Page last updated: 2024-09-04

pomalidomide and ribociclib

pomalidomide has been researched along with ribociclib in 1 studies

Compound Research Comparison

Studies
(pomalidomide)
Trials
(pomalidomide)
Recent Studies (post-2010)
(pomalidomide)
Studies
(ribociclib)
Trials
(ribociclib)
Recent Studies (post-2010) (ribociclib)
62312155233056322

Protein Interaction Comparison

ProteinTaxonomypomalidomide (IC50)ribociclib (IC50)
Cyclin-T1Homo sapiens (human)1.1228
Cyclin-dependent kinase 4Homo sapiens (human)0.0156
G1/S-specific cyclin-D1Homo sapiens (human)0.0235
G1/S-specific cyclin-D3Homo sapiens (human)0.0352
Cyclin-dependent kinase 9Homo sapiens (human)1.1228
Cyclin-dependent kinase 6Homo sapiens (human)0.0393

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, S; Cao, Y; Dong, Z; Li, M; Li, Y; Liu, Y; Ruan, H; Song, W; Tang, Z; Wang, J; Wang, Y; Wei, M; Wei, Y; Yang, C; Yang, G; Zhao, R; Zhou, Y1

Other Studies

1 other study(ies) available for pomalidomide and ribociclib

ArticleYear
First orally bioavailable prodrug of proteolysis targeting chimera (PROTAC) degrades cyclin-dependent kinases 2/4/6 in vivo.
    European journal of medicinal chemistry, 2021, Jan-01, Volume: 209

    Topics: Administration, Oral; Aminopyridines; Animals; Antineoplastic Agents; Apoptosis; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinases; Humans; Mice, Inbred C57BL; Neoplasms, Experimental; Prodrugs; Proteolysis; Purines; Structure-Activity Relationship; Transcription Factors

2021