Karolina Sloczynska

Medyczna 9 St
Krakow, MA 30688, Poland

Last Updated: 09/26/2026

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Found 48 publications

Biotransformation of common NSAIDs by Cunninghamella species and resulting metabolite toxicity.

Biotransformation of common NSAIDs by Cunninghamella species and resulting metabolite toxicity.

Journal: Scientific reports

Published: March 18, 2026

Phase II metabolism in xenobiotic biotransformation: general mechanisms and the underestimated role of microbial systems.

Phase II metabolism in xenobiotic biotransformation: general mechanisms and the underestimated role of microbial systems.

Journal: Drug metabolism reviews

Published: November 03, 2025

Targeting GABAergic Hypofunction Associated with Schizophrenia: Identification of α1β2γ2GABA-A Receptor Ligands with Neuroprotective and Antipsychotic Properties.

Targeting GABAergic Hypofunction Associated with Schizophrenia: Identification of α1β2γ2GABA-A Receptor Ligands with Neuroprotective and Antipsychotic Properties.

Journal: ACS chemical neuroscience

Published: June 06, 2025

Preferential Synaptic Type of GABA-A Receptor Ligands Enhancing Neuronal Survival and Facilitating Functional Recovery After Ischemic Stroke.

Preferential Synaptic Type of GABA-A Receptor Ligands Enhancing Neuronal Survival and Facilitating Functional Recovery After Ischemic Stroke.

Journal: Journal of medicinal chemistry

Published: December 13, 2024

Biotransformation of oxybenzone and 3-(4-methylbenzylidene)camphor in Cunninghamella species: Potential for environmental clean-up of widely used sunscreen agents.

Biotransformation of oxybenzone and 3-(4-methylbenzylidene)camphor in Cunninghamella species: Potential for environmental clean-up of widely used sunscreen agents.

Journal: Journal of hazardous materials

Published: October 20, 2024

In vitro safety evaluation of (6-methoxy-9-oxo-9H-xanthen-2-yl)methyl (E)-3-(2,4-dimethoxyphenyl)acrylate (K-116) - the novel potential UV filter designed by means of a double chromophore strategy.

In vitro safety evaluation of (6-methoxy-9-oxo-9H-xanthen-2-yl)methyl (E)-3-(2,4-dimethoxyphenyl)acrylate (K-116) - the novel potential UV filter designed by means of a double chromophore strategy.

Journal: Xenobiotica; the fate of foreign compounds in biological systems

Published: May 31, 2024

Discovery of (E)-3-(4-chlorophenyl)-N-(5-hydroxypentyl)acrylamide among N-substituted cinnamamide derivatives as a novel cosmetic ingredient for hyperpigmentation.

Discovery of (E)-3-(4-chlorophenyl)-N-(5-hydroxypentyl)acrylamide among N-substituted cinnamamide derivatives as a novel cosmetic ingredient for hyperpigmentation.

Journal: Bioorganic chemistry

Published: February 15, 2024

Synthesis, Antimicrobial and Mutagenic Activity of a New Class of d-Xylopyranosides.

Synthesis, Antimicrobial and Mutagenic Activity of a New Class of d-Xylopyranosides.

Journal: Antibiotics (Basel, Switzerland)

Published: April 18, 2023

In silico and in vitro evaluation of a safety profile of a cosmetic ingredient: 4-methoxychalcone (4-MC).

In silico and in vitro evaluation of a safety profile of a cosmetic ingredient: 4-methoxychalcone (4-MC).

Journal: Toxicology in vitro : an international journal published in association with BIBRA

Published: February 21, 2023

Antidepressant pharmaceuticals in aquatic systems, individual-level ecotoxicological effects: growth, survival and behavior.

Antidepressant pharmaceuticals in aquatic systems, individual-level ecotoxicological effects: growth, survival and behavior.

Journal: Aquatic toxicology (Amsterdam, Netherlands)

Published: December 15, 2022

In silico and in vitro ADME-Tox analysis and in vivo pharmacokinetic study of representative pan-PDE inhibitors from the group of 7,8-disubstituted derivatives of 1,3-dimethyl-7H-purine-2,6-dione.

In silico and in vitro ADME-Tox analysis and in vivo pharmacokinetic study of representative pan-PDE inhibitors from the group of 7,8-disubstituted derivatives of 1,3-dimethyl-7H-purine-2,6-dione.

Journal: Toxicology and applied pharmacology

Published: August 12, 2022

Cinnamamide derivatives with 4-hydroxypiperidine moiety enhance effect of doxorubicin to cancer cells and protect cardiomyocytes against drug-induced toxicity through CBR1 inhibition mechanism.

Cinnamamide derivatives with 4-hydroxypiperidine moiety enhance effect of doxorubicin to cancer cells and protect cardiomyocytes against drug-induced toxicity through CBR1 inhibition mechanism.

Journal: Life sciences

Published: February 24, 2022

Showing 1-12 of 48

Last Updated: 09/26/2026