Drug intelligence / Profile preview

LHT-7

Development stage
Preclinical
Lead developer
Kyungpook National University
Modality
Biodegradable Polymers → Polymer-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous, Subcutaneous, Topical
01

Overview

LHT-7 (heparin-taurocholate conjugate) is a low molecular weight heparin derivative developed as a multi-targeting anti-angiogenic agent for the treatment of solid tumors, including breast cancer, pancreatic cancer, and glioblastoma. It is synthesized by covalently conjugating low molecular weight heparin with taurocholic acid (a bile acid), which significantly reduces its anticoagulant activity while enhancing its binding affinity to multiple angiogenic growth factors. LHT-7 exerts its therapeutic effects by binding to and blocking key pro-angiogenic growth factors, including vascular endothelial growth factor (VEGF), fibroblast growth factor 2 (FGF2), and platelet-derived growth factor B (PDGF-B), thereby inhibiting the phosphorylation of their respective receptors (VEGFR2, FGFR1, and PDGFR-beta) and suppressing tumor angiogenesis and metastasis.

Other names
heparin-taurocholate conjugateheparin-taurocholic acid conjugatelow molecular weight heparin-taurocholate conjugatelow molecular weight heparin-taurocholic acid conjugate
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFA (Vascular endothelial growth factor A)PDGFRB (Platelet-derived growth factor receptor beta)FGFR1 (Fibroblast growth factor receptor 1)PDGFB (PDGF-B)FGF2

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