BDBM50384599 CHEMBL2036790::US9744172, Compound UNC00000479A

SMILES: CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1ccc(F)nc1

InChI Key: InChIKey=ADELQQCPARGKLR-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50384599   

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
Tyrosine-protein kinase receptor UFO (Homo sapiens (Human))	BDBM50384599 (CHEMBL2036790 | US9744172, Compound UNC00000479A) Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1ccc(F)nc1 |(25.93,-29.7,;27.27,-30.47,;28.6,-29.7,;28.6,-28.15,;29.93,-27.38,;31.27,-28.15,;32.74,-27.67,;33.65,-28.92,;32.74,-30.18,;33.22,-31.64,;32.19,-32.79,;30.68,-32.45,;29.65,-33.59,;30.12,-35.06,;29.09,-36.2,;31.63,-35.38,;32.66,-34.24,;31.27,-29.7,;29.93,-30.47,;33.22,-26.2,;32.19,-25.07,;32.66,-23.61,;34.17,-23.28,;34.64,-21.81,;35.2,-24.43,;34.72,-25.89,)| Show InChI InChI=1S/C18H22FN7/c1-21-18-23-9-14-16(12-4-7-15(19)22-8-12)25-26(17(14)24-18)10-11-2-5-13(20)6-3-11/h4,7-9,11,13H,2-3,5-6,10,20H2,1H3,(H,21,23,24)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	610	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Axl using KKKKEEIYFFF-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assay				ACS Med Chem Lett 3: 129-134 (2012) Article DOI: 10.1021/ml200239k BindingDB Entry DOI: 10.7270/Q2F76DMC
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Mer (Homo sapiens (Human))	BDBM50384599 (CHEMBL2036790 | US9744172, Compound UNC00000479A) Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1ccc(F)nc1 |(25.93,-29.7,;27.27,-30.47,;28.6,-29.7,;28.6,-28.15,;29.93,-27.38,;31.27,-28.15,;32.74,-27.67,;33.65,-28.92,;32.74,-30.18,;33.22,-31.64,;32.19,-32.79,;30.68,-32.45,;29.65,-33.59,;30.12,-35.06,;29.09,-36.2,;31.63,-35.38,;32.66,-34.24,;31.27,-29.7,;29.93,-30.47,;33.22,-26.2,;32.19,-25.07,;32.66,-23.61,;34.17,-23.28,;34.64,-21.81,;35.2,-24.43,;34.72,-25.89,)| Show InChI InChI=1S/C18H22FN7/c1-21-18-23-9-14-16(12-4-7-15(19)22-8-12)25-26(17(14)24-18)10-11-2-5-13(20)6-3-11/h4,7-9,11,13H,2-3,5-6,10,20H2,1H3,(H,21,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	US Patent	n/a	n/a	550	n/a	n/a	n/a	n/a	n/a	n/a
The University of North Carolina at Chapel Hill US Patent					Assay Description The ectopic expression of Mer receptor tyrosine kinase (Mer) has been identified as a tumor cell survival gene product in Acute Lymphoblastic Leukemi...				US Patent US9744172 (2017) BindingDB Entry DOI: 10.7270/Q2PR7Z30
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Mer (Homo sapiens (Human))	BDBM50384599 (CHEMBL2036790 | US9744172, Compound UNC00000479A) Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1ccc(F)nc1 |(25.93,-29.7,;27.27,-30.47,;28.6,-29.7,;28.6,-28.15,;29.93,-27.38,;31.27,-28.15,;32.74,-27.67,;33.65,-28.92,;32.74,-30.18,;33.22,-31.64,;32.19,-32.79,;30.68,-32.45,;29.65,-33.59,;30.12,-35.06,;29.09,-36.2,;31.63,-35.38,;32.66,-34.24,;31.27,-29.7,;29.93,-30.47,;33.22,-26.2,;32.19,-25.07,;32.66,-23.61,;34.17,-23.28,;34.64,-21.81,;35.2,-24.43,;34.72,-25.89,)| Show InChI InChI=1S/C18H22FN7/c1-21-18-23-9-14-16(12-4-7-15(19)22-8-12)25-26(17(14)24-18)10-11-2-5-13(20)6-3-11/h4,7-9,11,13H,2-3,5-6,10,20H2,1H3,(H,21,23,24)	PDB MMDB 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
TBA Curated by ChEMBL					Assay Description Inhibition of Mer expressed in Escherichia coli BL21 (DE3) cells using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electr...				ACS Med Chem Lett 3: 129-134 (2012) Article DOI: 10.1021/ml200239k BindingDB Entry DOI: 10.7270/Q2F76DMC
					More data for this Ligand-Target Pair
Tyrosine-protein kinase receptor TYRO3 (Homo sapiens (Human))	BDBM50384599 (CHEMBL2036790 | US9744172, Compound UNC00000479A) Show SMILES CNc1ncc2c(nn(CC3CCC(N)CC3)c2n1)-c1ccc(F)nc1 |(25.93,-29.7,;27.27,-30.47,;28.6,-29.7,;28.6,-28.15,;29.93,-27.38,;31.27,-28.15,;32.74,-27.67,;33.65,-28.92,;32.74,-30.18,;33.22,-31.64,;32.19,-32.79,;30.68,-32.45,;29.65,-33.59,;30.12,-35.06,;29.09,-36.2,;31.63,-35.38,;32.66,-34.24,;31.27,-29.7,;29.93,-30.47,;33.22,-26.2,;32.19,-25.07,;32.66,-23.61,;34.17,-23.28,;34.64,-21.81,;35.2,-24.43,;34.72,-25.89,)| Show InChI InChI=1S/C18H22FN7/c1-21-18-23-9-14-16(12-4-7-15(19)22-8-12)25-26(17(14)24-18)10-11-2-5-13(20)6-3-11/h4,7-9,11,13H,2-3,5-6,10,20H2,1H3,(H,21,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Tyro3 using EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluid capillary electrophoresis assay				ACS Med Chem Lett 3: 129-134 (2012) Article DOI: 10.1021/ml200239k BindingDB Entry DOI: 10.7270/Q2F76DMC
					More data for this Ligand-Target Pair