Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096172 (1-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096172 (1-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 2 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Inhibition of human recombinant AMPD3 | ACS Med Chem Lett 1: 286-289 (2010) Article DOI: 10.1021/ml100092a BindingDB Entry DOI: 10.7270/Q2X0683X | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096166 (1-Benzyloxy-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 9 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096165 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 15 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096165 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | 15 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Inhibition of human recombinant AMPD3 | ACS Med Chem Lett 1: 286-289 (2010) Article DOI: 10.1021/ml100092a BindingDB Entry DOI: 10.7270/Q2X0683X | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096169 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 20 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087401 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 29 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096170 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 30 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096167 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087407 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 40 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087409 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 41 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096164 (1,3-Dichloro-4-[2-(8-hydroxy-7,8-dihydro-6H-imidaz...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 50 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096171 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 90 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087411 (2-Benzyl-2-[4-(8-hydroxy-7,8-dihydro-6H-imidazo[4,...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 170 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096175 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 220 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087408 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 250 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087295 (2-(2-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 300 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096162 (1,3-Dichloro-4-[2-(8-hydroxy-7,8-dihydro-6H-imidaz...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 300 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096168 (1-Benzyloxy-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 300 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087414 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 360 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087405 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 360 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087332 (2-Benzyl-6-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5-d...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 410 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087332 (2-Benzyl-6-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5-d...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 410 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087377 (3-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096157 (1,3-Dichloro-4-[2-(8-hydroxy-7,8-dihydro-6H-imidaz...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087328 (2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 790 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087304 (2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 800 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087304 (2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 800 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087331 (6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 860 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087404 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 900 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087291 (6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 920 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096177 (6-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 960 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087321 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 970 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096174 (1-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087296 (2-(4-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087402 (6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096178 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087417 (2-(4-Chloro-benzylcarbamoyl)-6-(8-hydroxy-7,8-dihy...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087290 (2-(3-Chloro-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-im...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087310 (2-(4-Chloro-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-im...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096173 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087298 (6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087418 (6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096163 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087410 (2-Benzylcarbamoyl-6-(8-hydroxy-7,8-dihydro-6H-imid...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087329 (2-(3-Bromo-phenyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50096176 (4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50087413 (2-Benzyl-2-[4-(8-hydroxy-7,8-dihydro-6H-imidazo[4,...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibitory activity against porcine heart or recombinant human E-type AMPDA | J Med Chem 43: 1519-24 (2000) BindingDB Entry DOI: 10.7270/Q2PK0FC0 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 3 (Homo sapiens (Human)) | BDBM50003602 ((2R,3S,5R)-2-((R)-8-Hydroxy-7,8-dihydro-6H-imidazo...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Inhibition of recombinant human E-type adenylate deaminase | J Med Chem 44: 613-8 (2001) BindingDB Entry DOI: 10.7270/Q2BZ659R | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
AMP deaminase 2 (Homo sapiens (Human)) | BDBM50087324 (2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...) | PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Metabasis Therapeutics Inc. Curated by ChEMBL | Assay Description Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA) | J Med Chem 43: 1495-507 (2000) BindingDB Entry DOI: 10.7270/Q2Z31XWJ | |||||||||||
More data for this Ligand-Target Pair |
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