EST73502

CAS No. 2307458-82-6

EST73502( —— )

Catalog No. M28219 CAS No. 2307458-82-6

EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 285 Get Quote
10MG 407 Get Quote
25MG 671 Get Quote
50MG 945 Get Quote
100MG 1251 Get Quote
200MG Get Quote Get Quote
500MG 2547 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    EST73502
  • Note
    Research use only, not for human use.
  • Brief Description
    EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity.
  • Description
    EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity.(In Vivo):In CD1 male mice, EST73502 (10-40 mg/kg; p.o.) shows a dose-response analgesic effect reaching a maximum of 64% and an EC50 of 14 mg/kg in the paw pressure test. EST73502 (5 mg/kg; i.p.) attenuated the expression of mechanical allodynia induced by PSNL, reaching a maximal effect of 56%.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    Wnt
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2307458-82-6
  • Formula Weight
    388.88
  • Molecular Formula
    C19H27ClF2N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CCN1CC2(CCN(CCC3=CC(F)=CC=C3F)CC2)O[C@H](C)C1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.James E Tarver Jr, et al. Stimulation of cortical bone formation with thienopyrimidine based inhibitors of Notum Pectinacetylesterase. Bioorg Med Chem Lett. 2016 Mar 15;26(6):1525-1528.
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