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Found 54 with Last Name = 'schuber' and Initial = 'f'
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051375((6S,8aS)-5,5,8a-Trimethyl-2-((E)-1,5,9-trimethyl-d...)
Affinity DataKi:  300nMAssay Description:Binding affinity towards competitive inhibition against rat microsomal Oxidosqualene-lanosterol cyclaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051375((6S,8aS)-5,5,8a-Trimethyl-2-((E)-1,5,9-trimethyl-d...)
Affinity DataKi:  400nMAssay Description:Binding affinity towards noncompetetive inhibition against rat microsomal Oxidosqualene-lanosterol cyclaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051383((4aR,6S,8aS)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-...)
Affinity DataIC50:  100nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051371(1,1,4a-Trimethyl-5-(4,8,12-trimethyl-trideca-3,7,1...)
Affinity DataIC50:  600nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051372((6R,8aR)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-5,5,...)
Affinity DataIC50:  600nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051372((6R,8aR)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-5,5,...)
Affinity DataIC50:  600nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051375((6S,8aS)-5,5,8a-Trimethyl-2-((E)-1,5,9-trimethyl-d...)
Affinity DataIC50:  600nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051366((E)-1-((6S,8aS)-6-Hydroxy-5,5,8a-trimethyl-3,5,6,7...)
Affinity DataIC50:  680nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051380((4aS,6S,8aS)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-...)
Affinity DataIC50:  700nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051376((4aR,6S,8aS)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-...)
Affinity DataIC50:  900nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051368((6S,8aS)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-5,5,...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051373((6S,8aS)-2-Dodecyl-5,5,8a-trimethyl-1,2,3,5,6,7,8,...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051379((6S,8aS)-5,5,8a-Trimethyl-2-tetradecyl-1,2,3,5,6,7...)
Affinity DataIC50:  2.90E+3nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347144(LUTEOLINIDIN)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347135(Cyanidin-3-glucoside (M8) | KUROMANIN)
Affinity DataIC50:  6.30E+3nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051370((6S,8aS)-5,5,8a-Trimethyl-2-((Z)-1,5,9-trimethyl-d...)
Affinity DataIC50:  6.80E+3nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM7459(2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  8.20E+3nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid lipase/cholesteryl ester hydrolase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287472(1-((S)-10,13-Dimethyl-17-octyl-hexadecahydro-cyclo...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of ancreatic cholesterol esterase using using p-nitrophenylacetate or cholesteryl [1-14C]-oleate as substratesMore data for this Ligand-Target Pair
In DepthDetails Article
TargetLysosomal acid lipase/cholesteryl ester hydrolase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287473(3,3,4,4,4-Pentafluoro-1-((2S,4aS,8aS)-4a-methyl-de...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of ancreatic cholesterol esterase using using p-nitrophenylacetate or cholesteryl [1-14C]-oleate as substratesMore data for this Ligand-Target Pair
In DepthDetails Article
TargetLysosomal acid lipase/cholesteryl ester hydrolase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287471(1-(4-tert-Butyl-cyclohexyl)-3,3,4,4,4-pentafluoro-...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of ancreatic cholesterol esterase using using p-nitrophenylacetate or cholesteryl [1-14C]-oleate as substratesMore data for this Ligand-Target Pair
In DepthDetails Article
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50081942(CHEMBL3422364)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of human CD38 by HPLC analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347139(QUERCETAGETINIDIN)
Affinity DataIC50:  1.42E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)
Affinity DataIC50:  1.46E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50326998(CHEMBL591036 | Pelargonidin)
Affinity DataIC50:  1.63E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051382((6S,8aS)-2-Dodecyl-8a-methyl-1,2,3,5,6,7,8,8a-octa...)
Affinity DataIC50:  1.64E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347138(MALVIDIN)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051367((6S,8aS)-2-(1,5-Dimethyl-hex-4-enyl)-5,5,8a-trimet...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051381((6R,8aS)-2-((E)-5,9-Dimethyl-deca-4,8-dienyl)-5,5,...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347140(PEONIDIN)
Affinity DataIC50:  2.09E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50241503(2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopy...)
Affinity DataIC50:  2.18E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM15236(3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chr...)
Affinity DataIC50:  2.48E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051378((6S,8aS)-2-Benzyl-5,5,8a-trimethyl-1,2,3,5,6,7,8,8...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051377((4aR,8aS)-2-Dodecyl-5,5-dimethyl-decahydro-isoquin...)
Affinity DataIC50: >2.50E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051365((6S,8aS)-5,5,8a-Trimethyl-2-(3-phenyl-propyl)-1,2,...)
Affinity DataIC50: >2.50E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50003030((2S,4aS,8aR)-1,1,4a-Trimethyl-decahydro-naphthalen...)
Affinity DataIC50: >2.50E+4nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50081943(CHEMBL3422366)
Affinity DataIC50:  2.60E+4nMAssay Description:Inhibition of human CD38 by HPLC analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347141(DIOSMETINIDIN)
Affinity DataIC50:  3.21E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50033767(3,3',4',5',7-pentahydroxy flavone | 3,7,3',4',5'-P...)
Affinity DataIC50:  3.79E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)
Affinity DataIC50:  3.79E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347142(PETUNIDIN)
Affinity DataIC50:  3.92E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM23408(2-(3,4-dihydroxyphenyl)-3,5,6,7-tetrahydroxy-4H-ch...)
Affinity DataIC50:  4.86E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50347143(FISETINIDIN)
Affinity DataIC50:  7.03E+4nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051369((6S,8aS)-5,5,8a-Trimethyl-2-octadecyl-1,2,3,5,6,7,...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLanosterol synthase(Rattus norvegicus)
Laboratoires Fournier

Curated by ChEMBL
LigandPNGBDBM50051374((6S,8aS)-5,5,8a-Trimethyl-1,2,3,5,6,7,8,8a-octahyd...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid lipase/cholesteryl ester hydrolase(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287474(3,3-Difluoro-1-((2S,4aS,8aS)-4a-methyl-decahydro-n...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of ancreatic cholesterol esterase using using p-nitrophenylacetate or cholesteryl [1-14C]-oleate as substratesMore data for this Ligand-Target Pair
In DepthDetails Article
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM23416(α-CA inhibitor, 3 | (+)-Catechin | (2R,3S)-2-...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM23926((E)-resveratrol | 5-[(E)-2-(4-hydroxyphenyl)etheny...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50045936((E)-4-(3,5-dihydroxystyryl)benzene-1,2-diol | (E)-...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50049400((+/-) taxifolin | (+/-)-Dihydroquercetin | (+/-)-t...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human CD38 using 20 uM 1, N6-etheno NAD+ as substrate by continuous fluorimetric methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1(Homo sapiens (Human))
University Of Strasburg

Curated by ChEMBL
LigandPNGBDBM50081939(CHEMBL3422360)
Affinity DataIC50:  1.03E+5nMAssay Description:Inhibition of human CD38 by HPLC analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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