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EST64454: a Highly Soluble σ 1 Receptor Antagonist Clinical Candidate for Pain Management.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2020 Dec 10; Vol. 63 (23), pp. 14979-14988. Date of Electronic Publication: 2020 Nov 25. - Publication Year :
- 2020
-
Abstract
- The synthesis and pharmacological activity of a new series of pyrazoles that led to the identification of 1-(4-(2-((1-(3,4-difluorophenyl)-1 H -pyrazol-3-yl)methoxy)ethyl)piperazin-1-yl)ethanone ( 9k , EST64454) as a σ <subscript>1</subscript> receptor (σ <subscript>1</subscript> R) antagonist clinical candidate for the treatment of pain are reported. The compound 9k is easily obtained through a five-step synthesis suitable for the production scale and shows an outstanding aqueous solubility, which together with its high permeability in Caco-2 cells will allow its classification as a BCS class I compound. It also shows high metabolic stability in all species, linked to an adequate pharmacokinetic profile in rodents, and antinociceptive properties in the capsaicin and partial sciatic nerve ligation models in mice.
- Subjects :
- Analgesics chemical synthesis
Analgesics pharmacokinetics
Animals
Caco-2 Cells
Humans
Mice
Molecular Structure
Piperazines chemical synthesis
Piperazines pharmacokinetics
Pyrazoles chemical synthesis
Pyrazoles pharmacokinetics
Rats, Wistar
Structure-Activity Relationship
Sigma-1 Receptor
Analgesics therapeutic use
Pain drug therapy
Piperazines therapeutic use
Pyrazoles therapeutic use
Receptors, sigma antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 63
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 33237785
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.0c01575