Yeonwoo Cho, Chinmayee Bawkar, Jung Mi Hyun, Myung Jin Song, Kwiwan Jeong and Yeon-Ju Lee*,
{"title":"来自海洋海绵 Diacarnus spinipoculum 的去甲萜环状过氧化物,瞬时受体电位 Ankyrin 1 的抑制剂。","authors":"Yeonwoo Cho, Chinmayee Bawkar, Jung Mi Hyun, Myung Jin Song, Kwiwan Jeong and Yeon-Ju Lee*, ","doi":"10.1021/acs.jnatprod.3c01104","DOIUrl":null,"url":null,"abstract":"<p >Bioassay-guided isolation of the extract from the marine sponge <i>Diacarnus spinipoculum</i> showing inhibitory activity against human transient receptor potential ankyrin 1 (hTRPA1) resulted in the isolation of 12 norditerpene cyclic peroxides (<b>1</b>–<b>12</b>) and eight norsesterterpene cyclic peroxides (<b>13</b>–<b>20</b>). Among these, 10 (<b>5</b>–<b>7</b>, <b>11</b>, <b>12</b>, <b>16</b>–<b>20</b>) are unprecedented analogs. Compounds with either a hydroxy (<b>5</b>, <b>11</b>) or a methoxy (<b>6</b>, <b>12</b>) group attached to the cyclohexanone moiety were obtained as epimeric mixtures at C-11, while compounds <b>4</b>, <b>6</b>, <b>10</b>, and <b>12</b> are likely the artifacts of isolation. The absolute configurations of the new compounds were established based on an NMR-based empirical method and comparison of specific rotation values. Mosher ester analysis revealed the absolute configurations of compounds <b>17</b>–<b>20</b>. The inhibitory activity of the isolated compounds against hTRPA1 varied significantly depending on their structures, with the norsesterterpenoid <b>19</b> displaying the most potent activity (IC<sub>50</sub> 2.0 μM).</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"87 2","pages":"358–364"},"PeriodicalIF":3.6000,"publicationDate":"2024-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Norterpene Cyclic Peroxides from the Marine Sponge Diacarnus spinipoculum, Inhibitors of Transient Receptor Potential Ankyrin 1\",\"authors\":\"Yeonwoo Cho, Chinmayee Bawkar, Jung Mi Hyun, Myung Jin Song, Kwiwan Jeong and Yeon-Ju Lee*, \",\"doi\":\"10.1021/acs.jnatprod.3c01104\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Bioassay-guided isolation of the extract from the marine sponge <i>Diacarnus spinipoculum</i> showing inhibitory activity against human transient receptor potential ankyrin 1 (hTRPA1) resulted in the isolation of 12 norditerpene cyclic peroxides (<b>1</b>–<b>12</b>) and eight norsesterterpene cyclic peroxides (<b>13</b>–<b>20</b>). Among these, 10 (<b>5</b>–<b>7</b>, <b>11</b>, <b>12</b>, <b>16</b>–<b>20</b>) are unprecedented analogs. Compounds with either a hydroxy (<b>5</b>, <b>11</b>) or a methoxy (<b>6</b>, <b>12</b>) group attached to the cyclohexanone moiety were obtained as epimeric mixtures at C-11, while compounds <b>4</b>, <b>6</b>, <b>10</b>, and <b>12</b> are likely the artifacts of isolation. The absolute configurations of the new compounds were established based on an NMR-based empirical method and comparison of specific rotation values. Mosher ester analysis revealed the absolute configurations of compounds <b>17</b>–<b>20</b>. The inhibitory activity of the isolated compounds against hTRPA1 varied significantly depending on their structures, with the norsesterterpenoid <b>19</b> displaying the most potent activity (IC<sub>50</sub> 2.0 μM).</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\"87 2\",\"pages\":\"358–364\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-02-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Products \",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jnatprod.3c01104\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.3c01104","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Norterpene Cyclic Peroxides from the Marine Sponge Diacarnus spinipoculum, Inhibitors of Transient Receptor Potential Ankyrin 1
Bioassay-guided isolation of the extract from the marine sponge Diacarnus spinipoculum showing inhibitory activity against human transient receptor potential ankyrin 1 (hTRPA1) resulted in the isolation of 12 norditerpene cyclic peroxides (1–12) and eight norsesterterpene cyclic peroxides (13–20). Among these, 10 (5–7, 11, 12, 16–20) are unprecedented analogs. Compounds with either a hydroxy (5, 11) or a methoxy (6, 12) group attached to the cyclohexanone moiety were obtained as epimeric mixtures at C-11, while compounds 4, 6, 10, and 12 are likely the artifacts of isolation. The absolute configurations of the new compounds were established based on an NMR-based empirical method and comparison of specific rotation values. Mosher ester analysis revealed the absolute configurations of compounds 17–20. The inhibitory activity of the isolated compounds against hTRPA1 varied significantly depending on their structures, with the norsesterterpenoid 19 displaying the most potent activity (IC50 2.0 μM).
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.