(H,24,25)/b10-6+/t8-,11-,12-,13+,14+,15+,16-,17-,21-,22+/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Uppsala University Curated by ChEMBL					Assay Description Inhibition of COX2				J Nat Prod 68: 985-91 (2005) Article DOI: 10.1021/np049655u BindingDB Entry DOI: 10.7270/Q27S7PN5
					More data for this Ligand-Target Pair