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Found 53 with Last Name = 'sarma' and Initial = 'd'
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480493(CHEMBL539209 | acs.jmedchem.1c00409_ST.302 | jm5b0...)
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453878(CHEMBL371380)
Affinity DataKi:  3.80E+3nMAssay Description:Competitive inhibition of Caulobacter vibrioides full length wild type cell cycle histidine kinase CckA deltaTM Escherichia coli BL21-AI in presence ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480488(CHEMBL555061 | acs.jmedchem.1c00409_ST.606 | med.2...)
Affinity DataKi:  2.10E+4nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480495(CHEMBL555220)
Affinity DataKi:  3.41E+4nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480499(CHEMBL541707 | acs.jmedchem.1c00409_ST.696)
Affinity DataKi:  4.52E+4nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480500(CHEMBL538957 | acs.jmedchem.1c00409_ST.704)
Affinity DataKi:  4.93E+4nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480496(CHEMBL555221)
Affinity DataKi:  1.12E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480487(CHEMBL551569 | acs.jmedchem.1c00409_ST.759 | med.2...)
Affinity DataKi:  1.16E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480501(CHEMBL553172 | acs.jmedchem.1c00409_ST.765)
Affinity DataKi:  1.35E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480489(CHEMBL557699 | acs.jmedchem.1c00409_ST.767)
Affinity DataKi:  1.59E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480490(CHEMBL537916 | acs.jmedchem.1c00409_ST.792)
Affinity DataKi:  2.97E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480498(CHEMBL539208 | acs.jmedchem.1c00409_ST.799)
Affinity DataKi:  3.63E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480494(CHEMBL551504 | acs.jmedchem.1c00409_ST.804)
Affinity DataKi:  4.62E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480492(CHEMBL555062 | acs.jmedchem.1c00409_ST.805)
Affinity DataKi:  4.78E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480491(CHEMBL551181 | acs.jmedchem.1c00409_ST.808)
Affinity DataKi:  5.84E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetReplicase polyprotein 1ab(Human SARS coronavirus (SARS-CoV) (Severe acute re...)
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50480497(CHEMBL557291 | acs.jmedchem.1c00409_ST.809)
Affinity DataKi:  6.14E+5nMAssay Description:Inhibition of SARS coronavirus 3CL protease pretreated for 10 mins before substrate additionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50277598(CHEMBL453211 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  9nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50277599(CHEMBL507541 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  10nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50277597(CHEMBL501242 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  13nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50277595(CHEMBL445281 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  15nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50277594(CHEMBL448015 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  22nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50277596(CHEMBL504917 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  24nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50234644(CHEMBL400043 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  50nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50495215(CHEMBL3105743)
Affinity DataIC50:  79nMAssay Description:Inhibition of recombinant human BACE1 using (7-methoxycoumarin-4-yl)acetyl-SEVNL*DAEFRK(2,4-dinitrophenyl)-RR-NH2) as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50495216(CHEMBL3105741)
Affinity DataIC50:  89nMAssay Description:Inhibition of recombinant human BACE1 using (7-methoxycoumarin-4-yl)acetyl-SEVNL*DAEFRK(2,4-dinitrophenyl)-RR-NH2) as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50234646(2-(((2S,3S)-4-(3-(2H-tetrazol-5-yl)phenylamino)-3-...)
Affinity DataIC50:  96nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50234643(CHEMBL399839 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  140nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50495217(CHEMBL3105738)
Affinity DataIC50:  151nMAssay Description:Inhibition of recombinant human BACE1 using (7-methoxycoumarin-4-yl)acetyl-SEVNL*DAEFRK(2,4-dinitrophenyl)-RR-NH2) as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50234645(CHEMBL253865 | N-((2S,3S)-4-(3-(2H-tetrazol-5-yl)p...)
Affinity DataIC50:  360nMAssay Description:Inhibition of human recombinant Arg235 region of BACE1 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM20926(5-[2,4-dihydroxy-5-(propan-2-yl)phenyl]-N-ethyl-4-...)
Affinity DataIC50:  7.30E+3nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM15364(4-chloro-6-[4-(2,3-dihydro-1,4-benzodioxin-6-yl)-5...)
Affinity DataIC50:  1.12E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453878(CHEMBL371380)
Affinity DataIC50:  1.23E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPhosphate regulon sensor protein PhoR(Escherichia coli (strain K12))
Williams College

Curated by ChEMBL
LigandPNGBDBM50453879(CHEMBL4202687)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibition of Escherichia coli DHp-catalytic domain PhoR autophosphorylation expressed in Escherichia coli RIL in presence of gamma-32P-ATP by SDS-PA...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50409992(CHEMBL364882)
Affinity DataIC50:  1.75E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453882(CHEMBL4218027)
Affinity DataIC50:  1.86E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSensor protein kinase WalK(Staphylococcus epidermidis (strain ATCC 35984 / RP...)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453880(CHEMBL3343945)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of recombinant Staphylococcus epidermidis ATCC 35984 N-terminal GB1-tagged YycG expressed in Escherichia coli BL21 (DE3) preincubated for ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSensor protein kinase WalK(Staphylococcus epidermidis (strain ATCC 35984 / RP...)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453886(CHEMBL4215525)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of recombinant Staphylococcus epidermidis ATCC 35984 N-terminal GB1-tagged YycG expressed in Escherichia coli BL21 (DE3) preincubated for ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453881(CCT018159 | CHEBI:41656 | CHEMBL399530)
Affinity DataIC50:  2.80E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50409996(CHEMBL191228)
Affinity DataIC50:  3.23E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453884(CHEMBL4217100)
Affinity DataIC50:  3.27E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453883(CHEMBL4204469)
Affinity DataIC50:  3.36E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM15365(3-(2,4-Dihydroxyphenyl)-4-(4-methoxyphenyl)-5-meth...)
Affinity DataIC50:  4.60E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453887(CHEMBL1551662)
Affinity DataIC50:  5.69E+4nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Streptococcus pneumoniae PCS8203)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453885(CHEMBL4209595)
Affinity DataIC50:  7.50E+4nMAssay Description:Inhibition of Streptococcus pneumoniae VicK preincubated for 30 mins followed by [gamma-33P]ATP addition after 30 mins by SDS-PAGE methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChemotaxis protein CheA(Escherichia coli (strain K12))
Williams College

Curated by ChEMBL
LigandPNGBDBM7459(2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  1.11E+5nMAssay Description:Inhibition of Escherichia coli CheA preincubated for 30 mins followed by [gamma-33P]ATP addition after 30 mins by SDS-PAGE methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistidine kinase(Caulobacter vibrioides)
Williams College

Curated by ChEMBL
LigandPNGBDBM227589(Radicicol)
Affinity DataIC50:  1.84E+5nMAssay Description:Inhibition of recombinant Caulobacter vibrioides cell cycle histidine kinase CckA deltaTM mutant DHp domain (70 to 691 residues) expressed in Escheri...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSensor protein kinase WalK(Staphylococcus aureus subsp. aureus CN1)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453879(CHEMBL4202687)
Affinity DataIC50:  2.12E+5nMAssay Description:Inhibition of Staphylococcus aureus DHp-catalytic domain PhoR autophosphorylation expressed in Escherichia coli RIL in presence of gamma-32P-ATP by S...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistidine kinase(Streptococcus pneumoniae PCS8203)
Williams College

Curated by ChEMBL
LigandPNGBDBM7459(2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  2.16E+5nMAssay Description:Inhibition of Streptococcus pneumoniae VicK preincubated for 30 mins followed by [gamma-33P]ATP addition after 30 mins by SDS-PAGE methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVirulence sensor histidine kinase PhoQ(Salmonella typhimurium (strain LT2 / SGSC1412 / AT...)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453878(CHEMBL371380)
Affinity DataIC50:  2.38E+5nMAssay Description:Inhibition of recombinant Salmonella typhimurium N-terminal His6-SUMO-tagged DHp-catalytic domain PhoQ (257 to 487 residues) autophosphorylation expr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetVirulence sensor histidine kinase PhoQ(Salmonella typhimurium (strain LT2 / SGSC1412 / AT...)
Williams College

Curated by ChEMBL
LigandPNGBDBM50453881(CCT018159 | CHEBI:41656 | CHEMBL399530)
Affinity DataIC50:  2.61E+5nMAssay Description:Inhibition of recombinant Salmonella typhimurium N-terminal His6-SUMO-tagged DHp-catalytic domain PhoQ (257 to 487 residues) autophosphorylation expr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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