Compile Data Set for Download or QSAR
Found 172 with Last Name = 'wattanasin' and Initial = 's'
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469565(CHEMBL4082918)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106090((S)-3-(3,4-Dimethoxy-phenyl)-3-[2-((4-methoxy-buty...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469558(CHEMBL4061041)copy SMILEScopy InChI
Affinity DataIC50: 1.46nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106091((S)-3-Benzo[1,3]dioxol-5-yl-3-((S)-4-methyl-2-{2-[...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50249583(CHEMBL4097399)copy SMILEScopy InChI
Affinity DataIC50: 3.13nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469562(CHEMBL4069725)copy SMILEScopy InChI
Affinity DataIC50: 3.56nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469559(CHEMBL4063087)copy SMILEScopy InChI
Affinity DataIC50: 4.15nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469555(CHEMBL4090716)copy SMILEScopy InChI
Affinity DataIC50: 4.19nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106083((S)-3-(4-Methoxy-phenyl)-3-[2-((3-methoxy-propyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 4.70nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106086((S)-3-(3,4-Dimethoxy-phenyl)-3-[2-((3-methoxy-prop...)copy SMILEScopy InChI
Affinity DataIC50: 7.10nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106085((E)-(S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-...)copy SMILEScopy InChI
Affinity DataIC50: 7.70nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by mouse Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106085((E)-(S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-...)copy SMILEScopy InChI
Affinity DataIC50: 7.90nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to fibronectin by Very late antigen 4 (VLA-4)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106082((S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-urei...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469560(CHEMBL4083624)copy SMILEScopy InChI
Affinity DataIC50: 12.5nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106086((S)-3-(3,4-Dimethoxy-phenyl)-3-[2-((3-methoxy-prop...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to fibronectin by Very late antigen 5 (VLA-5)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106082((S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-urei...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to fibronectin by Very late antigen 4 (VLA-4)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106085((E)-(S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469563(CHEMBL4079368)copy SMILEScopy InChI
Affinity DataIC50: 16.4nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106098((R)-3-((S)-4-Methyl-2-{2-[4-(3-o-tolyl-ureido)-phe...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469550(CHEMBL4070478)copy SMILEScopy InChI
Affinity DataIC50: 19.7nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106093((S)-3-(3,4-Dimethoxy-phenyl)-3-[2-((3-methyl-butyl...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106085((E)-(S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by rat Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106086((S)-3-(3,4-Dimethoxy-phenyl)-3-[2-((3-methoxy-prop...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by rat Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106082((S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-urei...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by mouse Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-L/Intercellular adhesion molecule 1(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50161080((S)-2-[(S)-3-Isobutyl-2,5-dioxo-4-((E)-3-pyridin-4...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:In vitro inhibitory concentrationfor Lymphocyte function associated antigen 1/Intercellular adhesion molecule 1 (LFA-1/ICAM-1)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20Z72S2PubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106082((S)-3-[2-((3-Methoxy-propyl)-{2-[4-(3-o-tolyl-urei...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by rat Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106083((S)-3-(4-Methoxy-phenyl)-3-[2-((3-methoxy-propyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by rat Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106086((S)-3-(3,4-Dimethoxy-phenyl)-3-[2-((3-methoxy-prop...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by mouse Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106099(CHEMBL321739 | Lithium; (S)-3-[2-((3-methyl-butyl)...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106083((S)-3-(4-Methoxy-phenyl)-3-[2-((3-methoxy-propyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to fibronectin by Very late antigen 5 (VLA-5)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469557(CHEMBL4091408)copy SMILEScopy InChI
Affinity DataIC50: 37.5nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469554(CHEMBL4061854)copy SMILEScopy InChI
Affinity DataIC50: 39nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372752(CHEMBL272547)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106102((E)-(S)-3-[2-((3-Methyl-butyl)-{2-[4-(3-o-tolyl-ur...)copy SMILEScopy InChI
Affinity DataIC50: 45nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106083((S)-3-(4-Methoxy-phenyl)-3-[2-((3-methoxy-propyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 52nMAssay Description:Inhibition of fluorescent Ramos cell adhesion to VCAM-1 by mouse Very late antigen 4 (VLA-4) integrinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372771(CHEMBL404127)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetIntegrin alpha-L/Intercellular adhesion molecule 1(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50161067((2R)-2-[3-ISOBUTYL-2,5-DIOXO-4-(QUINOLIN-3-YLMETHY...)copy SMILEScopy InChI
Affinity DataIC50: 69nMAssay Description:In vitro inhibitory concentrationfor Lymphocyte function associated antigen 1/Intercellular adhesion molecule 1 (LFA-1/ICAM-1)More data for this Ligand-Target Pair
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372754(CHEMBL272054)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetIntegrin alpha-L/Intercellular adhesion molecule 1(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50123241((S)-2-[(3S,5R)-3-Isobutyl-5-methyl-2-oxo-4-(2-quin...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:In vitro inhibitory concentrationfor Lymphocyte function associated antigen 1/Intercellular adhesion molecule 1 (LFA-1/ICAM-1)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20Z72S2PubMed
TargetIntegrin alpha-L/Integrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50123241((S)-2-[(3S,5R)-3-Isobutyl-5-methyl-2-oxo-4-(2-quin...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of LFA-1/ICAM-1 interaction in ELISAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49K4PubMed
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372766(CHEMBL271482)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469553(CHEMBL4102769)copy SMILEScopy InChI
Affinity DataIC50: 81.4nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIntegrin alpha-4/beta-1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50106097(3-{[2-((3-Methyl-butyl)-{2-[4-(3-o-tolyl-ureido)-p...)copy SMILEScopy InChI
Affinity DataIC50: 98nMAssay Description:In vitro Very late antigen 4 cell adhesion inhibitory activity measured by binding of fluorescently labeled Ramos cells to immobilized VCAM-1.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20001CZPubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469552(CHEMBL4072428)copy SMILEScopy InChI
Affinity DataIC50: 98nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372750(CHEMBL272914)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetIntegrin alpha-L/Integrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Novartis Institute for Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50123239((S)-2-[(3S,5R)-3-Isobutyl-5-methyl-2-oxo-4-(2-quin...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of LFA-1/ICAM-1 interaction in ELISAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29K49K4PubMed
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372751(CHEMBL256222)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50469548(CHEMBL4073216)copy SMILEScopy InChI
Affinity DataIC50: 116nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FN18MZPubMed
TargetIsoprenyl transferase(Streptococcus pneumoniae)
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50372760(CHEMBL257948)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of Streptococcus pneumoniae UPPSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CF9QZ5PubMed
TargetIntegrin alpha-L/Intercellular adhesion molecule 1(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50161072((S)-2-((S)-3-Isobutyl-2,5-dioxo-4-quinolin-6-yl-[1...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:In vitro inhibitory concentrationfor Lymphocyte function associated antigen 1/Intercellular adhesion molecule 1 (LFA-1/ICAM-1)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20Z72S2PubMed
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