BindingDB PrimarySearch

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153085(CHEMBL364836 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 0.230nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153083(CHEMBL441502 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 0.330nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50131892(CHEMBL421252 | N-(3-tert-Butyl-2,5-dioxo-1,4diaza-...)

Ki: 0.670nMAssay Description:Binding affinity against Co(II)-substituted E. coli peptide deformylase was determinedMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153086(CHEMBL188671 | N-[(1R,2S)-3-(4-Amino-butyl)-2,5-di...)

Ki: 3nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50104501((R)-2-[(Formyl-hydroxy-amino)-methyl]-hexanoic aci...)

Ki: 11nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

CHEMBL DrugBank MMDB PC cid PC sid PDB Patents Similars

Details Article PubMed PDB

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153084(CHEMBL361449 | N-(4-{(3R,14S)-14-[(Formyl-hydroxy-...)

Ki: 12nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153087(CHEMBL188894 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 13.7nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153080((R)-2-[(Formyl-hydroxy-amino)-methyl]-hexanoic aci...)

Ki: 23nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

CHEMBL PC cid PC sid Patents

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153081(CHEMBL365910 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 25nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153079(CHEMBL364979 | N-[(3S,6R)-3-(4-Amino-butyl)-2,5-di...)

Ki: 36nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by AAP assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153087(CHEMBL188894 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 63nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153082((R)-2-[(Formyl-hydroxy-amino)-methyl]-heptanoic ac...)

Ki: 74nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

CHEMBL PC cid PC sid Patents Similars

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153088(CHEMBL365416 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 77nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153086(CHEMBL188671 | N-[(1R,2S)-3-(4-Amino-butyl)-2,5-di...)

Ki: 92nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153085(CHEMBL364836 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 96nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153083(CHEMBL441502 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 109nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153079(CHEMBL364979 | N-[(3S,6R)-3-(4-Amino-butyl)-2,5-di...)

Ki: 258nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50186746((2S)-2-AMINO-4-[(2R,3R)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 370nMAssay Description:Inhibition of cobalt substituted Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50186746((2S)-2-AMINO-4-[(2R,3R)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 430nMAssay Description:Inhibition of ferrous substituted Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304165(CHEMBL593446 | S-(5-Deoxy-D-xylofuranos-5-yl)-L-ho...)

Ki: 430nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair

ChEBI
CHEMBL PC cid PC sid Similars

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304168((2S)-2-amino-4-(((2S,3S,4S)-3-fluoro-4,5-dihydroxy...)

Ki: 700nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153084(CHEMBL361449 | N-(4-{(3R,14S)-14-[(Formyl-hydroxy-...)

Ki: 710nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50186747((2S)-2-AMINO-4-[(2R,3S)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 720nMAssay Description:Inhibition of ferrous substituted Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50186747((2S)-2-AMINO-4-[(2R,3S)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 720nMAssay Description:Inhibition of cobalt substituted Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304169((2S)-2-amino-4-(((2R,3S,4S)-3-bromo-4,5-dihydroxyt...)

Ki: 1.40E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/TrEMBL
B.MOAD GoogleScholar

Peptide deformylase(Escherichia coli)
The Ohio State University

Curated by ChEMBL

BDBM50153081(CHEMBL365910 | N-((3S,6R)-3-tert-Butyl-2,5-dioxo-1...)

Ki: 2.10E+3nMAssay Description:Inhibitory effect against E. coli peptide deformylase (PDF) by DPPI assayMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304166(CHEMBL593447 | S-(3,5-Dideoxy-3-fluoro-D-xylofuran...)

Ki: 2.80E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair

PDB MMDB NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50119679(2-[(S)-2-(2-{2-[4-(2-Bromo-acetyl)-phenoxy]-acetyl...)

Ki: 2.80E+3nMAssay Description:Dissociation constant of the compound towards Protein-tyrosine phosphatase 1B receptor-inhibitor complex was determined using PNP as substrateMore data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
GoogleScholar

S-ribosylhomocysteine lyase(Escherichia coli (strain K12))
The Ohio State University

Curated by ChEMBL

BDBM50186747((2S)-2-AMINO-4-[(2R,3S)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 3.20E+3nMAssay Description:Inhibition of cobalt substituted Escherichia coli LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304165(CHEMBL593446 | S-(5-Deoxy-D-xylofuranos-5-yl)-L-ho...)

Ki: 4.20E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair

ChEBI
CHEMBL PC cid PC sid Similars

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304166(CHEMBL593447 | S-(3,5-Dideoxy-3-fluoro-D-xylofuran...)

Ki: 7.70E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304169((2S)-2-amino-4-(((2R,3S,4S)-3-bromo-4,5-dihydroxyt...)

Ki: 7.90E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304167(CHEMBL610483 | S-(3,5-Dideoxy-3-fluoro-1-O-methyl-...)

Ki: 8.80E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair

KEGG
UniProtKB/SwissProt
GoogleScholar

S-ribosylhomocysteine lyase(Vibrio harveyi (strain ATCC BAA-1116 / BB120))
The Ohio State University

Curated by ChEMBL

BDBM50186747((2S)-2-AMINO-4-[(2R,3S)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 9.70E+3nMAssay Description:Inhibition of cobalt substituted Vibrio harveyi LuxSMore data for this Ligand-Target Pair

PDB MMDB NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50119683(2-[(S)-2-(2-{[4'-(2-Bromo-acetyl)-biphenyl-2-carbo...)

Ki: 9.90E+3nMAssay Description:Dissociation constant of the compound towards Protein-tyrosine phosphatase 1B receptor-inhibitor complex was determined using PNP as substrateMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304168((2S)-2-amino-4-(((2S,3S,4S)-3-fluoro-4,5-dihydroxy...)

Ki: 1.06E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50186746((2S)-2-AMINO-4-[(2R,3R)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 1.06E+4nMAssay Description:Inhibition of zinc substituted Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
GoogleScholar

S-ribosylhomocysteine lyase(Escherichia coli (strain K12))
The Ohio State University

Curated by ChEMBL

BDBM50186746((2S)-2-AMINO-4-[(2R,3R)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 1.27E+4nMAssay Description:Inhibition of cobalt substituted Escherichia coli LuxSMore data for this Ligand-Target Pair

KEGG
UniProtKB/SwissProt
GoogleScholar

S-ribosylhomocysteine lyase(Vibrio harveyi (strain ATCC BAA-1116 / BB120))
The Ohio State University

Curated by ChEMBL

BDBM50186746((2S)-2-AMINO-4-[(2R,3R)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 1.28E+4nMAssay Description:Inhibition of cobalt substituted Vibrio harveyi LuxSMore data for this Ligand-Target Pair

PDB MMDB NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50119685(2-Bromo-1-(4-trifluoromethyl-phenyl)-ethanone | CH...)

Ki: 1.40E+4nMAssay Description:Dissociation constant of the compound towards Protein-tyrosine phosphatase 1B receptor-inhibitor complex was determined using PNP as substrateMore data for this Ligand-Target Pair

PDB MMDB NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM7880(2-bromo-1-(4-phenylphenyl)ethan-1-one | CHEMBL4130...)

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50186747((2S)-2-AMINO-4-[(2R,3S)-2,3-DIHYDROXY-3-N-HYDROXYC...)

Ki: 1.96E+4nMAssay Description:Inhibition of zinc substituted Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50119682(2-Bromo-1-naphthalen-2-yl-ethanone | CHEMBL101423)

Ki: 2.50E+4nMAssay Description:Dissociation constant of the compound towards Protein-tyrosine phosphatase 1B receptor-inhibitor complex was determined using PNP as substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 6(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50119679(2-[(S)-2-(2-{2-[4-(2-Bromo-acetyl)-phenoxy]-acetyl...)

Ki: 2.90E+4nMAssay Description:Dissociation constant of the compound towards SHP 1 receptor-inhibitor complex was determined using PNP as substrateMore data for this Ligand-Target Pair

PDB MMDB Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Methionine aminopeptidase 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50137352((S)-2-Amino-hexanoic acid hydroxy-[(2-pyridin-2-yl...)

Ki: 3.30E+4nMAssay Description:Inhibitory activity of the compound against Methionine aminopeptidase 1More data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

Peptide deformylase(Escherichia coli (strain K12))
Ohio State University

Curated by ChEMBL

BDBM50291695(CHEMBL84822 | H-PHOSPHONATE DERIVATIVE)

Ki: 3.70E+4nMAssay Description:Compound was evaluated for inhibitory activity against Peptide deformylaseMore data for this Ligand-Target Pair

CHEMBL KEGG PC cid PC sid Similars

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304164(CHEMBL611818 | S-(5-Deoxy-3-O-methyl-D-ribofuranos...)

Ki: 4.20E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

S-ribosylhomocysteine lyase(Bacillus subtilis)
The Ohio State University

Curated by ChEMBL

BDBM50304167(CHEMBL610483 | S-(3,5-Dideoxy-3-fluoro-1-O-methyl-...)

Ki: 4.20E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair

PDB MMDB NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar

Tyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
The Ohio State University

Curated by ChEMBL

BDBM50119687(2-Bromo-1-(4-hydroxy-phenyl)-ethanone | CHEMBL1029...)

Ki: 4.30E+4nMAssay Description:Dissociation constant of the compound towards Protein-tyrosine phosphatase 1B receptor-inhibitor complex was determined using PNP as substrateMore data for this Ligand-Target Pair