Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/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 | 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)) | 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)) | 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 | 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)) | 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)) | 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)) | 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)) | 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)) | 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 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)) | 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)) | 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 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)) | 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)) | 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 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)) | 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 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 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 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 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 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 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 3 (Homo sapiens (Human)) | BDBM50096161 (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 | 3.80E+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 3 (Homo sapiens (Human)) | BDBM50087412 (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 | 4.20E+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)) | BDBM50096159 (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 | 5.00E+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 3 (Homo sapiens (Human)) | BDBM50087399 (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 | 5.10E+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)) | BDBM50087403 (2-Cyclohexylcarbamoyl-6-(8-hydroxy-7,8-dihydro-6H-...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 5.20E+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)) | BDBM50087400 (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 | 5.20E+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)) | BDBM50087406 (2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL KEGG PC cid PC sid UniChem Similars | PubMed | 6.00E+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 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)) | BDBM50087415 (2-Carbamoyl-6-(8-hydroxy-7,8-dihydro-6H-imidazo[4,...) | KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | 7.80E+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 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)) | BDBM50096158 (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 | 1.40E+4 | 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)) | BDBM50096160 (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 | 3.50E+4 | 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)) | BDBM50087416 (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 | 4.48E+4 | 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 |