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Compile Data Set for Download or QSAR
maximum 50k data
Found
16
Enz. Inhib. hit(s) with all data for assayid = 1 entry = 50031804
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50229973
((4-(2-Amino-4-methylthiazol-5-yl)pyrimidin-2-yl)-(...)
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Affinity Data
Ki: 2nM
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
Purchase
CHEMBL
DrugBank
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
MMDB
PDB
3D Structure (crystal)
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Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319620
(CHEMBL1084715 | N-(4-(4-(2-(Ethylamino)-4-methylth...)
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Affinity Data
Ki: 32nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319617
(CHEMBL1084630 | N-Ethyl-4-methyl-5-(2-(4-morpholin...)
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Copy InChI
Affinity Data
Ki: 151nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319618
(CHEMBL1084629 | N,4-Dimethyl-5-(2-(4-morpholinophe...)
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Affinity Data
Ki: 156nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319624
(Aminopyrimidine, 4 | CHEMBL1084454 | N1-(4-(2,4-Di...)
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Affinity Data
Ki: 168nM
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
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319623
(4-(2,4-Dimethylthiazol-5-yl)-N-(3,4,5-trimethoxyph...)
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Affinity Data
Ki: 239nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM8066
(2-Anilino-4-(thiazol-5-yl)pyrimidine deriv. 37 | 4...)
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Affinity Data
Ki: 251nM
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
DrugBank
MMDB
PC cid
PC sid
PDB
Patents
Similars
In Depth
Details
Article
PubMed
MMDB
PDB
3D Structure (crystal)
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319622
(CHEMBL1083152 | N,4-Dimethyl-5-(2-(3,4,5-trimethox...)
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Affinity Data
Ki: 256nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319625
(CHEMBL1083150 | N1-(4-(2,4-Dimethylthiazol-5-yl)py...)
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Affinity Data
Ki: 286nM
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
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319615
(1-(4-(4-(4-(4-Methyl-2-(methylamino)thiazol-5-yl)p...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 297nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50277583
(2-amino-4-methyl-1,3-thiazol-5-yl)-N-[4-(morpholin...)
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Copy InChI
Affinity Data
Ki: 390nM
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
Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
MMDB
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319627
(1-(4-(4-(4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-y...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 432nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319621
(CHEMBL1086088 | N-Ethyl-4-methyl-5-(2-(3,4,5-trime...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 463nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319616
(1-(4-(4-(4-(2-Amino-4-methylthiazol-5-yl)pyrimidin...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 522nM
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319619
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-morpholinophenyl...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.04E+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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.97E+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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI