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Development of an analytical method for multi-residue quantification of 18 anthelmintics in various animal-based food products using liquid chromatography-tandem mass spectrometry.

Journal of pharmaceutical analysis

Yoo KH, Park DH, Abd El-Aty AM, Kim SK, Jung HN, Jeong DH, Cho HJ, Hacimüftüoğlu A, Shim JH, Jeong JH, Shin HC.
PMID: 33717613
J Pharm Anal. 2021 Feb;11(1):68-76. doi: 10.1016/j.jpha.2020.03.008. Epub 2020 Mar 21.

In this study, we developed a simple screening procedure for the determination of 18 anthelmintics (including benzimidazoles, macrocyclic lactones, salicylanilides, substituted phenols, tetrahydropyrimidines, and imidazothiazoles) in five animal-derived food matrices (chicken muscle, pork, beef, milk, and egg) using liquid...

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Yoo KH, Park DH, Abd El-Aty AM, et al. Development of an analytical method for multi-residue quantification of 18 anthelmintics in various animal-based food products using liquid chromatography-tandem mass spectrometry. J Pharm Anal. 2020;11(1):68-76doi: 10.1016/j.jpha.2020.03.008.
Yoo, K. H., Park, D. H., Abd El-Aty, A. M., Kim, S. K., Jung, H. N., Jeong, D. H., Cho, H. J., Hacimüftüoğlu, A., Shim, J. H., Jeong, J. H., & Shin, H. C. (2021). Development of an analytical method for multi-residue quantification of 18 anthelmintics in various animal-based food products using liquid chromatography-tandem mass spectrometry. Journal of pharmaceutical analysis, 11(1), 68-76. https://doi.org/10.1016/j.jpha.2020.03.008
Yoo, Kyung-Hee, et al. "Development of an analytical method for multi-residue quantification of 18 anthelmintics in various animal-based food products using liquid chromatography-tandem mass spectrometry." Journal of pharmaceutical analysis vol. 11,1 (2021): 68-76. doi: https://doi.org/10.1016/j.jpha.2020.03.008
Yoo KH, Park DH, Abd El-Aty AM, Kim SK, Jung HN, Jeong DH, Cho HJ, Hacimüftüoğlu A, Shim JH, Jeong JH, Shin HC. Development of an analytical method for multi-residue quantification of 18 anthelmintics in various animal-based food products using liquid chromatography-tandem mass spectrometry. J Pharm Anal. 2021 Feb;11(1):68-76. doi: 10.1016/j.jpha.2020.03.008. Epub 2020 Mar 21. PMID: 33717613; PMCID: PMC7930640.
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Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants.

ACS infectious diseases

Li H, Mattingly AE, Jania LA, Smith R, Melander RJ, Ernst RK, Koller BH, Melander C.
PMID: 34752055
ACS Infect Dis. 2021 Dec 10;7(12):3303-3313. doi: 10.1021/acsinfecdis.1c00463. Epub 2021 Nov 09.

Multidrug-resistant bacterial infections have become a global threat. We recently disclosed that the known IKK-β inhibitor IMD-0354 and subsequent analogues abrogate colistin resistance in several Gram-negative strains. Herein, we report the activity of a second-generation library of IMD-0354 analogues...

Cite
Li H, Mattingly AE, Jania LA, et al. Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants. ACS Infect Dis. 2021;7(12):3303-3313doi: 10.1021/acsinfecdis.1c00463.
Li, H., Mattingly, A. E., Jania, L. A., Smith, R., Melander, R. J., Ernst, R. K., Koller, B. H., & Melander, C. (2021). Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants. ACS infectious diseases, 7(12), 3303-3313. https://doi.org/10.1021/acsinfecdis.1c00463
Li, Haoting, et al. "Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants." ACS infectious diseases vol. 7,12 (2021): 3303-3313. doi: https://doi.org/10.1021/acsinfecdis.1c00463
Li H, Mattingly AE, Jania LA, Smith R, Melander RJ, Ernst RK, Koller BH, Melander C. Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants. ACS Infect Dis. 2021 Dec 10;7(12):3303-3313. doi: 10.1021/acsinfecdis.1c00463. Epub 2021 Nov 09. PMID: 34752055.
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Gelation-induced enhanced fluorescence emission from organogels of salicylanilide-containing compounds exhibiting excited-state intramolecular proton transfer: synthesis and self-assembly.

Chemistry (Weinheim an der Bergstrasse, Germany)

Nayak MK, Kim BH, Kwon JE, Park S, Seo J, Chung JW, Park SY.
PMID: 20491121
Chemistry. 2010 Jul 05;16(25):7437-47. doi: 10.1002/chem.200902615.

Self-assembly structure, stability, hydrogen-bonding interaction, and optical properties of a new class of low molecular weight organogelators (LMOGs) formed by salicylanilides 3 and 4 have been investigated by field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), UV/Vis absorption and...

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Nayak MK, Kim BH, Kwon JE, et al. Gelation-induced enhanced fluorescence emission from organogels of salicylanilide-containing compounds exhibiting excited-state intramolecular proton transfer: synthesis and self-assembly. Chemistry. 2010;16(25):7437-47doi: 10.1002/chem.200902615.
Nayak, M. K., Kim, B. H., Kwon, J. E., Park, S., Seo, J., Chung, J. W., & Park, S. Y. (2010). Gelation-induced enhanced fluorescence emission from organogels of salicylanilide-containing compounds exhibiting excited-state intramolecular proton transfer: synthesis and self-assembly. Chemistry (Weinheim an der Bergstrasse, Germany), 16(25), 7437-47. https://doi.org/10.1002/chem.200902615
Nayak, Manoj Kumar, et al. "Gelation-induced enhanced fluorescence emission from organogels of salicylanilide-containing compounds exhibiting excited-state intramolecular proton transfer: synthesis and self-assembly." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 16,25 (2010): 7437-47. doi: https://doi.org/10.1002/chem.200902615
Nayak MK, Kim BH, Kwon JE, Park S, Seo J, Chung JW, Park SY. Gelation-induced enhanced fluorescence emission from organogels of salicylanilide-containing compounds exhibiting excited-state intramolecular proton transfer: synthesis and self-assembly. Chemistry. 2010 Jul 05;16(25):7437-47. doi: 10.1002/chem.200902615. PMID: 20491121.
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Corrigendum to "Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity" [Bioorg. Med. Chem. 25 (2017) 1524-1532].

Bioorganic & medicinal chemistry

Paraskevopoulos G, Monteiro S, Vosátka R, Krátký M, Navrátilová L, Trejtnar F, Stolaříková J, Vinšová J.
PMID: 28285926
Bioorg Med Chem. 2017 Apr 15;25(8):2530. doi: 10.1016/j.bmc.2017.02.053. Epub 2017 Mar 10.

No abstract available.

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Paraskevopoulos G, Monteiro S, Vosátka R, et al. Corrigendum to "Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity" [Bioorg. Med. Chem. 25 (2017) 1524-1532]. Bioorg Med Chem. 2017;25(8):2530doi: 10.1016/j.bmc.2017.02.053.
Paraskevopoulos, G., Monteiro, S., Vosátka, R., Krátký, M., Navrátilová, L., Trejtnar, F., Stolaříková, J., & Vinšová, J. (2017). Corrigendum to "Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity" [Bioorg. Med. Chem. 25 (2017) 1524-1532]. Bioorganic & medicinal chemistry, 25(8), 2530. https://doi.org/10.1016/j.bmc.2017.02.053
Paraskevopoulos, Georgios, et al. "Corrigendum to "Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity" [Bioorg. Med. Chem. 25 (2017) 1524-1532]." Bioorganic & medicinal chemistry vol. 25,8 (2017): 2530. doi: https://doi.org/10.1016/j.bmc.2017.02.053
Paraskevopoulos G, Monteiro S, Vosátka R, Krátký M, Navrátilová L, Trejtnar F, Stolaříková J, Vinšová J. Corrigendum to "Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity" [Bioorg. Med. Chem. 25 (2017) 1524-1532]. Bioorg Med Chem. 2017 Apr 15;25(8):2530. doi: 10.1016/j.bmc.2017.02.053. Epub 2017 Mar 10. PMID: 28285926.
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Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants.

ACS infectious diseases

Li H, Mattingly AE, Jania LA, Smith R, Melander RJ, Ernst RK, Koller BH, Melander C.
PMID: 34752055
ACS Infect Dis. 2021 Dec 10;7(12):3303-3313. doi: 10.1021/acsinfecdis.1c00463. Epub 2021 Nov 09.

Multidrug-resistant bacterial infections have become a global threat. We recently disclosed that the known IKK-β inhibitor IMD-0354 and subsequent analogues abrogate colistin resistance in several Gram-negative strains. Herein, we report the activity of a second-generation library of IMD-0354 analogues...

Cite
Li H, Mattingly AE, Jania LA, et al. Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants. ACS Infect Dis. 2021;7(12):3303-3313doi: 10.1021/acsinfecdis.1c00463.
Li, H., Mattingly, A. E., Jania, L. A., Smith, R., Melander, R. J., Ernst, R. K., Koller, B. H., & Melander, C. (2021). Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants. ACS infectious diseases, 7(12), 3303-3313. https://doi.org/10.1021/acsinfecdis.1c00463
Li, Haoting, et al. "Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants." ACS infectious diseases vol. 7,12 (2021): 3303-3313. doi: https://doi.org/10.1021/acsinfecdis.1c00463
Li H, Mattingly AE, Jania LA, Smith R, Melander RJ, Ernst RK, Koller BH, Melander C. Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants. ACS Infect Dis. 2021 Dec 10;7(12):3303-3313. doi: 10.1021/acsinfecdis.1c00463. Epub 2021 Nov 09. PMID: 34752055.
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Bio-evaluation of fluoro and trifluoromethyl-substituted salicylanilides against multidrug-resistant .

Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents

Lal J, Kaul G, Akhir A, Ansari SB, Chopra S, Reddy DN.
PMID: 34720564
Med Chem Res. 2021 Oct 27;1-15. doi: 10.1007/s00044-021-02808-4. Epub 2021 Oct 27.

Methicillin-resistant

Cite
Lal J, Kaul G, Akhir A, et al. Bio-evaluation of fluoro and trifluoromethyl-substituted salicylanilides against multidrug-resistant . Med Chem Res. 2021;1-15doi: 10.1007/s00044-021-02808-4.
Lal, J., Kaul, G., Akhir, A., Ansari, S. B., Chopra, S., & Reddy, D. N. (2021). Bio-evaluation of fluoro and trifluoromethyl-substituted salicylanilides against multidrug-resistant . Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents, 1-15. https://doi.org/10.1007/s00044-021-02808-4
Lal, Jhajan, et al. "Bio-evaluation of fluoro and trifluoromethyl-substituted salicylanilides against multidrug-resistant ." Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents vol. (2021): 1-15. doi: https://doi.org/10.1007/s00044-021-02808-4
Lal J, Kaul G, Akhir A, Ansari SB, Chopra S, Reddy DN. Bio-evaluation of fluoro and trifluoromethyl-substituted salicylanilides against multidrug-resistant . Med Chem Res. 2021 Oct 27;1-15. doi: 10.1007/s00044-021-02808-4. Epub 2021 Oct 27. PMID: 34720564; PMCID: PMC8548355.
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Showing 1 to 6 of 6 entries