Planta Med 2019; 85(18): 1485
DOI: 10.1055/s-0039-3399888
Main Congress Poster
Poster Session 1
© Georg Thieme Verlag KG Stuttgart · New York

Immunosuppressant flavonoids from Scutellaria baicalensis

N Syafni
1   Pharmaceutical Biology, Department of Pharmaceutical Sciences, University of Basel,, Klingelbergstrasse 50, Basel, Switzerland
2   Faculty of Pharmacy, Sumatran Biota Laboratory, University of Andalas,, Kampus Limau Manis, Padang, West Sumatra, Indonesia
,
AM Klemd
3   Center for Complementary Medicine, Institute for Infection Prevention and Hospital Epidemiology, Faculty of Medicine, University of Freiburg,, Breisacher Strasse 115 B, Freiburg, Germany
,
JK Reinhardt
1   Pharmaceutical Biology, Department of Pharmaceutical Sciences, University of Basel,, Klingelbergstrasse 50, Basel, Switzerland
,
O Danton
1   Pharmaceutical Biology, Department of Pharmaceutical Sciences, University of Basel,, Klingelbergstrasse 50, Basel, Switzerland
,
C Gründemann
3   Center for Complementary Medicine, Institute for Infection Prevention and Hospital Epidemiology, Faculty of Medicine, University of Freiburg,, Breisacher Strasse 115 B, Freiburg, Germany
,
M Hamburger
1   Pharmaceutical Biology, Department of Pharmaceutical Sciences, University of Basel,, Klingelbergstrasse 50, Basel, Switzerland
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Publikationsverlauf

Publikationsdatum:
20. Dezember 2019 (online)

 

A library of 435 extracts from plants used in Traditional Chinese Medicine was screened for their inhibitory potential on the proliferation of human T-lymphocytes in vitro. A dichloromethane extract from roots of Scutellaria baicalensis Georgi (Lamiaceae) inhibited T-lymphocyte proliferation with an IC50 of 12.9 μg/mL. To localize compounds responsible for the activity, 600 μg of the extract was submitted to HPLC-based activity profiling. Of the 33 one-minute micro-fractions collected, suppression of T-cell lymphocyte proliferation was detected in micro-fractions at rT 10, 14 and 17 minutes, respectively.

Preparative isolation led to seventeen flavonoids. Twelve compounds (2, and 5-15) were localized in the active time windows, and structurally related flavones 4, 16, and 17, and flavanones 1 and 3 were isolated from fractions adjacent to the active time windows. All flavonoids possess an unusual substitution pattern on the B-ring, with absence of substituents at C-3 and C-4.

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Fig. 1