Zobrazeno 1 - 10
of 12
pro vyhledávání: '"S. Sree Kanth"'
Autor:
S. Sree Kanth, M. Vijjulatha
Publikováno v:
E-Journal of Chemistry, Vol 5, Iss 3, Pp 584-592 (2008)
A series of novel tetrahydroxy cyclic urea molecules as HIV-1 protease inhibitors were designed using computational techniques. The designed molecules were compared with the known cyclic urea molecules by performing docking studies on six of wild typ
Externí odkaz:
https://doaj.org/article/c21d78104398469f8ba52b6f8fa7093e
Publikováno v:
E-Journal of Chemistry, Vol 7, Iss S1, Pp S75-S84 (2010)
To understand the structural requirements of HIV-1 integrase inhibitors and to design new ligands against human HIV-1 integrase with enhanced inhibitory potency, a 3D QSAR (quantitative structure-activity relationship) study with comparative molecula
Externí odkaz:
https://doaj.org/article/f48d83b3c63a42f8863581f349ab2217
Autor:
Manga Vijjulatha, Dongamanti Ashok, M. Sarasija, N. Sai Krishna, S. Sree Kanth, Someswar Rao Sagurthi, E. V. L. Madhuri, Akkiraju Anjini Gayatri
Publikováno v:
Russian Journal of General Chemistry. 89:2129-2135
Biaryl derivatives of spirofurochromanones have been synthesised from 4-bromophenyl derivatives of spirofurochromanones upon catalysis by Pd/C in water. Structures of the synthesised compounds are derived from IR, NMR and HRMS spectral data. The comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fd0fdd710f11c5682fb4d5c6caf5cb9
https://doi.org/10.1134/s1070363219100220
https://doi.org/10.1134/s1070363219100220
Autor:
Manga Vijjulatha, Deva Das Manwal, Ayub Shaik, Rambabu Aveli, S. Sree Kanth, Vani Kondaparthy
Publikováno v:
Inorganic Chemistry Communications. 126:108499
Evidence from biochemical, genetic, and pharmacological studies strongly suggest that inhibition of Protein Tyrosine Phosphatase-1B (PTP-1B) enzyme could address both diabetes and obesity and thus making PTP-1B as an exciting target for drug developm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9893c3bd6f835eba3cf379d6316e4aea
https://doi.org/10.1016/j.inoche.2021.108499
https://doi.org/10.1016/j.inoche.2021.108499
Autor:
Malini Devi Alaparthi, Manga Vijjulatha, Dongamanti Ashok, Someswar Rao Sagurthi, E. V. L. Madhuri, M. Sarasija, S. Sree Kanth
Publikováno v:
RSC Advances. 7:25710-25724
A series of 2′-substituted-3′-methylspiro[cyclohexane-1,7′-furo[3,2-g]chroman]-5′(7′H)-one, 5a–i and 7a–u have been synthesized using an eco-friendly approach to attain good yields in a shorter reaction time. The structures of novel com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f25ca012ff341acf44f975a2b9e492ff
https://doi.org/10.1039/c7ra01550j
https://doi.org/10.1039/c7ra01550j
Autor:
Manga Vijjulatha, S. Sree Kanth
Publikováno v:
Open Chemistry, Vol 5, Iss 4, Pp 1064-1072 (2007)
A series of novel cyclic urea molecules 5,6-dihydroxy-1,3-diazepane-2,4,7-trione as HIV-1 protease inhibitors were designed using computational techniques. The designed molecules were compared with the known cyclic urea molecules by performing dockin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80c0b5e24dbdd26bfc32fd584956d3e7
https://doi.org/10.2478/s11532-007-0040-x
https://doi.org/10.2478/s11532-007-0040-x
Publikováno v:
E-Journal of Chemistry, Vol 7, Iss S1, Pp S75-S84 (2010)
To understand the structural requirements of HIV-1 integrase inhibitors and to design new ligands against human HIV-1 integrase with enhanced inhibitory potency, a 3D QSAR (quantitative structure-activity relationship) study with comparative molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7007bfb51d11d1a661a6c171c4cc2f3c
https://doaj.org/article/f48d83b3c63a42f8863581f349ab2217
https://doaj.org/article/f48d83b3c63a42f8863581f349ab2217
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