Ghent University Academic Bibliography

Journal Article
A1
open access

Synthesis and cancer cell cytotoxicity of 6-, 7-, or 8-substituted 2-(hetero)aryl-4-(4-(hetero)aryl-2-oxobut-3-en-1-ylidene)benzothiazepanes

Katarina Magdalenic (UGent) , Donatien Morillon, Steven De Jonghe, Leentje Persoons, Dominique Schols, Kristof Van Hecke (UGent) , Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2025) JOURNAL OF HETEROCYCLIC CHEMISTRY. 62(2). p.249-256

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Synthesis and functional screening of novel inhibitors targeting the HDAC6 zinc finger ubiquitin-binding domain

Silke Geurs (UGent) , Eleni Staessens (UGent) , Kato Bredael (UGent) , Stefaan Borghgraef, Jordy De Ridder, Leentje Persoons, Steven De Jonghe, Dominique Schols, Mandeep K. Mann, Rachel J. Harding, et al.

(2025) EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. 285.

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Journal Article
A1
open access

Synthesis and cancer cell cytotoxicity of 2-heteroaryl-4-(4-heteroaryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes

Katarina Magdalenic (UGent) , Felien Morlion (UGent) , Steven De Jonghe, Leentje Persoons, Dominique Schols, Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2024) TETRAHEDRON. 154.

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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Katarina Magdalenic (UGent) , Felien Morlion (UGent) , Ulrike Ronse (UGent) , Steven De Jonghe, Leentje Persoons, Dominique Schols, Julie De Munck (UGent) , Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2024) 4th Alpine Winter Conference on Medicinal and Synthetic Chemistry, Abstracts.

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Synthesis and anticancer activity assessment of curcumin-inspired benzothiazepane derivatives

Katarina Magdalenic (UGent) , Felien Morlion (UGent) , Ulrike Ronse (UGent) , Steven De Jonghe, Leentje Persoons, Dominique Schols, Julie De Munck (UGent) , Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2024) 18th Belgian Organic Synthesis Symposium, Abstracts.

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Journal Article
A1
open access

Synthesis and cancer cell cytotoxicity of 2-aryl-4-(4-aryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes

Katarina Magdalenic (UGent) , Ulrike Ronse (UGent) , Steven De Jonghe, Leentje Persoons, Dominique Schols, Julie De Munck (UGent) , Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2023) PHYTOCHEMISTRY LETTERS. 55. p.117-123

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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Katarina Magdalenic (UGent) , Ulrike Ronse (UGent) , Felien Morlion (UGent) , Steven De Jonghe, Leentje Persoons, Dominique Schols, Julie De Munck (UGent) , Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2023) 5th International Congress (IRPES2023), Abstracts.

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Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Katarina Magdalenic (UGent) , Ulrike Ronse (UGent) , Felien Morlion (UGent) , Steven De Jonghe, Leentje Persoons, Dominique Schols, Julie De Munck (UGent) , Charlotte Grootaert (UGent) , John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2023) ACS Fall 2023, Abstracts.

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The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Katarina Magdalenic (UGent) , Ulrike Ronse (UGent) , Steven De Jonghe, John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2022) EFMC International Symposium on Medicinal Chemistry, 27th, Abstracts.

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The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Katarina Magdalenic (UGent) , Ulrike Ronse (UGent) , Steven De Jonghe, John Van Camp (UGent) and Matthias D'hooghe (UGent)

(2022) CRF-ChemCYS 2022, Abstracts.

Academic Bibliography

Synthesis and cancer cell cytotoxicity of 6-, 7-, or 8-substituted 2-(hetero)aryl-4-(4-(hetero)aryl-2-oxobut-3-en-1-ylidene)benzothiazepanes

Synthesis and functional screening of novel inhibitors targeting the HDAC6 zinc finger ubiquitin-binding domain

Synthesis and cancer cell cytotoxicity of 2-heteroaryl-4-(4-heteroaryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes

Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Synthesis and anticancer activity assessment of curcumin-inspired benzothiazepane derivatives

Synthesis and cancer cell cytotoxicity of 2-aryl-4-(4-aryl-2-oxobut-3-en-1-ylidene)-substituted benzothiazepanes

Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

Curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

The natural product curcumin as a source of inspiration for the development of novel benzothiazepane-based cancer cell cytotoxic agents

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