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PS75

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
PS75
Clinical data
ATC code
  • None
Identifiers
  • N-(pyridin-4-yl)-7-chloronaphthalen-1-amine
CAS Number
Chemical and physical data
FormulaC15H11ClN2
Molar mass254.72 g·mol−1
3D model (JSmol)
  • Clc1cc2c(cccc2cc1)Nc1ccncc1

PS75 is an experimentalanalgesic drug which acts as afunctionally selectivealpha-2A (α2A) adrenergicagonist, with a Ki of 8.2nM and an EC50 of 4.8nM at the α2A-adrenergic receptor. In animal studies it was found to produce analgesia but without thesedation typical of older drugs acting at this target such asdexmedetomidine. While PS75 itself is unlikely to be developed for medical use, the successful separation of analgesia from sedative effects makes it likely that related compounds may be developed as non-sedating, non-opioid analgesic medications.[1]

References

[edit]
  1. ^Fink EA, Xu J, Hübner H, Braz JM, Seemann P, Avet C, et al. (September 2022)."Structure-based discovery of nonopioid analgesics acting through the α2A-adrenergic receptor".Science.377 (6614): eabn7065.doi:10.1126/science.abn7065.PMC 10360211.PMID 36173843.
α1
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α2
Agonists
Antagonists
β
Agonists
Antagonists
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