Date published: 2025-12-14

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VU 0364739 hydrochloride (CAS 1244640-48-9)

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Alternate Names:
N-[2-[1-(3-Fluorophenyl)-4-oxo-1,3, 8-triazaspiro[4.5]dec-8-yl]ethyl]-2-naphthalenecar boxamide hydrochloride
Application:
VU 0364739 hydrochloride is a phospholipase D2 (PLD2) inhibitor
CAS Number:
1244640-48-9
Purity:
≥98%
Molecular Weight:
482.98
Molecular Formula:
C26H27FN4O2•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
Available in US only.
* Refer to Certificate of Analysis for lot specific data.

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VU 0364739 hydrochloride is a chemical compound widely utilized in scientific research for its potential to modulate neurotransmitter systems and investigate neurological disorders. Its mechanism of action primarily involves the allosteric modulation of metabotropic glutamate receptor subtype 5 (mGluR5), a G protein-coupled receptor (GPCR) involved in synaptic transmission and plasticity. By acting as a negative allosteric modulator (NAM) of mGluR5, VU 0364739 hydrochloride inhibits the receptor′s signaling pathway, leading to decreased intracellular calcium mobilization and downstream effects on synaptic transmission and neuronal excitability. In research, this compound has been instrumental in elucidating the role of mGluR5 in various neurological conditions, including schizophrenia, Alzheimer′s disease, Parkinson′s disease, and addiction. Additionally, studies have utilized VU 0364739 hydrochloride to explore the potential of targeting mGluR5 in the these disorders. Furthermore, its use extends to investigating the neurobiological mechanisms underlying synaptic plasticity, learning, and memory. As research in neuroscience continues to advance, VU 0364739 hydrochloride remains a valuable tool for probing the intricacies of neuronal function and identifying potential targets for neurological disorders.


VU 0364739 hydrochloride (CAS 1244640-48-9) References

  1. Protein kinase C and P2Y12 take center stage in thrombin-mediated activation of mammalian target of rapamycin complex 1 in human platelets.  |  Moore, SF., et al. 2014. J Thromb Haemost. 12: 748-60. PMID: 24612393
  2. Therapeutic inhibition of phospholipase D1 suppresses hepatocellular carcinoma.  |  Xiao, J., et al. 2016. Clin Sci (Lond). 130: 1125-36. PMID: 27129182
  3. Inhibition of PLD1 activity causes ER stress via regulation of COPII vesicle formation.  |  Nakagawa, H., et al. 2017. Biochem Biophys Res Commun. 490: 895-900. PMID: 28648601
  4. Co-ordinated activation of classical and novel PKC isoforms is required for PMA-induced mTORC1 activation.  |  Liu, M., et al. 2017. PLoS One. 12: e0184818. PMID: 28926616
  5. PLD-dependent phosphatidic acid microdomains are signaling platforms for podosome formation.  |  Bolomini-Vittori, M., et al. 2019. Sci Rep. 9: 3556. PMID: 30837487
  6. Preparation and Evaluation of Liposomes Co-Loaded with Doxorubicin, Phospholipase D Inhibitor 5-Fluoro-2-Indolyl Deschlorohalopemide (FIPI) and D-Alpha Tocopheryl Acid Succinate (α-TOS) for Anti-Metastasis.  |  Song, M., et al. 2019. Nanoscale Res Lett. 14: 138. PMID: 31001703
  7. Biased M1 receptor-positive allosteric modulators reveal role of phospholipase D in M1-dependent rodent cortical plasticity.  |  Moran, SP., et al. 2019. Sci Signal. 12: PMID: 31796631
  8. Diacylglycerol kinase and phospholipase D inhibitors alter the cellular lipidome and endosomal sorting towards the Golgi apparatus.  |  Lingelem, ABD., et al. 2021. Cell Mol Life Sci. 78: 985-1009. PMID: 32447426
  9. Parkin coordinates mitochondrial lipid remodeling to execute mitophagy.  |  Lin, CC., et al. 2022. EMBO Rep. 23: e55191. PMID: 36256516
  10. Phospholipase D1 activity is crucial for cytosolic phospholipase A2 -dependent prostaglandin E2 formation in murine osteoblastic MC3T3-E1 cells.  |  Leis, HJ. and Windischhofer, W. 2023. Prostaglandins Leukot Essent Fatty Acids. 198-199: 102592. PMID: 37951067

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

VU 0364739 hydrochloride, 10 mg

sc-363292
10 mg
$408.00
US: Only available in the US

VU 0364739 hydrochloride, 50 mg

sc-363292A
50 mg
$2040.00
US: Only available in the US