Sarleen G. Castro , Eisuke Hosoya , Mariko Kitajima , Hiroyuki Nakamura , Joe Anthony H. Manzano , Grecebio Jonathan D. Alejandro , Mario A. Tan , Hayato Ishikawa
{"title":"菲律宾长叶钩藤中钩藤素A-D、氧吲哚类生物碱及其抗淀粉样蛋白的性质","authors":"Sarleen G. Castro , Eisuke Hosoya , Mariko Kitajima , Hiroyuki Nakamura , Joe Anthony H. Manzano , Grecebio Jonathan D. Alejandro , Mario A. Tan , Hayato Ishikawa","doi":"10.1016/j.phytochem.2025.114585","DOIUrl":null,"url":null,"abstract":"<div><div>Eight oxindole alkaloids of the <em>Corynanthe</em>-type, including four previously undescribed compounds, uncamarins A–D (<strong>1</strong>–<strong>4</strong>), were isolated from the leaves of <em>Uncaria longiflora</em> (Poir.) Merr. (Rubiaceae family) collected in the Philippines. The structures of the previously undescribed compounds were elucidated based on extensive spectroscopic data such as NMR, ECD, UV, IR, and HRESIMS, whereas known compounds were identified by comparison with published literature. Their anti-amyloidogenic activity was evaluated using a thioflavin T (ThT) fluorescence assay at 100 μg/ml. All compounds exhibited inhibitory activity, with <strong>5</strong> (78.44 % ± 1.63) displaying the highest % inhibition, followed by <strong>4</strong> (77.91 % ± 0.22) and <strong>2</strong> (70.40 % ± 1.93), comparable to the positive control, phenol red (82.73 ± 0.84). These results were supported by molecular docking, where compounds <strong>2</strong> (−7.5 kcal/mol), <strong>4</strong> (−7.1 kcal/mol), and <strong>5</strong> (−7.2 kcal/mol) exhibited strong binding affinities to the dodecameric structure of the amyloid-β<sub>42</sub> protein. Notably, compound <strong>4</strong> also docked in silico to the active site of acetylcholinesterase, a key enzyme targeted in Alzheimer's disease (AD) therapy, thereby highlighting its potential for multitargeting in AD.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"238 ","pages":"Article 114585"},"PeriodicalIF":3.4000,"publicationDate":"2025-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Uncamarins A–D, oxindole alkaloids from Philippine Uncaria longiflora and their anti-amyloidogenic properties\",\"authors\":\"Sarleen G. Castro , Eisuke Hosoya , Mariko Kitajima , Hiroyuki Nakamura , Joe Anthony H. Manzano , Grecebio Jonathan D. Alejandro , Mario A. Tan , Hayato Ishikawa\",\"doi\":\"10.1016/j.phytochem.2025.114585\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Eight oxindole alkaloids of the <em>Corynanthe</em>-type, including four previously undescribed compounds, uncamarins A–D (<strong>1</strong>–<strong>4</strong>), were isolated from the leaves of <em>Uncaria longiflora</em> (Poir.) Merr. (Rubiaceae family) collected in the Philippines. The structures of the previously undescribed compounds were elucidated based on extensive spectroscopic data such as NMR, ECD, UV, IR, and HRESIMS, whereas known compounds were identified by comparison with published literature. Their anti-amyloidogenic activity was evaluated using a thioflavin T (ThT) fluorescence assay at 100 μg/ml. All compounds exhibited inhibitory activity, with <strong>5</strong> (78.44 % ± 1.63) displaying the highest % inhibition, followed by <strong>4</strong> (77.91 % ± 0.22) and <strong>2</strong> (70.40 % ± 1.93), comparable to the positive control, phenol red (82.73 ± 0.84). These results were supported by molecular docking, where compounds <strong>2</strong> (−7.5 kcal/mol), <strong>4</strong> (−7.1 kcal/mol), and <strong>5</strong> (−7.2 kcal/mol) exhibited strong binding affinities to the dodecameric structure of the amyloid-β<sub>42</sub> protein. Notably, compound <strong>4</strong> also docked in silico to the active site of acetylcholinesterase, a key enzyme targeted in Alzheimer's disease (AD) therapy, thereby highlighting its potential for multitargeting in AD.</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"238 \",\"pages\":\"Article 114585\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0031942225002080\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942225002080","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Uncamarins A–D, oxindole alkaloids from Philippine Uncaria longiflora and their anti-amyloidogenic properties
Eight oxindole alkaloids of the Corynanthe-type, including four previously undescribed compounds, uncamarins A–D (1–4), were isolated from the leaves of Uncaria longiflora (Poir.) Merr. (Rubiaceae family) collected in the Philippines. The structures of the previously undescribed compounds were elucidated based on extensive spectroscopic data such as NMR, ECD, UV, IR, and HRESIMS, whereas known compounds were identified by comparison with published literature. Their anti-amyloidogenic activity was evaluated using a thioflavin T (ThT) fluorescence assay at 100 μg/ml. All compounds exhibited inhibitory activity, with 5 (78.44 % ± 1.63) displaying the highest % inhibition, followed by 4 (77.91 % ± 0.22) and 2 (70.40 % ± 1.93), comparable to the positive control, phenol red (82.73 ± 0.84). These results were supported by molecular docking, where compounds 2 (−7.5 kcal/mol), 4 (−7.1 kcal/mol), and 5 (−7.2 kcal/mol) exhibited strong binding affinities to the dodecameric structure of the amyloid-β42 protein. Notably, compound 4 also docked in silico to the active site of acetylcholinesterase, a key enzyme targeted in Alzheimer's disease (AD) therapy, thereby highlighting its potential for multitargeting in AD.
期刊介绍:
Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.