Compile Data Set for Download or QSAR
Found 51 with Last Name = 'kirisits' and Initial = 'm'
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25558(4-arylamino-3-pyridinecarbonitrile, 4p | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataKi:  79nM ΔG°:  -40.1kJ/mole IC50: 70nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25543(4-[(3-bromophenyl)amino]-5-(3,4-dimethoxyphenyl)py...)copy SMILEScopy InChI
Affinity DataKi:  4.90E+3nM ΔG°:  -30.0kJ/mole IC50: 4.60E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25553(4-[(2,4-dichlorophenyl)amino]-5-(3,4-dimethoxyphen...)copy SMILEScopy InChI
Affinity DataIC50: 80nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326333(5-chloro-2-(4-nitrophenoxy)phenol | CHEMBL1240784)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137236(5-Acetylamino-2-{[2-(3-fluoro-4-trifluoromethyl-ph...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25554(4-arylamino-3-pyridinecarbonitrile, 4l | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 160nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326320(3-(2-Hydroxy-4-propylphenoxy)phenyl Boronic Acid |...)copy SMILEScopy InChI
Affinity DataIC50: 174nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137238(2-{[2-(3-Fluoro-4-trifluoromethyl-phenyl)-5-oxo-ox...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326323(4-(2,6-Dihydroxy-4-propylphenoxy)benzamide | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326334(5-chloro-2-(2-nitrophenoxy)phenol | CHEMBL1240785)copy SMILEScopy InChI
Affinity DataIC50: 290nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25551(4-arylamino-3-pyridinecarbonitrile, 4i | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 400nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25555(4-[(2,5-dichlorophenyl)amino]-5-(3,4-dimethoxyphen...)copy SMILEScopy InChI
Affinity DataIC50: 470nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326331(2-(biphenyl-4-yloxy)-5-chlorophenol | CHEMBL124302...)copy SMILEScopy InChI
Affinity DataIC50: 490nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137242(5-Methyl-2-{[5-oxo-2-(4-trifluoromethyl-phenyl)-ox...)copy SMILEScopy InChI
Affinity DataIC50: 830nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25550(4-arylamino-3-pyridinecarbonitrile, 4h | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 900nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137227(5-Chloro-2-{[2-(3-fluoro-4-trifluoromethyl-phenyl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137229(2-{[2-(4-Chloro-phenyl)-5-oxo-oxazol-(4E)-ylidenem...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25546(4-arylamino-3-pyridinecarbonitrile, 4d | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137234(5-Bromo-2-{[2-(3-fluoro-4-trifluoromethyl-phenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25544(4-arylamino-3-pyridinecarbonitrile, 4b | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137233(5-Fluoro-2-{[5-oxo-2-(4-trifluoromethyl-phenyl)-ox...)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25560(4-(2,3-dihydro-1H-inden-5-ylamino)-5-(3,4-dimethox...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326324(1-(2-chlorobenzyl)-4-(3-(9H-carbazol-9-yl)propoxy)...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326322(CHEMBL1243120 | Hexa-2,4-dienoic Acid(4-(2,4-Dichl...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137235(5-Bromo-4-chloro-2-{[5-oxo-2-(4-trifluoromethyl-ph...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326321(CHEMBL1243085 | Hexa-2,4-dienoic Acid(4-(4-Chloro-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137239(2-{[2-(4-Chloro-phenyl)-5-oxo-oxazol-(4E)-ylidenem...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25557(4-arylamino-3-pyridinecarbonitrile, 4o | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25559(4-arylamino-3-pyridinecarbonitrile, 4q | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25556(4-[(3,4-dichlorophenyl)amino]-5-(3,4-dimethoxyphen...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326319(5-chloro-2-(pyridin-3-yloxy)phenol | CHEMBL1240915)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25549(4-[(4-chlorophenyl)amino]-5-(3,4-dimethoxyphenyl)p...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326329(5-Chloro-2-(2,4-dichlorophenoxy)phenyl Pivaloate |...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137230(5-Bromo-2-{[2-(4-chloro-phenyl)-5-oxo-oxazol-(4E)-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25545(4-[(3-chlorophenyl)amino]-5-(3,4-dimethoxyphenyl)p...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137231(5-Methyl-2-{[5-oxo-2-(3-trifluoromethoxy-phenyl)-o...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+3nMAssay Description:In vitro inhibitory activity against acyl carrier protein synthase (AcpS) in Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25552(4-arylamino-3-pyridinecarbonitrile, 4j | 5-(3,4-di...)copy SMILEScopy InChI
Affinity DataIC50: 8.40E+3nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137240(2-{[2-(4-Chloro-phenyl)-5-oxo-oxazol-(4E)-ylidenem...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137237(5-Bromo-2-{[5-oxo-2-(3-trifluoromethoxy-phenyl)-ox...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326328(4-((4-(benzyloxy)-2-oxopyridin-1(2H)-yl)methyl)-3-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137228(5-Fluoro-2-{[2-(4-methoxy-phenyl)-5-oxo-oxazol-(4E...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326330(5-chloro-2-phenoxyaniline | CHEMBL1240673)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326327(1-(2-chlorobenzyl)-4-(4-methoxybenzyloxy)pyridin-2...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326326(1-(2-chlorobenzyl)-4-(benzyloxy)pyridin-2(1H)-one ...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326325(1-(2-chloro-4-nitrobenzyl)-4-(benzyloxy)pyridin-2(...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137232(5-Chloro-2-{[5-oxo-2-(3-trifluoromethoxy-phenyl)-o...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137243(2-{[5-Oxo-2-phenyl-oxazol-(4E)-ylidenemethyl]-amin...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetHolo-[acyl-carrier-protein] synthase(Bacillus subtilis)
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50137241(5-Bromo-4-chloro-2-{[2-(4-chloro-phenyl)-5-oxo-oxa...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:In vitro inhibitory activity against Holo-[acyl-carrier-protein] synthase was determined using Bacillus subtilis GST-Acp-HTRFassayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B27TPZPubMed
TargetEnoyl-acyl carrier reductase ENR(Toxoplasma gondii)
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50326332(2-Amino-N-(5-chloro-2-phenoxyphenyl)nicotinamide |...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of Toxoplasma gondii enoyl reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B858CMPubMed
TargetProtein kinase C theta type(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM25548(4-arylamino-3-pyridinecarbonitrile, 4f | 4-{[3-(be...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMpH: 7.2 T: 2°CAssay Description:All IC50s were measured by using a modified IMAP protocol from Molecular Devices. The kinase reaction was carried out in a Corning Costar 384 well pl...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5C8KPubMed
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