Naltrexone hydrochloride

CAS No. 16676-29-2

Naltrexone hydrochloride( NIH 8503 )

Catalog No. M12543 CAS No. 16676-29-2

A potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 37 In Stock
25MG 29 In Stock
50MG 34 In Stock
100MG 47 In Stock
200MG Get Quote In Stock
500MG 105 In Stock
1G 154 In Stock

Biological Information

  • Product Name
    Naltrexone hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively.
  • Description
    A potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively; also inhibits IL-6 and TNFα production in human immune cell subsets following stimulation with ligands for intracellular TLRs; a TLR-4 antognist that inhibits LPS-induced TLR4 downstream NO production in microglia BV-2 cells (IC50=105 uM).Alcoholism Approved.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    NIH 8503
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    OpioidReceptor
  • Research Area
    Neurological Disease
  • Indication
    Alcoholism

Chemical Information

  • CAS Number
    16676-29-2
  • Formula Weight
    377.8618
  • Molecular Formula
    C20H24ClNO4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 33 mg/mL
  • SMILES
    C1CC1CN2CC[C@]34[C@@H]5C(=O)CC[C@]3([C@H]2CC6=C4C(=C(C=C6)O)O5)O.Cl
  • Chemical Name
    Morphinan-6-one, 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-, hydrochloride (1:1), (5α)-

Shipping & Storage Information

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

Reference

1. Codd EE, et al. J Pharmacol Exp Ther. 1995 Sep;274(3):1263-70. 2. Cant R, et al. Front Immunol. 2017 Jul 11;8:809. 3. Selfridge BR, et al. J Med Chem. 2015 Jun 25;58(12):5038-52.
molnova catalog
related products
  • [Arg14,Lys15]Nocicep...

    Highly potent and selective NOP receptor agonist (EC50 = 1 nM). Displays > 875-fold selectivity over opioid receptors (IC50 values are 0.32, 280, > 10000 and 1500 for NOP, μ, δ and κ receptors respectively). Longer lasting and 30-fold more potent than nociceptin in vivo; pronociceptive and inhibits locomotor activity.

  • Hemorphin-7

    Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.

  • Bevenopran

    Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.