{"title":"Voagafries A-E,从 Voacanga africana 中提取的具有抗神经胶质瘤活性的吲哚生物碱。","authors":"Cai-Feng Ding , Ma-Long Qin , Kun-Ying Zhao , Wen Gao , Shan-Ze Yin , Xian-Guang Hu , Gui-Guang Cheng , Rong-Ping Zhang , Wei-Yan Hu","doi":"10.1016/j.phytochem.2024.114361","DOIUrl":null,"url":null,"abstract":"<div><div>Voagafries A–E, five undescribed monoterpenoid indole alkaloids (MIAs), were isolated from the stem bark of <em>Voacanga africana</em>. Voagafrie A (<strong>1</strong>) has a unique 6/5/5/6/6 spiral ring skeleton with an indolone-fused 9-oxo-3-aza-tricyclo[6,3,1,0<sup>3,7</sup>]-12-alkane-10-carbonyllactone. Voagafrie B (<strong>2</strong>) is a rare 5,6-seco diazine scaffold, whereas voagafrie C (<strong>3</strong>) possesses an octahydropyrrolo[2,3-b] pyrrole-fused 2,8-diazabicyclo[3.3.1] nonane. In addition, voagafrie D (<strong>4</strong>) represents an additional 3C ibogamine-type MIA. Their structures were elucidated using extensive spectroscopic and computational analyses and a plausible biosynthetic pathway originating from conopharyngine was proposed. Furthermore, voagafries B (<strong>2</strong>) and E (<strong>5</strong>) exhibited significant cytotoxicity against SH-SY5Y at 10 μmol/L with cell viabilities of 72.7 ± 3.8 and 79.5 ± 2.1, respectively, which were comparable to that of the positive drug paclitaxel (64.1 ± 0.9). Based on the research on several cell death-related factors, these compounds may be involved in apoptosis; therefore, it is necessary to advance our understanding of them through future studies.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"231 ","pages":"Article 114361"},"PeriodicalIF":3.2000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Voagafries A–E, undescribed indole alkaloids with anti-glioma activity from Voacanga africana\",\"authors\":\"Cai-Feng Ding , Ma-Long Qin , Kun-Ying Zhao , Wen Gao , Shan-Ze Yin , Xian-Guang Hu , Gui-Guang Cheng , Rong-Ping Zhang , Wei-Yan Hu\",\"doi\":\"10.1016/j.phytochem.2024.114361\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Voagafries A–E, five undescribed monoterpenoid indole alkaloids (MIAs), were isolated from the stem bark of <em>Voacanga africana</em>. Voagafrie A (<strong>1</strong>) has a unique 6/5/5/6/6 spiral ring skeleton with an indolone-fused 9-oxo-3-aza-tricyclo[6,3,1,0<sup>3,7</sup>]-12-alkane-10-carbonyllactone. Voagafrie B (<strong>2</strong>) is a rare 5,6-seco diazine scaffold, whereas voagafrie C (<strong>3</strong>) possesses an octahydropyrrolo[2,3-b] pyrrole-fused 2,8-diazabicyclo[3.3.1] nonane. In addition, voagafrie D (<strong>4</strong>) represents an additional 3C ibogamine-type MIA. Their structures were elucidated using extensive spectroscopic and computational analyses and a plausible biosynthetic pathway originating from conopharyngine was proposed. Furthermore, voagafries B (<strong>2</strong>) and E (<strong>5</strong>) exhibited significant cytotoxicity against SH-SY5Y at 10 μmol/L with cell viabilities of 72.7 ± 3.8 and 79.5 ± 2.1, respectively, which were comparable to that of the positive drug paclitaxel (64.1 ± 0.9). Based on the research on several cell death-related factors, these compounds may be involved in apoptosis; therefore, it is necessary to advance our understanding of them through future studies.</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"231 \",\"pages\":\"Article 114361\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-12-12\",\"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/S0031942224003984\",\"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/S0031942224003984","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}
Voagafries A–E, undescribed indole alkaloids with anti-glioma activity from Voacanga africana
Voagafries A–E, five undescribed monoterpenoid indole alkaloids (MIAs), were isolated from the stem bark of Voacanga africana. Voagafrie A (1) has a unique 6/5/5/6/6 spiral ring skeleton with an indolone-fused 9-oxo-3-aza-tricyclo[6,3,1,03,7]-12-alkane-10-carbonyllactone. Voagafrie B (2) is a rare 5,6-seco diazine scaffold, whereas voagafrie C (3) possesses an octahydropyrrolo[2,3-b] pyrrole-fused 2,8-diazabicyclo[3.3.1] nonane. In addition, voagafrie D (4) represents an additional 3C ibogamine-type MIA. Their structures were elucidated using extensive spectroscopic and computational analyses and a plausible biosynthetic pathway originating from conopharyngine was proposed. Furthermore, voagafries B (2) and E (5) exhibited significant cytotoxicity against SH-SY5Y at 10 μmol/L with cell viabilities of 72.7 ± 3.8 and 79.5 ± 2.1, respectively, which were comparable to that of the positive drug paclitaxel (64.1 ± 0.9). Based on the research on several cell death-related factors, these compounds may be involved in apoptosis; therefore, it is necessary to advance our understanding of them through future studies.
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.