Chemical components from (W.Hunter) Roxb. and their preliminary bioactivities in CDC25B phosphatase inhibition and vasodilatory activity.

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Hauptverfasser: Liu, Wenyan, Jin, Song, Wang, Ziming, Li, Xinyue, Li, Zheng, Xu, Yanqi, Wang, Wei, Wu, Yanchao, Huang, Li
Format: Artículo científico
Sprache:en
Veröffentlicht: Natural product research 2026
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author Liu, Wenyan
Jin, Song
Wang, Ziming
Li, Xinyue
Li, Zheng
Xu, Yanqi
Wang, Wei
Wu, Yanchao
Huang, Li
author_facet Liu, Wenyan
Jin, Song
Wang, Ziming
Li, Xinyue
Li, Zheng
Xu, Yanqi
Wang, Wei
Wu, Yanchao
Huang, Li
Liu, Wenyan
Jin, Song
Wang, Ziming
Li, Xinyue
Li, Zheng
Xu, Yanqi
Wang, Wei
Wu, Yanchao
Huang, Li
collection PubMed - marine biology
contents Chemical components from (W.Hunter) Roxb. and their preliminary bioactivities in CDC25B phosphatase inhibition and vasodilatory activity. Liu, Wenyan Jin, Song Wang, Ziming Li, Xinyue Li, Zheng Xu, Yanqi Wang, Wei Wu, Yanchao Huang, Li The endangered (W.Hunter) Roxb. () remains largely unexplored in chemical constituents and bioactivities. Therefore, fifteen compounds (-), comprising monoterpene indole alkaloids, lignans, flavonoids, triterpenoids, coumarins, and fatty acids, were isolated from this species. Their inhibitory effects against cell division cycle 25B (CDC25B) phosphatase and vasodilatory activities were then evaluated. Results showed that compound (strictosamide) exhibited a notable inhibitory effect on CDC25B phosphatase, with the IC value of 5.4 μM, comparable to the positive control (NaVO). Compound (3dihydrocadambine) effectively revealed strong vasodilatory activity with EC values of 2.4 μM and 2.1 μM, respectively, similar levels comparable to the positive control (verapamil). Interestingly, these activities of compounds and were evaluated for the first time in this work. Moreover, network pharmacology and molecular docking predicted compound to correlate with the p53-Hippo-TGF- antitumor signalling pathway and compound with the cAMP/cGMP-PKG cardiovascular signalling pathway. This work provides preliminary experimental data for the development of potential lead compounds from .
format Artículo científico
id pubmed_42176307
institution PubMed
language en
publishDate 2026
publisher Natural product research
record_format pubmed
spellingShingle Chemical components from (W.Hunter) Roxb. and their preliminary bioactivities in CDC25B phosphatase inhibition and vasodilatory activity.
Liu, Wenyan
Jin, Song
Wang, Ziming
Li, Xinyue
Li, Zheng
Xu, Yanqi
Wang, Wei
Wu, Yanchao
Huang, Li
Chemical components from (W.Hunter) Roxb. and their preliminary bioactivities in CDC25B phosphatase inhibition and vasodilatory activity. Liu, Wenyan Jin, Song Wang, Ziming Li, Xinyue Li, Zheng Xu, Yanqi Wang, Wei Wu, Yanchao Huang, Li The endangered (W.Hunter) Roxb. () remains largely unexplored in chemical constituents and bioactivities. Therefore, fifteen compounds (-), comprising monoterpene indole alkaloids, lignans, flavonoids, triterpenoids, coumarins, and fatty acids, were isolated from this species. Their inhibitory effects against cell division cycle 25B (CDC25B) phosphatase and vasodilatory activities were then evaluated. Results showed that compound (strictosamide) exhibited a notable inhibitory effect on CDC25B phosphatase, with the IC value of 5.4 μM, comparable to the positive control (NaVO). Compound (3dihydrocadambine) effectively revealed strong vasodilatory activity with EC values of 2.4 μM and 2.1 μM, respectively, similar levels comparable to the positive control (verapamil). Interestingly, these activities of compounds and were evaluated for the first time in this work. Moreover, network pharmacology and molecular docking predicted compound to correlate with the p53-Hippo-TGF- antitumor signalling pathway and compound with the cAMP/cGMP-PKG cardiovascular signalling pathway. This work provides preliminary experimental data for the development of potential lead compounds from .
title Chemical components from (W.Hunter) Roxb. and their preliminary bioactivities in CDC25B phosphatase inhibition and vasodilatory activity.
url https://pubmed.ncbi.nlm.nih.gov/42176307/