BDBM50424325 CHEMBL2314760

SMILES: N[C@@H]1CCN(C1)c1nc(N)nc2[nH]c(cc12)-c1ccc(F)cc1

InChI Key: InChIKey=PEQLQRNUKZZPNP-LLVKDONJSA-N

Data: 1 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 1 hit for monomerid = 50424325   

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
Histamine H4 receptor (Homo sapiens (Human))	BDBM50424325 (CHEMBL2314760) Show SMILES N[C@@H]1CCN(C1)c1nc(N)nc2[nH]c(cc12)-c1ccc(F)cc1 |r| Show InChI InChI=1S/C16H17FN6/c17-10-3-1-9(2-4-10)13-7-12-14(20-13)21-16(19)22-15(12)23-6-5-11(18)8-23/h1-4,7,11H,5-6,8,18H2,(H3,19,20,21,22)/t11-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.71E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
KU Leuven Curated by ChEMBL					Assay Description Displacement of [3H]Histamine from human histamine H4 receptor expressed in Sf9 cells co-expressing Galphai/o and Gbeta1gamma				Bioorg Med Chem Lett 23: 132-7 (2012) Article DOI: 10.1016/j.bmcl.2012.10.139 BindingDB Entry DOI: 10.7270/Q28P61TF
					More data for this Ligand-Target Pair