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Bioorganic & Medicinal Chemistry Letters|February 28, 2012
Catalysis by molecular iodine: a rapid synthesis of 1,8-dioxo-octahydroxanthenes and their evaluation as potential anticancer agentsNaveen Mulakayala, P V N S Murthy, D Rambabu, et al.Bioorganic Chemistry|February 19, 2022
Fe(III)-catalyzed regioselective and faster synthesis of isocoumarins with 3-oxoalkyl moiety at C-4: Identification of new inhibitors of PDE4B Thirupataiah, Harshavardhan Bhuktar, Guntipally Mounika, et al.Chemical Communications (Cambridge, England)|March 30, 2011
A new three-component reaction: green synthesis of novel isoindolo[2,1-a]quinazoline derivatives as potent inhibitors of TNF-αK Siva Kumar, P Mahesh Kumar, K Anil Kumar, et al.Organic & Biomolecular Chemistry|February 26, 2013
Novel N-indolylmethyl substituted olanzapine derivatives: their design, synthesis and evaluation as PDE4B inhibitorsDhilli Rao Gorja, Soumita Mukherjee, Chandana Lakshmi T Meda, et al.Bioorganic & Medicinal Chemistry Letters|August 9, 2012
Pd-mediated functionalization of polysubstituted pyrroles: their evaluation as potential inhibitors of PDE4T Bhaskar Kumar, Ch Sumanth, S Vaishaly, et al.Bioorganic & Medicinal Chemistry Letters|April 3, 2012
Conformationally restricted novel pyrazole derivatives: synthesis of 1,8-disubstituted 5,5-dimethyl-4,5-dihydro-1H-benzo[g]indazoles as a new class of PDE4 inhibitorsT Shyamsunder Reddy, K Shiva Kumar, Chandana L T Meda, et al.European Journal of Medicinal Chemistry|May 16, 2021
PdCl2-catalyzed synthesis of a new class of isocoumarin derivatives containing aminosulfonyl / aminocarboxamide moiety: First identification of a isocoumarin based PDE4 inhibitorB Thirupataiah, Guntipally Mounika, Gangireddy Sujeevan Reddy, et al.Iscience|June 9, 2025
Early preclinical development of Mycobacterium tuberculosis amino acid biosynthesis pathway inhibitor DRILS-1398 as a potential anti-TB drugDeepesh Biswas, Rebecca Kristina Edwin, K Shiva Kumar, et al.European Journal of Medicinal Chemistry|April 30, 2019
InCl3 mediated heteroarylation of indoles and their derivatization via CH activation strategy: Discovery of 2-(1H-indol-3-yl)-quinoxaline derivatives as a new class of PDE4B selective inhibitors for arthritis and/or multiple sclerosisRajnikanth Sunke, Ramudu Bankala, B Thirupataiah, et al.Chemical Communications (Cambridge, England)|June 7, 2011
Pd-mediated new synthesis of pyrroles: their evaluation as potential inhibitors of phosphodiesterase 4G Rajeshwar Reddy, T Ram Reddy, Suju C Joseph, et al.Pageof 13