PRE-084 hydrochloride

CAS No. 75136-54-8

PRE-084 hydrochloride( —— )

Catalog No. M22600 CAS No. 75136-54-8

PRE-084 hydrochloride is a selective agonist of σ1(IC50:44 nM, in the sigma receptor assay).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 33 In Stock
10MG 53 In Stock
25MG 111 In Stock
50MG 196 In Stock
100MG 350 In Stock
200MG 536 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PRE-084 hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    PRE-084 hydrochloride is a selective agonist of σ1(IC50:44 nM, in the sigma receptor assay).
  • Description
    PRE-084 hydrochloride is a selective agonist of σ1(IC50:44 nM, in the sigma receptor assay).
  • In Vitro
    PRE-084 hydrochloride (0.1-100 μM; 24 h) protects cultured cortical neurons against β-amyloid toxicity (maximally neuroprotective at 10 μM) and reduces the levels of proapoptotic protein Bax at 10 μM. Cell Viability AssayCell Line:Cortical cells (βAP(25-35)-induced neurotoxicity model)Concentration:0.1-100 μM Incubation Time:24 h Result:Reduced neuronal toxicity in a bell shaped-manner and is maximally neuroprotective at 10 μM.Western Blot Analysis Cell Line:Cortical cells (βAP(25-35)-induced neurotoxicity model)Concentration:10 μM Incubation Time:24 hResult:Reduced the levels of proapoptotic protein Bax in cortical neurons induced by βAP(25-35).
  • In Vivo
    PRE-084 hydrochloride (0.25 mg/kg; i.p.; 3 times a week for 8 weeks) displays beneficial effects on motor performance (improves motor neuron survival, ameliorates paw abnormality and grip strength performance) in wobbler mice, and shows neuroprotective effects (increases the levels of BDNF in the gray matter).PRE-084 hydrochloride (1 mg/kg; i.p.; single) protects the heart by activating the Akt eNOS pathway in myocardial infarction model. Animal Model:Wobbler mice (4-week-old).Dosage:0.25 mg/kg Administration:Intraperitoneal injection; 3 times a week for 8 weeks.Result:Significantly improved ameliorated paw abnormality from week 4, and notably improved paw grip strength at week 5.Reduced the number of reactive astrocytes whereas increased the number of pan-macrophage marker CD68-positive cells and CD206+ cells involved in tissue restoration.Animal Model:Adult male Sprague?Dawley rats (220-250 g; myocardial infarction model).Dosage:1 mg/kg Administration:Intraperitoneal injection; single.Result:Significantly decreased the degree of myocardial apoptosis.Led to significantly increased expression of p?Akt and p?eNOS.
  • Synonyms
    ——
  • Pathway
    Autophagy
  • Target
    Sigma receptor
  • Recptor
    σ1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    75136-54-8
  • Formula Weight
    353.88
  • Molecular Formula
    C19H28ClNO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:31 mg/mL (87.6mM)
  • SMILES
    Cl.O=C(OCCN1CCOCC1)C1(CCCCC1)c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Peviani M, et al. Neuroprotective effects of the Sigma-1 receptor (S1R) agonist PRE-084, in a mouse model of motor neuron disease not linked to SOD1 mutation. Neurobiol Dis. 2014 Feb;62:218-232.
molnova catalog
related products
  • Opipramol

    Opipramol (Ensidon) is a compound with antidepressant activity that attenuates cocaine-seeking behavior in a rat model of self-administration.

  • KSK67

    KSK67 is a selective dual antagonist of sigma-2 and histamine H3 receptors with inhibitory effects on H3 receptors, sigma-1, and sigma-2 receptors, with Ki values of 3.2, 1531, and 101 nM, respectively.

  • AF-710B

    AF-710B is a specific variant of M1 muscarinic and Sigma-1 receptor agonist used in the study of neurological disorders such as Alzheimer's disease dementia and schizophrenia.