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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
9
hits in this display
Target
G-protein coupled receptor 35
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
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Affinity Data
IC50: 564nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...
More data for this Ligand-Target Pair
Target Info
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Target
Nucleotide-binding oligomerization domain-containing protein 1
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
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Affinity Data
IC50: 607nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics Source Affiliation: Sanford-Burnham Medical Research Institute Network: NIH Molecular Lib...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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KEGG
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Target
G-protein coupled receptor 35
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
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Copy InChI
Affinity Data
IC50: 1.20E+3nM
Assay Description:
Data Source: Dr. Mary Abood Source Affiliation: Temple University Network: NIH Molecular Libraries Probe Production Centers Network (MLPCN) Grant Pro...
More data for this Ligand-Target Pair
Target Info
PDB
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Target
26S proteasome non-ATPase regulatory subunit 14
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
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Affinity Data
IC50: 1.77E+4nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford Burnham Medical Research Institute (SBMRI, La Jolla, CA...
More data for this Ligand-Target Pair
Target Info
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Target
Prothrombin
(Bos taurus (Bovine))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
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Affinity Data
IC50: 2.39E+4nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford Burnham Medical Research Institute (SBMRI, La Jolla, CA...
More data for this Ligand-Target Pair
Target Info
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Target
G-protein coupled receptor 55
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
Copy SMILES
Copy InChI
Affinity Data
IC50: >3.20E+4nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics(SSBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...
More data for this Ligand-Target Pair
Target Info
Reactome pathway
KEGG
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Target
DNA (cytosine-5)-methyltransferase 3A
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
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Affinity Data
IC50: 5.88E+4nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
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KEGG
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Target
Tyrosine-protein phosphatase non-receptor type 22
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
Copy SMILES
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Affinity Data
IC50: 9.59E+4nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, CA...
More data for this Ligand-Target Pair
Target Info
PDB
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antibodypedia
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Copy BDB DOI
Target
Tyrosine-protein phosphatase non-receptor type 22
(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by
PubChem BioAssay
Ligand
BDBM61654
(3-[4-[(5Z)-4-keto-2-thioxo-5-veratrylidene-thiazol...)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
Purchase
PC cid
PC sid
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In Depth
Details
PCBioAssay
Copy BDB DOI