Monoterpene indole glycoalkaloids from the hook-bearing branches of <i>Uncaria rhynchophylla</i>

Twelve monoterpene indole glycoalkaloids, comprising of three new ones, 19-<i>epi</i>-rhynchophylloside A (<b>1</b>), 7-<i>epi</i>-rhynchophylloside A (<b>2</b>), and 7-<i>epi</i>-anthocephalusine A (<b>3</b>), were isolated from the hook-bearing branches of <i>Uncaria rhynchophylla</i>. The structures and absolute configurations of <b>1-3</b> were elucidated by analysis of MS, NMR, ECD, and single-crystal X-ray diffraction or TDDFT-ECD calculations. Glycoalkaloids <b>1</b> and <b>3</b> showed significant immunosuppressive activity against the proliferation of B lymphocyte induced by LPS with broad selective index.

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Publication Details

Journal
Journal of Asian Natural Products Research
Published
2024-10-16
DOI
https://doi.org/10.1080/10286020.2024.2410460
Citations
2
Primary Topic
Alkaloids: synthesis and pharmacology
Type
article
Field-Weighted Citation Impact
0.93
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article

Monoterpene indole glycoalkaloids from the hook-bearing branches of Uncaria rhynchophylla

Shi‐Jin Qu, Chang‐Heng Tan, Jun‐Jie Tan, Lu Rao et al.
2 citations
Journal of Asian Natural Products Research
Alkaloids: synthesis and pharmacology
0.93
article

Monoterpene indole glycoalkaloids from the hook-bearing branches of Uncaria rhynchophylla

Shi‐Jin Qu, Chang‐Heng Tan, Jun‐Jie Tan, Lu Rao, Fei Chen, Ming-Hui Gao
article en
2 citations

Abstract

Twelve monoterpene indole glycoalkaloids, comprising of three new ones, 19-<i>epi</i>-rhynchophylloside A (<b>1</b>), 7-<i>epi</i>-rhynchophylloside A (<b>2</b>), and 7-<i>epi</i>-anthocephalusine A (<b>3</b>), were isolated from the hook-bearing branches of <i>Uncaria rhynchophylla</i>. The structures and absolute configurations of <b>1-3</b> were elucidated by analysis of MS, NMR, ECD, and single-crystal X-ray diffraction or TDDFT-ECD calculations. Glycoalkaloids <b>1</b> and <b>3</b> showed significant immunosuppressive activity against the proliferation of B lymphocyte induced by LPS with broad selective index.

Journal of Asian Natural Products ResearchVol. 27(1)
Nanjing University of Chinese Medicine (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Materia Medica (CN), University of Chinese Academy of Sciences (CN)
Life in Land
Openalex Percentile: Top 24%
Alkaloids: synthesis and pharmacology
0.93
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