Affinity DataKi: 0.440nMAssay Description:Binding affinity to human recombinant his-tagged MDM2 assessed as inhibition constant by fluorescence polarization based assayMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 5.80nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 5.80nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Affinity DataKi: 10nMAssay Description:Compound was evaluated for in vitro binding affinity towards Dopamine receptor D2 in rat striatum using [3H]- spiperone as radioligandMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 12nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
Affinity DataKi: 20nMAssay Description:Compound was evaluated for in vitro binding affinity towards serotonin 5-hydroxytryptamine 2 receptor in rat cortex using [3H]- spiperone as radiolig...More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 26nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Affinity DataKi: 40nMAssay Description:Compound was evaluated for in vitro binding affinity towards serotonin 5-hydroxytryptamine 1A receptor receptor in rat hippocampus using [3H]-8-OH-D...More data for this Ligand-Target Pair
Affinity DataKi: 50nMAssay Description:Compound was evaluated for in vitro binding affinity towards 5-hydroxytryptamine 2 receptor in rat cortex using [3H]- spiperone as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 60nMAssay Description:Compound was evaluated for in vitro binding affinity towards 5-hydroxytryptamine 2 receptor in rat cortex using [3H]- spiperone as radioligandMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 120nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 120nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 130nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 140nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 150nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 160nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 200nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 200nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 230nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 260nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 290nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 290nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 350nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 390nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Affinity DataKi: 520nMAssay Description:Compound was evaluated for in vitro binding affinity towards Dopamine receptor D2 in rat striatum using [3H]- spiperone as radioligandMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 520nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 540nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 570nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Affinity DataKi: 640nMAssay Description:Compound was evaluated for in vitro binding affinity towards 5-hydroxytryptamine 1A receptor in rat hippocampus using [3H]-8-OH-DPAT as radioligandMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 780nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 780nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Rattus norvegicus (rat))
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Affinity DataKi: 790nMAssay Description:Compound was evaluated for in vitro binding affinity towards Dopamine receptor D2 in rat striatum using [3H]- spiperone as radioligandMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 880nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 1.03E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
Affinity DataKi: 2.74E+3nMAssay Description:Compound was evaluated for in vitro binding affinity towards Dopamine receptor D1 in striatum using [3H]- SCH 23390 as radioligandMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University Of Virginia
Curated by ChEMBL
University Of Virginia
Curated by ChEMBL
Affinity DataKi: 3.67E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia L1 metallo beta lactamaseMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Hoechst-Roussel Pharmaceuticals
Curated by ChEMBL
Affinity DataKi: 5.75E+3nMAssay Description:Compound was evaluated for in vitro binding affinity towards 5-hydroxytryptamine 1A receptor in rat hippocampus using [3H]-8-OH-DPAT as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 1.44E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin) by competitive Lineweaver-burk plotMore data for this Ligand-Target Pair
Affinity DataIC50: >1nMAssay Description:Compound was tested in vitro for inhibition of rat brain mitochondrial monoamine oxidase BMore data for this Ligand-Target Pair
Affinity DataIC50: >1nMAssay Description:Compound was tested in vitro for inhibition of rat brain mitochondrial monoamine oxidase A.More data for this Ligand-Target Pair
Target6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3(Homo sapiens (Human))
Selvita
Curated by ChEMBL
Selvita
Curated by ChEMBL
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant human His-tagged PFKFB3 expressed in Escherichia coli using fructose-6-phosphate as substrate measured after 2 hrs by ADP-G...More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 receptor antagonism in gel filtered human platelets.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
Affinity DataIC50: 3.70nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine chloride as substrate incubated for 20 mins by DTNB reagent based Ellman's methodMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
Ligand Info
Affinity DataIC50: 4nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
Target6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3(Homo sapiens (Human))
Selvita
Curated by ChEMBL
Selvita
Curated by ChEMBL
Affinity DataIC50: 4nMAssay Description:Inhibition of recombinant human His-tagged PFKFB3 expressed in Escherichia coli using fructose-6-phosphate as substrate measured after 2 hrs by ADP-G...More data for this Ligand-Target Pair