Guanabenz

CAS No. 5051-62-7

Guanabenz( WY 8678 )

Catalog No. M14722 CAS No. 5051-62-7

Guanabenz (WY 8678) is an α2 adrenergic receptor agonist that is used as an antihypertensive agent.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 42 In Stock
5MG 61 In Stock
10MG 88 In Stock
25MG 158 In Stock
50MG 226 In Stock
100MG 339 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Guanabenz
  • Note
    Research use only, not for human use.
  • Brief Description
    Guanabenz (WY 8678) is an α2 adrenergic receptor agonist that is used as an antihypertensive agent.
  • Description
    Guanabenz (WY 8678) is an α2 adrenergic receptor agonist that is used as an antihypertensive agent, also has been proposed to exert protective effects against misfolding by interfering with eIF2α-P dephosphorylation through selective disruption of a PP1-PPP1R15A holophosphatase complex; also has antiparasitic activity against replicative stages of Toxoplasma.Multiple Sclerosis Phase 1 Clinical(In Vitro):Guanabenz hydrochloride (0.5-50 μM, 24 h) is treated with increasing concentrations for 24 hours not affect cell viability.Guanabenz hydrochloride (0.5-50 μM, 24 h) alone not affects the UPR targets, neither on mRNA or protein level nor the phosphorylation status of eIF2a. Guanabenz also not induces GADD34 or the constitutively active form CReP.Guanabenz hydrochloride (0.5-50 μM, 24 h) alone not induces ER stress in neonatal rat cardiomyocytes. (In Vivo):Guanabenz hydrochloride (5 mg/kg/day; i.p.; for 3 weeks) can reproducibly reduce brain cyst burden.Guanabenz hydrochloride (5 mg /kg/d, i.p., oral; 10 mg/kg/d, gavage; for 3 weeks) reverses Toxoplasma-induced hyperactivity in latently infected mice.Guanabenz hydrochloride (100 and 320 μg/kg and 1 mg/kg, i.v., over a period of 5 min at intervals of 40 min) reduces sympathetic outflow, heart rate and blood pressure in debuffered cats.
  • In Vitro
    Guanabenz (0.5-50 μM, 24 h) is treated with increasing concentrations for 24 hours not affect cell viability.Guanabenz (0.5-50 μM, 24 h) alone not affects the UPR targets, neither on mRNA or protein level nor the phosphorylation status of eIF2a. Guanabenz also not induces GADD34 or the constitutively active form CReP.Guanabenz (0.5-50 μM, 24 h) alone not induces ER stress in neonatal rat cardiomyocytes.Cell Viability Assay Cell Line:Neonatal rat cardiac myocytes (NRCM)Concentration:0.5–50 μM Incubation Time:24 hResult:Did not affect cell survival.RT-PCRCell Line:Neonatal rat cardiac myocytes (NRCM)Concentration:0.5–50 μM Incubation Time:24 h Result:Did not affect levels of UPR targets.Western Blot Analysis Cell Line:Neonatal rat cardiac myocytes (NRCM) Concentration:0.5–50 μM Incubation Time:24 h Result:Increased the levels of low panel concentration-dependent UPR targets proteins.
  • In Vivo
    Guanabenz (5 mg/kg/day; i.p.; for 3 weeks) can reproducibly reduce brain cyst burden.Guanabenz (5 mg /kg/d, i.p., oral; 10 mg/kg/d, gavage; for 3 weeks) reverses Toxoplasma-induced hyperactivity in latently infected mice.Guanabenz (100 and 320 μg/kg and 1 mg/kg, i.v., over a period of 5 min at intervals of 40 min) reduces sympathetic outflow, heart rate and blood pressure in debuffered cats. Animal Model:BALB/cJ mice Dosage:5 mg/kg Administration:5 mg/kg/day; i.p. ; for 3 weeks Result:Reduced the latent brain cysts in both male and female BALB/cJ mice.Animal Model:BALB/cJ mice Dosage:5 mg/kg; 10 mg/kg Administration:5 mg /kg/d, i.p., oral; 10 mg/kg/d, gavage; for 3 weeks Result:Reversed parasite-induced hyperactivity to near-baseline levels.Animal Model:Cats Dosage:100 and 320 μg/kg and 1 mg/kg Administration:100 and 320 μg/kg and 1 mg/kg, i.v., over a period of 5 min at intervals of 40 min Result:Declined markedly blood pressure and nerve activity.
  • Synonyms
    WY 8678
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Protein Phosphatase/PTP
  • Recptor
    Protein Phosphatase/PTP
  • Research Area
    Inflammation/Immunology
  • Indication
    Multiple Sclerosis

Chemical Information

  • CAS Number
    5051-62-7
  • Formula Weight
    231.08
  • Molecular Formula
    C8H8Cl2N4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    N/C(N)=N\N=C\C1=C(Cl)C=CC=C1Cl
  • Chemical Name
    2-[(E)-(2,6-dichlorophenyl)methylideneamino]guanidine

Shipping & Storage Information

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

Reference

1. Das I, et al. Science. 2015 Apr 10;348(6231):239-42. 2. Crespillo-Casado A, et al. Elife. 2017 Apr 27;6. pii: e26109. 3. Benmerzouga I, et al. Antimicrob Agents Chemother. 2015 Nov;59(11):6939-45.
molnova catalog
related products
  • LB-100

    LB-100 (LB100) is a potent serine/threonine protein phosphatase 2A (PP2A) inhibitor; exhibits inhibitory effect in HCC cell lines Huh-7, HepG2, Hep3B, and SNU-449 with mean IC50 of 10 uM.

  • JTT-551 sodium

    JTT-551 sodium (JTT551, JTT 551) is a novel potent, selective inhibitor of protein tyrosine phosphatase 1B (PTP1B) with Ki of 0.22 uM.

  • AQX 1125

    AQX 1125 (Rosiptor) is a specific, orally bioavailable SHIP1 activator.