Date published: 2026-3-18

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THIP hydrochloride (CAS 64603-91-4)

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Alternate Names:
Gaboxadol hydrochloride
Application:
THIP hydrochloride is a GABAA receptor agonist and GABAC receptor antagonist
CAS Number:
64603-91-4
Purity:
>98%
Molecular Weight:
176.60
Molecular Formula:
C6H8N2O2•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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THIP hydrochloride functions primarily through its interaction with the gamma-aminobutyric acid (GABA) system, specifically targeting GABAA and GABAC receptors where it acts as an antagonist. This chemical′s mechanism of action involves inhibiting the activity of these receptors, which play a role in mediating inhibitory neurotransmission in the central nervous system. By binding to these sites, THIP hydrochloride disrupts GABAergic signaling, leading to an increase in neuronal activity by preventing the typical inhibitory effects of GABA. This property has made it useful in neuroscientific research, offering insights into the functioning and pharmacological manipulation of GABAergic pathways. Researchers utilize THIP hydrochloride to study the complexities of the GABA system, elucidating the roles of inhibitory neurotransmission in various neurological processes and conditions. Its ability to selectively antagonize GABAA and GABAC receptors provides a means to dissect the contributions of these receptor subtypes to overall neural activity and behavior, thereby advancing our understanding of the intricate network of neurotransmission.


THIP hydrochloride (CAS 64603-91-4) References

  1. Involvement of GABAergic modulation of antinociception induced by morphine microinjected into the ventrolateral orbital cortex.  |  Qu, CL., et al. 2006. Brain Res. 1073-1074: 281-9. PMID: 16448630
  2. GABA(A) receptor modulation of 5-HT neuronal firing in the median raphe nucleus: implications for the action of anxiolytics.  |  Judge, SJ., et al. 2006. Eur Neuropsychopharmacol. 16: 612-9. PMID: 16531019
  3. GABAA receptor alpha 4 subunits mediate extrasynaptic inhibition in thalamus and dentate gyrus and the action of gaboxadol.  |  Chandra, D., et al. 2006. Proc Natl Acad Sci U S A. 103: 15230-5. PMID: 17005728
  4. The role of dopamine receptors in ventrolateral orbital cortex-evoked anti-nociception in a rat model of neuropathic pain.  |  Dang, YH., et al. 2010. Neuroscience. 169: 1872-80. PMID: 20599592
  5. Tonic GABAergic control of mouse dentate granule cells during postnatal development.  |  Holter, NI., et al. 2010. Eur J Neurosci. 32: 1300-9. PMID: 20846322
  6. Benzodiazepines modulate GABAA receptors by regulating the preactivation step after GABA binding.  |  Gielen, MC., et al. 2012. J Neurosci. 32: 5707-15. PMID: 22539833
  7. The role of GABAergic system on the inhibitory effect of ghrelin on food intake in neonatal chicks.  |  Jonaidi, H., et al. 2012. Neurosci Lett. 520: 82-6. PMID: 22613635
  8. Enantiotropically related polymorphs of gaboxadol hydrochloride.  |  Lopez de Diego, H., et al. 2013. Acta Crystallogr C. 69: 1234-7. PMID: 24192165
  9. Molecular and functional diversity of GABA-A receptors in the enteric nervous system of the mouse colon.  |  Seifi, M., et al. 2014. J Neurosci. 34: 10361-78. PMID: 25080596
  10. Specialized areas for value updating and goal selection in the primate orbitofrontal cortex.  |  Murray, EA., et al. 2015. Elife. 4: PMID: 26673891
  11. Effects of AMPA receptor antagonist, NBQX, and extrasynaptic GABAA agonist, THIP, on social behavior of adolescent and adult rats.  |  Dannenhoffer, CA., et al. 2018. Physiol Behav. 194: 212-217. PMID: 29800636
  12. Searching for New Microbiome-Targeted Therapeutics through a Drug Repurposing Approach.  |  Barone, M., et al. 2021. J Med Chem. 64: 17277-17286. PMID: 34846885

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

THIP hydrochloride, 50 mg

sc-204342
50 mg
$155.00