Zobrazeno 1 - 10
of 54
pro vyhledávání: '"D.R., Sherin"'
Autor:
Anuja Gracy Joseph, P. Sasikumar, Manojkumar K Thanathu, D.R. Sherin, Maniyamma Aswathy, Choudhary Harsha, Ajaikumar B. Kunnumakkara, Radhakrishnan Kokkuvayil Vasu, Kishore Banik, Dey Parama
Publikováno v:
ACS Pharmacology & Translational Science. 4:834-847
Triterpenoids are ubiquitously distributed secondary metabolites, primarily scrutinized as a source of medication and preventive measures for various chronic diseases. The ease of isolation and excellent pharmacological properties of triterpenoids ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3319decd99192f53a0910ddc86093f84
https://doi.org/10.1021/acsptsci.1c00011
https://doi.org/10.1021/acsptsci.1c00011
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Materials Today: Proceedings. 46:2898-2905
Normal cells’ genomic identity is protected by telomeres and sometimes chromosomal instability was observed due to shortening of telomerase because of successive cell divisions. Reports indicate that telomerase length is crucial in determining telo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::babda066d26f9c2812615ac9ee8f879d
https://doi.org/10.1016/j.matpr.2020.10.675
https://doi.org/10.1016/j.matpr.2020.10.675
Autor:
D.R. Sherin, T.K. Manojkumar
Publikováno v:
Materials Today: Proceedings. 33:1229-1233
The significance of five membered heterocycles in simple donor-acceptor system was elaboratively studied by density functional theory (DFT) and time dependent density functional theory (TDDFT). By effectively substituting eight different rings the HO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f44e62ab48db3d277609f8073395fbb9
https://doi.org/10.1016/j.matpr.2020.03.482
https://doi.org/10.1016/j.matpr.2020.03.482
Publikováno v:
Computational and Theoretical Chemistry. 1217:113894
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a7e449e014a6e278fcac1a9e5135db1
https://doi.org/10.1016/j.comptc.2022.113894
https://doi.org/10.1016/j.comptc.2022.113894
Autor:
Neethu, S, Govind, M.G., P.S., Vimalkumar, Biji, M, D.R, Sherin, Dan, Mathew, Radhakrishnan, K.V. *
Publikováno v:
In Phytochemistry Letters October 2021 45:72-76
Autor:
Girija K. Krishnapriya, Sreerekha V. Keerthi, Kallikat N. Rajasekharan, D.R. Sherin, T.K. Manojkumar, Maheswari R. Priya, Vijayan R. Akhila
Publikováno v:
Letters in Organic Chemistry. 16:560-568
The synthesis of 4-amino-2-arylamino-5-(benzofuran-2-oyl)thiazoles 4a-h, as example of 2,4-diaminothiazole-benzofuran hybrids and an evaluation of their antidiabetic activity, by in vitro and computational methods, are reported. The synthesis of thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::533fdb225a354631586e8cdcfa58d7c5
https://doi.org/10.2174/1570178615666180815124425
https://doi.org/10.2174/1570178615666180815124425
Publikováno v:
Computational Biology and Chemistry. 78:108-115
Serotonin receptor, 5-HT1AR, agonists and partial agonists have established drug candidates for psychiatric and neurologic disorders. Recently, we reported the synthesis and evaluation of arylpiperazine derivatives of 3,5-dioxo-(2H,4H)-1,2,4-triazine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2faba03ccf5f4da89f210b3f82cf227d
https://doi.org/10.1016/j.compbiolchem.2018.11.015
https://doi.org/10.1016/j.compbiolchem.2018.11.015
Publikováno v:
Chemphyschem : a European journal of chemical physics and physical chemistry. 21(20)
Among different possible non-classical structures, the stabilization of half-planar tetracoordinate carbon conformation is believed to be the most difficult one. Herein, we designed three types of half-planar tetracoordinate carbon compounds computat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81db5f8e6a15151c818d3c4fedfc94ce
https://pubmed.ncbi.nlm.nih.gov/32841480
https://pubmed.ncbi.nlm.nih.gov/32841480