Drug intelligence / Profile preview

KR-31831

Development stage
Phase 1
Lead developer
Hanlim Pharm. Co., Ltd.
Modality
Small Molecules
Administration
Oral, Topical (ophthalmic), Intravitreal, Intraperitoneal
01

Overview

KR-31831 is a **synthetic small molecule** with anti-angiogenic and radioprotective activities. It is a **benzopyran derivative** that inhibits angiogenesis by targeting multiple pathways involved in neovascularization, primarily through suppression of **VEGF signaling (downregulation of VEGFR-2/KDR)**, reduction of **FGFR-2** and **basic FGF (bFGF)** expression, and inhibition of **matrix metalloproteinase-2 (MMP-2)** activity, thus preventing proliferation, migration, and tube formation of endothelial cells[1][2][4][7]. In preclinical models, KR-31831 protects hematopoietic cells and radiosensitive tissues against radiation-induced injury, enhances bone marrow and peripheral blood cell recovery, and reduces apoptosis in response to whole-body irradiation, mainly by modulating apoptotic gene expression and the immune response[3][5]. Topical and systemic administration in animal models demonstrated efficacy in reducing corneal and choroidal neovascularization as well as subretinal neovascularization[7][5].

Brand names
HL-217HL217HL 217
Other names
benzopyran derivative KR-31831
02

Targets

PDGFRB (Platelet-derived growth factor receptor beta)VEGFR2 (Vascular endothelial growth factor receptor 2)MMP2 (Matrix metalloproteinase-2)FGFR2 (Keratinocyte growth factor receptor)

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