Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50541944   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Acidic mammalian chitinase (Homo sapiens (Human))	BDBM50541944 (CHEMBL4648162) Show SMILES Nc1nc(n[nH]1)N1CCC(CC1)N1Cc2ccncc2OC[C@@H]1Cc1ccc(Cl)cc1 |r| Show InChI InChI=1S/C22H26ClN7O/c23-17-3-1-15(2-4-17)11-19-14-31-20-12-25-8-5-16(20)13-30(19)18-6-9-29(10-7-18)22-26-21(24)27-28-22/h1-5,8,12,18-19H,6-7,9-11,13-14H2,(H3,24,26,27,28)/t19-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	55	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics S.A. Curated by ChEMBL					Assay Description Inhibition of full length recombinant C-terminal His-tagged human acidic mammalian chitinase expressed in CHOK1 cells assessed as reduction in chitin...				ACS Med Chem Lett 11: 1228-1235 (2020) Article DOI: 10.1021/acsmedchemlett.0c00092 BindingDB Entry DOI: 10.7270/Q2PV6PX3
					More data for this Ligand-Target Pair
Chitotriosidase-1 (Homo sapiens (Human))	BDBM50541944 (CHEMBL4648162) Show SMILES Nc1nc(n[nH]1)N1CCC(CC1)N1Cc2ccncc2OC[C@@H]1Cc1ccc(Cl)cc1 |r| Show InChI InChI=1S/C22H26ClN7O/c23-17-3-1-15(2-4-17)11-19-14-31-20-12-25-8-5-16(20)13-30(19)18-6-9-29(10-7-18)22-26-21(24)27-28-22/h1-5,8,12,18-19H,6-7,9-11,13-14H2,(H3,24,26,27,28)/t19-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics S.A. Curated by ChEMBL					Assay Description Inhibition of full length recombinant C-terminal His-taged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using ...				ACS Med Chem Lett 11: 1228-1235 (2020) Article DOI: 10.1021/acsmedchemlett.0c00092 BindingDB Entry DOI: 10.7270/Q2PV6PX3
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50541944 (CHEMBL4648162) Show SMILES Nc1nc(n[nH]1)N1CCC(CC1)N1Cc2ccncc2OC[C@@H]1Cc1ccc(Cl)cc1 |r| Show InChI InChI=1S/C22H26ClN7O/c23-17-3-1-15(2-4-17)11-19-14-31-20-12-25-8-5-16(20)13-30(19)18-6-9-29(10-7-18)22-26-21(24)27-28-22/h1-5,8,12,18-19H,6-7,9-11,13-14H2,(H3,24,26,27,28)/t19-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics S.A. Curated by ChEMBL					Assay Description Displacement of Tracer Red from human ERG by fluorescence polarization assay				ACS Med Chem Lett 11: 1228-1235 (2020) Article DOI: 10.1021/acsmedchemlett.0c00092 BindingDB Entry DOI: 10.7270/Q2PV6PX3
					More data for this Ligand-Target Pair