J 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
Name: CEITEC ? open access
Investor: Ministry of Education, Youth and Sports of the CR
90043, large research infrastructures
Name: CIISB