نتایج جستجو برای: isatin hydrazone
تعداد نتایج: 2792 فیلتر نتایج به سال:
Our previous research have identified a series of N-phenyl substituted isatin derivatives as antitumor agents in vitro. 5-Bromo isatin derivatives have been found to increase their cytotoxic activity and selectivity. A series of 5-bromo-N-phenyl isatin analogues were designed and synthesized about 40-80% overall yields. All of synthesized compounds have not been reported before. Their structure...
برهمکنش dna تیموس گاوی با isatin و دو مشتق سنتزی آن , isatin-?-thiosemicarbazone, ibt isonicotinylhydrazone(iinh) isatin-3- در ph فیزیولوژیکی مطالعه شد. برهمکنش ها با طیف سنجیuv-vis،طیف سنجی فوتومتری، آزمایشات رقابتی، دورنگ نمایی دورانی، تکنیک ویسکوزیمتری مطالعه شد. هیچ جابجایی قرمز و نقطه ایزوبستیک در طیف های جذبی مرئیisatin مشاهده نشد. یک واکنش خاموش شدن قوی فلوئوسانس isatin با dna مشاهده شد...
The condensation of isatin with pyridine carboxylic acid hydrazides in methanol give rise to hydrazone ligands. By the reactions of oxovanadium(IV) sulphate with hydrazones in presence of sodium hydroxide in methanol [VO(L)H2O] type complexes were obtained. The complexes were characterized by elemental analyses, conductances, magnetic moments, TGA and spectral (IR, Electronic and EPR) data. The...
4s-ferrugineone and 4s,5s-ferrugineol as pheromones of palm weevils were synthesized in 3 and 4 steps, respectively, starting from nonane-5-one employing samp-/ramp -hydrazone methodology. 5-nonanone is transformed to its corresponding ramp hydrazone by reaction with the enantiomerically pure hydrazine ramp. metalation with lithium diisopropylamide (lda) in ether to form azaenolate, followed by...
Previous studies have shown that (E)-5-styrylisatin and (E)-6-styrylisatin are reversible inhibitors of human monoamine oxidase (MAO) A and B. Both homologues are reported to exhibit selective binding to the MAO-B isoform with (E)-5-styrylisatin being the most potent inhibitor. To further investigate these structure-activity relationships (SAR), in the present study, additional C5- and C6-subst...
Marine organisms such as seaweeds, sponges and corals protect their own surfaces from fouling by their high anesthetic, repellant, and settlement inhibition properties. Within the marine ecosystem, evolution has allowed for the development of certain antifouling properties. Isatin is a biologically active chemical produced by an Alteromonas sp. strain inhibiting the surface of embryos of the ca...
An exceptionally mild method for the preparation of isatin derivatives has been developed using a sulfur ylide mediated carbonyl homologation sequence starting from anthranilic acid precursors. This method proceeds at ambient temperature via a sulfur ylide intermediate without the need for protection of the amine or chromatographic isolation of the intermediate ylide. Gentle oxidation of the su...
Isatin, previously shown to promote growth in green and etiolated pea stems, is converted mainly to anthranilate in those tissues; small quantities of isatate are also formed. Fed anthranilate is converted mainly to its beta-d-glucoside; smaller amounts are metabolized to anthranilamide, tryptophan and kynurenine. These data provide some basis for understanding the growth promoting activity of ...
Isatin is a heterocyclic molecule that belongs to one of the most important classes organic compounds known as indolines. Isatin, isatin analogs, and their Schiff bases have recently attracted lot attention in medicinal chemistry. itself, shows various biological activities such antiviral, anticancer, antimicrobial, anti-inflammatory, analgesic, antioxidant, anticonvulsant. Bis- containing moie...
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