Zobrazeno 1 - 10
of 54
pro vyhledávání: '"S. Venketesh"'
Autor:
R.S., Sai Murali, R.S., Sai Siddhardha, D., Rajesh Babu, S., Venketesh, R., Basavaraju, G., Nageswara Rao
Publikováno v:
In Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 5 June 2017 180:217-223
Autor:
Natarajan Arumugam, Abdulrahman I. Almansour, Thota Sai Manohar, S. Venketesh, D. Kotresha, Raju Suresh Kumar
Publikováno v:
Saudi Journal of Biological Sciences, Vol 28, Iss 1, Pp 754-761 (2021)
Saudi Journal of Biological Sciences
Saudi Journal of Biological Sciences
Two series of dimethoxyindanone imbedded novel fluorinated spiropyrrolidine heterocyclic hybrids were synthesized employing two different less explored azomethine ylides and were measured for their efficiency as inhibitors for Alzheimer’s disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d7a530ef064d9b915aa4c3959a58c9c
https://doi.org/10.1016/j.sjbs.2020.11.005
https://doi.org/10.1016/j.sjbs.2020.11.005
Autor:
V. Sai Muthukumar, K. B. R. Varma, S. Venketesh, B. Siva Kumar, Chelli Sai Manohar, Sai Pavan Prashanth Sadhu, Sai Krishna Srimadh
Publikováno v:
Nanotechnology Reviews, Vol 8, Iss 1, Pp 61-78 (2019)
BCZT (Ba0.85Ca0.15Zr0.1Ti0.9O3) is a recent class of lead-free ferroelectric material associated with high piezoelectric coefficient, making it suitable to inspire hydroxyapatite (HA)-BCZT ceramics for bone materials. Nano-crystalline hydroxyapatite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9c812231d9da40660d711028252a849
https://doaj.org/article/0889a731cbfc422580f5a717f0dd6962
https://doaj.org/article/0889a731cbfc422580f5a717f0dd6962
Autor:
S. Venketesh, D. Kotresha, Natarajan Arumugam, Thota Sai Manohar, Alireza Basiri, Abdullah M. Asiri, Raju Suresh Kumar, Abdulrahman I. Almansour, Dhaifallah M. Al-thamili, Mohammad Asad
Publikováno v:
Bioorganic Chemistry. 81:134-143
Novel highly functionalized 2-amino-4H-pyrans were achieved in excellent yields under simple grinding at ambient temperature and were assessed for their potential for treating Alzheimer’s disease (AD). The 2-amino-4H-pyran bearing nitro groups on b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::615052349f085ce686e62d9a60af9ee1
https://doi.org/10.1016/j.bioorg.2018.08.009
https://doi.org/10.1016/j.bioorg.2018.08.009
Autor:
Mohammad Altaf, Thota Sai Manohar, D. Kotresha, R. Padmanaban, Abdulrahman I. Almansour, S. Venketesh, Natarajan Arumugam, Popuri Sureshbabu, Gnanavel Angamuthu, Raju Suresh Kumar
Publikováno v:
Bioorganic Chemistry. 79:64-71
A regio and stereo- selective synthesis of hitherto unexplored hybrid heterocyclic system comprising spiropyrrolidine, indolizino[6,7-b]indole units in good to excellent yields, has been developed via three component 1,3-dipolar cycloaddition and con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f80c4733dd1ebf3bfc00ef0a95f98e2c
https://doi.org/10.1016/j.bioorg.2018.04.025
https://doi.org/10.1016/j.bioorg.2018.04.025
Autor:
Dhaifeallah Mohammed Qaide Althomili, S. Venketesh, Natarajan Arumugam, Abdulrahman I. Almansour, Alireza Basiri, Raju Suresh Kumar, D. Kotresha, Mohammed Altaf, Thota Sai Manohar
Publikováno v:
Bioorganic Chemistry. 77:263-268
A small library of novel spiropyrrolidine heterocyclic hybrids has been prepared regioselectively in 1-butyl-3-methylimidazoliumbromide ([bmim]Br) with good to excellent yields using a [3+2] cycloaddition reaction. These synthesized compounds were ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4e8d3d4f7958fc7c11f8005824518de
https://doi.org/10.1016/j.bioorg.2018.01.019
https://doi.org/10.1016/j.bioorg.2018.01.019
Autor:
S. Venketesh, R.S. Sai Siddhardha, G. Nageswara Rao, R. Basavaraju, R S Sai Murali, D Rajesh Babu
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 180:217-223
The present study brings out the interaction between vasicine, an alkaloid of Adhatoda vasica Nees with double stranded DNA [corrected]. The physico-chemical interaction between small molecules and nucleic acids is a major area of focus in screening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0482c8c432f7e0f979612631a65b7c73
https://doi.org/10.1016/j.saa.2017.03.016
https://doi.org/10.1016/j.saa.2017.03.016
Autor:
Natarajan Arumugam, Abdulrahman I. Almansour, R. Saiswaroop, Raju Suresh Kumar, D. Kotresha, S. Venketesh
Publikováno v:
Bioorganicmedicinal chemistry. 27(12)
A small library of new class of dispiropyrrolidinyl-piperidone tethered indono[1,2-b]quinoxaline heterocyclic hybrids 7a–j were synthesized employing multicomponent 1,3-dipolar cycloaddition strategy in [bmim]Br. The azomethine ylide employed is fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::094c1a9203189338f1a2b7a4836ddbc2
https://pubmed.ncbi.nlm.nih.gov/30952387
https://pubmed.ncbi.nlm.nih.gov/30952387
Autor:
Abdulrahman I. Almansour, R. Padmanaban, Thota Sai Manohar, Santhakumar Yeswanthkumar, S. Venketesh, Raju Suresh Kumar, Natarajan Arumugam, Y. Arun, Necmi Dege, Sevgi Kansiz
Publikováno v:
Journal of Molecular Structure. 1225:129165
A facile eco-friendly approach for the regio- and stereoselective synthesis of structurally intriguing novel spiropyrrolidinoquinoxaline tethered indole hybrid heterocycle has been accomplished via a cascade reaction sequence involving 1,3-dipolar cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd9f5f1e0b8d39401dc13241feb74398
https://doi.org/10.1016/j.molstruc.2020.129165
https://doi.org/10.1016/j.molstruc.2020.129165
Autor:
D. Kotresha, Natarajan Arumugam, S. Venketesh, Raju Suresh Kumar, Abdulrahman I. Almansour, Thota Sai Manohar
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 30:126789
A small library of structurally fascinating spiropyrrolidine tethered imidazole heterocylic hybrids has been synthesized regioselectively in good yields employing [bmim]Br mediated 1,3-diplar cycloaddition strategy. The new class of azomethine ylide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573ed7c55d1d01d6c07d052b5fd229af
https://doi.org/10.1016/j.bmcl.2019.126789
https://doi.org/10.1016/j.bmcl.2019.126789