Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sukumar Bepary"'
Publikováno v:
Indonesian Journal of Chemistry, Vol 24, Iss 5, Pp 1541-1555 (2024)
Several 2-phenoxyacetic acid derivatives and their isosteres were synthesized in moderate to high yield (57–96%) for searching newer and safer alternatives to these existing anti-inflammatory agents. The compounds were characterized by 1H-NMR, 13C-
Externí odkaz:
https://doaj.org/article/3ba6231a2e1d4ab1960d9af72ecb2c9f
Publikováno v:
Journal of Molecular Docking, Vol 1, Iss 2 (2021)
Acetamides (S30A1 and S30) were synthesized from benzo[d]thiazol-2-amine and 6-nitrobenzo[d]thiazol-2-amine by direct use of acetic acid instead of acetylating agents. The usual acetylating agents, acetic anhydride and acetyl chloride are very unstab
Externí odkaz:
https://doaj.org/article/843d95d63948448ba392e4620209bd81
Autor:
Shahenul Islam, Tran Quang De, Shamima Akhter, Rahen Mahmuda, Sukumar Bepary, Pranoy Saha, Khadija Akhter Poly, Negar Sultana Shoshi
Publikováno v:
Can Tho University Journal of Science. 12
Resorcinol with its two hydroxyl groups was derivatized in laboratory to observe the anti-inflammatory potential in vitro. Subsequently in silico docking analysis was done for observing the binding modes in cyclooxygenase enzyme to have idea about th
Synthesis and evaluation of PI3Kγ enzyme inhibitory activity of Novel (1H-pyrazol-4-yl)methanamines.
Publikováno v:
Thai Journal of Pharmaceutical Sciences. Apr-Jun2016, Vol. 40 Issue 2, p82-86. 5p.
Publikováno v:
Bulletin of the Korean Chemical Society. 37:2054-2057
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 26:51-54
Synthesis, SAR study and BACE1 inhibitory activity of (3S,4S)-4-aminopyrrolidine-3-ol derivatives (2) were described. The compound 7c exhibited more inhibition activity than 11a (IC50: 0.05μM vs 0.12μM, respectively), but the latter was more effect
Objective: This study was intended to evaluate the phytochemical, analgesic and anti-inflammatory activity of 70% ethanolic extracts of Ardisia colorata in swiss albino mice and long evans rats. Methods: The ethanolic extract of A. colorata stem and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1817bae6809583ddadc1dd183be59fa0
Publikováno v:
Synthetic Communications. 44:1876-1880
2-Aminoimidazolidin-4-ones have been synthesized by using di-2-pyridyl thiocarbonate (DPT), taking the thioureas tethered to amides as the starting materials. Both the primary amides and secondary amides have been subjected to this cyclization method
Publikováno v:
Bulletin of the Korean Chemical Society. 34:2829-2832
E-mail: yink@pcu.ac.krReceived May 30, 2013, Accepted June 25, 2013Key Words : Phenylpyrazole, PI3 kinase gamma, In vitro assay, SAR, Inhibitory activityPhosphatidylinositol-3-kinase gamma (PI3Kγ), with itscatalytic subunit P110γ and regulatory sub
Publikováno v:
Bulletin of the Korean Chemical Society. 31:3788-3790
solution using tetramethylsilane as internal standard. Analytical thin-layer chromatography was performed on precoated silica gel plates (0.25-mm 60 F-254 E. Merck). The products were pu rified by flash column chro-matography on silica gel 60 (Merck,