Drug intelligence / Profile preview

flonotinib

Development stage
Unknown
Lead developer
Zenitar
Modality
Small Molecules
Administration
Oral
01

Overview

Flonotinib (ZL-2102) is a potent and highly selective Janus kinase 2 (JAK2) inhibitor developed by Chengdu Zeling Biomedical Technology. It is specifically designed to target the JAK2/STAT3 signaling pathway, which is frequently dysregulated in myeloproliferative neoplasms. Unlike first-generation JAK inhibitors that often inhibit both JAK1 and JAK2, flonotinib's high selectivity for JAK2 is intended to reduce off-target toxicities such as anemia and thrombocytopenia associated with JAK1 inhibition. It is currently being evaluated in clinical trials for the treatment of intermediate-2 or high-risk myelofibrosis, including patients who are refractory, relapsed, or intolerant to prior JAK inhibitor therapies like ruxolitinib.

Other names
flonotinib maleate马来酸氟诺替尼
02

Targets

FLT3 (Fms related receptor tyrosine kinase 3)JAK2 (Janus kinase 2)JAK3 (Janus kinase 3)JAK1 (Janus kinase 1)TYK2 (Tyrosine kinase 2)

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