Search Results - "Gangula, Mohan Rao"

Investigation of manganese metal coordination in proteins: a comprehensive PDB analysis and quantum mechanical study by S., Udayalaxmi, Gangula, Mohan Rao, K., Ravikiran, P., Ettaiah

“…Manganese (Mn) is an important metal that is crucial in biological cell mechanism and function. However, its binding mechanism is poorly characterized. In the…”
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Regioselective synthesis of some new 1,4-disubstituted sulfonyl-1,2,3-triazoles and their antibacterial activity studies by Thirukovela, Narasimha Swamy, Kankala, Shravankumar, Kankala, Ranjith Kumar, Paidakula, Suresh, Gangula, Mohan Rao, Vasam, Chandra Sekhar, Vadde, Ravinder

“…Some new 1,4-disubstituted-sulfonyl-1,2,3-triazoles ( 3a – f , 5a – h , 7a – d , and 9a – e ) were regioselectively synthesized in high yields by Cu(I)…”
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Synthesis, characterization and evaluation of novel isoquinoline analogues as anticancer agents by Ambati, Anna Reddy, Gangula, Mohan Rao, Murahari, Kiran Kumar, Uppula, Purushotham, Tanneeru, Karunakar, Baru, Vijaya kumar

“…•Synthesis and characterisation of novel tetrahydrobenz[f]isoquinoles.•In-vitro cell viability assay using methotrexate as a standard drug•Molecular docking…”
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Regioselective synthesis of isoxazole–mercaptobenzimidazole hybrids and their in vivo analgesic and anti-inflammatory activity studies by Kankala, Shravankumar, Kankala, Ranjith Kumar, Gundepaka, Prasad, Thota, Niranjan, Nerella, Srinivas, Gangula, Mohan Rao, Guguloth, Hanmanthu, Kagga, Mukkanti, Vadde, Ravinder, Vasam, Chandra Sekhar

“…Regioselective synthesis of isoxazole–mercaptobenzimidazole hybrids and their efficiency in in vivo analgesic and anti-inflammatory activity was described. A…”
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Novel imidazophenoxazine-4-sulfonamides: Their synthesis and evaluation as potential inhibitors of PDE4 by Reddy, Seelam Venkata, Rao, Gangula Mohan, Kumar, Baru Vijaya, Meda, Chandana L.T., Deora, Girdhar Singh, Kumar, K. Shiva, Parsa, Kishore V.L., Pal, Manojit

“…A number of novel imidazophenoxazine-4-sulfonamides have been designed as potential inhibitors of PDE4. All these compounds were readily prepared via an…”
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