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Found 31 with Last Name = 'correia' and Initial = 'a'
TargetBeta-lactamase(Enterobacter cloacae)
University Of Aveiro

Curated by ChEMBL
LigandPNGBDBM50053173((2S,3S,5R)-3-Methyl-4,4,7-trioxo-3-[1,2,3]triazol-...)
Affinity DataIC50:  30nMAssay Description:Inhibition of Enterobacter cloacae IMI1 beta lactamase expressed in Escherichia coli DH5alpha by SDS-PAGEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbapenem-hydrolyzing beta-lactamase KPC(Klebsiella pneumoniae)
University Of Aveiro

Curated by ChEMBL
LigandPNGBDBM50053173((2S,3S,5R)-3-Methyl-4,4,7-trioxo-3-[1,2,3]triazol-...)
Affinity DataIC50:  374nMAssay Description:Inhibition of Klebsiella pneumoniae KPC-1 beta lactamase expressed in Escherichia coli DH5alpha by SDS-PAGEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Serratia fonticola)
University Of Aveiro

Curated by ChEMBL
LigandPNGBDBM50053173((2S,3S,5R)-3-Methyl-4,4,7-trioxo-3-[1,2,3]triazol-...)
Affinity DataIC50:  6.90E+3nMAssay Description:Inhibition of Serratia fonticola UTAD54 SFC1 beta lactamase expressed in Escherichia coli BL21(DE3) by SDS-PAGEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Serratia fonticola)
University Of Aveiro

Curated by ChEMBL
LigandPNGBDBM50021954((2S,5R)-3,3-Dimethyl-4,4,7-trioxo-4lambda*6*-thia-...)
Affinity DataIC50:  2.27E+4nMAssay Description:Inhibition of Serratia fonticola UTAD54 SFC1 beta lactamase expressed in Escherichia coli BL21(DE3) by SDS-PAGEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Serratia fonticola)
University Of Aveiro

Curated by ChEMBL
LigandPNGBDBM50021959(CHEMBL777 | MM 14151 | US9120808, Clavulanic acid ...)
Affinity DataIC50:  7.28E+4nMAssay Description:Inhibition of Serratia fonticola UTAD54 SFC1 beta lactamase expressed in Escherichia coli BL21(DE3) by SDS-PAGEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297597(4-(2-tert-butyl-1-(cyclopropylmethyl)-6,7-dihydro-...)
Affinity DataEC50:  5.10nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297598(1-(1-(cyclopropylmethyl)-2-neopentyl-6,7-dihydro-1...)
Affinity DataEC50:  1.02E+3nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297599(CHEMBL562149 | N-benzyl-2-tert-butyl-1-(cyclopropy...)
Affinity DataEC50:  637nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297600(CHEMBL564065 | N-benzyl-1-(cyclopropylmethyl)-N-me...)
Affinity DataEC50:  523nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297601(1-(2-tert-butyl-1-(cyclopropylmethyl)-6,7-dihydro-...)
Affinity DataEC50:  320nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297594(1-(cyclopropylmethyl)-5-(2-methoxyethylsulfonyl)-2...)
Affinity DataEC50:  1.40E+4nMAssay Description:Agonist activity at human recombinant CB1 receptor expressed in CHO cells by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297603(1-(cyclopropylmethyl)-2-neopentyl-5-(pyridin-3-yls...)
Affinity DataEC50:  24.5nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297604(2-tert-butyl-1-(cyclopropylmethyl)-5-(pyridin-3-yl...)
Affinity DataEC50:  14.2nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297605(1-(cyclopropylmethyl)-2-neopentyl-5-(phenylsulfony...)
Affinity DataEC50:  9.10nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297606(2-tert-butyl-1-(cyclopropylmethyl)-5-(phenylsulfon...)
Affinity DataEC50:  7.90nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297607(4-(1-(cyclopropylmethyl)-2-neopentyl-6,7-dihydro-1...)
Affinity DataEC50:  18.5nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297608(4-(2-tert-butyl-1-(cyclopropylmethyl)-6,7-dihydro-...)
Affinity DataEC50:  55.4nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297609(4-(1-(cyclopropylmethyl)-2-neopentyl-6,7-dihydro-1...)
Affinity DataEC50:  7nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297610(2-tert-butyl-1-(cyclopropylmethyl)-N-methyl-N-prop...)
Affinity DataEC50:  380nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297611(2-tert-butyl-1-(cyclopropylmethyl)-5-pentyl-4,5,6,...)
Affinity DataEC50:  878nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297612(1-(cyclopropylmethyl)-2-neopentyl-5-pentyl-4,5,6,7...)
Affinity DataEC50:  3.00E+3nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297613(CHEMBL561890 | propyl 1-(cyclopropylmethyl)-2-neop...)
Affinity DataEC50:  560nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297614(5-((5-bromo-2-methoxypyridin-3-yl)methyl)-2-tert-b...)
Affinity DataEC50:  295nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297597(4-(2-tert-butyl-1-(cyclopropylmethyl)-6,7-dihydro-...)
Affinity DataEC50:  7.50E+3nMAssay Description:Agonist activity at human recombinant CB1 receptor expressed in CHO cells by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297608(4-(2-tert-butyl-1-(cyclopropylmethyl)-6,7-dihydro-...)
Affinity DataEC50:  1.80E+4nMAssay Description:Agonist activity at human recombinant CB1 receptor expressed in CHO cells by FLIPR assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297596(5-(benzylsulfonyl)-1-(cyclopropylmethyl)-2-neopent...)
Affinity DataEC50:  13.4nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297595(2-tert-butyl-1-(cyclopropylmethyl)-5-(2-methoxyeth...)
Affinity DataEC50:  26.7nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297594(1-(cyclopropylmethyl)-5-(2-methoxyethylsulfonyl)-2...)
Affinity DataEC50:  21.5nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297593(2-tert-butyl-1-(cyclopropylmethyl)-5-(methylsulfon...)
Affinity DataEC50:  403nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297592(1-(cyclopropylmethyl)-5-(methylsulfonyl)-2-neopent...)
Affinity DataEC50:  439nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50297602(5-(benzylsulfonyl)-2-tert-butyl-1-(cyclopropylmeth...)
Affinity DataEC50:  21.8nMAssay Description:Agonist activity at human recombinant CB2 receptor expressed in CHO cells assessed as inhibition forskolin-induced cAMP releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed