dc.contributor.author |
Tsemeugne, Joseph
|
|
dc.contributor.author |
Bah, Yetiny A.
|
|
dc.contributor.author |
Dzoyem, Jean Paul
|
|
dc.contributor.author |
Dzoyem, Jean Paul
|
|
dc.contributor.author |
Ndefongang, Jerome N.
|
|
dc.contributor.author |
Famuyide, Ibukun Michael
|
|
dc.contributor.author |
McGaw, Lyndy Joy
|
|
dc.contributor.author |
Nangmo, Pamela K.
|
|
dc.contributor.author |
Ouahouo, Blandine M.W.
|
|
dc.contributor.author |
Mkounga, Pierre
|
|
dc.contributor.author |
Edwards, Giles
|
|
dc.contributor.author |
Simon, Peter F.W.
|
|
dc.contributor.author |
Tsopmo, Apollinaire
|
|
dc.contributor.author |
Sopbue, Emmanuel F.
|
|
dc.contributor.author |
Nkengfack, Augustin E.
|
|
dc.date.accessioned |
2023-04-24T08:17:57Z |
|
dc.date.available |
2023-04-24T08:17:57Z |
|
dc.date.issued |
2022 |
|
dc.description.abstract |
A series of novel tetrazine derivatives, containing benzothiazole framework, were prepared during the
coupling reactions of some diazotized 2-aminobenzo[d]thiazole derivatives with p-acetaminophen. Their
structures were elucidated based on NMR and MS spectrometry. The anticancer activity and the safety of the
synthesized compounds along with the entire precursors were assessed against three human cancer cell lines
and a normal cell line. All the synthesized compounds showed selective cytotoxic activity against the cancer
cell lines used in comparison to the normal Vero cell line. Their IC50 values varied from 2.02 to 171.67 μM. |
en_US |
dc.description.department |
Paraclinical Sciences |
en_US |
dc.description.librarian |
am2023 |
en_US |
dc.description.sponsorship |
The Cameroonian Ministry of Higher Education special research allocation, the German Academic Exchange Service (DAAD) and the University of Pretoria. |
en_US |
dc.description.uri |
https://www.arkat-usa.org/arkivoc-journal |
en_US |
dc.identifier.citation |
Tsemeugnehm, J., Bah, Y.A., Dzoyem, J.P. et al. 2022, 'Synthesis and anticancer activity evaluation of some new 1,2,3,5-tetrazine derivatives attached to benzothiazole moiety', Arkivoc, vol. 2022, no. ix, pp. 1-17, doi : 10.24820/ark.5550190.p011.866. |
en_US |
dc.identifier.issn |
1551-7012 (print) |
|
dc.identifier.issn |
1551-7004 (online) |
|
dc.identifier.other |
10.24820/ark.5550190.p011.866 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/90431 |
|
dc.language.iso |
en |
en_US |
dc.publisher |
ARKAT |
en_US |
dc.rights |
© Author(s). This paper is an open access article distributed under the terms of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
en_US |
dc.subject |
Tetrazine |
en_US |
dc.subject |
Benzothiazole |
en_US |
dc.subject |
Acetaminophen |
en_US |
dc.subject |
Azo dyes |
en_US |
dc.subject |
Anticancer activity |
en_US |
dc.title |
Synthesis and anticancer activity evaluation of some new 1,2,3,5-tetrazine derivatives attached to benzothiazole moiety |
en_US |
dc.type |
Article |
en_US |