BindingDB PrimarySearch

BDBM5416 4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-6-yl]phenoxy}ethyl)morpholine::CHEMBL324153::dorsomorphin (6K1)::pyrazolo[1,5-a]pyrimidine 4h

SMILES: C(CN1CCOCC1)Oc1ccc(cc1)-c1cnc2c(cnn2c1)-c1ccncc1

InChI Key: InChIKey=OOQJIJYKWXLQNC-UHFFFAOYSA-N

Data: 10 IC50 3 EC50

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 13 hits for monomerid = 5416
Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	k_off s^-1	k_on M^-1s^-1	pH	Temp °C
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	7.4	22
Merck Research Laboratories					Assay Description Activated KDR was incubated with 25 uM/10 uCi of [gamma-33P] ATP, poly-Glu/Tyr, and inhibitors in kinase buffer for 15 min at 22 °C. The reactio...				Bioorg Med Chem Lett 12: 2767-70 (2002) Article DOI: 10.1016/s0960-894x(02)00525-5 BindingDB Entry DOI: 10.7270/Q2NG4NTG
Merck Research Laboratories					More data for this Ligand-Target Pair
Bone morphogenetic protein (Danio rerio (Zebrafish))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a
Vanderbilt University					Assay Description The effects on zebrafish embryos with respect to the dorsoventral (DV) axis. For dorsalization, the EC100 (effective concentration 100%) represents t...				ACS Chem Biol 5: 245-53 (2010) Article DOI: 10.1021/cb9002865 BindingDB Entry DOI: 10.7270/Q2JW8C78
Vanderbilt University					More data for this Ligand-Target Pair
Bone morphogenetic protein (Danio rerio (Zebrafish))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	5.00E+3	n/a	n/a	n/a	n/a
Vanderbilt University					Assay Description For ISV disruption, the EC50 represents the concentration when the formation of about 50% of the ISVs is inhibited.				ACS Chem Biol 5: 245-53 (2010) Article DOI: 10.1021/cb9002865 BindingDB Entry DOI: 10.7270/Q2JW8C78
Vanderbilt University					More data for this Ligand-Target Pair
Bone morphogenetic protein (Danio rerio (Zebrafish))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a
Vanderbilt University					Assay Description For nonspecific toxicity, the EC100 represents the concentration when 100% of the treated embryos exhibit either early lethality within hours of comp...				ACS Chem Biol 5: 245-53 (2010) Article DOI: 10.1021/cb9002865 BindingDB Entry DOI: 10.7270/Q2JW8C78
Vanderbilt University					More data for this Ligand-Target Pair
Bone morphogenetic protein 4 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Inhibition of BMP4 (unknown origin)-induced phosphorylation of SMAD 1/5/8 by cytoblot cellular ELISA				Bioorg Med Chem Lett 18: 4388-92 (2008) Article DOI: 10.1016/j.bmcl.2008.06.052 BindingDB Entry DOI: 10.7270/Q2BR8S0V
Harvard Medical School Curated by ChEMBL					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of c-SRC by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
Ribosomal protein S6 kinase alpha 1 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of RSK1 by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 1 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	210	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of FLT1 by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of FLT3 by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	56	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of KDR by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of LCK by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
MAP kinase-interacting serine/threonine-protein kinase 1 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of MNK1 by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair
Ephrin type-A receptor 2 (Homo sapiens (Human))	BDBM5416 (4-(2-{4-[3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidin-...) Show SMILES Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Ansaris Curated by ChEMBL					Assay Description Inhibition of EphA2 by Hot Spot filtration binding assay				Bioorg Med Chem Lett 20: 6394-9 (2010) Article DOI: 10.1016/j.bmcl.2010.09.088 BindingDB Entry DOI: 10.7270/Q2NP24NB
Ansaris Curated by ChEMBL					More data for this Ligand-Target Pair