{"title":"四氢大麻酚丙基同源物:从大麻中分离、性质及合成","authors":"E. Gill","doi":"10.1039/J39710000579","DOIUrl":null,"url":null,"abstract":"The n-propyl homologue of Δ1-tetrahydrocannabinol (Δ1-THC) has been isolated from Cannabis sativa L. The structure of the compound was deduced by i.r., n.m.r., and mass spectroscopy, and was confirmed by synthesis. It has only one-fifth of the activity of Δ1-THC in the mouse catalepsy test, and although present in amounts comparable to Δ1-THC it probably makes only a small contribution to the effects produced by the consumption of crude cannabis.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"66 1","pages":"579-582"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"25","resultStr":"{\"title\":\"Propyl homologue of tetrahydrocannabinol: its isolation from Cannabis, properties, and synthesis\",\"authors\":\"E. Gill\",\"doi\":\"10.1039/J39710000579\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The n-propyl homologue of Δ1-tetrahydrocannabinol (Δ1-THC) has been isolated from Cannabis sativa L. The structure of the compound was deduced by i.r., n.m.r., and mass spectroscopy, and was confirmed by synthesis. It has only one-fifth of the activity of Δ1-THC in the mouse catalepsy test, and although present in amounts comparable to Δ1-THC it probably makes only a small contribution to the effects produced by the consumption of crude cannabis.\",\"PeriodicalId\":17245,\"journal\":{\"name\":\"Journal of The Chemical Society C: Organic\",\"volume\":\"66 1\",\"pages\":\"579-582\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"25\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society C: Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J39710000579\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society C: Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J39710000579","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Propyl homologue of tetrahydrocannabinol: its isolation from Cannabis, properties, and synthesis
The n-propyl homologue of Δ1-tetrahydrocannabinol (Δ1-THC) has been isolated from Cannabis sativa L. The structure of the compound was deduced by i.r., n.m.r., and mass spectroscopy, and was confirmed by synthesis. It has only one-fifth of the activity of Δ1-THC in the mouse catalepsy test, and although present in amounts comparable to Δ1-THC it probably makes only a small contribution to the effects produced by the consumption of crude cannabis.
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