BW 373U86

BW 373U86

Catalog Number:
L002370861APE
Mfr. No.:
APE-B5157
Price:
$705
  • Size:
    10mg
    Quantity:
    Add to Cart:
      • Overview
        • Please contact us at for specific academic pricing.

          Background

          Ki: 1.8, 15, 85 and 34 nM for delta, mu, epsilon and kappa receptor
          Opioid receptors are heterogeneous and at least four types, mu,.delta, kappa and epsilon, are known to exist. Currently, all clinically used opiates act through the mu receptor to induce analgesia; however, they also induce unwanted side effects such as respiratory depression, dependence, constipation and muscle rigidity.BW 373U86 is a novel, potent and selective nonpeptidic delta opioid receptor agonist. In vitro: BW 373U86 was a potent delta receptor-selective ligand in receptor binding assays. The Ki values were 1 .8 ± 0.4, 15 ± 3, 85 ± 4 and 34 ± 3 nM for delta, mu, epsilon and kappa receptor binding sites, respectively. BW 373U86 inhibited electncally evoked muscle contraction of mouse vas deferens with an ED50 value of 0.2 ± 0.06 nM [1]. In vivo: BW 373U86 inhibited the acoustic startle reflex after subcutaneous administration from 0.2- to 2-mg/kg doses in rats, and this inhibition was blocked by naltnndole. BW 373U86 also induced a dose-dependent increase of locomotor activity in rats at similar doses. This effect was inhibited by naltnndole [3].
          Clinical trial: Up to now, BW 373U86 is still in the preclinical development stage.

      • Properties
        • Categories
          Non-peptide delta agonist, potent and selective
          Alternative Name
          4-((R)-((2S,5R)-4-allyl-2,5-dimethylpiperazin-1-yl)(3-hydroxyphenyl)methyl)-N,N-diethylbenzamide
          CAS Number
          155836-50-3
          Molecular Formula
          C27H37N3O2
          Molecular Weight
          435.61
          Appearance
          Beige solid
          Purity
          98.00%
          Solubility
          <43.56mg/ml in 1eq. HCl
          Storage
          Store at -20°C
          SMILES
          OC1=CC([[email protected]@H](C2=CC=C(C(N(CC)CC)=O)C=C2)N3[[email protected]@H](C)CN(CC=C)[[email protected]](C)C3)=CC=C1

          * For Research Use Only

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