Oxidopamine hydrobromide

CAS No. 636-00-0

Oxidopamine hydrobromide( 6-Hydroxydopamine hydrobromide,6-OHDA hydrobromide )

Catalog No. M22559 CAS No. 636-00-0

Oxidopamine hydrobromide is a neurotransmitter dopamine?antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG 50 In Stock
200MG 74 In Stock
500MG 154 In Stock
1G 248 In Stock

Biological Information

  • Product Name
    Oxidopamine hydrobromide
  • Note
    Research use only, not for human use.
  • Brief Description
    Oxidopamine hydrobromide is a neurotransmitter dopamine?antagonist.
  • Description
    Oxidopamine hydrobromide is a neurotransmitter dopamine?antagonist.
  • In Vitro
    Cell Viability Assay Cell Line:Neuro-2a cells and SH-SY5Y cellsConcentration:0-500 μMIncubation Time:24 or 48 h Result:Induced neurotoxicity, caused cytotoxicity in both Neuro-2a cells and SH-SY5Y cells in a concentration dependent manner. EC50=111 μM for 24 h incubation and 109 μM for 48 h incubation in the Neuro-2a cells; EC50=118 μM for 24 h incubation and 107 μM for 48 h incubation in the SH-SY5Y cells.RT-PCR Cell Line:Neuro-2a cells and SH-SY5Y cellsConcentration:75 or 150?μM Incubation Time:0, 6 or 24 h Result:Quickly and robustly induced COX-2 in a time-dependent manner. Induced COX-2 activation characterized by expression induction and nuclear translocation. Substantially increased PGE2 in the culture medium by nearly 5-fold in Neuro-2a cells (at 75 μM) and 3-fold in SH-SY5Y cells (at 150?μM). Significantly upregulated the pro-inflammatory cytokine interleukin-1β (IL-1β) within Neuro-2a cells and SH-SY5Y cells.Apoptosis Analysis Cell Line:PC12 cells Concentration:0, 25, 50, 75, and 150 μM Incubation Time:0, 2, 4, 6, 12, and 20 h Result:Induced apoptosis of PC12 cells. Increased the activities of caspase-3, -8 and -9 in PC12 cells in a time- and concentration-dependent manner. Increased these caspase activities at 2-4 h and reached a maximum at 12 h. Decreased cells with high mitochondrial membrane potential (JC-1 aggregate) in a time- and concentration-dependent manner.Western Blot Analysis Cell Line:PC12 cells Concentration:75 μM Incubation Time:0, 3, 5, 6, 8, 10, and 12 h Result:Increased the level of p-p38 in a time-dependent manner.
  • In Vivo
    ——
  • Synonyms
    6-Hydroxydopamine hydrobromide,6-OHDA hydrobromide
  • Pathway
    GPCR/G Protein
  • Target
    Dopamine Receptor
  • Recptor
    neurotransmitter dopamine|Autophagy
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    636-00-0
  • Formula Weight
    250.09
  • Molecular Formula
    C8H12BrNO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:97 mg/mL (387.86mM); H2O:17 mg/mL (67.98mM; Need ultrasonic)
  • SMILES
    Br.NCCc1cc(O)c(O)cc1O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Fujita H et al. Cell-permeable cAMP analog suppresses 6-hydroxydopamine-induced apoptosis in PC12 cells through the activation of the Akt pathway. Brain Res. 2006 Oct 3;1113(1):10-23.
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