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Design and Synthesis of novel N-(5-substituted-1,3,4-thiadiazol-2-yl)benzenesulfonamide derivatives as potential anticancer agents
- At: 2017 FIP Congress in Stockholm (Sweden)
- Type: Poster
- By: BHONGADE, Bhoomendra (RAK College of Pharmaceutical Sciences, RAKMHSU, Pharmaceutical Chemistry, Ras Al Khaimah, United Arab Emirates)
- Co-author(s): Bhoomendra Bhongade: Pharmaceutical Chemistry, RAK College of Pharmaceutical Sciences, RAKMHSU, Ras Al Khaimah, United Arab Emirates
BackgroundsCancer represents a pathological manifestation of uncontrolled cell division. Several new classes of compounds including the specific enzyme inhibitors are being explored to overcome these problems. The heterocyclic 1,3,4-thiadiazoles represent one of the most biologically vibrant classes of compounds, possessing a wide spectrum of.. The access to the whole abstract and the presentation file is available to FIP members and to congress participants of that specific congress.
Last update 4 October 2019