{"title":"药用苯并噻唑缩合氧咔唑和氧杂氮咔唑的二氮卓类和喹啉类羧酸取代类似物合成新可能性的探索","authors":"V. Soni, Meenakshi Sharma, Vaishali Soni, S. Soni","doi":"10.9734/bpi/cacs/v1/2264f","DOIUrl":null,"url":null,"abstract":"Heterocyclic systems containing benzothiazoles, carbazole (and azacarbazole) moieties have attracted the attention of chemists owing to these nuclei having been identified in the literature as most promising pharmacophores in drug design and synthesis. Based on these observations, it could be anticipated that incorporation of the bioactive azepine moiety and quinoline moiety into the molecular framework of benzothiazoles fused to carbazole (and azacarbazoles) could produce interesting series of compounds 9-12 with enhanced biological activities, whose structure was unequivocally established from its micro analyses and spectral data.","PeriodicalId":9698,"journal":{"name":"Challenges and Advances in Chemical Science Vol. 1","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploration of Newer Possibilities to the Synthesis of Diazepine and Quinoline Carboxylic Acid Substituted Analogues of Benzothiazolo Condensed Oxocarbazoles and Oxoazacarbazoles of Medicinal Interest\",\"authors\":\"V. Soni, Meenakshi Sharma, Vaishali Soni, S. Soni\",\"doi\":\"10.9734/bpi/cacs/v1/2264f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Heterocyclic systems containing benzothiazoles, carbazole (and azacarbazole) moieties have attracted the attention of chemists owing to these nuclei having been identified in the literature as most promising pharmacophores in drug design and synthesis. Based on these observations, it could be anticipated that incorporation of the bioactive azepine moiety and quinoline moiety into the molecular framework of benzothiazoles fused to carbazole (and azacarbazoles) could produce interesting series of compounds 9-12 with enhanced biological activities, whose structure was unequivocally established from its micro analyses and spectral data.\",\"PeriodicalId\":9698,\"journal\":{\"name\":\"Challenges and Advances in Chemical Science Vol. 1\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Challenges and Advances in Chemical Science Vol. 1\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/bpi/cacs/v1/2264f\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Challenges and Advances in Chemical Science Vol. 1","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/bpi/cacs/v1/2264f","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Exploration of Newer Possibilities to the Synthesis of Diazepine and Quinoline Carboxylic Acid Substituted Analogues of Benzothiazolo Condensed Oxocarbazoles and Oxoazacarbazoles of Medicinal Interest
Heterocyclic systems containing benzothiazoles, carbazole (and azacarbazole) moieties have attracted the attention of chemists owing to these nuclei having been identified in the literature as most promising pharmacophores in drug design and synthesis. Based on these observations, it could be anticipated that incorporation of the bioactive azepine moiety and quinoline moiety into the molecular framework of benzothiazoles fused to carbazole (and azacarbazoles) could produce interesting series of compounds 9-12 with enhanced biological activities, whose structure was unequivocally established from its micro analyses and spectral data.