Drug intelligence / Profile preview

THX-B

Development stage
Preclinical
Lead developer
McGill University
Modality
Small Molecules
Administration
Intravenous, Intraperitoneal, Oral, Subcutaneous, Transdermal, Topical, Intravitreal
01

Overview

THX-B is a potent, non-peptidic small molecule antagonist of the p75 neurotrophin receptor (p75NTR, also known as NGFR or CD271). It acts as a competitive blocker of pro-nerve growth factor (proNGF) binding to p75NTR, thereby inhibiting both proNGF-induced and ligand-independent p75NTR signaling pathways. Developed by researchers at McGill University, THX-B has demonstrated therapeutic potential in preclinical models for several conditions, including diabetic retinopathy, diabetic voiding dysfunction, age-related bladder remodeling, retinitis pigmentosa, and metastatic melanoma. By blocking p75NTR, THX-B reduces neuroinflammation, prevents neuronal apoptosis (such as retinal ganglion cell death), and limits tumor lymphangiogenesis and distal metastasis.

Other names
1,3-diisopropyl-1-[2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-purin-7-yl)-acetyl]-urea2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)-N-isopropyl-N-(isopropylcarbamoyl)acetamide
02

Targets

NGFR (p75NTR)

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