{"title":"9-苄基嘌呤抗鼻病毒活性的量子QSAR。","authors":"Y S Prabhakar","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The antirhinoviral activity of previously described 9-benzylpurines was quantitatively analysed using Huckel molecular orbital generated electronic parameters and physicochemical properties of substituents. Correlations with the activity against each of several serotypes of the virus were obtained but very few common requirements emerged. Our results emphasise the difficulties in identifying a compound with optimum structural features for broad spectrum antirhinovirus activity.</p>","PeriodicalId":11271,"journal":{"name":"Drug design and delivery","volume":"7 3","pages":"227-39"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quantum QSAR of the antirhinoviral activity of 9-benzylpurines.\",\"authors\":\"Y S Prabhakar\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The antirhinoviral activity of previously described 9-benzylpurines was quantitatively analysed using Huckel molecular orbital generated electronic parameters and physicochemical properties of substituents. Correlations with the activity against each of several serotypes of the virus were obtained but very few common requirements emerged. Our results emphasise the difficulties in identifying a compound with optimum structural features for broad spectrum antirhinovirus activity.</p>\",\"PeriodicalId\":11271,\"journal\":{\"name\":\"Drug design and delivery\",\"volume\":\"7 3\",\"pages\":\"227-39\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1991-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug design and delivery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug design and delivery","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Quantum QSAR of the antirhinoviral activity of 9-benzylpurines.
The antirhinoviral activity of previously described 9-benzylpurines was quantitatively analysed using Huckel molecular orbital generated electronic parameters and physicochemical properties of substituents. Correlations with the activity against each of several serotypes of the virus were obtained but very few common requirements emerged. Our results emphasise the difficulties in identifying a compound with optimum structural features for broad spectrum antirhinovirus activity.