Naloxone hydrochloride

CAS No. 357-08-4

Naloxone hydrochloride( N-Allyldihydro-14-hydroxynormorphinone | NIH 7890 )

Catalog No. M14225 CAS No. 357-08-4

Naloxone hydrochloride is an opioid inverse agonist drug used to counter the effects of opiate overdose.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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200MG 56 In Stock
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Biological Information

  • Product Name
    Naloxone hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Naloxone hydrochloride is an opioid inverse agonist drug used to counter the effects of opiate overdose.
  • Description
    Naloxone hydrochloride is an opioid inverse agonist drug used to counter the effects of opiate overdose.
  • In Vitro
    ——
  • In Vivo
    Naloxone (2.0 mg/kg with constant infusion of 1.7 mg/kg/h) causes a significant improvement in neurobehavioral outcome which persists up to 4 weeks postinjury in rat. Naloxone treatment causes a modest and nonsignificant increase in mean arterial blood pressure (MAP). Naloxone (0.4 mg/kg) causes memory facilitation and antagonizes the amnestic effect of ACTH and epinephrine in rat. Naloxone treatment diminishes the strength of the initial tetanus in a dose-related manner in cats. Naloxone (5 or 10 mg/kg, i.v.) causes subsequent doses of morphine to produce less PTP depression but has no effect on maximal twitch depression.
  • Synonyms
    N-Allyldihydro-14-hydroxynormorphinone | NIH 7890
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    Opioid Receptor
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    357-08-4
  • Formula Weight
    363.84
  • Molecular Formula
    C19H21NO4·HCl
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 73 mg/mL (200.63 mM); DMSO: 73 mg/mL (200.63 mM)
  • SMILES
    C=CCN1CC[C@]23[C@@H]4C(=O)CC[C@]2([C@H]1CC5=C3C(=C(C=C5)O)O4)O.Cl
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Liu B, et al. J Pharmacol Exp Ther, 2000, 293(2), 607-617.
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