[Cereblon as a primary target of IMiDs].


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
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

Pagination

1013-1019

Auteurs

Takumi Ito (T)

Department of Nanoparticle Translational Research, Tokyo Medical University.
PRESTO, JST.

Hiroshi Handa (H)

Department of Nanoparticle Translational Research, Tokyo Medical University.

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Classifications MeSH