{"title":"趋化基团的药理学易感性","authors":"Luv Kush","doi":"10.22270/ajprd.v10i6.1194","DOIUrl":null,"url":null,"abstract":"The drugs target the pathological proteins for the pharmacological intervention through their vunerability of chemophoric and congate groups 1-3 at therapeutic level. They are essential for binding affinity, intrinsic efficacy and bioavailability. They are introduced in bioactive molecules by replacement of hydrogen atoms. They are implicated in SAR modifications and interactional participation with receptor or enzyme or target protein. The pharmacological influence of them is delineated here. \n ","PeriodicalId":8526,"journal":{"name":"Asian Journal of Pharmaceutical Research and Development","volume":"101 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pharmacological Vunerability of Chemophoric Groups\",\"authors\":\"Luv Kush\",\"doi\":\"10.22270/ajprd.v10i6.1194\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The drugs target the pathological proteins for the pharmacological intervention through their vunerability of chemophoric and congate groups 1-3 at therapeutic level. They are essential for binding affinity, intrinsic efficacy and bioavailability. They are introduced in bioactive molecules by replacement of hydrogen atoms. They are implicated in SAR modifications and interactional participation with receptor or enzyme or target protein. The pharmacological influence of them is delineated here. \\n \",\"PeriodicalId\":8526,\"journal\":{\"name\":\"Asian Journal of Pharmaceutical Research and Development\",\"volume\":\"101 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Pharmaceutical Research and Development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.22270/ajprd.v10i6.1194\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Pharmaceutical Research and Development","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22270/ajprd.v10i6.1194","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Pharmacological Vunerability of Chemophoric Groups
The drugs target the pathological proteins for the pharmacological intervention through their vunerability of chemophoric and congate groups 1-3 at therapeutic level. They are essential for binding affinity, intrinsic efficacy and bioavailability. They are introduced in bioactive molecules by replacement of hydrogen atoms. They are implicated in SAR modifications and interactional participation with receptor or enzyme or target protein. The pharmacological influence of them is delineated here.