Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Basavaraj Padmashali"'
Autor:
Katharigatta N. Venugopala, Sandeep Chandrashekharappa, Pran Kishore Deb, Christophe Tratrat, Melendhran Pillay, Deepak Chopra, Nizar A. Al-Shar’i, Wafa Hourani, Lina A. Dahabiyeh, Pobitra Borah, Rahul D. Nagdeve, Susanta K. Nayak, Basavaraj Padmashali, Mohamed A. Morsy, Bandar E. Aldhubiab, Mahesh Attimarad, Anroop B. Nair, Nagaraja Sreeharsha, Michelyne Haroun, Sheena Shashikanth, Viresh Mohanlall, Raghuprasad Mailavaram
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1471-1486 (2021)
A series of 1,2,3-trisubstituted indolizines (2a–2f, 3a–3d, and 4a–4c) were screened for in vitro whole-cell anti-tubercular activity against the susceptible H37Rv and multidrug-resistant (MDR) Mycobacterium tuberculosis (MTB) strains. Compound
Externí odkaz:
https://doaj.org/article/317149f295104f1dbe7c0e6553495828
Autor:
Vijayakumar Uppar, Sandeep Chandrashekharappa, Chandan Shivamallu, Sushma P, Shiva Prasad Kollur, Joaquín Ortega-Castro, Juan Frau, Norma Flores-Holguín, Atiyaparveen I. Basarikatti, Mallikarjun Chougala, Mrudula Mohan M, Govindappa Banuprakash, Jayadev, Katharigatta N. Venugopala, Belakatte P. Nandeshwarappa, Ravindra Veerapur, Abdulaziz A. Al-Kheraif, Abdallah M. Elgorban, Asad Syed, Kiran K. Mudnakudu-Nagaraju, Basavaraj Padmashali, Daniel Glossman-Mitnik
Publikováno v:
Molecules, Vol 26, Iss 9, p 2722 (2021)
Candida albicans, an opportunistic fungal pathogen, frequently colonizes immune-compromised patients and causes mild to severe systemic reactions. Only few antifungal drugs are currently in use for therapeutic treatment. However, evolution of a drug-
Externí odkaz:
https://doaj.org/article/9e2cfb7e49a44d0a9a663a5a87642fba
Autor:
Katharigatta N. Venugopala, Vijayakumar Uppar, Sandeep Chandrashekharappa, Hassan H. Abdallah, Melendhran Pillay, Pran Kishore Deb, Mohamed A. Morsy, Bandar E. Aldhubiab, Mahesh Attimarad, Anroop B. Nair, Nagaraja Sreeharsha, Christophe Tratrat, Abdulmuttaleb Yousef Jaber, Rashmi Venugopala, Raghu Prasad Mailavaram, Bilal A. Al-Jaidi, Mahmoud Kandeel, Michelyne Haroun, Basavaraj Padmashali
Publikováno v:
Antibiotics, Vol 9, Iss 5, p 233 (2020)
A series of ethyl 1-(substituted benzoyl)-5-methylpyrrolo[1,2-a]quinoline-3-carboxylates 4a–f and dimethyl 1-(substituted benzoyl)-5-methylpyrrolo[1,2-a]quinoline-2,3-dicarboxylates 4g–k have been synthesized and evaluated for their anti-tubercul
Externí odkaz:
https://doaj.org/article/f25c1a746c5a4cdb8c1931de74c7a524
Publikováno v:
Journal of Advanced Pharmaceutical Technology & Research, Vol 1, Iss 2, Pp 236-244 (2010)
Some novel substituted pyramidinopyrazoles and pyrimidinotriazoles have been synthesized by using 6-anisyl-5-cyano-2-hydrazino-3-N-methyl-3, 4-dihydropyrimidine-4-one as the starting material. Structures of these compounds have been established by IR
Externí odkaz:
https://doaj.org/article/2510617458374ea88ab9d3fc3bf59b39
Publikováno v:
Journal of Advanced Pharmaceutical Technology & Research, Vol 1, Iss 2, Pp 236-244 (2010)
Some novel substituted pyramidinopyrazoles and pyrimidinotriazoles have been synthesized by using 6-anisyl-5-cyan-2-hydrazine-3-N-methyl-3, 4-dihydropyrimidine-4-one as the starting material. Structures of these compounds have been established by IR,
Externí odkaz:
https://doaj.org/article/89ae71f0a132416ba82f4ac6a72c3a32
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 6, Pp o654-o654 (2014)
In the title compound, C10H7BrF3N3O, the dihedral angle between the benzene and triazole rings is 23.17 (12)° and the C atom of the –CF3 group deviates from its attached ring plane by 1.147 (3) Å. In the crystal, molecules are linked by C—H...N
Externí odkaz:
https://doaj.org/article/eedbea4b751f4b46a34c46ef4954531d
Publikováno v:
Molbank, Vol 2012, Iss 3, p M774 (2012)
2-[(4-Bromophenylimino)methyl]-5-pentadecylphenol has been synthesized by reaction of 2-hydroxy-4-pentadecylbenzaldehyde with 4-bromoaniline in 1,4-dioxane and its IR, 1H-NMR, 13C-NMR and MS spectroscopic data are presented.
Externí odkaz:
https://doaj.org/article/a9ed3b12faa2482e8375d08333ca5d35
Publikováno v:
Molbank, Vol 2009, Iss 4, p M641 (2009)
The title compound, [1-(4-chlorophenyl)cyclopropyl](piperazin-1-yl)methanone, was synthesized and characterized by elemental analysis, IR, 1H NMR, 13C NMR and mass spectral data.
Externí odkaz:
https://doaj.org/article/04cd8194fb184ab0a74cb3bc5831748c
Autor:
Dilip Kamble Soumyashree, Dinesh Shrikant Reddy, Honnappa Nagarajaiah, Lohit Naik, Hemantkumar Mohanchand Savanur, Choradi Devendrappa Shilpa, Mayanna Sunitha Kumari, Hamzad Shanavaz, Basavaraj Padmashali
Publikováno v:
Archiv der Pharmazie.
Autor:
Mahesh Attimarad, Rahul D. Nagdeve, Deepak Chopra, Mohamed A. Morsy, Katharigatta N. Venugopala, Basavaraj Padmashali, Lina A. Dahabiyeh, Nizar A. Al-Shar’i, Wafa Hourani, Raghuprasad Mailavaram, Nagaraja Sreeharsha, Pobitra Borah, Sheena Shashikanth, Anroop B. Nair, Melendhran Pillay, Christophe Tratrat, Viresh Mohanlall, Pran Kishore Deb, Bandar E. Al-Dhubiab, Susanta K. Nayak, Sandeep Chandrashekharappa, Michelyne Haroun
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
article-version (VoR) Version of Record
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1471-1486 (2021)
article-version (VoR) Version of Record
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1471-1486 (2021)
A series of 1,2,3-trisubstituted indolizines (2a–2f, 3a–3d, and 4a–4c) were screened for in vitro whole-cell anti-tubercular activity against the susceptible H37Rv and multidrug-resistant (MDR) Mycobacterium tuberculosis (MTB) strains. Compound