N-tert-butyl-α-Phenylnitrone

CAS No. 3376-24-7

N-tert-butyl-α-Phenylnitrone( (Z)-N-benzylidene-2-Methylpropan-2-aMine oxide )

Catalog No. M27667 CAS No. 3376-24-7

N-tert-butyl-α-Phenylnitrone inhibits COX2 catalytic activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 32 In Stock
50MG 43 In Stock
100MG 65 In Stock
200MG 102 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    N-tert-butyl-α-Phenylnitrone
  • Note
    Research use only, not for human use.
  • Brief Description
    N-tert-butyl-α-Phenylnitrone inhibits COX2 catalytic activity.
  • Description
    N-tert-butyl-α-Phenylnitrone inhibits COX2 catalytic activity. N-tert-butyl-α-Phenylnitrone possesses potent reactive oxygen species scavenging, anti-inflammatory, neuroprotective, anti-aging, and anti-diabetic activities, and can penetrate the blood-brain barrier.(In Vitro):Treatment of 25-100 μM N-tert-butyl-α-Phenylnitrone significantly reduces 2,2'-azobis (2-amidinopropane) dihydrochloride (AAPH)-induced intracellular ROS accumulation. N-tert-butyl-α-Phenylnitrone also attenuates AAPH-induced cytotoxicity, matrix degradation, and apoptosis, inhibiting AAPH-induced ERK/MAPK pathway activation. (In Vivo):In C57Bl/6 mice induced by lipopolysaccharide (LPS), intraperitoneal injection of 100 mg/kg N-tert-butyl-α-Phenylnitrone twice a day (on gestational day 8) abolishes LPS-induced lipid peroxidation, nitrate tyrosine residue levels and GSH depletion, and reduces the incidence of external malformations.
  • In Vitro
    N-tert-Butyl-α-phenylnitrone (PBN) (25-100 μM) treatment leads to a significant decrease in 2,2'-azobis (2-amidinopropane) dihydrochloride (AAPH)-induced intracellular ROS accumulation. N-tert-Butyl-α-phenylnitrone also attenuates AAPH-induced cytotoxicity, matrix degradation, and apoptosis. N-tert-Butyl-α-phenylnitrone suppresses AAPH-induced activation of ERK/MAPK pathway. N-tert-Butyl-α-phenylnitrone has the potenial for intervertebral disc degeneration (IDD) research.
  • In Vivo
    N-tert-Butyl-α-phenylnitrone (PBN; 100 mg/kg; intraperitoneal injection; twice a day; C57Bl/6 mice) treatment not only abolishes the LPS-induced lipid peroxidation, nitrotyrosine residue levels, and GSH depletion, but also decreases the incidence of external malformations. Animal Model:C57Bl/6 mice induced by lipopolysaccharide (LPS) Dosage:100 mg/kg Administration:Intraperitoneal injection; twice a day (on gestational day 8)Result:Abolished LPS-induced lipid peroxidation, nitrotyrosine residues, and GSH depletion.
  • Synonyms
    (Z)-N-benzylidene-2-Methylpropan-2-aMine oxide
  • Pathway
    Immunology/Inflammation
  • Target
    ROS
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    3376-24-7
  • Formula Weight
    177.247
  • Molecular Formula
    C11H15NO
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (564.21 mM)
  • SMILES
    CC(C)(C)[N+](\[O-])=C\c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Hong XX, et al. New steroidal saponins from the bulbs of Lilium brownii var. viridulum. Carbohydr Res. 2012 Nov 1;361:19-26.
molnova catalog
related products
  • SFI003

    SFI003 is a novel SRSF3 inhibitor that exerts anticancer activity against colorectal cancer by modulating the SRSF3 / DHCR24 / ROS axis and driving apoptosis in CRC cells through the SRSF3 / DHCR24 / reactive oxygen species (ROS) axis.

  • ROS inducer 1

    ROS inducer 1 is a small molecule compound with bactericidal activity that inhibits the production of ROS in Xanthomonas axonopodis pv. citri (Xac), Xanthomonas oryzae pv. oryzae (Xoo) and Pseudomonas syringae pv. actinidiae (Psa).

  • Cyfluthrin

    Cyfluthrin binds to voltage-sensitive sodium channel such as Nav 1.8 sodium channel and modify their gating kinetics, thereby disrupting nerve function of pests.