Compile Data Set for Download or QSAR
Found 38 of ki for UniProtKB: P50750
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81433(CDK Inhibitor, 6)copy SMILEScopy InChI
Affinity DataKi:  0.290nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81441(CDK Inhibitor, 14)copy SMILEScopy InChI
Affinity DataKi:  0.380nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81430(CDK Inhibitor, 3)copy SMILEScopy InChI
Affinity DataKi:  0.800nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81434(CDK Inhibitor, 7)copy SMILEScopy InChI
Affinity DataKi:  0.960nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81439(CDK Inhibitor, 12)copy SMILEScopy InChI
Affinity DataKi:  1.90nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM5655(2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydr...)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Inhibition of CDK9 (unknown origin)More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50229973((4-(2-Amino-4-methylthiazol-5-yl)pyrimidin-2-yl)-(...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM5931(BMS-387072 | CHEMBL296468 | N-(5-{[(5-tert-butyl-1...)copy SMILEScopy InChI
Affinity DataKi:  4nMAssay Description:Inhibition of CDK9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8N18PubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81432(CDK Inhibitor, 5)copy SMILEScopy InChI
Affinity DataKi:  4.30nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81431(CDK Inhibitor, 4)copy SMILEScopy InChI
Affinity DataKi:  4.30nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81429(CDK Inhibitor, 2)copy SMILEScopy InChI
Affinity DataKi:  4.5nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM8061(2-Anilino-4-(thiazol-5-yl)pyrimidine deriv. 32 | 4...)copy SMILEScopy InChI
Affinity DataKi:  4.60nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81440(CDK Inhibitor, 13)copy SMILEScopy InChI
Affinity DataKi:  5.90nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81435(CDK Inhibitor, 8)copy SMILEScopy InChI
Affinity DataKi:  5.90nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319622(CHEMBL1083152 | N,4-Dimethyl-5-(2-(3,4,5-trimethox...)copy SMILEScopy InChI
Affinity DataKi:  6nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM498187(US11014911, Example 15 | US11718603, Example 15)copy SMILES
Affinity DataKi:  6.30nMAssay Description:The purpose of CDK2/Cyclin E1 assay is to evaluate the inhibition (% inhibition, Kiapp and Ki values) of small molecule inhibitors by using a fluores...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23N26H2US Patent
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81436(CDK Inhibitor, 9)copy SMILEScopy InChI
Affinity DataKi:  6.70nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81437(CDK Inhibitor, 10)copy SMILEScopy InChI
Affinity DataKi:  8.5nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319620(CHEMBL1084715 | N-(4-(4-(2-(Ethylamino)-4-methylth...)copy SMILEScopy InChI
Affinity DataKi:  9nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319623(4-(2,4-Dimethylthiazol-5-yl)-N-(3,4,5-trimethoxyph...)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM81438(CDK Inhibitor, 11)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Kinase assay using cyclin-dependant kinases (CDK).More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F3QPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50193090(CHEMBL3895785)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Inhibition of human CDK9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G73GP8PubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50261273(CHEMBL4076947)copy SMILEScopy InChI
Affinity DataKi:  108nMAssay Description:Inhibition of CDK9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RF5XG8PubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50434821(CHEMBL2387224)copy SMILEScopy InChI
Affinity DataKi:  111nMAssay Description:Inhibition of CDK9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2416ZGBPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM498185(US11014911, Example 13 | US11718603, Example 13 | ...)copy SMILES
Affinity DataKi:  177nMAssay Description:The purpose of CDK2/Cyclin E1 assay is to evaluate the inhibition (% inhibition, Kiapp and Ki values) of small molecule inhibitors by using a fluores...More data for this Ligand-Target Pair
Ligand InfoMCE
PC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23N26H2US Patent
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319616(1-(4-(4-(4-(2-Amino-4-methylthiazol-5-yl)pyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  264nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319624(Aminopyrimidine, 4 | CHEMBL1084454 | N1-(4-(2,4-Di...)copy SMILEScopy InChI
Affinity DataKi:  337nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319625(CHEMBL1083150 | N1-(4-(2,4-Dimethylthiazol-5-yl)py...)copy SMILEScopy InChI
Affinity DataKi:  348nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319615(1-(4-(4-(4-(4-Methyl-2-(methylamino)thiazol-5-yl)p...)copy SMILEScopy InChI
Affinity DataKi:  448nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50277583(2-amino-4-methyl-1,3-thiazol-5-yl)-N-[4-(morpholin...)copy SMILEScopy InChI
Affinity DataKi:  480nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319617(CHEMBL1084630 | N-Ethyl-4-methyl-5-(2-(4-morpholin...)copy SMILEScopy InChI
Affinity DataKi:  559nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319621(CHEMBL1086088 | N-Ethyl-4-methyl-5-(2-(3,4,5-trime...)copy SMILEScopy InChI
Affinity DataKi:  564nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM8066(2-Anilino-4-(thiazol-5-yl)pyrimidine deriv. 37 | 4...)copy SMILEScopy InChI
Affinity DataKi:  575nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319627(1-(4-(4-(4-(2,4-Dimethylthiazol-5-yl)pyrimidin-2-y...)copy SMILEScopy InChI
Affinity DataKi:  1.15E+3nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319626(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)copy SMILEScopy InChI
Affinity DataKi:  1.47E+3nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50224883(7-chloro-3-oxo-8-[(thiazol-5-ylmethyl)-amino]-11,1...)copy SMILEScopy InChI
Affinity DataKi: >1.64E+3nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X067WTPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319618(CHEMBL1084629 | N,4-Dimethyl-5-(2-(4-morpholinophe...)copy SMILEScopy InChI
Affinity DataKi:  2.61E+3nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed
TargetCyclin-dependent kinase 9(Homo sapiens (Human))
Cyclacel Limited

LigandPNGBDBM50319619(4-(2,4-Dimethylthiazol-5-yl)-N-(4-morpholinophenyl...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Inhibition of CDK9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930T9DPubMed