Výsledky vyhledávání - "Jhimli Sengupta"

Akademický článek

Detection of a bibenzyl core scaffold in 28 common mangrove and associate species of the Indian Sundarbans: potential signature molecule for mangrove salinity stress acclimation

Autor: Bhanumati Sarkar, Hemendra Nath Kotal, Chayan Kumar Giri, Anup Mandal, Nandagopal Hudait, Nithar Ranjan Madhu, Subhajit Saha, Sandip Kumar Basak, Jhimli Sengupta, Krishna Ray

Publikováno v: Frontiers in Plant Science, Vol 14 (2024)

Bibenzyl derivatives comprising two benzene rings are secondary plant metabolites with significant therapeutic value. To date, bibenzyl derivatives in the Plant kingdom have been primarily identified in bryophytes, orchids, and Cannabis sativa. The m

Externí odkaz: https://doaj.org/article/52fcd33e685f4a9bac27f4cf0488ae3e

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Host assisted molecular recognition by human serum albumin: Study of molecular recognition controlled protein/drug mimic binding in a microfluidic channel

Autor: Dipanjan Mukherjee, Rami J. Obaid, Ranjan Das, Debanjona Singh Roy, Samir Kumar Pal, Jhimli Sengupta, Uttam Pal, Saleh A. Ahmed, Soumendra Singh, Subhankar Singha, Priya Singh, Tanusri Saha Dasgupta

Publikováno v: International Journal of Biological Macromolecules. 176:137-144

Human serum albumin (HSA) plays a pivotal role in drug release from its delivery vehicles such as cyclodextrins (CDs) by binding to the drugs. Here molecular recognition and binding of a drug mimic (CD1) to HSA have been explored in a microfluidic ch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bb8e5bc5623a44d565363ef47dc4076
https://doi.org/10.1016/j.ijbiomac.2021.02.002

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Optimal dose of vitamin-D supplement reduces death risk in covid patients – A review

Autor: Jhimli Sengupta, Arpan Basu, Nandagopal Hudait

Department of Chemistry, West Bengal State University, Barasat, Kolkata-700 126, India E-mail: jhimli.sengupta@gmail.com Manuscript received online 29 November 2020, revised and accepted 27 December 2020 An impasse in the realm of public health has b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f3c5352a9b3673920d46f72a0085d3f

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Synthesis and characterization of new carbohydrate-based organic Schiff bases

Autor: Jhimli Sengupta, Nandagopal Hudait

Department of Chemistry, West Bengal State University, Barasat, Kolkata-700 126, India E-mail: jhimli.sengupta@gmail.com Manuscript received online 12 October 2020, revised and accepted 30 November 2020 Carbohydrate-based organic Schiff bases having

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b93a953b6910656e498efd508f1d49b

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Deciphering the response of asymmetry in the hydrophobic chains of novel cationic lipids towards biological function

Autor: Theja Parassini Puthiyapurayil, Tatini Rakshit, Samir Kumar Pal, Ranjan Das, Priya Singh, Dipanjan Mukherjee, Praveen Kumar Vemula, Jhimli Sengupta

Publikováno v: Physical chemistry chemical physics : PCCP. 22(3)

Cationic liposomes, a type of non-viral vectors, often play the important biological function of delivering nucleic acids during cell transfection. Variations in the molecular architecture of di-alkyl dihydroxy ethyl ammonium chloride-based cationic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867afab8917276a77bd3b8e583238146
https://pubmed.ncbi.nlm.nih.gov/31898698

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A sensitive fluorescent probe for the polar solvation dynamics at protein–surfactant interfaces

Autor: Subhankar Singha, Priya Singh, Samir Kumar Pal, Jhimli Sengupta, Sandipan Chakraborty, Susobhan Choudhury, Kyo Han Ahn, Ranjan Das, Yong Woong Jun

Publikováno v: Physical Chemistry Chemical Physics. 19:12237-12245

Relaxation dynamics at the surface of biologically important macromolecules is important taking into account their functionality in molecular recognition. Over the years it has been shown that the solvation dynamics of a fluorescent probe at biomolec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2e86c27ed82d26f18dfedc5a931fc6
https://doi.org/10.1039/c6cp08804j

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Synthesis of Ether-Linked Oligoribo- and Xylonucleosides from 3,5′-Ether-Linked Pseudosaccharides

Autor: Anup Bhattacharjya, Jhimli Sengupta

Publikováno v: The Journal of Organic Chemistry. 73:6860-6863

First examples of di- and trinucleosides with ribose and xylose stereochemistry having internucleoside ether linkage were synthesized from 3,5'-ether-linked pseudosaccharides. The synthetic protocol involved removal of 1,2-isopropylidene protecting g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7221065258c5feae5d552c87abe941e0
https://doi.org/10.1021/jo8007429

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Bis- and Trisuracil Nucleosides with Nucleobases Anchored to 11-, 12-, and 16-Membered Macrocyclic Scaffolds: Synthesis and Aggregation Study

Autor: Ranjan Mukhopadhyay, Jhimli Sengupta, Anup Bhattacharjya

Publikováno v: The Journal of Organic Chemistry. 72:4621-4625

Bis- and trisuracil nucleosides, in which the nucleobases are anchored to isoxazoline ring-fused 11-, 12-, and 16-membered macrooxacycles, were synthesized by nucleosidation of 1,2-isopropylidenefuranose ring-fused macrocycles. The nucleosides exhibi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::860e8949126bbecf650b11b7d075d9e6
https://doi.org/10.1021/jo062554b

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