Date published: 2026-5-27

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Lurasidone Hydrochloride (CAS 367514-88-3)

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Alternate Names:
(3aR,4S,7R,7aS)-2-[[(1R,2R)-2-[[4-(1,2-Benzisothiazol-3-yl)-1-piperazinyl]methyl]cyclohexyl]methyl]hexahydro-4,7-methano-1H-isoindole-1,3(2H)-dione Hydrochloride
CAS Number:
367514-88-3
Molecular Weight:
529.14
Molecular Formula:
C28H37ClN4O2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Lurasidone Hydrochloride is a synthetic compound notable for its affinity and antagonistic activity towards a variety of neurotransmitter receptors, including dopamine D2, serotonin 5-HT2A, and 5-HT7, among others, in the central nervous system. This specific receptor profile allows it to modulate neurotransmitter signaling, affecting the dopaminergic and serotonergic systems, which are in understanding a wide range of neurobiological processes. In research applications, Lurasidone Hydrochloride′s ability to cross the blood-brain barrier and its high receptor selectivity make it useful for investigating the underlying mechanisms of neurotransmission and its impact on neural circuits. Its action at the D2 receptor, for instance, provides insights into dopamine′s role in cognition and behavior, while its effects on serotonin receptors help elucidate the complex interplay between different neurotransmitter systems. By altering neurotransmitter activity, Lurasidone Hydrochloride serves as a critical asset in neuroscientific studies, enabling researchers to dissect the neuropharmacological basis of behavior and neural function, and to explore the molecular underpinnings of neurological conditions.


Lurasidone Hydrochloride (CAS 367514-88-3) References

  1. Solubility enhancement studies on lurasidone hydrochloride using mixed hydrotropy.  |  Madan, JR., et al. 2015. Int J Pharm Investig. 5: 114-20. PMID: 25838997
  2. Pharmacokinetics and Pharmacodynamics of Lurasidone Hydrochloride, a Second-Generation Antipsychotic: A Systematic Review of the Published Literature.  |  Greenberg, WM. and Citrome, L. 2017. Clin Pharmacokinet. 56: 493-503. PMID: 27722855
  3. Charge-assisted bond N+H mediates the gelation of amorphous lurasidone hydrochloride during dissolution.  |  Qian, S., et al. 2017. Int J Pharm. 518: 335-341. PMID: 28043915
  4. Optimization of Nanostructured Lipid Carriers of Lurasidone Hydrochloride Using Box-Behnken Design for Brain Targeting: In Vitro and In Vivo Studies.  |  Jazuli, I., et al. 2019. J Pharm Sci. 108: 3082-3090. PMID: 31077685
  5. Lurasidone compared to other atypical antipsychotic monotherapies for adolescent schizophrenia: a systematic literature review and network meta-analysis.  |  Arango, C., et al. 2020. Eur Child Adolesc Psychiatry. 29: 1195-1205. PMID: 31758359
  6. Coamorphization combined with complexation enhances dissolution of lurasidone hydrochloride and puerarin with synchronized release.  |  Wang, S., et al. 2020. Int J Pharm. 588: 119793. PMID: 32827676
  7. Lurasidone, olanzapine, and quetiapine extended-release for bipolar depression: A systematic review and network meta-analysis of phase 3 trials in Japan.  |  Kishi, T., et al. 2020. Neuropsychopharmacol Rep. 40: 417-422. PMID: 32902200
  8. Stable solid dispersion of lurasidone hydrochloride with augmented physicochemical properties for the treatment of schizophrenia and bipolar disorder.  |  Pardhi, VP. and Flora, S. 2020. Biopharm Drug Dispos. 41: 334-351. PMID: 33080060
  9. Influence of the pK a Value of Cinnamic Acid and P-Hydroxycinnamic Acid on the Solubility of a Lurasidone Hydrochloride-Based Coamorphous System.  |  Hu, Y., et al. 2021. ACS Omega. 6: 3106-3119. PMID: 33553927
  10. Lurasidone for Adolescents With Complex Mental Disorders: A Case Series.  |  Mole, TB., et al. 2022. J Pharm Pract. 35: 800-804. PMID: 33757374
  11. Systematic Review and Network Meta-analysis: Efficacy and Safety of Second-Generation Antipsychotics in Youths With Bipolar Depression.  |  DelBello, MP., et al. 2022. J Am Acad Child Adolesc Psychiatry. 61: 243-254. PMID: 34420839
  12. Inclusion complex of lurasidone hydrochloride with Sulfobutylether-β-cyclodextrin has enhanced oral bioavailability and no food effect.  |  Wang, J., et al. 2022. Am J Transl Res. 14: 1495-1506. PMID: 35422944
  13. Lurasidone-induced hyperosmolar hyperglycemic syndrome: A case report.  |  Hanyu, S., et al. 2022. Neuropsychopharmacol Rep. 42: 377-379. PMID: 35609885
  14. Effect of sodium lauryl sulfate-mediated gelation on the suppressed dissolution of crystalline lurasidone hydrochloride and a strategy to mitigate the gelation.  |  Lin, Z., et al. 2022. Int J Pharm. 624: 122035. PMID: 35863597
  15. Improving Lurasidone Hydrochloride's Solubility and Stability by Higher-Order Complex Formation with Hydroxypropyl-β-cyclodextrin.  |  Gamboa-Arancibia, ME., et al. 2023. Pharmaceutics. 15: PMID: 36678861

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Lurasidone Hydrochloride, 5 mg

sc-489135
5 mg
$350.00