Zobrazeno 1 - 10
of 29
pro vyhledávání: '"D. S. Prasanna"'
Autor:
Dinesh Rangappa, Vijaya V. Shanbhag, T.R. Shashi Shekhar, Ramachandra Naik, H. Nagabhushana, K.M. Girish, D. S. Prasanna, S.C. Prashantha, S. Ashwini
Publikováno v:
Ceramics International. 47:10346-10354
Systematic analysis of SiO2@CaTiO3:Dy3+(3 mol %):Li+(0.25–1 mol %) core shell nanoparticles (C–S NPs) were carried out. CaTiO3:Dy3+ (3 mol %), Li+ (0.25–1 mol %) NPs were prepared using low temperature solution combustion method. C–S structur
Autor:
V.S. Amrutha, G.P. Darshan, H. Nagabhushana, K. Ashwini, Y.S. Vidya, K.S. Anantharaju, Dinesh Rangappa, Krushitha Shetty, D. S. Prasanna
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 1, Pp 1449-1465 (2020)
The present study reveals a simple and efficient method for the green reduction of graphene oxide (GO) employing Emblica officinalis fruit extract as a reducing agent. Here, a green sol–gel method has been reported for the preparation of ZnFe2O4 an
Autor:
D.M.K. Siddeswara, K.R. Vishnu Mahesh, T. Venkatesh, N. V. Raghavendra, M. Sathish Kumar, Dinesh Rangappa, M. Mylarappa, D. S. Prasanna
Publikováno v:
Materials Today: Proceedings. 4:11915-11922
The present research was mainly focused on an efficient approach for the synthesis of MnO 2 /Graphene/Multiwalled carbon nano tubes/nanocomposite (MnO 2 /Graphene/MWCNTs). The MnO 2 /Graphene/MWCNTs nanocomposite was characterized by using X-Ray Diff
Publikováno v:
Synthetic Communications. 43:2756-2762
A simple and convenient procedure for the synthesis of nitriles by dehydration of aldoximes using a PCC (pyridiniumchlorochromate) has been developed. A variety of aromatic, heteroaromatic, and aliphatic aldoximes are converted. Supplementary materia
Autor:
Kanchugarakoppal S. Rangappa, Bibha Choudhary, Sathees C. Raghavan, Vidya Gopalakrishnan, Mahesh Hegde, Supriya V. Vartak, Hanumappa Ananda, D. S. Prasanna, C. V. Kavitha
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Chemically synthesized small molecules play important role in anticancer therapy. Several chemical compounds have been reported to damage the DNA, either directly or indirectly slowing down the cancer cell progression by causing a cell cycle arrest.
Autor:
Toreshettahally R. Swaroop, Kyathegowdanadoddi Srinivas Balaji, Shankar Jayarama, Lokesh Siddalingaiah, Kanchugarakoppal S. Rangappa, D. S. Prasanna, Preethi Saligrama Devegowda
Publikováno v:
Medicinal chemistry. 6
Quinazolines are very important class of heterocyclic compounds with antitumor properties. In search of novel anti-tumour agents, a series of 4-anilinoquinazolines were synthesized and characterized using proton and carbon-13 nuclear magnetic resonan
Autor:
D. S. Prasanna, C. V. Kavitha, S. R. Ranganatha, Kanchugarakoppal S. Rangappa, S. Chandrappa, Sathees C. Raghavan, K. Vinaya
Publikováno v:
Chemical Biology & Drug Design. 79:360-367
A series of novel 2-(4-(2,4-dimethoxybenzoyl)phenoxy)-1-(4-(3-(piperidin-4-yl)propyl) piperidin-1-yl)ethanone derivatives 9(ae) and 10(ag) were synthesized and characterized by 1H NMR, IR, mass spectral, and elemental analysis. These novel compounds
Publikováno v:
Letters in Drug Design & Discovery. 8:988-995
A series of novel 2-methyl-3-(2-(piperazin-1-yl)ethyl)-6,7,8,9-tetrahydro-4H-pyrido1,2- a]pyrimidin-4-one sulfonamide and carboxamide derivatives were synthesized in good yield. The synthesized compounds were characterized by H-1-NMR, FTIR and elemen
Autor:
Kanchugarakoppal S. Rangappa, C. V. Kavitha, Sathees C. Raghavan, D. S. Prasanna, K. Vinaya, S. Chandrappa
Publikováno v:
Chemical Biology & Drug Design. 78:622-630
To explore the anticancer effect associated with the piperidine framework, several (substituted phenyl) {4-[3-(piperidin-4-yl)propyl]piperidin-1-yl} methanone derivatives 3(a-i) were synthesized. Variation in the functional group at N-terminal of the
Autor:
Hanumegowda Raju, S. Chandrappa, Kanchugarakoppal S. Rangappa, Sonnahallipura M. Byregowda, Hanumappa Ananda, Tandaga S. Nagamani, D. S. Prasanna
Publikováno v:
Recent Patents on Anti-Cancer Drug Discovery. 6:186-195
In search of synthetic chemotherapeutic substances capable of inhibiting, retarding, or reversing the process of multistage carcinogenesis, we synthesised a series of novel 1-(4-methoxybenzyl)-3-cyclopropyl-1H-pyrazol-5-amine derivatives 9(a-h) by a