Guanqun Zhan, Kailing Yang, Tao Yang, Xiaolei Li, Ruixi Zhou, Rongkun Miao, Yuyan Guan, Y. Teng, Zengjun Guo
{"title":"吐茅茎中一种新的单萜生物碱","authors":"Guanqun Zhan, Kailing Yang, Tao Yang, Xiaolei Li, Ruixi Zhou, Rongkun Miao, Yuyan Guan, Y. Teng, Zengjun Guo","doi":"10.25135/rnp.353.2204.2432","DOIUrl":null,"url":null,"abstract":": One new monoterpene alkaloid ( 1 ) and eight known compounds ( 2 – 9 ), belonging to two monoterpene alkaloids ( 1 – 2 ), one pyridine alkaloid ( 3 ), four phenylpropanoid derivatives ( 4 – 7 ), and two matrine-type alkaloids ( 8 – 9 ), were isolated from Rauvolfia vomitoria Afzel. The structure of new compound 1 was determined by extensive spectroscopic analysis and electronic circular dichroism (ECD) calculation. Notably, this is the first reported monoterpene alkaloids from R. vomitoria . Besides, compounds 3 , 5 , and 7 – 9 were first discovered in the Apocynaceae family and compounds 4 and 6 were first reported in the Rauvolfia genus. This is also the first example of matrine-type alkaloids reported in the Apocynaceae family, indicating that matrine-type alkaloids are not unique to the Leguminosae/Fabaceae family. All isolated compounds were evaluated for their anti-acetylcholinesterase, anti-α-glucosidase, and antioxidant activities. Compound 6 showed significant α-glucosidase inhibitory activity and remarkable DPPH radical scavenging capacity, both of which are superior to the positive controls. Molecular docking of compound 6 with α-glucosidase was further performed, suggesting that compound 6 could form hydrogen bonds with residues ALA-292, ASN-259, and ARG-263.","PeriodicalId":21053,"journal":{"name":"Records of Natural Products","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2022-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A New Monoterpene Alkaloid From the Stems of Rauvolfia vomitoria\",\"authors\":\"Guanqun Zhan, Kailing Yang, Tao Yang, Xiaolei Li, Ruixi Zhou, Rongkun Miao, Yuyan Guan, Y. Teng, Zengjun Guo\",\"doi\":\"10.25135/rnp.353.2204.2432\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": One new monoterpene alkaloid ( 1 ) and eight known compounds ( 2 – 9 ), belonging to two monoterpene alkaloids ( 1 – 2 ), one pyridine alkaloid ( 3 ), four phenylpropanoid derivatives ( 4 – 7 ), and two matrine-type alkaloids ( 8 – 9 ), were isolated from Rauvolfia vomitoria Afzel. The structure of new compound 1 was determined by extensive spectroscopic analysis and electronic circular dichroism (ECD) calculation. Notably, this is the first reported monoterpene alkaloids from R. vomitoria . Besides, compounds 3 , 5 , and 7 – 9 were first discovered in the Apocynaceae family and compounds 4 and 6 were first reported in the Rauvolfia genus. This is also the first example of matrine-type alkaloids reported in the Apocynaceae family, indicating that matrine-type alkaloids are not unique to the Leguminosae/Fabaceae family. All isolated compounds were evaluated for their anti-acetylcholinesterase, anti-α-glucosidase, and antioxidant activities. Compound 6 showed significant α-glucosidase inhibitory activity and remarkable DPPH radical scavenging capacity, both of which are superior to the positive controls. Molecular docking of compound 6 with α-glucosidase was further performed, suggesting that compound 6 could form hydrogen bonds with residues ALA-292, ASN-259, and ARG-263.\",\"PeriodicalId\":21053,\"journal\":{\"name\":\"Records of Natural Products\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2022-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Records of Natural Products\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.25135/rnp.353.2204.2432\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Records of Natural Products","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.25135/rnp.353.2204.2432","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
A New Monoterpene Alkaloid From the Stems of Rauvolfia vomitoria
: One new monoterpene alkaloid ( 1 ) and eight known compounds ( 2 – 9 ), belonging to two monoterpene alkaloids ( 1 – 2 ), one pyridine alkaloid ( 3 ), four phenylpropanoid derivatives ( 4 – 7 ), and two matrine-type alkaloids ( 8 – 9 ), were isolated from Rauvolfia vomitoria Afzel. The structure of new compound 1 was determined by extensive spectroscopic analysis and electronic circular dichroism (ECD) calculation. Notably, this is the first reported monoterpene alkaloids from R. vomitoria . Besides, compounds 3 , 5 , and 7 – 9 were first discovered in the Apocynaceae family and compounds 4 and 6 were first reported in the Rauvolfia genus. This is also the first example of matrine-type alkaloids reported in the Apocynaceae family, indicating that matrine-type alkaloids are not unique to the Leguminosae/Fabaceae family. All isolated compounds were evaluated for their anti-acetylcholinesterase, anti-α-glucosidase, and antioxidant activities. Compound 6 showed significant α-glucosidase inhibitory activity and remarkable DPPH radical scavenging capacity, both of which are superior to the positive controls. Molecular docking of compound 6 with α-glucosidase was further performed, suggesting that compound 6 could form hydrogen bonds with residues ALA-292, ASN-259, and ARG-263.
期刊介绍:
Records of Natural Products is a journal of natural product chemistry. Reviews, book reviews, research papers and short reports are considered on the substances of plants, microbes and animals.
Discussions on the structure elucidation, synthesis of naturally occurring compounds and biological activity of natural compounds and plant extracts, biosynthesis of natural products and essential oils of aromatic plants as well as chemotaxonomy in the field of plants are welcomed in the journal.
All published research articles in Records of Natural Products have undergone rigorous peer review, based on initial editor screening and anonymized refereeing by expert referees.