Form of presentation | Articles in Russian journals and collections |
Year of publication | 2023 |
Язык | английский |
|
Aymaletdinov Aleksandr Maazovich, author
Bondar Oksana Viktorovna, author
Kayumov Ayrat Rashitovich, author
Pavelev Roman Sergeevich, author
Pugachev Mikhail Vladimirovich, author
Shtyrlin Yuriy Grigorevich, author
|
|
Karut Rauda , postgraduate kfu
|
|
Mokhammad Taraa , author
Ygayev Beksultan Baktybekovich, author
|
Bibliographic description in the original language |
.V. Bondar, R. Karwt, T. Mohammad, R.S. Pavelyev, M.V. Pugachev, Be.B. Ygaiev, A.R. Kayumov, A.M. Aimaletdinov, and Y.G. Shtyrlin. Structural Analogs of Dehydrozingerone Containing a Pyridoxine Fragment Exhibit Membrane-Modulating Properties and Synergistically Enhance the Antitumor Activity of Cytostatics // Russian Journal of Bioorganic Chemistry, 2023, 49 (4), P. 797-814. ISSN 1068-1620. DOI: 10.1134/S106816202304009X |
Annotation |
Previously we synthesized 10 novel structural analogs of dehydrozingerone based on the pyridoxine
(vitamin B6) scaffold. Two lead compounds (compound (I) and compound (II)) expressed good cytotoxic
activity against tumor cells and have shown higher selectivity than doxorubicin. In the present study, the
mechanism of action of the leading analogues of dehydrozingerone, as well as the efficiency of their combinations
with known cytostatics, was studied in more detail. We revealed a synergistic effect of leader dehydrozingerone
analogs combinations with known cytostatics—doxorubicin, vinblastine and paclitaxel. It was
established, that test compounds (I) and (II), as well as curcumin and dehydrozingerone, possess membranedamaging
activity: cause cytoplasmic membrane depolarization and reduction in its microviscosity, which
can explain the increase in toxicity of cytostatics. In addition, the test compounds were found to increase the
ATPase activity of P-glycoproteins, likely acting as their substrates. It was also revealed that the test compounds
increase the expression of BAX and E-cadherin, decrease the expression of Bcl-2 in cancer cells.
Compound (I) does not cause blood cells hemolysis, does not possess DNA-damaging and mutagenic activity,
and when administered intravenously to mice, the LD50 was 65 mg/kg. The investigated compounds are
promising drug candidates to be further tested on animals with grafted tumors. |
Keywords |
pyridoxine, dehydrozingerone, curcumin, compositions with cytostatics, membrane-damaging activity |
The name of the journal |
Биоорганическая химия
|
URL |
https://link.springer.com/article/10.1134/S106816202304009X |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=292856&p_lang=2 |
Resource files | |
|
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Aymaletdinov Aleksandr Maazovich |
ru_RU |
dc.contributor.author |
Bondar Oksana Viktorovna |
ru_RU |
dc.contributor.author |
Kayumov Ayrat Rashitovich |
ru_RU |
dc.contributor.author |
Pavelev Roman Sergeevich |
ru_RU |
dc.contributor.author |
Pugachev Mikhail Vladimirovich |
ru_RU |
dc.contributor.author |
Shtyrlin Yuriy Grigorevich |
ru_RU |
dc.contributor.author |
Mokhammad Taraa |
ru_RU |
dc.contributor.author |
Ygayev Beksultan Baktybekovich |
ru_RU |
dc.contributor.author |
Karut Rauda |
ru_RU |
dc.date.accessioned |
2023-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2023-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2023 |
ru_RU |
dc.identifier.citation |
.V. Bondar, R. Karwt, T. Mohammad, R.S. Pavelyev, M.V. Pugachev, Be.B. Ygaiev, A.R. Kayumov, A.M. Aimaletdinov, and Y.G. Shtyrlin. Structural Analogs of Dehydrozingerone Containing a Pyridoxine Fragment Exhibit Membrane-Modulating Properties and Synergistically Enhance the Antitumor Activity of Cytostatics // Russian Journal of Bioorganic Chemistry, 2023, 49 (4), P. 797-814. ISSN 1068-1620. DOI: 10.1134/S106816202304009X |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=292856&p_lang=2 |
ru_RU |
dc.description.abstract |
Биоорганическая химия |
ru_RU |
dc.description.abstract |
Previously we synthesized 10 novel structural analogs of dehydrozingerone based on the pyridoxine
(vitamin B6) scaffold. Two lead compounds (compound (I) and compound (II)) expressed good cytotoxic
activity against tumor cells and have shown higher selectivity than doxorubicin. In the present study, the
mechanism of action of the leading analogues of dehydrozingerone, as well as the efficiency of their combinations
with known cytostatics, was studied in more detail. We revealed a synergistic effect of leader dehydrozingerone
analogs combinations with known cytostatics—doxorubicin, vinblastine and paclitaxel. It was
established, that test compounds (I) and (II), as well as curcumin and dehydrozingerone, possess membranedamaging
activity: cause cytoplasmic membrane depolarization and reduction in its microviscosity, which
can explain the increase in toxicity of cytostatics. In addition, the test compounds were found to increase the
ATPase activity of P-glycoproteins, likely acting as their substrates. It was also revealed that the test compounds
increase the expression of BAX and E-cadherin, decrease the expression of Bcl-2 in cancer cells.
Compound (I) does not cause blood cells hemolysis, does not possess DNA-damaging and mutagenic activity,
and when administered intravenously to mice, the LD50 was 65 mg/kg. The investigated compounds are
promising drug candidates to be further tested on animals with grafted tumors. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
pyridoxine |
ru_RU |
dc.subject |
dehydrozingerone |
ru_RU |
dc.subject |
curcumin |
ru_RU |
dc.subject |
compositions with cytostatics |
ru_RU |
dc.subject |
membrane-damaging activity |
ru_RU |
dc.title |
Structural Analogs of Dehydrozingerone Containing a Pyridoxine Fragment Exhibit Membrane-Modulating Properties and Synergistically Enhance the Antitumor Activity of Cytostatics |
ru_RU |
dc.type |
Articles in Russian journals and collections |
ru_RU |
|