Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Dihydrokainate (DHK) is a synthetic derivative of kainic acid that serves as a potent and selective inhibitor of the **Excitatory Amino Acid Transporter 2 (EAAT2)**, also known as **Glutamate Transporter 1 (GLT-1)** in rodents. Unlike its parent compound, DHK exhibits negligible activity at ionotropic glutamate receptors (AMPA, kainate, or NMDA) at concentrations that effectively block glutamate transport. By selectively inhibiting the primary transporter responsible for clearing glutamate from the synaptic cleft in the mammalian central nervous system, DHK is a vital pharmacological tool for investigating the role of glutamate homeostasis in synaptic plasticity and neurotoxicity. It is frequently employed in disease models of **Amyotrophic Lateral Sclerosis (ALS)** and epilepsy, where impaired EAAT2 function is a recognized pathological feature.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on dihydrokainate.