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Found 18 with Last Name = 'mitchell' and Initial = 'da'
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388903(CHEMBL2063253)
Affinity DataKi:  250nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388906(CHEMBL2063256)
Affinity DataKi:  450nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388903(CHEMBL2063253)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of Staphylococcus aureus isolate WT CrtM-mediated staphyloxanthin synthesis after 72 hrs by spectrophotometryMore data for this Ligand-Target Pair
TargetGeranylgeranyl pyrophosphate synthase(Homo sapiens (Human))
University Of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50388398(CHEMBL561057 | SQ-109)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibition of human geranylgeranyl diphosphate synthaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388904(CHEMBL2063254)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388903(CHEMBL2063253)
Affinity DataIC50:  2.40E+4nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388906(CHEMBL2063256)
Affinity DataIC50:  3.30E+4nMAssay Description:Inhibition of Staphylococcus aureus isolate WT CrtM-mediated staphyloxanthin synthesis after 72 hrs by spectrophotometryMore data for this Ligand-Target Pair
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388906(CHEMBL2063256)
Affinity DataIC50:  4.53E+4nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388908(CHEMBL2063258)
Affinity DataIC50:  6.70E+4nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50011480(CHEMBL3261881)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of Staphylococcus aureus CrtMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50011479(CHEMBL3261880)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of Staphylococcus aureus CrtMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSqualene synthase(Homo sapiens (Human))
University Of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50011479(CHEMBL3261880)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of human SQSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSqualene synthase(Homo sapiens (Human))
University Of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50388398(CHEMBL561057 | SQ-109)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of human SQSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSqualene synthase(Homo sapiens (Human))
University Of Illinois At Urbana-Champaign

Curated by ChEMBL
LigandPNGBDBM50011480(CHEMBL3261881)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of human SQSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388398(CHEMBL561057 | SQ-109)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of Staphylococcus aureus CrtMMore data for this Ligand-Target Pair
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388909(CHEMBL2063259)
Affinity DataIC50: >3.00E+5nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388905(CHEMBL2063255)
Affinity DataIC50: >3.00E+5nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target4,4'-diapophytoene synthase(Staphylococcus aureus)
TBA

Curated by ChEMBL
LigandPNGBDBM50388907(CHEMBL2063257)
Affinity DataIC50: >3.00E+5nMAssay Description:Inhibition of Staphylococcus aureus His6-tagged CrtM expressed in Escherichia coli BL21(DE3) using Farnesyl pyrophosphate as substrate incubated for ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed