Page last updated: 2024-09-04

pomalidomide and THZ531

pomalidomide has been researched along with THZ531 in 1 studies

Compound Research Comparison

Studies
(pomalidomide)
Trials
(pomalidomide)
Recent Studies (post-2010)
(pomalidomide)
Studies
(THZ531)
Trials
(THZ531)
Recent Studies (post-2010) (THZ531)
62312155219018

Protein Interaction Comparison

ProteinTaxonomypomalidomide (IC50)THZ531 (IC50)
Cyclin-T1Homo sapiens (human)0.5135
Cyclin-KHomo sapiens (human)0.2656
Cyclin-A2Homo sapiens (human)1.3
Cyclin-dependent kinase 2Homo sapiens (human)1.3
Cyclin-dependent kinase 7Homo sapiens (human)4.4025
Cyclin-dependent kinase 9Homo sapiens (human)0.5135
Cyclin-HHomo sapiens (human)5.8173
CDK-activating kinase assembly factor MAT1Homo sapiens (human)8.5
Cyclin-dependent kinase 13Homo sapiens (human)0.265
Cyclin-dependent kinase 12Homo sapiens (human)2.3247

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Cao, J; Chen, X; Dong, X; He, Q; Hong, J; Jiang, L; Li, K; Niu, T; Yang, B; Zhou, Z; Zhu, CL1

Other Studies

1 other study(ies) available for pomalidomide and THZ531

ArticleYear
Noncovalent CDK12/13 dual inhibitors-based PROTACs degrade CDK12-Cyclin K complex and induce synthetic lethality with PARP inhibitor.
    European journal of medicinal chemistry, 2022, Jan-15, Volume: 228

    Topics: CDC2 Protein Kinase; Cell Line, Tumor; Cyclin-Dependent Kinases; Cyclins; Dose-Response Relationship, Drug; Humans; Models, Molecular; Molecular Structure; Poly(ADP-ribose) Polymerase Inhibitors; Poly(ADP-ribose) Polymerases; Protein Kinase Inhibitors; Proteolysis; Structure-Activity Relationship

2022