TY - JOUR
T1 - Where Is Bacosine in Commercially Available Bacopa monnieri ?
AU - Ritter, Stefanie
AU - Urmann, Corinna
AU - Herzog, Rainer
AU - Glaser, Jan
AU - Bieringer, Sebastian
AU - Geisberger, Thomas
AU - Eisenreich, Wolfgang
AU - Riepl, Herbert
N1 - Publisher Copyright:
© 2020 Georg Thieme Verlag. All rights reserved.
PY - 2020/5/1
Y1 - 2020/5/1
N2 - Bacopa monnieri is an Ayurvedic plant with rising interest in the pharmacological effects of its extract and constituents, including flavonoids, saponins, and triterpenes such as cucurbitacins, betulinic acid, and bacosine. The latter two compounds are isomeric 3-hydroxy lupenoic acids, which vary only in the arrangement of the carboxylic acid group and the methyl group at C-27 and C-28 and the orientation of the hydroxy group at C-3. In this study, we have reinvestigated the contents of betulinic acid and bacosine, respectively, in extracts from various commercially available B. monnieri powders and food supplements. To our surprise, HPLC-ion trap time-of-flight analyses identified only betulinic acid, but not bacosine, in all extracts under study, which was verified by GC-MS, HPLC-ELSD, 1D NMR (1 H, 13 C), and 2D NMR (1 H, 1 H COSY, 1 H, 13 C HMBC, 1 H, 13 C HSQC, 1 H, 1 H NOESY) experiments. Moreover, it turned out that commercially available reference samples of bacosine were structurally identical with betulinic acid.
AB - Bacopa monnieri is an Ayurvedic plant with rising interest in the pharmacological effects of its extract and constituents, including flavonoids, saponins, and triterpenes such as cucurbitacins, betulinic acid, and bacosine. The latter two compounds are isomeric 3-hydroxy lupenoic acids, which vary only in the arrangement of the carboxylic acid group and the methyl group at C-27 and C-28 and the orientation of the hydroxy group at C-3. In this study, we have reinvestigated the contents of betulinic acid and bacosine, respectively, in extracts from various commercially available B. monnieri powders and food supplements. To our surprise, HPLC-ion trap time-of-flight analyses identified only betulinic acid, but not bacosine, in all extracts under study, which was verified by GC-MS, HPLC-ELSD, 1D NMR (1 H, 13 C), and 2D NMR (1 H, 1 H COSY, 1 H, 13 C HMBC, 1 H, 13 C HSQC, 1 H, 1 H NOESY) experiments. Moreover, it turned out that commercially available reference samples of bacosine were structurally identical with betulinic acid.
KW - Bacopa monnieri
KW - Brahmi
KW - Plantaginaceae
KW - bacosine
KW - betulinic acid
KW - constitutional isomers
KW - triterpene
UR - http://www.scopus.com/inward/record.url?scp=85085538771&partnerID=8YFLogxK
U2 - 10.1055/a-1137-4289
DO - 10.1055/a-1137-4289
M3 - Article
C2 - 32325509
AN - SCOPUS:85085538771
SN - 0032-0943
VL - 86
SP - 565
EP - 570
JO - Planta Medica
JF - Planta Medica
IS - 8
ER -