Výsledky vyhledávání - "Madhavi, Madhavaram"

High-throughput virtual screening, ADME analysis, and estimation of MM/GBSA binding-free energies of azoles as potential inhibitors of Mycobacterium tuberculosis H37Rv

Autor: Parthasarathy Tigulla, Suresh Gangadhari, Manoj Kumar Palnati, Madhavi Madhavaram, Venkatesh Nampally

Publikováno v: Journal of Receptors and Signal Transduction. 39:312-320

Isoniazid, also known as isonicotinyl hydrazide (INH), was used as a frontline drug to treat Mycobacterium tuberculosis. The in silico virtual screening is used to identify the effective in...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e37275115de5dbc24e630ecb4cec95d3
https://doi.org/10.1080/10799893.2019.1660895

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A conventional and solid-state synthesis, biological activity, and molecular docking studies of 6-arylbenzo[4,5]imidazo[1,2-a] [1,8]naphthyridin-10-ols

Autor: Kurumanna Adem, Govan Maloth, Parthasarathy T, Sakram Boda, Ravi Dharavath, Madhu Palithapu, Madhavi Madhavaram

Publikováno v: Synthetic Communications. 49:1-11

An effective, practical, and simple approach toward the preparation of highly-substituted 6-arylbenzo[4, 5]imidazo[1,2-a][1,8]naphthyridin-10-ols 6(a-h) by the reaction of 3-aryl-1,8-naphthyridin-2-amines 3(a-h) with benzoquinone 4 in acid catalyzed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d654898f3ed94db4d1a70ab0454472e
https://doi.org/10.1080/00397911.2018.1509349

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3D QSAR and molecular docking studies of 4-alkoxy- and 4-acyloxy –phenyl ethylene thiosemicarbazone derivatives as tyrosinase inhibitors

Autor: Parthasarathy Tigulla, Madhavi Madhavaram

Publikováno v: Medicinal Chemistry Research. 26:3125-3135

Three-dimensional quantitative structural–activity relationship studies were carried out to understand the factors affecting the activity of 4-alkoxy- and 4-acyloxy –phenyl ethylene thiosemicarbazone analogs. The quantitative structural activity

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff8316cee9655874359a726fbdea175c
https://doi.org/10.1007/s00044-017-2007-6

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High-throughput virtual screening, ADME analysis, and estimation of MM/GBSA binding-free energies of azoles as potential inhibitors of

Autor: Madhavi, Madhavaram, Venkatesh, Nampally, Suresh, Gangadhari, Manoj Kumar, Palnati, Parthasarathy, Tigulla

Publikováno v: Journal of receptor and signal transduction research. 39(4)

Isoniazid, also known as isonicotinyl hydrazide (INH), was used as a frontline drug to treat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::465a7839077c22e65b1d8cba7ccf1245
https://pubmed.ncbi.nlm.nih.gov/31658859

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