BindingDB PrimarySearch

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469558(CHEMBL4061041)

IC50: 1.46nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: 3.13nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

Details Article PubMed PDB

3D Structure (crystal)

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469562(CHEMBL4069725)

IC50: 3.56nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469559(CHEMBL4063087)

IC50: 4.15nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469555(CHEMBL4090716)

IC50: 4.19nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469560(CHEMBL4083624)

IC50: 12.5nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469563(CHEMBL4079368)

IC50: 16.4nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469550(CHEMBL4070478)

IC50: 19.7nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469557(CHEMBL4091408)

IC50: 37.5nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469554(CHEMBL4061854)

IC50: 39nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469553(CHEMBL4102769)

IC50: 81.4nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469552(CHEMBL4072428)

IC50: 98nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469548(CHEMBL4073216)

IC50: 116nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

DNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50197073(3-amino-7-((R)-3-((S)-1-aminoethyl)pyrrolidin-1-yl...)

IC50: 200nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair

CHEMBL MMDB PC cid PC sid PDB Patents Similars

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469549(CHEMBL4092311)

IC50: 268nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469551(CHEMBL4064630)

IC50: 342nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469561(CHEMBL4065657)

IC50: 362nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

DNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50542206(CHEMBL4640061)

IC50: 430nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

DNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM21690(1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,...)

IC50: 490nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair

Purchase ChEBI
CHEMBL DrugBank MCE
KEGG MMDB PC cid PC sid PDB Patents Similars

Details Article PubMed DrugBank

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469556(CHEMBL4087085)

IC50: 899nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

DNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50542207(CHEMBL4634552)

IC50: 1.25E+3nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair

PC cid PC sid PDB

PDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

UDP-3-O-acyl-N-acetylglucosamine deacetylase(Pseudomonas aeruginosa)
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50469564(CHEMBL4100062)

IC50: 1.64E+3nMAssay Description:Inhibition of Pseudomonas aeruginosa LpxC using UDP-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine as substrate preincubated for 30 mins followed by sub...More data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566539(CHEMBL4860033)

IC50: 2.70E+3nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

PDB MMDB KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar

DNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50542205(CHEMBL4643875)

IC50: 2.91E+3nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566543(CHEMBL4864037)

IC50: 8.00E+3nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566538(CHEMBL4875315)

IC50: 1.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566541(CHEMBL4867915)

IC50: 1.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566542(CHEMBL4878164)

IC50: 1.20E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566546(CHEMBL4875871)

IC50: 1.30E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566544(CHEMBL4852170)

IC50: 1.70E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566545(CHEMBL4861495)

IC50: 1.80E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566510(CHEMBL4860105)

IC50: 2.50E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566540(CHEMBL4877922)

IC50: 2.90E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Histone deacetylase 3(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC3More data for this Ligand-Target Pair

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

Histone deacetylase 6(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair

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

Histone deacetylase 8(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC8More data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566514(CHEMBL4865462)

IC50: >3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar

Histone deacetylase 11(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC11More data for this Ligand-Target Pair

Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar

Histone deacetylase 5(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC5More data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566535(CHEMBL4860370)

IC50: >3.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566513(CHEMBL4869164)

IC50: >3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Histone deacetylase 7(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC7More data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566549(CHEMBL4856534)

IC50: >3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566548(CHEMBL4861063)

IC50: >3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566547(CHEMBL4869998)

IC50: >3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair

Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar

Histone deacetylase 9(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC9More data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566517(CHEMBL4873798)

IC50: >3.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair

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

Potassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50566519(CHEMBL4868731)

IC50: >3.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair

NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia GoogleScholar

Polyamine deacetylase HDAC10(Homo sapiens (Human))
Novartis Institutes For Biomedical Research

Curated by ChEMBL

BDBM50249583(CHEMBL4097399)

IC50: >3.00E+4nMAssay Description:Inhibition of human HDAC10More data for this Ligand-Target Pair