Drug intelligence / Profile preview

JNJ-7706621

Development stage
Preclinical
Lead developer
Johnson & Johnson
Modality
Small Molecules
Administration
Oral, Intraperitoneal
01

Overview

**JNJ-7706621** is a small molecule, dual inhibitor targeting both cyclin-dependent kinases (CDKs) and Aurora kinases. It potently inhibits CDK1/cyclin B, CDK2/cyclin A, CDK2/cyclin E, and Aurora kinase A/B, resulting in disruption of cell cycle progression. In preclinical studies, JNJ-7706621 blocks tumor cell proliferation by causing G2/M phase arrest, endoreduplication, and apoptotic cell death, while showing reduced toxicity toward normal cells. The drug has demonstrated antitumor activity in xenograft models across multiple cancer types and can synergistically overcome resistance to radioimmunotherapy in activated B cell–like diffuse large B cell lymphoma. JNJ-7706621 has not progressed to clinical trials[1][3][5][7].

Other names
Aurora Kinase Inhibitor II4-(4'-Benzamidoanilino)-6,7-dimethoxyquinazoline
02

Targets

AURKA (Aurora kinase A)AURKB (Aurora kinase B)Cyclin-dependent kinase 2-cyclin E/A complexCDK3 (Cyclin-dependent kinase 3)CDK4 (Cyclin-dependent kinase 4)Cyclin-dependent kinase 6–cyclin D1 complexFGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)GSK3 (Glycogen synthase kinase 3 beta)JAK2 JH2 (Janus kinase 2 (JAK2) JH2 pseudokinase domain)TEK (Tie2)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)CDK1 (Cyclin-dependent kinase 1)CDK2 (Cyclin-dependent kinase 2)

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