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Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
17
hits in this display
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: 150nM
Assay Description:
Inhibition of CDK1
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
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Article
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Target
Protein kinase C delta type
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: 1.70E+3nM
Assay Description:
Inhibition of PKCd
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
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PC sid
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Article
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Target
Ephrin type-B receptor 3
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of EPHB3
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
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In Depth
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Article
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Target
Glycogen synthase kinase-3
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of GSKp1
More data for this Ligand-Target Pair
Target Info
PDB
UniProtKB/SwissProt
antibodypedia
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
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In Depth
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Article
PubMed
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Target
Cyclin-dependent kinase 4
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of CDK4
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
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PC sid
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In Depth
Details
Article
PubMed
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Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: 2.00E+3nM
Assay Description:
Inhibition of CDK2
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
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In Depth
Details
Article
PubMed
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Target
Protein kinase C alpha type
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of PKCa
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
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In Depth
Details
Article
PubMed
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Target
RAC-alpha/RAC-beta/RAC-gamma serine/threonine-protein kinase
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of AKT
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
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Target
Mitogen-activated protein kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of ERK
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Ribosomal protein S6 kinase alpha-3
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of PKAP1
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
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In Depth
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Article
PubMed
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Target
Tyrosine-protein kinase Fyn
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
Ki: >2.00E+3nM
Assay Description:
Inhibition of FYN
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
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In Depth
Details
Article
PubMed
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Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
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Affinity Data
IC50: 1.28E+3nM
Assay Description:
Antiproliferative activity against human MDA435 cells
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 1.82E+3nM
Assay Description:
Antiproliferative activity against human H460a cells
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 1.86E+3nM
Assay Description:
Antiproliferative activity against human RKO cells
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 2.53E+3nM
Assay Description:
Antiproliferative activity against human HCT116 cells
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 2.84E+3nM
Assay Description:
Antiproliferative activity against human SJSA1 cells
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Roche Research Center
Curated by
ChEMBL
Ligand
BDBM50205468
((Z)-2-amino-5-(quinolin-6-ylmethylene)thiazol-4(5H...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 3.10E+3nM
Assay Description:
Antiproliferative activity against human SW480 cells
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI