Zobrazeno 1 - 10
of 29
pro vyhledávání: '"M.S. Bethu"'
Autor:
Praveen Choppara, Y.V. Prasad, C.V. Rao, K. Hari Krishna, G. Trimoorthulu, G.U. Maheswara Rao, J. Venkateswara Rao, M.S. Bethu, Y.L.N. Murthy
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2328-2335 (2019)
A series of novel N-1 and C-3 substituted indole derivatives (5a–f) were designed, synthesized and evaluated for their cytotoxic properties, viz Brine Shrimp Lethality Bioassay (BSLB) besides 5-Lipoxygenase (5-LOX) inhibitory activities through in
Externí odkaz:
https://doaj.org/article/3307db68f4844e02a2f82414953469cc
Autor:
Praveen Choppara, M.S. Bethu, Y. Vara Prasad, J. Venkateswara Rao, T.J. Uday Ranjan, G.V. Siva Prasad, Rajitha Doradla, Y.L.N. Murthy
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2721-2731 (2019)
Two series of novel bis(indole) analogues viz., N′-((5-substituted-1H-indol-3-yl)methylene)-n-(1H-indol-3-yl)alkanehydrazides (7a–f) and N′-((5-substituted-1-(3-methylbut-2-enyl)-1H-indol-3-yl)methylene)-n-(1H-indol-3-yl)acetohydrazide (8a–f)
Externí odkaz:
https://doaj.org/article/e0a952fdcbd742d0881176a2b49ead73
Autor:
Y. Vara Prasad, M.S. Bethu, Rajitha Doradla, J. Venkateswara Rao, G.V. Siva Prasad, T.J. Uday Ranjan, Praveen Choppara, Y.L.N. Murthy
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2721-2731 (2019)
Two series of novel bis(indole) analogues viz., N′-((5-substituted-1H-indol-3-yl)methylene)-n-(1H-indol-3-yl)alkanehydrazides (7a–f) and N′-((5-substituted-1-(3-methylbut-2-enyl)-1H-indol-3-yl)methylene)-n-(1H-indol-3-yl)acetohydrazide (8a–f)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d0dba112a458ae17c0460e22526f3af
http://www.sciencedirect.com/science/article/pii/S187853521500163X
http://www.sciencedirect.com/science/article/pii/S187853521500163X
Autor:
G. Trimoorthulu, Y.L.N. Murthy, M.S. Bethu, C.V. Rao, Praveen Choppara, Y. V. S. S. Prasad, G.U. Maheswara Rao, K. Hari Krishna, J. Venkateswara Rao
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2328-2335 (2019)
A series of novel N-1 and C-3 substituted indole derivatives (5a–f) were designed, synthesized and evaluated for their cytotoxic properties, viz Brine Shrimp Lethality Bioassay (BSLB) besides 5-Lipoxygenase (5-LOX) inhibitory activities through in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b38337c1967a32f919164c27b0bec88
https://doi.org/10.1016/j.arabjc.2015.02.006
https://doi.org/10.1016/j.arabjc.2015.02.006
Autor:
Latha Domdi, M.S. Bethu, Sindhu G. Reddy, Venkata Subbaiah Kotakdi, Vijaya Tartte, K. V. Saritha, Suman Bukke, S. Soneya, Vasudeva Reddy Netala
Publikováno v:
Artificial Cells, Nanomedicine, and Biotechnology. 46:1138-1148
The present study reports the biosynthesis of silver nanoparticles (IH-AgNPs) using aqueous leaf extract of Indigofera hisruta L. The biosynthesized IH-AgNPs were found to be FCC crystals, 5-10 nm in size, spherical in shape and stable. The biosynthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0f004525dc75348b26cea20757210c
https://doi.org/10.1080/21691401.2018.1446967
https://doi.org/10.1080/21691401.2018.1446967
Publikováno v:
Artificial Cells, Nanomedicine, and Biotechnology. 46:104-114
The present study reports a simple and eco-friendly synthesis of silver nanoparticles (AgNPs) using leaf extract of Rhynchosia suaveolens. UV-Vis analysis of R. suaveolens synthesized AgNPs (RS-AgNPs) showed surface plasmon resonance (SPR) peak at 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50da579764af7835b389106b76270285
https://doi.org/10.1080/21691401.2017.1414824
https://doi.org/10.1080/21691401.2017.1414824
Autor:
Vidya Katangoor, Suresh Poudapally, M.S. Bethu, Venkateswara Rao Janapala, Vijaya Bhaskara Reddy Iska, Narender Pottabathini, Somesh Sharma, Subhabrata Sen, Loka Reddy Velatooru, Shankar Battu
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:1923-1928
A robust economic approach to N-(quinazoline-4-yl)sulfonamides was developed and synthesized different aryl, hetero aryl, alkyl and cyclopropyl sulfonamides in excellent yields. All the compounds were evaluated for cytotoxic affinity to SKOV3, DU145,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc9cae08b4173f654cdcc041a4257d1
https://doi.org/10.1016/j.bmcl.2017.03.042
https://doi.org/10.1016/j.bmcl.2017.03.042
Autor:
M.S. Bethu, Venkateswara Rao J, T. Chiranjeevi, Biplab Sarkar, A. Uma, Debojit Kumar Deb, Werner Kaminsky, Basava Punna Rao A, Mohan Rao Kollipara
Publikováno v:
Journal of Organometallic Chemistry. 824:131-139
Synthesis, characterization and biological activity of mono, bi and tri nuclear pentamethylcyclopentadienyl rhodium and iridium complexes with 1,3,5-tris(di-2-pyridylaminomethyl)benzene (L) ligand have been described. These complexes have general for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfd61874facc1c7ae808d0a11422550f
https://doi.org/10.1016/j.jorganchem.2016.10.018
https://doi.org/10.1016/j.jorganchem.2016.10.018
Autor:
M.S. Bethu, Krishna Mohan Poluri, T. Chiranjeevi, A. Uma, A. Basava Punna Rao, J. Venkateswara Rao, Mohan Rao Kollipara, B. Yashwanth
Publikováno v:
Inorganica Chimica Acta. 453:284-291
Ruthenium based complexes are growing as a promising formulations for the cure of cancer with their distinct activity and less side effects. In the present study, a series of mono, di and trinuclear octahedral arene ruthenium complexes containing 1,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3017041c315819cfe2046a31019d6801
https://doi.org/10.1016/j.ica.2016.08.031
https://doi.org/10.1016/j.ica.2016.08.031
Autor:
Vijaya Tartte, M.S. Bethu, Vasudeva Reddy Netala, Bobbu Pushpalatha, Sani Aishwarya, Vijaya Bhaskar Baki, J. Venkateswara Rao
Publikováno v:
International Journal of Nanomedicine. 11:5683-5696
An endophytic fungal strain isolated from the leaves of Gymnema sylvestre was identified as Pestalotiopsis microspora VJ1/VS1 based on nucleotide sequencing of internal transcribed spacer region (ITS 1-5.8S-ITS 2) of 18S rRNA gene (NCBI accession num
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::325989b522a59bf1564f6cbbe01302e8
https://doi.org/10.2147/ijn.s112857
https://doi.org/10.2147/ijn.s112857