Date published: 2026-4-5

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UBP 296 (CAS 745055-86-1)

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Alternate Names:
(RS)-1-(2-Amino-2-carboxyethyl)-3-(2-carboxybenzyl)pyrimidine-2,4-dione
Application:
UBP 296 is a selective GluR5-subunit containing kainate receptor antagonist
CAS Number:
745055-86-1
Molecular Weight:
333.30
Molecular Formula:
C15H15N3O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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UBP 296 is a potent and selective GluR5-subunit containing kainate receptor antagonist (apparent KD = 1.09 mM). It displays ~ 90-fold selectivity over both AMPA receptors and recombinant human GluR6- and KA2-containing kainate receptors and shows little to no action at NMDA or group I mGlu receptors. UBP 296 selectively blocks kainate receptor-mediated LTP induction in rat hippocampal mossy fibers. UBP 296 garners significant interest owing to its potential applications across diverse scientific domains. This compound, derived from benzoic acid, comprises a pair of carboxylic groups alongside an amine group. Researchers have meticulously examined this compound for its physiological and biochemical impacts, as well as its promising roles in advancing scientific investigations. The precise mode of action of UBP 296 remains partially elusive. Nonetheless, it is postulated that the compound functions as a chelating agent, forming complexes with metal ions, thereby hampering the enzymatic and protein activities.


UBP 296 (CAS 745055-86-1) References

  1. Characterisation of UBP296: a novel, potent and selective kainate receptor antagonist.  |  More, JC., et al. 2004. Neuropharmacology. 47: 46-64. PMID: 15165833
  2. Synthesis and pharmacology of willardiine derivatives acting as antagonists of kainate receptors.  |  Dolman, NP., et al. 2005. J Med Chem. 48: 7867-81. PMID: 16302825
  3. Retigabine-induced population primary afferent hyperpolarisation in vitro.  |  Rivera-Arconada, I. and Lopez-Garcia, JA. 2006. Neuropharmacology. 51: 756-63. PMID: 16844148
  4. Low-frequency stimulation of the direct cortical input to area CA1 induces homosynaptic LTD and heterosynaptic LTP in the rat hippocampal-entorhinal cortex slice preparation.  |  Wöhrl, R., et al. 2007. Eur J Neurosci. 25: 251-8. PMID: 17241286
  5. Ethanol inhibition of kainate receptor-mediated excitatory neurotransmission in the rat basolateral nucleus of the amygdala.  |  Läck, AK., et al. 2008. Neuropharmacology. 55: 661-8. PMID: 18617194
  6. Chronic ethanol and withdrawal effects on kainate receptor-mediated excitatory neurotransmission in the rat basolateral amygdala.  |  Läck, AK., et al. 2009. Alcohol. 43: 25-33. PMID: 19185207
  7. Coactivation of thalamic and cortical pathways induces input timing-dependent plasticity in amygdala.  |  Cho, JH., et al. 2011. Nat Neurosci. 15: 113-22. PMID: 22158512
  8. Chondroitin Sulfate Induces Depression of Synaptic Transmission and Modulation of Neuronal Plasticity in Rat Hippocampal Slices.  |  Albiñana, E., et al. 2015. Neural Plast. 2015: 463854. PMID: 26075099
  9. Kainate receptors have different modulatory effect in seizure-like events and slow rhythmic activity in entorhinal cortex ex vivo.  |  Szádeczky-Kardoss, K., et al. 2019. Brain Res Bull. 153: 279-288. PMID: 31550521
  10. Epileptiform Events and Kainate Receptor Activity Changes Considerably during Entorhinal Cortex Development: An ex vivo Study.  |  Májer, T., et al. 2022. Dev Neurosci. 44: 508-517. PMID: 35640552

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

UBP 296, 1 mg

sc-204366
1 mg
$190.00

UBP 296, 10 mg

sc-204366A
10 mg
$900.00