BDBM50234035 CHEMBL4070008

SMILES: C(Oc1cccc2ccccc12)[C@H]1CCCN1c1ncnc2[nH]cnc12

InChI Key: InChIKey=DUYDXTWDEKJZHW-OAHLLOKOSA-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 = 50234035   

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
Microtubule-associated protein 2 (Homo sapiens (Human))	BDBM50234035 (CHEMBL4070008) Show SMILES C(Oc1cccc2ccccc12)[C@H]1CCCN1c1ncnc2[nH]cnc12 |r| Show InChI InChI=1S/C20H19N5O/c1-2-8-16-14(5-1)6-3-9-17(16)26-11-15-7-4-10-25(15)20-18-19(22-12-21-18)23-13-24-20/h1-3,5-6,8-9,12-13,15H,4,7,10-11H2,(H,21,22,23,24)/t15-/m1/s1	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	450	n/a	n/a	n/a	n/a	n/a	n/a
Merck KGaA Curated by ChEMBL					Assay Description Inhibition of recombinant human N-terminal His tagged MetAP-2 using tripeptide Met-Ala-Ser as substrate preincubated for 15 mins followed by substrat...				Bioorg Med Chem Lett 27: 551-556 (2017) BindingDB Entry DOI: 10.7270/Q2V98BB4
					More data for this Ligand-Target Pair