Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity
Zhi Nan Xiang
1
,
Jun Cheng Su
2
,
Yihui Liu
3
,
Bin Deng
3
,
Ning Zhao
4
,
Jun Pan
1
,
Zhuo Fan Hu
1
,
Fei-Hong Chen
1
,
Bing Yu Cheng
1
,
Jiachun Chen
1
,
Luo Sheng Wan
1
Publication type: Journal Article
Publication date: 2021-04-01
scimago Q1
wos Q1
SJR: 0.786
CiteScore: 8.3
Impact factor: 4.7
ISSN: 00452068, 10902120
PubMed ID:
33652163
Organic Chemistry
Drug Discovery
Biochemistry
Molecular Biology
Abstract
Extensive phytochemical study of the methanol extract of twigs and leaves of Buxus sempervirens resulted in the identification of 17 Buxus alkaloids, including 12 new ones, namely buxusemines A–L ( 1 – 12 ). Their structures were delineated by detailed analysis of the HRESIMS and NMR data, as well as quantum chemical NMR calculations. Buxusemine A ( 1 ) represents the second Buxus alkaloid with a unique spiro[4.6]undecatriene moiety, buxusemines B–C ( 2 – 3 ) are a rarely occurring class of Buxus alkaloids featured with an additional five-membered ring through the ether or lactone linkage between C-10 and C-23, and buxusemines D–F ( 4 – 6 ) are another rare type of Buxus alkaloids with an epoxy motif. In the assessment of their bioactivities, buxusemine F ( 6 ) and buxanoldine ( 17 ) displayed more potent protective effects than the positive control cyclovirobuxinum D in the doxorubicin-induced cardiac injury model. • 17 Buxus alkaloids, including 12 new ones, were isolated from B. sempervirens . • Buxusemine A represents the second Buxus alkaloid with a spiro motif. • Buxusemines B−F are also members of two rare occurring substructures of Buxus alkaloids. • All the isolates were evaluated for their cardioprotective activities. • Preliminary structure-activity relationships were discussed. Extensive phytochemical study of the methanol extract of twigs and leaves of Buxus sempervirens resulted in the identification of 17 Buxus alkaloids, including 12 new ones, namely buxusemines A–L ( 1 – 12 ). Their structures were delineated by detailed analysis of the HRESIMS and NMR data, as well as quantum chemical NMR calculations. Buxusemine A ( 1 ) represents the second Buxus alkaloid with a unique spiro[4.6]undecatriene moiety, buxusemines B–C ( 2 – 3 ) are a rarely occurring class of Buxus alkaloids featured with an additional five-membered ring through the ether or lactone linkage between C-10 and C-23, and buxusemines D–F ( 4 – 6 ) are another rare type of Buxus alkaloids with an epoxy motif. In the assessment of their bioactivities, buxusemine F ( 6 ) and buxanoldine ( 17 ) displayed more potent protective effects than the positive control cyclovirobuxinum D in the doxorubicin-induced cardiac injury model.
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Total citations:
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Citations from 2024:
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(37%)
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GOST
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Xiang Z. N. et al. Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity // Bioorganic Chemistry. 2021. Vol. 109. p. 104753.
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Xiang Z. N., Su J. C., Liu Y., Deng B., Zhao N., Pan J., Hu Z. F., Chen F., Cheng B. Yu., Chen J., Wan L. S. Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity // Bioorganic Chemistry. 2021. Vol. 109. p. 104753.
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TY - JOUR
DO - 10.1016/j.bioorg.2021.104753
UR - https://doi.org/10.1016/j.bioorg.2021.104753
TI - Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity
T2 - Bioorganic Chemistry
AU - Xiang, Zhi Nan
AU - Su, Jun Cheng
AU - Liu, Yihui
AU - Deng, Bin
AU - Zhao, Ning
AU - Pan, Jun
AU - Hu, Zhuo Fan
AU - Chen, Fei-Hong
AU - Cheng, Bing Yu
AU - Chen, Jiachun
AU - Wan, Luo Sheng
PY - 2021
DA - 2021/04/01
PB - Elsevier
SP - 104753
VL - 109
PMID - 33652163
SN - 0045-2068
SN - 1090-2120
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2021_Xiang,
author = {Zhi Nan Xiang and Jun Cheng Su and Yihui Liu and Bin Deng and Ning Zhao and Jun Pan and Zhuo Fan Hu and Fei-Hong Chen and Bing Yu Cheng and Jiachun Chen and Luo Sheng Wan},
title = {Structurally diverse alkaloids from Buxus sempervirens with cardioprotective activity},
journal = {Bioorganic Chemistry},
year = {2021},
volume = {109},
publisher = {Elsevier},
month = {apr},
url = {https://doi.org/10.1016/j.bioorg.2021.104753},
pages = {104753},
doi = {10.1016/j.bioorg.2021.104753}
}