Compile Data Set for Download or QSAR
Found 49 Enz. Inhib. hit(s) with Target = 'Arylamine N-acetyltransferase 1'
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014986(CHEMBL3262086)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50275074((Z)-5-(3',5'-Diiodo-4'-hydroxybenzylidene)-2-thiox...)copy SMILEScopy InChI
Affinity DataIC50: 138nMAssay Description:Inhibition of NAT1 in human ZR75 cell lysate assessed as acetylation of aryl amine using PABA as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50275074((Z)-5-(3',5'-Diiodo-4'-hydroxybenzylidene)-2-thiox...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014944(CHEMBL3262085)copy SMILEScopy InChI
Affinity DataIC50: 540nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274853((Z)-5-(3'-Hydroxybenzylidene)-2-thioxothiazolidin-...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014914(CHEMBL3262049)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50368688(CHEMBL2047717)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of Homo sapiens (human) arylamine N-acetyltransferase 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X351BT
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50092273((Z)-5-(2'-Hydroxybenzylidene)-2-thioxothiazolidin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274890((Z)-3-Amino-5-(4'-hydroxy-3',5-diiodobenzylidene)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014912(CHEMBL1568345)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014924(CHEMBL3262055)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014943(CHEMBL3262084)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014922(CHEMBL3262053)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274887((Z)-5-(3',4'-Dichlorobenzylidene)-2-thioxothiazoli...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50240730((Z)-5-(4'-Hydroxy-3',5'-diiodobenzylidene)thiazoli...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274886((Z)-5-(2'-Methylbenzylidene)-2-thioxothiazolidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014913(CHEMBL3262048)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014942(CHEMBL3262082)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50181730((Z)-5-(4'-Chlorobenzylidene)-2-thioxothiazolidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014987(CHEMBL3262087)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014938(CHEMBL3262077)copy SMILEScopy InChI
Affinity DataIC50: 6.60E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274889((Z)-5-(4'-Hydroxy-3',5'-diiodobenzylidene)-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014925(CHEMBL3262056)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274888((Z)-5-(4'-Biphenylmethylene)-2-thioxothiazolidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 8.10E+3nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014928(CHEMBL3262059)copy SMILEScopy InChI
Affinity DataIC50: 8.40E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014930(CHEMBL3262061)copy SMILEScopy InChI
Affinity DataIC50: 9.60E+3nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014932(CHEMBL3262073)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014931(CHEMBL3262062)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014929(CHEMBL3262060)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014923(CHEMBL3262054)copy SMILEScopy InChI
Affinity DataIC50: 1.21E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014927(CHEMBL3262058)copy SMILEScopy InChI
Affinity DataIC50: 1.21E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50241154((Z)-5-(4'-Fluorobenzylidene)-2-thioxothiazolidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50092271((Z)-5-Benzylidene-2-thioxothiazolidin-4-one | (Z)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014926(CHEMBL3262057)copy SMILEScopy InChI
Affinity DataIC50: 1.45E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50247599((Z)-5-(4'-Hydroxybenzylidene)-2-thioxothiazolidin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.69E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274855((Z)-5-(3'-Methylbenzylidene)-2-thioxothiazolidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50274854((Z)-5-(2'-Methoxybenzylidene)-2-thioxothiazolidin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.76E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014933(CHEMBL3262074)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014937(CHEMBL3262076)copy SMILEScopy InChI
Affinity DataIC50: 1.93E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014934(CHEMBL3262075)copy SMILEScopy InChI
Affinity DataIC50: 2.21E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014916(CHEMBL3262050)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014920(CHEMBL3262051)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014921(CHEMBL3262052)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50241156((Z)-5-(4'-Methylbenzylidene)-2-thioxothiazolidin-4...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50241489((Z)-5-(3'-Methoxybenzylidene)-2-thioxothiazolidin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014941(CHEMBL3262081)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014940(CHEMBL3262080)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50014939(CHEMBL3262078)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NAT1 assessed as rate of free thiol coenzyme A production using arylamine and AcCoA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75HVGPubMed
TargetArylamine N-acetyltransferase 1(Homo sapiens (Human))
University of Oxford

Curated by ChEMBL
LigandPNGBDBM50241157((Z)-5-(4'-Methoxybenzylidene)-2-thioxothiazolidin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human recombinant NAT1 assessed as hydrolysis of acetyl coA using PABA as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ58Q3PubMed