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| Main Authors: | , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Marine drugs
2026
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| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/41590748/ |
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Table of Contents:
- Isolation, Structural Elucidation, and Biological Evaluation of Pyrrole-Based Alkaloids from Sea Anemone-Associated sp. S1502. Zhang, Xin Yang, Qihong Zhou, Le Chen, Yingying Ju, Jianhua Ma, Junying Humans Streptomyces Animals Alkaloids Antineoplastic Agents Cell Line, Tumor Pyrroles Sea Anemones Cell Proliferation Methicillin-Resistant Staphylococcus aureus Molecular Structure Crystallography, X-Ray Anti-Bacterial Agents Three new pyrrole alkaloids, streptopyrroles D-F (-), along with four known analogs (-) were isolated from Sea Anemone-Associated sp. S1502 via an OSMAC (One Strain Many Compounds)-based strategy. Their structures were elucidated through comprehensive spectroscopic analyses, including HRESIMS and 1D/2D NMR experiments (COSY, HSQC, and HMBC), and further confirmed by X-ray crystallography. Biological evaluation identified streptopyrrole () as an anti-MRSA (methicillin-resistant ) agent, while and displayed broad-spectrum cytotoxicity and good selectivity against a panel of human cancer cell lines. Notably, and showed particularly potent activity against the lung cancer cell lines H1299, SW1573, and A549, with IC values ranging from 5.43 to 16.24 μM. Further mechanistic investigation revealed that both compounds suppress the proliferation of lung cancer cells by inducing cell cycle arrest at the G/G phase and impair metastatic potential by inhibiting migration and invasion. These findings not only expand the structural diversity of marine-derived pyrrole alkaloids but also reveal the anticancer mechanisms of and , highlighting their promise as active candidates for further antitumor drug development, particularly in lung cancer.