Zobrazeno 1 - 10
of 191
pro vyhledávání: '"Nagula Shankaraiah"'
Autor:
Stephy Elza John, Darshana Bora, Vivek Dhiman, Ramya Tokala, Gananadhamu Samanthula, Nagula Shankaraiah
Publikováno v:
ACS Omega, Vol 7, Iss 1, Pp 1299-1310 (2021)
Externí odkaz:
https://doaj.org/article/ffa980a599e145eaaf74506b1d4a209a
Publikováno v:
New Journal of Chemistry. 47:4687-4697
The currently designed molecules demonstrated potential anti-cancer activity by the induction of apoptosis and tubulin polymerization inhibition.
Autor:
Jay Prakash Soni, Shrilekha Chilvery, Anamika Sharma, G. Nikitha Reddy, Chandraiah Godugu, Nagula Shankaraiah
Publikováno v:
RSC Medicinal Chemistry. 14:549-562
The present work demonstrates the design and synthesis of new indolo–pyrazole derivatives, their cytotoxic evaluation, tubulin polymerization inhibition, and molecular modeling studies.
Akademický článek
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Publikováno v:
Current Medicinal Chemistry. 29:3530-3556
Abstract: Cancer is a silent killer and remains to pose major health problems globally. Amongst the several biological targets, DNA is one of the most striking targets in cancer chemotherapy. Owing to its planar structure, phenanthrene and its deriva
Publikováno v:
Arkivoc. 2023
Autor:
Kritika Laxmikeshav, Mone Sayali, Geetanjali Devabattula, Durgesh G. Valapil, Ashutosh Mahale, Pravesh Sharma, Joel George, Regur Phanindranath, Chandraiah Godugu, Onkar P. Kulkarni, Narayana Nagesh, Nagula Shankaraiah
Publikováno v:
Archiv der Pharmazie. 356
Publikováno v:
Current Organic Chemistry. 26:382-398
Abstract: Organic azides are in the interphase between chemistry, biology, medicine, and materials science. Their uses in peptide chemistry, combinatorial chemistry, and the synthesis of heterocycles are extensively explored. In this review, the focu
Autor:
Stephy Elza John, Darshana Bora, Sowmya Dastari, Durgesh Gurukkala Valapil, Nagula Shankaraiah
Publikováno v:
New Journal of Chemistry. 46:19722-19730
The protocol represents the efficiency of a C–H activation strategy in the construction of pharmacophoric and chromophoric structures employing cis-stilbene acids as directing groups.
Publikováno v:
Green Chemistry. 24:1259-1269
Microwave-assisted dithiocarbamation of various imidazoheterocycles with in situ generated dithiocarbamates via a water-soluble Cu(i) catalyst using benign solvent, enabling catalyst recyclability, scalability, less reaction time and high yields.