BDBM50279555 CHEMBL4168853

SMILES: [H][C@@]1(C[C@]2([H])C(=CO[C@@]([H])(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@]2([H])[C@H](C)O1)C(=O)OC)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]1([H])OC=C(C(=O)OC)[C@@]2([H])C[C@H](OC)O[C@@H](C)[C@@]12[H]

InChI Key: InChIKey=CLWBZMLPBZRTKE-SACIIBEWSA-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 = 50279555   

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
Signal transducer and activator of transcription 3 (Homo sapiens (Human))	BDBM50279555 (CHEMBL4168853) Show SMILES [H][C@@]1(C[C@]2([H])C(=CO[C@@]([H])(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@]2([H])[C@H](C)O1)C(=O)OC)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]1([H])OC=C(C(=O)OC)[C@@]2([H])C[C@H](OC)O[C@@H](C)[C@@]12[H] |r,c:5,t:50| Show InChI InChI=1S/C35H52O21/c1-12-22-14(6-20(45-3)50-12)16(30(43)46-4)10-49-33(22)56-35-29(27(41)25(39)19(9-37)53-35)54-21-7-15-17(31(44)47-5)11-48-32(23(15)13(2)51-21)55-34-28(42)26(40)24(38)18(8-36)52-34/h10-15,18-29,32-42H,6-9H2,1-5H3/t12-,13-,14+,15+,18+,19+,20+,21-,22+,23+,24+,25+,26-,27-,28+,29+,32-,33-,34-,35-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Beijing University of Chinese Medicine Curated by ChEMBL					Assay Description Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...				J Nat Prod 80: 3103-3111 (2017) Article DOI: 10.1021/acs.jnatprod.6b01127 BindingDB Entry DOI: 10.7270/Q2QV3Q11
					More data for this Ligand-Target Pair