TargetCatechol O-methyltransferase(Sus scrofa)
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Affinity DataKi: 1.35E+4nMAssay Description:Compound was evaluated for reversible inhibition of Catechol O-methyltransferase with variable AdoMet and saturating catechol as substrate (mixed inh...More data for this Ligand-Target Pair
TargetCatechol O-methyltransferase(Sus scrofa)
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Affinity DataKi: 1.72E+4nMAssay Description:Compound was evaluated for reversible inhibition of Catechol O-methyltransferase with saturating AdoMet and variable catechol as substrate (noncompet...More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 0.00200nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 0.100nMAssay Description:Inhibition of BLK (unknown origin) incubated for 1 hr in presence of ATP by Z'LYTE assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.900nMAssay Description:Inhibition of BTK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
Ligand Info
Affinity DataIC50: 0.900nMAssay Description:Inhibition of BMX (unknown origin) incubated for 1 hr in presence of ATP by Z'LYTE assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.20nMAssay Description:Inhibition of BMX (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADantibodypediaGoogleScholar
Ligand Info
Affinity DataIC50: 1.40nMAssay Description:Inhibition of BLK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 1.5nMAssay Description:Inhibition of BTK (unknown origin) using Blk/Lyntide as substrate preincubated for 1 hr followed by substrate addition and measured after 2 hrs in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 4.90nMAssay Description:Inhibition of ITK (unknown origin) using Blk/Lyntide as substrate preincubated for 1 hr followed by substrate addition and measured after 2 hrs in pr...More data for this Ligand-Target Pair
Affinity DataIC50: 5.30nMAssay Description:Inhibition of EGFR (unknown origin) incubated for 1 hr in presence of ATP by Z'LYTE assayMore data for this Ligand-Target Pair
Affinity DataIC50: 5.70nMAssay Description:Inhibition of BMX (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADantibodypediaGoogleScholar
Ligand Info
Affinity DataIC50: 13nMAssay Description:Inhibition of BTK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
Ligand Info
Affinity DataIC50: 29nMAssay Description:Inhibition of HCK (unknown origin) incubated for 1 hr in presence of ATP by Z'LYTE assayMore data for this Ligand-Target Pair
Affinity DataIC50: 30nMAssay Description:Inhibition of HCK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 33nMAssay Description:Inhibition of JAK3 (unknown origin) incubated for 1 hr in presence of ATP by Z'LYTE assayMore data for this Ligand-Target Pair
Affinity DataIC50: 34nMAssay Description:Inhibition of SRC (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 36nMAssay Description:Inhibition of BLK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 44nMAssay Description:Covalent inhibition of NanoLuc fused BTK (unknown origin) expressed in HEK293 cells incubated for 90 mins by NanoBRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: 109nMAssay Description:Covalent inhibition of NanoLuc fused BTK (unknown origin) expressed in HEK293 cells incubated for 90 mins by NanoBRET assayMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
Ligand Info
Affinity DataIC50: 114nMAssay Description:Inverse agonist activity at RARalpha (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 197nMAssay Description:Inhibition of EGFR (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 210nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 226nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 308nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 314nMAssay Description:Covalent inhibition of NanoLuc fused BTK (unknown origin) expressed in HEK293 cells incubated for 90 mins by NanoBRET assayMore data for this Ligand-Target Pair
Target InfoPDBMMDBNCI pathwayReactome pathwayKEGG
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
UniProtKB/SwissProt
B.MOADDrugBankantibodypediaGoogleScholar
Ligand Info
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 318nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 344nMAssay Description:Inhibition of ITK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 654nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 874nMAssay Description:Inhibition of JAK3 (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 1.28E+3nMAssay Description:Antagonist activity at Gal4-fused RARalpha (unknown origin) transfected in HEK293 cells assessed as inhibition of ATRA-induced transcriptional activi...More data for this Ligand-Target Pair
TargetCatechol O-methyltransferase(Sus scrofa)
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibition of Catechol-O-methyltransferase (COMT) from isolated partially purified pig liver enzymeMore data for this Ligand-Target Pair
TargetCatechol O-methyltransferase(Sus scrofa)
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibition of Catechol-O-methyltransferase (COMT) from isolated partially purified pig liver enzymeMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 1.61E+3nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.71E+3nMAssay Description:Inhibition of SRC (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
TargetCatechol O-methyltransferase(Sus scrofa)
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibition of Catechol-O-methyltransferase (COMT) from isolated partially purified pig liver enzymeMore data for this Ligand-Target Pair
TargetCatechol O-methyltransferase(Sus scrofa)
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Instituto De QuíMica OrgáNica General (Csic)
Curated by ChEMBL
Affinity DataIC50: 2.10E+3nMAssay Description:In vitro inhibition of Catechol-O-methyltransferase (COMT) from isolated partially purified pig liver enzymeMore data for this Ligand-Target Pair
Affinity DataIC50: 2.31E+3nMAssay Description:Inhibition of HCK (unknown origin) by Z'LYTE assayMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 2.65E+3nMAssay Description:Antagonist activity at Gal4-fused RARalpha (unknown origin) transfected in HEK293 cells assessed as inhibition of ATRA-induced transcriptional activi...More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 3.16E+3nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Universidade De Vigo
Curated by ChEMBL
Universidade De Vigo
Curated by ChEMBL
Affinity DataIC50: 3.37E+3nMAssay Description:Inhibition of recombinant IKKbeta (unknown origin) using ulight-IkappaomegaBalpha as substrate after 2 hrs by LANCE ultra TR-FRET assayMore data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Universidade De Vigo
Curated by ChEMBL
Universidade De Vigo
Curated by ChEMBL
Affinity DataIC50: 4.43E+3nMAssay Description:Inhibition of recombinant IKKbeta (unknown origin) using ulight-IkappaomegaBalpha as substrate after 2 hrs by LANCE ultra TR-FRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.47E+3nMAssay Description:Antagonist activity at Gal4-fused RARalpha (unknown origin) transfected in HEK293 cells assessed as inhibition of ATRA-induced transcriptional activi...More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase LMTK3(Homo sapiens)
San Diego State University
Curated by ChEMBL
San Diego State University
Curated by ChEMBL
Affinity DataIC50: 4.65E+3nMAssay Description:Inhibition of LMTK3 (unknown origin)More data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Universidade De Vigo
Curated by ChEMBL
Universidade De Vigo
Curated by ChEMBL
Affinity DataIC50: 4.75E+3nMAssay Description:Inhibition of recombinant IKKbeta (unknown origin) using ulight-IkappaomegaBalpha as substrate after 2 hrs by LANCE ultra TR-FRET assayMore data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Universidade De Vigo
Curated by ChEMBL
Universidade De Vigo
Curated by ChEMBL
Affinity DataIC50: 4.78E+3nMAssay Description:Inhibition of recombinant IKKbeta (unknown origin) using ulight-IkappaomegaBalpha as substrate after 2 hrs by LANCE ultra TR-FRET assayMore data for this Ligand-Target Pair
TargetNuclear receptor ROR-gamma(Mus musculus)
Torrey Pines Institute For Molecular Studies
Curated by ChEMBL
Torrey Pines Institute For Molecular Studies
Curated by ChEMBL
Affinity DataIC50: 5.10E+3nMAssay Description:Antagonist activity at mouse Gal4-fused DBD RORgamma LBD (Pro-261-end) expressed in TRex-CHOK1 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Universidade De Vigo
Curated by ChEMBL
Universidade De Vigo
Curated by ChEMBL
Affinity DataIC50: 5.16E+3nMAssay Description:Inhibition of recombinant IKKbeta (unknown origin) using ulight-IkappaomegaBalpha as substrate after 2 hrs by LANCE ultra TR-FRET assayMore data for this Ligand-Target Pair
TargetNuclear receptor ROR-gamma(Mus musculus)
Torrey Pines Institute For Molecular Studies
Curated by ChEMBL
Torrey Pines Institute For Molecular Studies
Curated by ChEMBL
Affinity DataIC50: 5.60E+3nMAssay Description:Antagonist activity at mouse Gal4-fused DBD RORgamma LBD (Pro-261-end) expressed in TRex-CHOK1 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
TargetNuclear receptor ROR-gamma(Mus musculus)
Torrey Pines Institute For Molecular Studies
Curated by ChEMBL
Torrey Pines Institute For Molecular Studies
Curated by ChEMBL
Affinity DataIC50: 5.80E+3nMAssay Description:Antagonist activity at mouse Gal4-fused DBD RORgamma LBD (Pro-261-end) expressed in TRex-CHOK1 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair