Product Details of 93-02-7. Authors Ilyina, IV; Patrusheva, OS; Zarubaev, VV; Misiurina, MA; Slita, AV; Esaulkova, IL; Korchagina, DV; Gatilov, YV; Borisevich, SS; Volcho, KP; Salakhutdinov, NF in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Ilyina, Irina V.; Patrusheva, Oksana S.; Korchagina, Dina V.; Gatilov, Yuri V.; Volcho, Konstantin P.; Salakhutdinov, Nariman F.] Russian Acad Sci, Siberian Branch, Novosibirsk Organ Chem Inst, Lavrentjev Av 9, Novosibirsk 630090, Russia; [Zarubaev, Vladimir V.; Misiurina, Maria A.; Slita, Alexander V.; Esaulkova, Iana L.] Pasteur Inst Epidemiol & Microbiol, 14 Mira Str, St Petersburg 197101, Russia; [Borisevich, Sophia S.] Ufa Fed Res Ctr, Ufa Chem Inst, Chem Phys Lab, 71 Octyabrya Pr, Ufa 450054, Russia in 2021, Cited 24. The Name is 2,5-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 93-02-7
We synthesized fluoroand hydroxy-containing octahydro-2H-chromenes by the Prins reaction starting from a monoterpenoid (-)-isopulegol and a wide range of aromatic aldehydes in the presence of the BF3.Et2O/H2O system acting as both an acid catalyst and a fluorine source. Activity of the produced compounds against the influenza A/Puerto Rico/8/34 (H1N1) virus was studied. The highest activity was demonstrated by fluoro(11i) and hydroxy-containing (10i) derivatives of 2,4,6-trimethoxybenzaldehyde. The most pronounced virus inhibiting effect of compounds 10i and 11i was observed at an early stage of infection. These compounds were supposed to be capable of binding to viral hemagglutinin, which is an agreement with data on the effect of compounds 10i and 11i on the viral fusogenic activity as well as by molecular docking studies.
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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com