نتایج جستجو برای: isopropoxy carbothioyldisulfanylethanethioate iide

تعداد نتایج: 111  

2015
Marianne Lucas-Hourani Hélène Munier-Lehmann Farah El Mazouni Nicholas A. Malmquist Jane Harpon Eloi P. Coutant Sandrine Guillou Olivier Helynck Anne Noel Artur Scherf Margaret A. Phillips Frédéric Tangy Pierre-Olivier Vidalain Yves L. Janin

Following our discovery of human dihydroorotate dehydrogenase (DHODH) inhibition by 2-(3-alkoxy-1H-pyrazol-1-yl)pyrimidine derivatives as well as 2-(4-benzyl-3-ethoxy-5-methyl-1H-pyrazol-1-yl)-5-methylpyridine, we describe here the syntheses and evaluation of an array of azine-bearing analogues. As in our previous report, the structure-activity study of this series of human DHODH inhibitors was...

Journal: :Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2014
Norikazu Sakakibara

This review describes the synthesis and evaluation of novel nucleic acid derivatives performed by our research group to date. We developed a new method for the synthesis of 2-alkoxyadenosine analogs via nonaqueous diazotization-dediazoniation reactions. By applying these reactions, we effectively synthesized four types of carbocyclic oxetanocin analogs (2-alkoxy-C.OXT-A). The angiogenic activit...

Journal: :The Journal of organic chemistry 2003
Junlin He Igor Mikhailopulo Frank Seela

The nucleobase anion glycosylation of 3-bromo-4-isopropoxy-1H-pyrazolo[3,4-d]pyrimidin-6-amine (6) with 3,5-di-O-benzoyl-2-deoxy-2-fluoro-alpha-d-arabinofuranosyl bromide (5) furnished the protected N(1)-beta-d-nucleosides 7 (60%) and 8 (ca. 2%) along with the N(2)-beta-d-regioisomer 9 (9%). Debenzoylation of compounds 7 and 9 yielded the nucleosides 10 (81%) and 11 (76%). Compound 10 was trans...

Journal: :Journal of Fungi 2023

The development of new anti-ureolytic compounds is great interest due to the newly discovered role urease inhibitors in crop protection. Purine degradation and generation ammonium by are required for full virulence biotrophic hemibiotrophic fungal plant pathogens. Accordingly, chemicals displaying inhibitor activity may be used as a novel class fungicides. Several belonging different chemical c...

Journal: :European journal of medicinal chemistry 2021

P-glycoprotein (P-gp)-mediated multidrug resistance (MDR) is a phenomenon in which cells become resistant to structurally and mechanistically unrelated drugs resulting low intracellular drug concentrations. It one of the noteworthy problems malignant tumor clinical therapeutics. So P-gp protein ideal targets solve MDR. Based on lead compound 5m obtained from our previous work, series furan deri...

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