Detailed Information on Publication Record
2016
Identification of metabolites of selected benzophenanthridine alkaloids and their toxicity evaluation
SÁNDOR, Roman, Adam MIDLIK, Kristýna ŠEBRLOVÁ, Gabriela DOVRTĚLOVÁ, Kristýna NOSKOVÁ et. al.Basic information
Original name
Identification of metabolites of selected benzophenanthridine alkaloids and their toxicity evaluation
Authors
SÁNDOR, Roman (703 Slovakia, belonging to the institution), Adam MIDLIK (703 Slovakia, belonging to the institution), Kristýna ŠEBRLOVÁ (203 Czech Republic, belonging to the institution), Gabriela DOVRTĚLOVÁ (203 Czech Republic, belonging to the institution), Kristýna NOSKOVÁ (203 Czech Republic, belonging to the institution), Jan JUŘICA (203 Czech Republic, belonging to the institution), Iva SLANINOVÁ (203 Czech Republic, belonging to the institution), Eva TÁBORSKÁ (203 Czech Republic, belonging to the institution) and Ondřej PEŠ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Journal of Pharmaceutical and Biomedical Analysis, Amsterdam, Elsevier Science BV, 2016, 0731-7085
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10600 1.6 Biological sciences
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.255
RIV identification code
RIV/00216224:14110/16:00089320
Organization unit
Faculty of Medicine
UT WoS
000371187100021
Keywords in English
benzophenanthridines; metabolites; rat liver microsomes; mass spectrometry; isolation
Tags
International impact, Reviewed
Změněno: 2/8/2016 13:26, Ing. Mgr. Věra Pospíšilíková
Abstract
V originále
Selected benzo[c]phenathridine alkaloids were biotransformed using rat liver microsomes and identified by liquid chromatography and mass spectrometry. While the metabolites of commercially available sanguinarine and chelerythrine have been studied in detail, data about the metabolism of the minor alkaloids remained unknown. Reactions involved in transformation include single and/or double O-demethylation, demethylenation, reduction, and hydroxylation. Two metabolites, when isolated, purified and tested for toxicity, were found to be less toxic than the original compounds.
Links
LH12176, research and development project |
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MUNI/A/1116/2014, interní kód MU |
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MUNI/A/1123/2014, interní kód MU |
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MUNI/A/1195/2014, interní kód MU |
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