Deutsche Forschungsgemeinschaft. Grant Numbers: He 1376/38-1, SA 2902/2-1

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Deutsche Forschungsgemeinschaft. Grant Numbers: He 1376/38-1, SA 2902/2-1

Authors

Publications

Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines.

Buzharevski, Antonio; Paskas, Svetlana; Sárosi, Menyhárt‐Botond; Laube, Markus; Lönnecke, Peter; Neumann, Wilma; Mijatović, Sanja; Maksimović-Ivanić, Danijela; Pietzsch, Jens; Hey-Hawkins, Evamarie

(2019)

TY  - JOUR
AU  - Buzharevski, Antonio
AU  - Paskas, Svetlana
AU  - Sárosi, Menyhárt‐Botond
AU  - Laube, Markus
AU  - Lönnecke, Peter
AU  - Neumann, Wilma
AU  - Mijatović, Sanja
AU  - Maksimović-Ivanić, Danijela
AU  - Pietzsch, Jens
AU  - Hey-Hawkins, Evamarie
PY  - 2019
UR  - https://onlinelibrary.wiley.com/doi/abs/10.1002/cmdc.201800685
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3254
AB  - Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most common way of treating inflammatory disorders. Their widespread use helped reveal their other modes of action as pharmaceuticals, such as a profound effect on various cancers. Celecoxib has proven to be a very prominent member of this group with cytostatic activities. On the other hand, the highly dynamic field of drug design is constantly searching for new ways of modifying known structures to obtain more powerful and less harmful drugs. A very interesting development is the implementation of carboranes in pharmacologically active structures, mostly as phenyl mimetics. Herein we report the synthesis of three carborane-containing derivatives of the COX-2-selective NSAID celecoxib. The new compounds proved to have promising cytostatic potential against various melanoma and colorectal adenocarcinoma cell lines. Inhibited proliferation accompanied by caspase-independent apoptotic cell death was found to be the main cause of decreased cell viability upon treatment with the most efficient celecoxib analogue, 3 b (4-[5-(1,7-dicarba-closo-dodecaboranyl)-3-trifluoromethyl-1H-pyrazol-1-yl]-1-methylsulfonylbenzene).
T2  - ChemMedChem
T1  - Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines.
IS  - 3
VL  - 14
DO  - 10.1002/cmdc.201800685
SP  - 315
EP  - 321
ER  - 
@article{
author = "Buzharevski, Antonio and Paskas, Svetlana and Sárosi, Menyhárt‐Botond and Laube, Markus and Lönnecke, Peter and Neumann, Wilma and Mijatović, Sanja and Maksimović-Ivanić, Danijela and Pietzsch, Jens and Hey-Hawkins, Evamarie",
year = "2019",
abstract = "Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most common way of treating inflammatory disorders. Their widespread use helped reveal their other modes of action as pharmaceuticals, such as a profound effect on various cancers. Celecoxib has proven to be a very prominent member of this group with cytostatic activities. On the other hand, the highly dynamic field of drug design is constantly searching for new ways of modifying known structures to obtain more powerful and less harmful drugs. A very interesting development is the implementation of carboranes in pharmacologically active structures, mostly as phenyl mimetics. Herein we report the synthesis of three carborane-containing derivatives of the COX-2-selective NSAID celecoxib. The new compounds proved to have promising cytostatic potential against various melanoma and colorectal adenocarcinoma cell lines. Inhibited proliferation accompanied by caspase-independent apoptotic cell death was found to be the main cause of decreased cell viability upon treatment with the most efficient celecoxib analogue, 3 b (4-[5-(1,7-dicarba-closo-dodecaboranyl)-3-trifluoromethyl-1H-pyrazol-1-yl]-1-methylsulfonylbenzene).",
journal = "ChemMedChem",
title = "Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines.",
number = "3",
volume = "14",
doi = "10.1002/cmdc.201800685",
pages = "315-321"
}
Buzharevski, A., Paskas, S., Sárosi, M., Laube, M., Lönnecke, P., Neumann, W., Mijatović, S., Maksimović-Ivanić, D., Pietzsch, J.,& Hey-Hawkins, E.. (2019). Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines.. in ChemMedChem, 14(3), 315-321.
https://doi.org/10.1002/cmdc.201800685
Buzharevski A, Paskas S, Sárosi M, Laube M, Lönnecke P, Neumann W, Mijatović S, Maksimović-Ivanić D, Pietzsch J, Hey-Hawkins E. Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines.. in ChemMedChem. 2019;14(3):315-321.
doi:10.1002/cmdc.201800685 .
Buzharevski, Antonio, Paskas, Svetlana, Sárosi, Menyhárt‐Botond, Laube, Markus, Lönnecke, Peter, Neumann, Wilma, Mijatović, Sanja, Maksimović-Ivanić, Danijela, Pietzsch, Jens, Hey-Hawkins, Evamarie, "Carboranyl Analogues of Celecoxib with Potent Cytostatic Activity against Human Melanoma and Colon Cancer Cell Lines." in ChemMedChem, 14, no. 3 (2019):315-321,
https://doi.org/10.1002/cmdc.201800685 . .
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