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Found 264 with Last Name = 'manfredini' and Initial = 's'
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50004566(9-Chloro-2-furan-2-yl-[1,2,4]triazolo[1,5-c]quinaz...)
Affinity DataKi:  1.20nMAssay Description:Dissplacement of [3H]-CGS- from Adenosine A2a receptor of rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051232(8-(4-Fluoro-benzyl)-2-furan-2-yl-8H-pyrazolo[4,3-e...)
Affinity DataKi:  1.20nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051234(2-(furan-2-yl)-8-phenethyl-8H-pyrazolo[4,3-e][1,2,...)
Affinity DataKi:  1.40nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50007848(8-Cyclopropyl-1,3-dipropyl-3,7-dihydro-purine-2,6-...)
Affinity DataKi:  1.5nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)
Affinity DataKi:  1.90nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50048466(2-(furan-2-yl)-7-phenethyl-7H-pyrazolo[4,3-e][1,2,...)
Affinity DataKi:  2.30nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051242(8-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,2,4]tria...)
Affinity DataKi:  2.40nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283532(2-(4-Fluoro-benzyl)-8-furan-2-yl-2H-[1,2,3]triazol...)
Affinity DataKi:  2.5nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051232(8-(4-Fluoro-benzyl)-2-furan-2-yl-8H-pyrazolo[4,3-e...)
Affinity DataKi:  3.30nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283529(3-Benzyl-8-furan-2-yl-3H-[1,2,3]triazolo[4,5-e][1,...)
Affinity DataKi:  4.60nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051234(2-(furan-2-yl)-8-phenethyl-8H-pyrazolo[4,3-e][1,2,...)
Affinity DataKi:  4.70nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283526(3-(3-Fluoro-benzyl)-8-furan-2-yl-3H-[1,2,3]triazol...)
Affinity DataKi:  4.90nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50094688(2-(furan-2-yl)-8-isopentyl-8H-pyrazolo[4,3-e][1,2,...)
Affinity DataKi:  5.60nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283529(3-Benzyl-8-furan-2-yl-3H-[1,2,3]triazolo[4,5-e][1,...)
Affinity DataKi:  6.10nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50004566(9-Chloro-2-furan-2-yl-[1,2,4]triazolo[1,5-c]quinaz...)
Affinity DataKi:  6.40nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283528(8-Furan-2-yl-3-phenethyl-3H-[1,2,3]triazolo[4,5-e]...)
Affinity DataKi:  6.90nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051227(7-Butyl-2-furan-2-yl-7H-pyrazolo[4,3-e][1,2,4]tria...)
Affinity DataKi:  8.90nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283527(3-(2-Fluoro-benzyl)-8-furan-2-yl-3H-[1,2,3]triazol...)
Affinity DataKi:  10.4nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283530(2-Furan-2-yl-7-(3-methyl-butyl)-7H-pyrazolo[4,3-e]...)
Affinity DataKi:  12nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283527(3-(2-Fluoro-benzyl)-8-furan-2-yl-3H-[1,2,3]triazol...)
Affinity DataKi:  13.7nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283531(3-(4-Fluoro-benzyl)-8-furan-2-yl-3H-[1,2,3]triazol...)
Affinity DataKi:  13.7nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283532(2-(4-Fluoro-benzyl)-8-furan-2-yl-2H-[1,2,3]triazol...)
Affinity DataKi:  18.3nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283526(3-(3-Fluoro-benzyl)-8-furan-2-yl-3H-[1,2,3]triazol...)
Affinity DataKi:  19nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051242(8-Butyl-2-furan-2-yl-8H-pyrazolo[4,3-e][1,2,4]tria...)
Affinity DataKi:  30.4nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283528(8-Furan-2-yl-3-phenethyl-3H-[1,2,3]triazolo[4,5-e]...)
Affinity DataKi:  42.4nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283531(3-(4-Fluoro-benzyl)-8-furan-2-yl-3H-[1,2,3]triazol...)
Affinity DataKi:  61.2nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051243(2-Furan-2-yl-7-methyl-7H-pyrazolo[4,3-e][1,2,4]tri...)
Affinity DataKi:  101nMAssay Description:Binding ability of adenosine A2a receptor by using [3H]-CGS- as radioligand in rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50283530(2-Furan-2-yl-7-(3-methyl-butyl)-7H-pyrazolo[4,3-e]...)
Affinity DataKi:  116nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50048466(2-(furan-2-yl)-7-phenethyl-7H-pyrazolo[4,3-e][1,2,...)
Affinity DataKi:  121nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051227(7-Butyl-2-furan-2-yl-7H-pyrazolo[4,3-e][1,2,4]tria...)
Affinity DataKi:  236nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A1(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50051243(2-Furan-2-yl-7-methyl-7H-pyrazolo[4,3-e][1,2,4]tri...)
Affinity DataKi:  651nMAssay Description:Binding ability of adenosine A1 receptor by using [3H]-CHA as radioligand in rat whole brain homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50007848(8-Cyclopropyl-1,3-dipropyl-3,7-dihydro-purine-2,6-...)
Affinity DataKi:  706nMAssay Description:Dissplacement of [3H]-CGS- from Adenosine A2a receptor of rat striatal homogenateMore data for this Ligand-Target Pair
In DepthDetails Article
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116890(CHEMBL3613038)
Affinity DataIC50:  160nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116902(CHEMBL3613026)
Affinity DataIC50:  180nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116895(CHEMBL3613033)
Affinity DataIC50:  200nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116903(CHEMBL3613025)
Affinity DataIC50:  470nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50000541((+-)-1-(1-Benzo[b]thien-2-ylethyl)-1-hydroxyurea |...)
Affinity DataIC50:  540nMAssay Description:Inhibition of 5-LOX in human neutrophils assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 15 mins before A23187 and arachidon...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116891(CHEMBL3613037)
Affinity DataIC50:  600nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116904(CHEMBL3613024)
Affinity DataIC50:  920nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50000541((+-)-1-(1-Benzo[b]thien-2-ylethyl)-1-hydroxyurea |...)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116899(CHEMBL3613029)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116905(CHEMBL3613023)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116889(CHEMBL3613039)
Affinity DataIC50:  2.60E+3nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116896(CHEMBL3613032)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibition of human 5-LOX expressed in Escherichia coli Bl21 (DE3) assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 10 mins b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Varicella-zoster virus (strain Dumas) (HHV-3) (Hum...)
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50206491(1-beta-D-arabinofuranosyl-5-(2-bromovinyl)uracil |...)
Affinity DataIC50:  3.20E+3nMAssay Description:Inhibition of VZV TK assessed as [methyl-3H]dThd phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50116895(CHEMBL3613033)
Affinity DataIC50:  3.20E+3nMAssay Description:Inhibition of 5-LOX in human neutrophils assessed as reduction in LTB4 and 5-H(P)ETE) formation pre-incubated for 15 mins before A23187 and arachidon...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Varicella-zoster virus (strain Dumas) (HHV-3) (Hum...)
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50366680(CHEMBL605255)
Affinity DataIC50:  3.30E+3nMAssay Description:Inhibitory concentration against Varicella- zoster virus thymidine kinase(VZV TK)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Varicella-zoster virus (strain Dumas) (HHV-3) (Hum...)
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50206497(1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]...)
Affinity DataIC50:  3.60E+3nMAssay Description:Inhibition of VZV TK assessed as [methyl-3H]dThd phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase(Human herpesvirus 1 (strain SC16) (HHV-1) (Human h...)
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50206491(1-beta-D-arabinofuranosyl-5-(2-bromovinyl)uracil |...)
Affinity DataIC50:  3.60E+3nMAssay Description:Inhibition of HSV1 TK assessed as [methyl-3H]dThd phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidine kinase 2, mitochondrial(Homo sapiens (Human))
University Of Ferrara

Curated by ChEMBL
LigandPNGBDBM50206507(1-[2'-O-(N-Boc-12-aminododecanoyl)-beta-D-arabinof...)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of human TK2 assessed as [methyl-3H]dThd phosphorylationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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