Niina Jalava
Turku, 20360, Finland
Last Updated: 09/26/2026
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Found 9 publications
5-HT6 receptor antagonists. Design, synthesis, and structure-activity relationship of substituted 2-(1-methyl-4-piperazinyl)pyridines.
Journal: Bioorganic & medicinal chemistry letters
Published: August 30, 2023
Inhibition of Canonical Transient Receptor Potential Channels 4/5 with Highly Selective and Potent Small-Molecule HC-070 Alleviates Mechanical Hypersensitivity in Rat Models of Visceral and Neuropathic Pain.
Journal: International journal of molecular sciences
Published: January 05, 2023
Tasipimidine-the pharmacological profile of a novel orally active selective α2A-adrenoceptor agonist.
Journal: European journal of pharmacology
Published: March 09, 2022
2,3-Dihydrobenzo-dioxine piperidine derivatives as potent and selective α2c antagonists.
Journal: Bioorganic & medicinal chemistry letters
Published: March 04, 2022
Development of benzodioxine-heteroarylpiperazines as highly potent and selective α2c antagonists.
Journal: Bioorganic & medicinal chemistry letters
Published: March 04, 2022
Ongoing pain in streptozotocin model of diabetes in the rat: correlation with cutaneous cheminociception.
Journal: Journal of physiology and pharmacology : an official journal of the Polish Physiological Society
Published: September 05, 2019
TRPA1 Antagonists for Pain Relief.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: October 01, 2018
1-Sulfonyl-6-Piperazinyl-7-Azaindoles as potent and pseudo-selective 5-HT6 receptor antagonists.
Journal: Bioorganic & medicinal chemistry letters
Published: February 19, 2016
TRPA1: a transducer and amplifier of pain and inflammation.
Journal: Basic & clinical pharmacology & toxicology
Published: May 31, 2013
Showing 1-9 of 9
Last Updated: 09/26/2026