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Report error Found 23 Enz. Inhib. hit(s) with all data for entry = 50005253
TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50230540(CHEMBL5285953)
Affinity DataIC50:  45nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50079203(CHEMBL3416669)
Affinity DataIC50:  160nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAmine oxidase [flavin-containing] B(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50161760(CHEMBL3786378)
Affinity DataIC50:  226nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAmine oxidase [flavin-containing] A(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50161755(CHEMBL3263556)
Affinity DataIC50:  271nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50229337(CHEMBL5267000)
Affinity DataIC50:  348nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAmine oxidase [flavin-containing] B(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50161755(CHEMBL3263556)
Affinity DataIC50:  393nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50079189(CHEMBL3416658)
Affinity DataIC50:  422nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50229338(CHEMBL5272095)
Affinity DataIC50:  545nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50079190(CHEMBL3416657)
Affinity DataIC50:  643nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAmine oxidase [flavin-containing] B(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50161759(CHEMBL3785406)
Affinity DataIC50:  703nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetAcetylcholinesterase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50079193(CHEMBL3416654)
Affinity DataIC50:  845nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetCyclin-dependent kinase 2(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50540102(CHEMBL4637085)
Affinity DataIC50:  1.11E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed

TargetCyclin-dependent kinase 2(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM5446(CHEMBL553 | ERLOTINIB HYDROCHLORIDE | Erlotinib | ...)
Affinity DataIC50:  1.14E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNitric oxide synthase, inducible(Mouse)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50229335(CHEMBL5284763)
Affinity DataIC50:  5.22E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNitric oxide synthase, inducible(Mouse)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50229334(CHEMBL5268641)
Affinity DataIC50:  8.09E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNitric oxide synthase, inducible(Mouse)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50227385(CHEMBL5277141)
Affinity DataIC50:  8.41E+3nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNitric oxide synthase, inducible(Mouse)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50229336(CHEMBL5284184)
Affinity DataIC50:  1.08E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50230541(CHEMBL5289805)
Affinity DataIC50:  1.13E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNitric oxide synthase, inducible(Mouse)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50227386(CHEMBL5274680)
Affinity DataIC50:  1.19E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetNitric oxide synthase, inducible(Mouse)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50227387(CHEMBL5288910)
Affinity DataIC50:  1.22E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetDiacylglycerol O-acyltransferase 1(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50230541(CHEMBL5289805)
Affinity DataIC50:  3.52E+4nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzyme in rabbit lung, using hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetMaltase-glucoamylase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50230542(CHEMBL5274141)
Affinity DataIC50:  6.21E+4nMAssay Description:Evaluated for norepinephrine as agonist.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetMaltase-glucoamylase(Human)
Northwest A&F University

Curated by ChEMBL
LigandPNGBDBM50230541(CHEMBL5289805)
Affinity DataIC50:  7.38E+4nMAssay Description:In vitro relative blocking action (pA2) of the post-synaptic Alpha adrenergic receptor from rat and rabbit aorta.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed