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Antibiotics (Basel, Switzerland)|July 27, 2024
Bacterial Histidine Kinase and the Development of Its Inhibitors in the 21st CenturyRagib Ahsan, Sumaiya Kifayat, Krishan Kumar Pooniya, et al.European Journal of Medicinal Chemistry|March 9, 2018
Synthesis, molecular modeling and evaluation of α-glucosidase inhibition activity of 3,4-dihydroxy piperidinesSiva Prasad Kasturi, Sujatha Surarapu, Srinivas Uppalanchi, et al.Archiv Der Pharmazie|September 19, 2022
Synthesis and biological evaluation of coumarin-thiazole hybrids as selective carbonic anhydrase IX and XII inhibitorsPavitra S Thacker, Vaishnavi Newaskar, Andrea Angeli, et al.European Journal of Medicinal Chemistry|June 27, 2017
Synthesis of thiazole linked indolyl-3-glyoxylamide derivatives as tubulin polymerization inhibitorsSravanthi Devi Guggilapu, Lalita Guntuku, T Srinivasa Reddy, et al.European Journal of Medicinal Chemistry|May 31, 2022
Design, synthesis of DNA-interactive 4-thiazolidinone-based indolo-/pyrroloazepinone conjugates as potential cytotoxic and topoisomerase I inhibitorsManasa Kadagathur, Sandip Patra, Geetanjali Devabattula, et al.Bioorganic & Medicinal Chemistry Letters|May 13, 2017
Synthesis and α-glucosidase inhibition activity of dihydroxy pyrrolidinesSivaprasad Kasturi, Sujatha Surarapu, Srinivas Uppalanchi, et al.Bioorganic Chemistry|July 20, 2020
Design and synthesis of β-carboline linked aryl sulfonyl piperazine derivatives: DNA topoisomerase II inhibition with DNA binding and apoptosis inducing abilityKesari Lakshmi Manasa, Sowjanya Thatikonda, Dilep Kumar Sigalapalli, et al.Bioorganic Chemistry|March 3, 2022
Synthesis of indolo/pyrroloazepinone-oxindoles as potential cytotoxic, DNA-intercalating and Topo I inhibitorsManasa Kadagathur, Arbaz Sujat Shaikh, Biswajit Panda, et al.Medchemcomm|August 16, 2018
Synthesis, molecular modeling and biological evaluation of aza-flavanones as α-glucosidase inhibitorsSivaprasad Kasturi, Sujatha Surarapu, Chandra Chary Bathoju, et al.Chemmedchem|December 13, 2021
Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII InhibitorsPriti Singh, Dilep Kumar Sigalapalli, Nerella Sridhar Goud, et al.Pageof 4