Why do aromatic interactions matter of compound:1-(4-Nitrophenyl)ethanone

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In 2020.0 ARCH PHARM published article about PROTEIN-KINASE-C; IN-VITRO; CANCER; DERIVATIVES; INHIBITORS; RECEPTOR; COMPLEX; MODEL in [Corsini, Emanuela; Esposito, Sara] Univ Milan, Lab Toxicol, Dipartimento Sci Polit & Ambientali, Milan, Italy; [Facchetti, Giorgio; Rimoldi, Isabella; Christodoulou, Michael S.] Univ Milan, DISFARM, Sez Chim Gen & Organ A Marchesini, Via Venezian 21, I-20133 Milan, Italy; [Maddalon, Ambra] Univ Milan, Lab Toxicol, Dipartimento Sci Farmacol & Biomol, Milan, Italy in 2020.0, Cited 38.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 100-19-6

In this study, a series of 20 chalcone derivatives was synthesized, and their antiproliferative activity was tested against the human T cell acute lymphoblastic leukemia-derived cell line, CCRF-CEM. On the basis of the structural features of the most active compounds, a new library of chalcone derivatives, according to the structure-activity relationship design, was synthesized, and their antiproliferative activity was tested against the same cancer cell line. Furthermore, four of these derivatives (compounds 3, 4, 8, 28), based on lower IC50 values (between 6.1 and 8.9 mu M), were selected for further investigation regarding the modulation of the protein expression of RACK1 (receptor for activated C kinase), protein kinase C (PKC)alpha and PKC beta, and their action on the cell cycle level. The cell cycle analysis indicated a block in the G0/G1 phase for all four compounds, with a statistically significant decrease in the percentage of cells in the S phase, with no indication of apoptosis (sub-G0/G1 phase). Compounds 4 and 8 showed a statistically significant reduction in the expression of PKC alpha and an increase in PKC beta, which together with the demonstration of an antiproliferative role of PKC beta, as assessed by treating cells with a selective PKC beta activator, indicated that the observed antiproliferative effect is likely to be mediated through PKC beta induction.

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Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem