Compile Data Set for Download or QSAR
Found 163 with Last Name = 'nakano' and Initial = 'h'
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232782(CHEMBL4083975)copy SMILEScopy InChI
Affinity DataIC50: 0.280nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232778(CHEMBL4062256)copy SMILEScopy InChI
Affinity DataIC50: 0.400nMAssay Description:Inhibition of full length recombinant human N-terminal GST-tagged PIM3 (1 to 326 end residues) expressed in baculovirus infected sf21 cells using S6K...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232778(CHEMBL4062256)copy SMILEScopy InChI
Affinity DataIC50: 0.410nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232778(CHEMBL4062256)copy SMILEScopy InChI
Affinity DataIC50: 0.490nMAssay Description:Inhibition of full length recombinant human N-terminal His-tagged PIM1 (1 to 313 end residues) expressed in baculovirus infected sf21 cells using S6K...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232779(CHEMBL4060711)copy SMILEScopy InChI
Affinity DataIC50: 0.640nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499276(CHEMBL3735861)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391948(CHEMBL2147767)copy SMILEScopy InChI
Affinity DataIC50: 0.840nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232780(CHEMBL4061176)copy SMILEScopy InChI
Affinity DataIC50: 0.880nMAssay Description:Inhibition of full length recombinant human N-terminal GST-tagged PIM3 (1 to 326 end residues) expressed in baculovirus infected sf21 cells using S6K...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232785(CHEMBL4074201)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499277(CHEMBL3735633)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232780(CHEMBL4061176)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Inhibition of full length recombinant human N-terminal His-tagged PIM1 (1 to 313 end residues) expressed in baculovirus infected sf21 cells using S6K...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391948(CHEMBL2147767)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232780(CHEMBL4061176)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499281(CHEMBL3735816)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232786(CHEMBL4092704)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499279(CHEMBL3735890)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Inhibition of PIM1 (unknown origin) by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232777(CHEMBL4102902)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391946(CHEMBL2147763)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391948(CHEMBL2147767)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232787(CHEMBL4073609)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499279(CHEMBL3735890)copy SMILEScopy InChI
Affinity DataIC50: 2.5nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391938(CHEMBL2147845)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499282(CHEMBL3735657)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232776(CHEMBL4084953)copy SMILEScopy InChI
Affinity DataIC50: 3.80nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499275(CHEMBL3736117)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232784(CHEMBL4094705)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391947(CHEMBL2147764)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391938(CHEMBL2147845)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of PIM1 by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499279(CHEMBL3735890)copy SMILEScopy InChI
Affinity DataIC50: 6.10nMAssay Description:Inhibition of GSK3beta (unknown origin) by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499280(CHEMBL3735412)copy SMILEScopy InChI
Affinity DataIC50: 6.40nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50162967(CHEMBL3792850)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of human N-terminal GST-tagged FLT3 cytoplasmic domain (564 to 993 residues) expressed in baculovirus expression system using fluorescence...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3H89PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50162967(CHEMBL3792850)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human N-terminal GST-tagged FLT3 cytoplasmic domain (564 to 993 residues) expressed in baculovirus expression system using 5-FAM-peptid...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3H89PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391942(CHEMBL2147765)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetDeath-associated protein kinase 1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499279(CHEMBL3735890)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of DAPK1 (unknown origin) by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391938(CHEMBL2147845)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of PIM3 by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232781(CHEMBL4065023)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50232783(CHEMBL4100433)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of PIM1 (unknown origin) using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58PK5PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391939(CHEMBL2147760)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50499278(CHEMBL3735628)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391941(CHEMBL2147762)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50162968(CHEMBL3793843)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human N-terminal GST-tagged FLT3 cytoplasmic domain (564 to 993 residues) expressed in baculovirus expression system using fluorescence...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3H89PubMed
TargetSerine/threonine-protein kinase pim-3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391938(CHEMBL2147845)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of PIM3 (unknown origin) using FL-Peptide 1 (5-FAM-AKRRRLSSLRA-COOH) substrate incubated for 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD50SXPubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50089857(Argadin)copy SMILES
Affinity DataIC50: 33nMAssay Description:Inhibition of Serratia marcescens chitinase ChiBMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50089857(Argadin)copy SMILES
Affinity DataIC50: 33nMAssay Description:Inhibition of Serratia marcescens chitinase ChiBMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50162968(CHEMBL3793843)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Inhibition of human N-terminal GST-tagged FLT3 cytoplasmic domain (564 to 993 residues) expressed in baculovirus expression system using 5-FAM-peptid...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3H89PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50089847(CHEMBL3577620)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of Serratia marcescens chitinase ChiB assessed as reduction in chitinolytic activity using 4MU-(GlcNAc)2 substrate by fluorescence based a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50089847(CHEMBL3577620)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of Serratia marcescens chitinase ChiB assessed as reduction in chitinolytic activity using 4MU-(GlcNAc)2 substrate by fluorescence based a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50162971(CHEMBL3793804)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibition of human N-terminal GST-tagged FLT3 cytoplasmic domain (564 to 993 residues) expressed in baculovirus expression system using 5-FAM-peptid...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3H89PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50163005(CHEMBL3793847)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Inhibition of human N-terminal GST-tagged FLT3 cytoplasmic domain (564 to 993 residues) expressed in baculovirus expression system using 5-FAM-peptid...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TX3H89PubMed
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50391943(CHEMBL2147766)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Inhibition of PIM1 using 5-FAM-RSRHSSYPAGT-CONH2 as substrate after 2 hrs by electrophoretic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33G8PubMed
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