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Devashish Sengupta

Researcher at Assam University

Publications -  13
Citations -  95

Devashish Sengupta is an academic researcher from Assam University. The author has contributed to research in topics: Porphyrin & Chemistry. The author has an hindex of 4, co-authored 9 publications receiving 59 citations. Previous affiliations of Devashish Sengupta include North Eastern Hill University.

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Reactions of 1,3-diaza-1,3-butadienes with haloketenes - rearrangements accompanying [4+2] cycloaddition reactions.

TL;DR: In this article, 1-Aryl-2-phenyl-(methylthio) -4-dimethylamino-1, 3-butadienes 1 gave different pyrimidones with different haloketenes (chloro, bromo and iodo).
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meso-Thiophenium Porphyrins and Their Zn(II) Complexes: A New Category of Cationic Photosensitizers.

TL;DR: The DFT calculations of the singlet-triplet energy gap (ΔE) of all the four hydrophilic thiophenium porphyrin derivatives establish the potential applicability of these cationic photosensitizers as PDT agents.
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Benzamide porphyrins with directly conjugated and distal pyridyl or pyridinium groups substituted to the porphyrin macrocycles: Study of the photosensitising abilities as inducers of apoptosis in cancer cells under photodynamic conditions

TL;DR: It was found that B.3, having a pyridinium group attached to the meso-position of the macrocycle along with three distal cationic pyrinium groups, independent of the porphyrinic electron delocalisation cycle, showed better photocytotoxic efficacy and higher potential to promote apoptosis and hence better efficacy as PS towards cancer photodynamic therapy (PDT).
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Cancer photocytotoxicity and anti-inflammatory response of cis-A2B2 type meso-p-nitrophenyl and p-hydroxyphenyl porphyrin and its zinc(II) complex: a synthetic alternative to the THPP synthon

TL;DR: In this paper, the cis-A2B2 type porphyrin derivative, synthesized by replacing two p-hydroxyphenyl groups at the meso-positions with two pnitrophenyl moieties, 5,10-bis-(4-oxymethyl)-15,20-bis-porphyrin PN2(OH)2 and its zinc(II) 2Zn have more promising photosensitizing and photobiological activities.