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Discovery of Scalarane Sesterterpenoids From the Mollusk Glossodoris hikuerensis Exhibiting Anticancer Effects Against Drug-resistant Lung Cancer Cells.

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Chemistry & biodiversity 2026 Vol.23(1) p. e03257
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출처

Xiao X, Zhang LT, Du CL, Zhang C, Lu YM, Su MZ, Li SW, Guo YW

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A new scalarane-type sesterterpene (1), along with four known related compounds (2-5), was isolated from the nudibranch mollusk Glossodoris hikuerensis.

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APA Xiao X, Zhang LT, et al. (2026). Discovery of Scalarane Sesterterpenoids From the Mollusk Glossodoris hikuerensis Exhibiting Anticancer Effects Against Drug-resistant Lung Cancer Cells.. Chemistry & biodiversity, 23(1), e03257. https://doi.org/10.1002/cbdv.202503257
MLA Xiao X, et al.. "Discovery of Scalarane Sesterterpenoids From the Mollusk Glossodoris hikuerensis Exhibiting Anticancer Effects Against Drug-resistant Lung Cancer Cells.." Chemistry & biodiversity, vol. 23, no. 1, 2026, pp. e03257.
PMID 41237174

Abstract

A new scalarane-type sesterterpene (1), along with four known related compounds (2-5), was isolated from the nudibranch mollusk Glossodoris hikuerensis. Compound 6 was also obtained from 4 by chemical conversion. Their structures were established by extensive spectroscopic analysis, chemical conversion, and by the comparison of their spectroscopic data with those reported in the literature. In bioassay, compound 1 inhibited the proliferation of human leukemia U937 cells with a half-maximal inhibitory concentration (IC) value of 7.1 µM. Compounds 2, 3, and 6 exhibited inhibitory activities against a variety of human cancer cell lines, including U937, K562, A549, HCC827, and gefitinib-resistant HCC827 cells, with IC values 0.7-10.1 µM. Furthermore, compound 6 significantly induced apoptosis, reduced mitochondrial membrane potential, and suppressed cellular invasion and migration by inhibiting EGFR/PI3K signaling pathway.

MeSH Terms

Humans; Antineoplastic Agents; Sesterterpenes; Cell Proliferation; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Animals; Apoptosis; Lung Neoplasms; Cell Line, Tumor; Structure-Activity Relationship; Membrane Potential, Mitochondrial; Molecular Structure; Dose-Response Relationship, Drug; Drug Discovery; Cell Movement; ErbB Receptors; Mollusca; Phosphatidylinositol 3-Kinases

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