Anna Furgala

9 Medyczna St
Krakow, MA 30688, Poland

Last Updated: 09/26/2026

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Found 13 publications

Novel mouse GABA uptake inhibitors with enhanced inhibitory activity toward mGAT3/4 and their effect on pain threshold in mice.

Novel mouse GABA uptake inhibitors with enhanced inhibitory activity toward mGAT3/4 and their effect on pain threshold in mice.

Journal: European journal of medicinal chemistry
Published: September 07, 2019

Acute cold allodynia induced by oxaliplatin is attenuated by amitriptyline.

Acute cold allodynia induced by oxaliplatin is attenuated by amitriptyline.

Journal: Acta neurobiologiae experimentalis
Published: January 10, 2019

Interventional and preventive effects of aripiprazole and ceftriaxone used alone or in combination on oxaliplatin-induced tactile and cold allodynia in mice.

Interventional and preventive effects of aripiprazole and ceftriaxone used alone or in combination on oxaliplatin-induced tactile and cold allodynia in mice.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: October 12, 2018

Searching for analgesic drug candidates alleviating oxaliplatin-induced cold hypersensitivity in mice.

Searching for analgesic drug candidates alleviating oxaliplatin-induced cold hypersensitivity in mice.

Journal: Chemical biology & drug design
Published: August 16, 2018

Time-shifted co-administration of sub-analgesic doses of ambroxol and pregabalin attenuates oxaliplatin-induced cold allodynia in mice.

Time-shifted co-administration of sub-analgesic doses of ambroxol and pregabalin attenuates oxaliplatin-induced cold allodynia in mice.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: June 24, 2018

Enhanced pharmacological efficacy of sumatriptan due to modification of its physicochemical properties by inclusion in selected cyclodextrins.

Enhanced pharmacological efficacy of sumatriptan due to modification of its physicochemical properties by inclusion in selected cyclodextrins.

Journal: Scientific reports
Published: May 22, 2018

Thiazoles with cyclopropyl fragment as antifungal, anticonvulsant, and anti-Toxoplasma gondii agents: synthesis, toxicity evaluation, and molecular docking study.

Thiazoles with cyclopropyl fragment as antifungal, anticonvulsant, and anti-Toxoplasma gondii agents: synthesis, toxicity evaluation, and molecular docking study.

Journal: Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents
Published: March 26, 2018

Synthesis and activity of di- or trisubstituted N-(phenoxyalkyl)- or N-{2-[2-(phenoxy)ethoxy]ethyl}piperazine derivatives on the central nervous system.

Synthesis and activity of di- or trisubstituted N-(phenoxyalkyl)- or N-{2-[2-(phenoxy)ethoxy]ethyl}piperazine derivatives on the central nervous system.

Journal: Bioorganic & medicinal chemistry letters
Published: January 18, 2018

Evaluation of cebranopadol, a dually acting nociceptin/orphanin FQ and opioid receptor agonist in mouse models of acute, tonic, and chemotherapy-induced neuropathic pain.

Evaluation of cebranopadol, a dually acting nociceptin/orphanin FQ and opioid receptor agonist in mouse models of acute, tonic, and chemotherapy-induced neuropathic pain.

Journal: Inflammopharmacology
Published: July 25, 2017

Antinociceptive, antiallodynic and antihyperalgesic effects of the 5-HT1A receptor selective agonist, NLX-112 in mouse models of pain.

Antinociceptive, antiallodynic and antihyperalgesic effects of the 5-HT1A receptor selective agonist, NLX-112 in mouse models of pain.

Journal: Neuropharmacology
Published: April 11, 2017

Synthesis, antimicrobial and anticonvulsant screening of small library of tetrahydro-2H-thiopyran-4-yl based thiazoles and selenazoles.

Synthesis, antimicrobial and anticonvulsant screening of small library of tetrahydro-2H-thiopyran-4-yl based thiazoles and selenazoles.

Journal: Journal of enzyme inhibition and medicinal chemistry
Published: May 20, 2016

Synthesis and evaluation of anticonvulsant properties of new N-Mannich bases derived from 3-(1-phenylethyl)- and 3-benzyl-pyrrolidine-2,5-dione.

Synthesis and evaluation of anticonvulsant properties of new N-Mannich bases derived from 3-(1-phenylethyl)- and 3-benzyl-pyrrolidine-2,5-dione.

Journal: Bioorganic & medicinal chemistry letters
Published: January 29, 2016
Showing 1-12 of 13

Last Updated: 09/26/2026