Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Geethavani, Meka"'
Publikováno v:
Results in Chemistry, Vol 5, Iss , Pp 100783- (2023)
Medicinal chemistry is a basic science that involves identification, synthesis and development of new drugs for therapeutic use. Biological importance of heterocycles makes them more crucial in pharmaceutical industries.In this work heterocyclics lik
Externí odkaz:
https://doaj.org/article/0a3b07ed6b834f3a933396c743b47ea6
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 6, Iss 1, Pp 1-6 (2020)
Abstract Background The o-phenylenediamine is a versatile starting material for several compounds. Synthesized o-phenylenediamine and amino acids (glycine, alanine, aspartic acid, and l-proline) undergo condensation via Phillips reaction. The synthes
Externí odkaz:
https://doaj.org/article/301b82a2db2e42cc91981cc0929bb6c1
Publikováno v:
Journal of Young Pharmacists. Apr-Jun2022, Vol. 14 Issue 2, p174-178. 5p.
Autor:
Rajavardhana Thamineni, Ramalingam Peraman, Jayakumar Chenniah, Geethavani Meka, Ashok Kumar Munagala, Vijayakumar Thangavel Mahalingam, Rajanandh Muhasaparur Ganesan
Publikováno v:
Tropical Medicine & International Health. 27:1013-1023
Tuberculosis (TB) patients on the National Tuberculosis Elimination Program (NTEP) treatment protocol receive daily doses without health professional-supervised drug intake as during the previous directly observed treatment short-course (DOTS) regime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faae7d03ab41ead7ce07cb892970571f
https://doi.org/10.1111/tmi.13824
https://doi.org/10.1111/tmi.13824
Publikováno v:
Journal of Pharmaceutical Research International. :128-139
Various biologically important Stilbene analogues were competently synthesized using inexpensive, non-toxic, and readily available amino acids and Stilbene; the systematic study was carried out to characterize parameters such as TLC, melting point, I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b12eb42f9aeca8b1beaaf5e4b325d31a
https://doi.org/10.9734/jpri/2021/v33i39b32189
https://doi.org/10.9734/jpri/2021/v33i39b32189
Autor:
Vinay Kumar Kutagulla, Geethavani Meka, Saloni Malla, Padmanabha Reddy Yiragamreddy, Naresh Babu Chilamakuru, Amit K. Tiwari, Ramalingam Peraman, Charles R. Ashby
Publikováno v:
New Journal of Chemistry. 45:10683-10692
Novel scaffolds of stilbene were identified as inhibitors of Mycobacterium tuberculosis by targeting the nucleoid-associated protein, HU, using molecular docking. Based on the proposed combinatorial libraries I to VI, structures I and III had signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00ba46813813e0c14f3ba25c45d9a13a
https://doi.org/10.1039/d0nj05947a
https://doi.org/10.1039/d0nj05947a