Results 101 to 110 of about 22,537 (233)

N-(4-Chlorophenyl)benzamide

open access: yes, 2008
The structure of the title compound, C13H10ClNO, resembles those of N-phenylbenzamide, N-(2-chlorophenyl)benzamide and other benzanilides, with similar bond parameters.
B. P. Sowmya   +4 more
core   +1 more source

Synthetic pathway of 2-fluoro-N,N-diphenylbenzamide with opto-electrical properties: NMR, FT-IR, UV-Vis spectroscopic, and DFT computational studies of the first-order nonlinear optical organic single crystal

open access: yesGreen Processing and Synthesis, 2022
Raveendiran C.   +8 more
doaj   +1 more source

Substrate‐Selective Inhibition of the SARS‐CoV‐2 Papain‐Like Protease: Inhibition of Hydrolysis of Human Over Viral Substrates

open access: yesChemistry – A European Journal, Volume 32, Issue 36, 24 September 2026.
The SARS‐CoV‐2 papain‐like protease (PLpro) is a medicinal chemistry target. Here we report mass spectrometry assays employing oligopeptide substrates based on the sequences of the viral polyproteins 1a/1ab and on an ISG15‐modified human protein, which enabled the identification of substrate‐selective PLpro inhibitors.
Sakshi Sharma   +13 more
wiley   +1 more source

Crystal structure of N-(2-hydroxy-5-methylphenyl)benzamide

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
In the title compound, C14H13NO2, the mean plane of the non-H atoms of the central amide fragment C—N—C(=O)—C (r.m.s. deviation = 0.029 Å) forms dihedral angles of 5.63 (6) and 10.20 (5)° with the phenyl and hydroxyphenyl rings, respectively.
Rodolfo Moreno-Fuquen   +2 more
doaj   +1 more source

Crystal structure of 4-methoxy-N-(piperidine-1-carbonothioyl)benzamide

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2017
In the title compound, C14H18N2O2S, the piperidine ring has a chair conformation. Its mean plane is twisted with respect to the 4-methoxybenzoyl ring, with a dihedral angle of 63.0 (3)°.
Khairi Suhud   +4 more
doaj   +1 more source

Selective Photoinduced α‐Amino C(sp3)–H Alkylation Mediated by NHC–Borane

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 17, 1 September 2026.
Herein, we report a selective photoinduced functionalization of α‐amino C(sp3)─H bonds mediated by NHC–boranes. This reaction proceeds efficiently without the need for any external radical initiator or photoredox catalyst. Mechanistic studies reveal that the reaction proceeds via an efficient radical chain, featuring the formation of an aryl radical ...
Gabin Lalande   +2 more
wiley   +1 more source

Ordered aggregation of benzamide crystals induced using a motif capper additive

open access: yes, 2013
This paper reports on the growth of benzamide crystals in the presence of 2â?²-aminoacetophenone. The resulting self-replicating intergrowth of benzamide crystals gives rise to ordered crystal aggregates in which individuals share a common c*.
R. J. Davey (1812265)   +4 more
core   +4 more sources

Antiglycation and Amyloid‐β Inhibitory Activities of Pandanus odorifer Extracts and Isolated Constituents: In Vitro and Molecular Docking Insights

open access: yesChemistry &Biodiversity, Volume 23, Issue 9, September 2026.
Pandanus odorifer methanolic extract exhibited strong antiglycation activity, moderate antioxidant capacity, and high flavonoid content. Three isolated compounds reduced Aβ‐associated ThT fluorescence, with blumenol C glucoside showing the greatest effect.
Patricia Marie P. Oliva   +4 more
wiley   +1 more source

Synthesis, characterization and biological evaluation of tryptamine based benzamide derivatives

open access: yes, 2016
Benzamides and tryptamine are biologically significant compounds, therefore, various benzamide analogous of tryptamine have been efficiently synthesized using tryptamine and different benzoyl chlorides, in order to find new biologically active compounds.
Kiran Aftab
core   +1 more source

Heterocyclic‐Based Fungicides: Emerging Strategies for Viable Plant Disease Control

open access: yesChemistry &Biodiversity, Volume 23, Issue 9, September 2026.
Heterocyclic compounds have attracted considerable attention because of their structural diversity, potent antifungal activity, and ability to interact with multiple fungal targets, offering broad‐spectrum protection against phytopathogens. Synthetic and semisynthetic/part‐natural scaffolds, particularly azole, quinoline, indole, cyclotryptamine, and ...
Sumit Tahlan   +4 more
wiley   +1 more source

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