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Found 238 with Last Name = 'baker' and Initial = 'sj'
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339869(5-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl...)
Affinity DataKi:  20nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339868(4-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl...)
Affinity DataKi:  20nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339870(2-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl...)
Affinity DataKi:  80nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase mTOR(Homo sapiens (Human))
Piramed Pharma

LigandPNGBDBM25028(4-[2-(1H-indazol-4-yl)-6-[(4-methanesulfonylpipera...)
Affinity DataKi:  580nM ΔG°:  -35.6kJ/molepH: 7.5 T: 2°CAssay Description:Mammalian target of rapamycin (mTOR) was assayed by monitoring phosphorylation of GFP-4EBP using a homogeneous time-resolved fluorescence resonance e...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339846(6-phenoxybenzo[c][1,2]oxaborol-1(3H)-ol | CHEMBL17...)
Affinity DataKi:  710nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339856(6-(3-methoxyphenoxy)benzo[c][1,2]oxaborol-1(3H)-ol...)
Affinity DataKi:  1.35E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339862(3-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl...)
Affinity DataKi:  1.44E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeucine--tRNA ligase, cytoplasmic(Saccharomyces cerevisiae S288c)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50370987(TAVABOROLE)
Affinity DataKi:  1.85E+3nMAssay Description:Inhibition of Saccharomyces cerevisiae cytoplasmic leucyl-tRNA synthetase after 20 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339860(6-(3-(benzyloxy)phenoxy)benzo[c][1,2]oxaborol-1(3H...)
Affinity DataKi:  2.27E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339857(6-(3-aminophenoxy)benzo[c][1,2]oxaborol-1(3H)-ol |...)
Affinity DataKi:  2.75E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339859(6-(3-(aminomethyl)phenoxy)benzo[c][1,2]oxaborol-1(...)
Affinity DataKi:  3.33E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339855(6-(phenylamino)benzo[c][1,2]oxaborol-1(3H)-ol | CH...)
Affinity DataKi:  4.73E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339867(CHEMBL1761273 | ethyl 4-(1-hydroxy-1,3-dihydrobenz...)
Affinity DataKi:  5.55E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339863(6-(4-methoxyphenoxy)benzo[c][1,2]oxaborol-1(3H)-ol...)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339850(6-(hydroxy(phenyl)methyl)benzo[c][1,2]oxaborol-1(3...)
Affinity DataKi:  7.28E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339861(6-(3-((dimethylamino)methyl)phenoxy)benzo[c][1,2]o...)
Affinity DataKi:  7.72E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339858(6-(3-(hydroxymethyl)phenoxy)benzo[c][1,2]oxaborol-...)
Affinity DataKi:  8.40E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339864(6-(4-aminophenoxy)benzo[c][1,2]oxaborol-1(3H)-ol |...)
Affinity DataKi:  8.73E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339847(6-(phenylthio)benzo[c][1,2]oxaborol-1(3H)-ol | CHE...)
Affinity DataKi:  9.09E+3nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339865(6-(4-(aminomethyl)phenoxy)benzo[c][1,2]oxaborol-1(...)
Affinity DataKi:  1.33E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339854(6-((phenylaminooxy)carbonyl)benzo[c][1,2]oxaborol-...)
Affinity DataKi:  1.60E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089572(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi:  1.70E+4nMAssay Description:In vitro inhibitory activity against Aminoimidazole carboxamide ribonucleotide transformylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339848(6-benzylbenzo[c][1,2]oxaborol-1(3H)-ol | CHEMBL176...)
Affinity DataKi:  1.98E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339849((1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)(...)
Affinity DataKi:  2.85E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeucine--tRNA ligase, cytoplasmic(Saccharomyces cerevisiae S288c)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50370987(TAVABOROLE)
Affinity DataKi:  3.14E+4nMAssay Description:Inhibition of Saccharomyces cerevisiae cytoplasmic leucyl-tRNA synthetase after 2 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrifunctional purine biosynthetic protein adenosine-3(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089585(2,6-Diamino-5-[2-(4,5-difluoro-2-nitro-phenylamino...)
Affinity DataKi:  3.50E+4nMAssay Description:In vitro inhibitory activity against Glycinamide ribonucleotide transformylase (GAR Tfase) after 3 min at 250 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339866(6-(4-((dimethylamino)methyl)phenoxy)benzo[c][1,2]o...)
Affinity DataKi:  4.06E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrifunctional purine biosynthetic protein adenosine-3(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089594(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi:  4.50E+4nMAssay Description:In vitro inhibitory activity against Glycinamide ribonucleotide transformylase (GAR Tfase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339853(CHEMBL1761258 | N-(1-hydroxy-1,3-dihydrobenzo[c][1...)
Affinity DataKi:  4.66E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBifunctional purine biosynthesis protein ATIC(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089594(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi:  5.20E+4nMAssay Description:In vitro inhibitory activity against Aminoimidazole carboxamide ribonucleotide transformylaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339851(6-(phenylsulfinyl)benzo[c][1,2]oxaborol-1(3H)-ol |...)
Affinity DataKi:  5.80E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Enterobacter cloacae)
Anacor Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50339852(6-(phenylsulfonyl)benzo[c][1,2]oxaborol-1(3H)-ol |...)
Affinity DataKi:  6.32E+4nMAssay Description:Inhibition of Enterobacter cloacae P99 beta-lactamase AmpC P99 using nitrocefin as substrate after 30 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTrifunctional purine biosynthetic protein adenosine-3(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50089572(2-{4-[(2-Amino-4-oxo-3,4-dihydro-quinazolin-6-ylme...)
Affinity DataKi: >1.00E+5nMAssay Description:In vitro inhibitory activity against Glycinamide ribonucleotide transformylase (GAR Tfase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101068(4-Chloro-10,10-dioxo-9,10-dihydro-10lambda*6*-thio...)
Affinity DataIC50:  0.0900nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101051(4,5-Dichloro-9H-xanthene-9-carboxylic acid [(2R,3R...)
Affinity DataIC50:  0.100nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101050(10,10-Dioxo-9,10-dihydro-10lambda*6*-thioxanthene-...)
Affinity DataIC50:  0.110nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101069(10,10-Bis-trifluoromethyl-9,10-dihydro-anthracene-...)
Affinity DataIC50:  0.110nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101045(9H-Xanthene-9-carboxylic acid [(2R,3R,4S,5R)-5-(5-...)
Affinity DataIC50:  0.110nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101053(9H-Xanthene-9-carboxylic acid [(2R,3S,5R)-5-(5-eth...)
Affinity DataIC50:  0.130nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101071(10,10-Dioxo-9,10-dihydro-10lambda*6*-thioxanthene-...)
Affinity DataIC50:  0.130nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101058(4-Phenyl-9H-xanthene-9-carboxylic acid [(2R,3R,4S,...)
Affinity DataIC50:  0.140nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101060(4-Trifluoromethyl-9H-xanthene-9-carboxylic acid [(...)
Affinity DataIC50:  0.140nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101048(4-Chloro-9H-xanthene-9-carboxylic acid [(2R,3R,4S,...)
Affinity DataIC50:  0.140nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101047(4-Methyl-9H-xanthene-9-carboxylic acid [(2R,3R,4S,...)
Affinity DataIC50:  0.190nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101067((S)-2-(2,4-Dichloro-5-methoxy-phenoxy)-N-[(2R,3R,4...)
Affinity DataIC50:  0.190nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 1 (strain SC16) (HHV-1) (Human h...)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101069(10,10-Bis-trifluoromethyl-9,10-dihydro-anthracene-...)
Affinity DataIC50:  0.190nMAssay Description:Inhibitory activity against HSV-1 Thymidine Kinase (HSV-1 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101074(4-Methoxy-9H-xanthene-9-carboxylic acid [(2R,3R,4S...)
Affinity DataIC50:  0.210nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101062(4-Chloro-9H-thioxanthene-9-carboxylic acid [(2R,3R...)
Affinity DataIC50:  0.210nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 1 (strain SC16) (HHV-1) (Human h...)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101068(4-Chloro-10,10-dioxo-9,10-dihydro-10lambda*6*-thio...)
Affinity DataIC50:  0.270nMAssay Description:Inhibitory activity against HSV-1 Thymidine Kinase (HSV-1 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 2)
Roche Discovery Welwyn

Curated by ChEMBL
LigandPNGBDBM50101049(10,10-Dimethyl-9,10-dihydro-anthracene-9-carboxyli...)
Affinity DataIC50:  0.280nMAssay Description:Inhibitory activity against HSV-2 Thymidine Kinase (HSV-2 TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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