Currently, tissue plasminogen activator (tPA) is the gold standard for ischemic stroke in clinical practice. However, a shorter therapeutic window of opportunity limits the utility of tPA. Secondary brain damage from stroke is also a pressing issue. Many organizations have invested significant funds and resources in the development of new drugs to improve quality of life, but most have failed in clinical practice. In addition, the traditional process of stroke drug development is very costly and has a high failure rate. In conclusion, the development of stroke drugs is very urgent and necessary.
Fig. 1. Ischemic stroke translational research: from basic investigation to clinical application. (Chen et al., 2024)
Ace Therapeutics is a leading provider of preclinical stroke research services, specializing in providing comprehensive and customized stroke drug development services to pharmaceutical companies, biotech firms, and academic researchers. With one-stop services from target discovery and validation to preclinical evaluation, we aim to accelerate our clients' stroke therapy development programs.
Our team employs a multi-faceted approach that integrates advanced genomic, proteomic, and bioinformatics tools to identify and validate potential targets that play a key role in stroke pathogenesis, such as those involved in inflammation, oxidative stress, and neuronal cell death.
Categories | Promising therapeutic targets |
Targeting excitotoxicity | NMDA receptor (NMDAR), AMPA receptor (AMPAR), metabotropic glutamate receptor (mGluR), glutamate receptor, γ-amino butyric acid (GABA) receptor, PSD-95, etc. |
Targeting oxidative stress | Superoxide dismutase (SOD), catalase (CAT), peroxidase, glutathione peroxidase (GSH-Px), etc. |
Targeting apoptosis | Bcl-2 protein family, p53 gene, caspase family, Fas gene, JAK2/STAT3 signaling pathway, etc. |
Targeting autophagy | HIF-1α/BNIP3, PINK1/Parkin, PKC/JNK, PI3K/Akt-mTOR, AMPK/mTORC1, etc. |
Targeting inflammation | Interleukin 1β (IL-1β), IL-6, tumor necrosis factor-α (TNF-α), NLRP3, etc. |
Targeting angiogenesis | Vascular endothelial growth factor (VEGF), angiogenin, platelet-derived growth factor (PDGF), transforming growth factor (TGF), basic fibroblast growth factor (bFGF), matrix metalloproteinases (MMPs), hepatocyte growth factor (HGF), nitric oxide (NO), etc. |
Targeting neurogenesis | Brain-derived neurotrophic factor (BDNF) pathway, Notch pathway, Wnt/β-Catenin pathway, bone morphogenetic protein (BMP) pathway, etc. |
Our team can help clients conduct detailed PK/PD studies to assess the absorption, distribution, metabolism, and excretion (ADME) of potential stroke therapeutics. These include assessing bioavailability, tissue penetration (e.g., across the blood-brain barrier), and metabolic stability.
At Ace Therapeutics, we understand the complexities of stroke pathophysiology and the challenges associated with developing effective therapeutics. With deep expertise in discovery informatics, computational chemistry, molecular modeling, medicinal chemistry, structural biology, in vitro and in vivo pharmacology, and translational science in the field of stroke, Ace Therapeutics provides end-to-end support for stroke drug development.
By Drug Modality | |
By Drug Action |
Ace Therapeutics provide one-stop drug development services designed to help clients rapidly achieve key milestones in the development of innovative stroke therapeutics. If you are looking for a high-quality solution with best practices in the field of stroke drug development, please feel free to contact us.