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Found 65 with Last Name = 'schillaci' and Initial = 'd'
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506709(CHEMBL3218456)
Affinity DataIC50:  140nMAssay Description:Inhibition of biotinylated polymeric fucose binding to Pseudomonas aeruginosa LecB expressed in Escherichia coli BL21(DE3) preincubated for 1 hr foll...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50505593(CHEMBL4453855)
Affinity DataIC50:  340nMAssay Description:Inhibition of N-(Fluorescein-5-yl)-N'-(alpha-L-fucopyranosyl ethylen)thiocarbamide binding to Pseudomonas aeruginosa PA14 LecB after 22 to 24 hrs by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50505613(CHEMBL4441817)
Affinity DataIC50:  440nMAssay Description:Inhibition of N-(Fluorescein-5-yl)-N'-(alpha-L-fucopyranosyl ethylen)thiocarbamide binding to Pseudomonas aeruginosa PA14 LecB after 22 to 24 hrs by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50505593(CHEMBL4453855)
Affinity DataIC50:  970nMAssay Description:Inhibition of N-(Fluorescein-5-yl)-N'-(alpha-L-fucopyranosyl ethylen)thiocarbamide binding to Pseudomonas aeruginosa PAO1 LecB after 22 to 24 hrs by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50505613(CHEMBL4441817)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of N-(Fluorescein-5-yl)-N'-(alpha-L-fucopyranosyl ethylen)thiocarbamide binding to Pseudomonas aeruginosa PAO1 LecB after 22 to 24 hrs by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQuinolone resistance protein NorA(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50245850(CHEMBL4071003)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of Staphylococcus aureus 1199B NorA assessed as reduction in ethidium bromide efflux by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)
Affinity DataIC50:  5.80E+3nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)
Affinity DataIC50:  6.90E+3nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
TargetQuinolone resistance protein NorA(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50017712((-)-reserpine | (3beta,16beta,17alpha,18beta,20alp...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of Staphylococcus aureus 1199B NorA assessed as reduction in ethidium bromide efflux by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371165(CHEMBL236237)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)
Affinity DataIC50:  1.06E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)
Affinity DataIC50:  1.65E+4nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQuinolone resistance protein NorA(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50245849(CHEMBL4059669)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibition of Staphylococcus aureus 1199B NorA assessed as reduction in ethidium bromide efflux by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)
Affinity DataIC50:  1.98E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFucose-binding lectin PA-IIL(Pseudomonas aeruginosa)
Universit£

Curated by ChEMBL
LigandPNGBDBM50505627(CHEMBL4450053)
Affinity DataIC50:  1.99E+4nMAssay Description:Inhibition of Pseudomonas aeruginosa LecBMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)
Affinity DataIC50:  3.40E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506711(CHEMBL4453279)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506703(CHEMBL4464532)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506706(CHEMBL4442189)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506710(CHEMBL4521808)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506704(CHEMBL4517713)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506705(CHEMBL4585170)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371167(CHEMBL236030)
Affinity DataIC50:  7.00E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506707(CHEMBL4552582)
Affinity DataIC50:  7.50E+4nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371164(CHEMBL413980)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371173(CHEMBL397792)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50203126(3,4-dimethoxy-6,7-dihydro-[1,3]dioxolo[4,5-g]pyrid...)
Affinity DataIC50:  1.20E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50203126(3,4-dimethoxy-6,7-dihydro-[1,3]dioxolo[4,5-g]pyrid...)
Affinity DataIC50:  1.20E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371166(CHEMBL236444)
Affinity DataIC50:  1.29E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530362(CHEMBL4436646)
Affinity DataIC50:  1.30E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530362(CHEMBL4436646)
Affinity DataIC50:  1.30E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530360(CHEMBL4088841)
Affinity DataIC50:  1.30E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530360(CHEMBL4088841)
Affinity DataIC50:  1.30E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530361(CHEMBL4061442)
Affinity DataIC50:  1.40E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530361(CHEMBL4061442)
Affinity DataIC50:  1.40E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530358(CHEMBL4548402)
Affinity DataIC50:  1.60E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50530358(CHEMBL4548402)
Affinity DataIC50:  1.60E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtA using dabcyl-QALPETGEE-edans as substrate preincubated for 1 hr followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Universit£

Curated by ChEMBL
LigandPNGBDBM50506708(CHEMBL4471174)
Affinity DataIC50:  1.92E+5nMAssay Description:Inhibition of Staphylococcus aureus SrtAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371162(CHEMBL394393)
Affinity DataIC50:  2.09E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371171(CHEMBL235586)
Affinity DataIC50:  2.09E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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