Paruch K - Search Results

1

New benzenesulphonohydrazide derivatives as potential antitumour agents.

Popiołek Ł, Gawrońska-Grzywacz M, Berecka-Rycerz A, Paruch K, Piątkowska-Chmiel I, Natorska-Chomicka D, Herbet M, Gumieniczek A, Dudka J, Wujec M. Popiołek Ł, et al. Among authors: paruch k. Oncol Lett. 2020 Nov;20(5):136. doi: 10.3892/ol.2020.12047. Epub 2020 Sep 2. Oncol Lett. 2020. PMID: 32934704 Free PMC article.

2

Synthesis and in vitro antimicrobial activity screening of new pipemidic acid derivatives.

Popiołek Ł, Biernasiuk A, Paruch K, Malm A, Wujec M. Popiołek Ł, et al. Among authors: paruch k. Arch Pharm Res. 2018 Jun;41(6):633-645. doi: 10.1007/s12272-018-1025-3. Epub 2018 Apr 4. Arch Pharm Res. 2018. PMID: 29619676 Free PMC article.

3

Synthesis and in Vitro Antimicrobial Activity Screening of New 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazoline Derivatives.

Popiołek Ł, Biernasiuk A, Paruch K, Malm A, Wujec M. Popiołek Ł, et al. Among authors: paruch k. Chem Biodivers. 2019 Jun;16(6):e1900082. doi: 10.1002/cbdv.201900082. Epub 2019 May 3. Chem Biodivers. 2019. PMID: 31050208

4

Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines: Synthesis and Biological Activity.

Paruch K, Popiołek Ł, Biernasiuk A, Hordyjewska A, Malm A, Wujec M. Paruch K, et al. Molecules. 2020 Dec 10;25(24):5844. doi: 10.3390/molecules25245844. Molecules. 2020. PMID: 33322054 Free PMC article.

5

Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines.

Paruch K, Biernasiuk A, Berecka-Rycerz A, Hordyjewska A, Popiołek Ł. Paruch K, et al. Int J Mol Sci. 2021 Dec 20;22(24):13669. doi: 10.3390/ijms222413669. Int J Mol Sci. 2021. PMID: 34948461 Free PMC article.

6

Synthesis, Biological Activity and Molecular Docking Studies of Novel Nicotinic Acid Derivatives.

Paruch K, Biernasiuk A, Khylyuk D, Paduch R, Wujec M, Popiołek Ł. Paruch K, et al. Int J Mol Sci. 2022 Mar 4;23(5):2823. doi: 10.3390/ijms23052823. Int J Mol Sci. 2022. PMID: 35269966 Free PMC article.

7

Effect of Linker Elongation on the VGSC Affinity and Anticonvulsant Activity among 4-Alkyl-5-aryl-1,2,4-triazole-3-thione Derivatives.

Paruch K, Kaproń B, Łuszczki JJ, Paneth A, Plech T. Paruch K, et al. Molecules. 2023 Jul 7;28(13):5287. doi: 10.3390/molecules28135287. Molecules. 2023. PMID: 37446948 Free PMC article.

8

Inhibition of Chk1 stimulates cytotoxic action of platinum-based drugs and TRAIL combination in human prostate cancer cells.

Krkoška M, Paruch K, Šošolíková T, Vázquez-Gómez G, Herůdková J, Novotný J, Ovesná P, Sova P, Hyršlová Vaculová A. Krkoška M, et al. Among authors: paruch k. Biol Chem. 2024 Mar 8. doi: 10.1515/hsz-2023-0111. Online ahead of print. Biol Chem. 2024. PMID: 38452398

9

Author Correction: Characterization of an RNA binding protein interactome reveals a context-specific post-transcriptional landscape of MYC-amplified medulloblastoma.

Kameda-Smith MM, Zhu H, Luo EC, Suk Y, Xella A, Yee B, Chokshi C, Xing S, Tan F, Fox RG, Adile AA, Bakhshinyan D, Brown K, Gwynne WD, Subapanditha M, Miletic P, Picard D, Burns I, Moffat J, Paruch K, Fleming A, Hope K, Provias JP, Remke M, Lu Y, Reya T, Venugopal C, Reimand J, Wechsler-Reya RJ, Yeo GW, Singh SK. Kameda-Smith MM, et al. Among authors: paruch k. Nat Commun. 2023 Jan 10;14(1):136. doi: 10.1038/s41467-023-35816-6. Nat Commun. 2023. PMID: 36627300 Free PMC article. No abstract available.

10

Discovery of Potent and Exquisitely Selective Inhibitors of Kinase CK1 with Tunable Isoform Selectivity.

Němec V, Khirsariya P, Janovská P, Moyano PM, Maier L, Procházková P, Kebková P, Gybel' T, Berger BT, Chaikuad A, Reinecke M, Kuster B, Knapp S, Bryja V, Paruch K. Němec V, et al. Among authors: paruch k. Angew Chem Int Ed Engl. 2023 Mar 6;62(11):e202217532. doi: 10.1002/anie.202217532. Epub 2023 Feb 2. Angew Chem Int Ed Engl. 2023. PMID: 36625768

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