Detailed Information on Publication Record
2019
New diterpenoid glucoside and flavonoids from Plectranthus scutellarioides (L.) R. Br.
KUBÍNOVÁ, Renata, Markéta GAZDOVÁ, Zuzana HANÁKOVÁ, Sabína JUSKOVÁ, Acqua S DALL et. al.Basic information
Original name
New diterpenoid glucoside and flavonoids from Plectranthus scutellarioides (L.) R. Br.
Authors
KUBÍNOVÁ, Renata (203 Czech Republic), Markéta GAZDOVÁ (203 Czech Republic), Zuzana HANÁKOVÁ (203 Czech Republic), Sabína JUSKOVÁ (203 Czech Republic), Acqua S DALL (380 Italy), Josef CVAČKA (203 Czech Republic) and Otakar HUMPA (203 Czech Republic, guarantor, belonging to the institution)
Edition
SOUTH AFRICAN JOURNAL OF BOTANY, AMSTERDAM, ELSEVIER SCIENCE BV, 2019, 0254-6299
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10401 Organic chemistry
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 1.792
RIV identification code
RIV/00216224:14740/19:00109325
Organization unit
Central European Institute of Technology
UT WoS
000456314600038
Keywords in English
Plectranthus scutellarioides; Diterpene glucoside; Flavonoids; Hyaluronidase; ORAC values; Acetylcholinesterase and butyrylcholinesterase; inhibitory activities
Tags
Tags
International impact, Reviewed
Změněno: 30/10/2024 14:07, Ing. Martina Blahová
Abstract
V originále
Three new compounds, diterpenoid glucoside (13S, 15S)-6 beta, 7 alpha, 12 alpha-trihydroxy-13 beta, 16-cyclo-8-abietene11,14- dione 7-O-beta-D-glucoside 1, flavonoids apigenin 7-O-(3''-O-acetyl)-beta-D-glucuronide 2 and apigenin 5-O( 3''-O-acetyl)-beta-D-glucuronide 3, together with known compounds caffeic acid 4, luteolin 5-O-beta-D-glucoside 5 and rosmarinic acid 6 were isolated from the aerial parts of Plectranthus scutellarioides (L.) R. Br. The structures of the new compounds were elucidated by spectroscopic and mass-spectrometric analyses, including 1D-and 2D-NMR. Compound 1 inhibited hyaluronidase by 25% at the concentration of 200 mu M, compounds 2 and 3 showed inhibitory activity on butyrylcholinesterase better than standard galanthamine at the concentration of 100 mu M, and compound 6 is a potent antioxidant with an ORAC value of 2.15 +/- 0.12. (c) 2018 SAAB. Published by Elsevier B. V. All rights reserved.
Links
LM2011020, research and development project |
| ||
90043, large research infrastructures |
|