[Cereblon as a primary target of IMiDs].
Adaptor Proteins, Signal Transducing
Heterocyclic Compounds, 4 or More Rings
/ pharmacology
Humans
Immunomodulation
Lupus Erythematosus, Systemic
/ drug therapy
Lymphoma, Large B-Cell, Diffuse
/ drug therapy
Morpholines
Peptide Hydrolases
/ pharmacology
Phthalimides
Piperidones
Protease Inhibitors
Substrate Specificity
Ubiquitin-Protein Ligases
/ antagonists & inhibitors
Cereblon
IMiDs
PROTACs
Thalidomide
Journal
[Rinsho ketsueki] The Japanese journal of clinical hematology
ISSN: 0485-1439
Titre abrégé: Rinsho Ketsueki
Pays: Japan
ID NLM: 2984782R
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
11
10
2019
pubmed:
11
10
2019
medline:
28
10
2019
Statut:
ppublish
Résumé
Various derivatives of thalidomide, a drug that is well-known for its teratogenicity, have recently been developed; among them, lenalidomide and pomalidomide, known as immunomodulatory drugs (IMiDs), have potent anticancer activity. These drugs have been approved by Food and Drug Administration for the treatment of several diseases, including multiple myeloma, under strict control. The primary direct target protein of thalidomide and IMiDs is cereblon (CRBN), a substrate receptor of Cullin-RING ligase 4 (CRL4). CRL4
Identifiants
pubmed: 31597822
doi: 10.11406/rinketsu.60.1013
doi:
Substances chimiques
Adaptor Proteins, Signal Transducing
0
CRBN protein, human
0
Heterocyclic Compounds, 4 or More Rings
0
Morpholines
0
Phthalimides
0
Piperidones
0
Protease Inhibitors
0
iberdomide
8V66F27X44
Ubiquitin-Protein Ligases
EC 2.3.2.27
Peptide Hydrolases
EC 3.4.-
Types de publication
Journal Article
Review
Langues
jpn
Sous-ensembles de citation
IM