نتایج جستجو برای: indoleamine 2

تعداد نتایج: 2526824  

Journal: :Organic letters 2009
Gavin Carr Wendy Tay Helen Bottriell Sarah K Andersen A Grant Mauk Raymond J Andersen

Laboratory cultures of the fungus Plectosphaerella cucumerina obtained from marine sediments collected in Barkley Sound, British Columbia, yielded the novel alkaloids plectosphaeroic acids A (1) to C (3). The alkaloids 1-3 are inhibitors of indoleamine 2,3-dioxygenase (IDO).

Journal: :The Biochemical journal 1989
E R Werner G Werner-Felmayer D Fuchs A Hausen G Reibnegger H Wachter

In all of eight tested human cells and cell lines with inducible indoleamine 2,3-dioxygenase (EC 1.13.11.17) tetrahydrobiopterin biosynthesis was activated by interferon-gamma. This was demonstrated by GTP cyclohydrolase I (EC 3.5.4.16) activities and intracellular neopterin and biopterin concentrations. Pteridine synthesis was influenced by extracellular tryptophan. In T 24-cell extracts, subm...

Journal: :International Journal of Medical Sciences 2017

Journal: :Journal of medicinal chemistry 2013
Raffaele Pasceri David Siegel David Ross Christopher J Moody

A range of 2-aminophenoxazin-3-ones has been prepared by oxidative cyclocondensation of 2-aminophenols, including the natural products exfoliazone and chandrananimycin A, both synthesized for the first time. The compounds were evaluated for their ability to inhibit indoleamine 2,3-dioxygenase. Compounds containing additional electron-withdrawing carboxylate groups, such as cinnabarinic acid, sh...

Journal: :Bioorganic & medicinal chemistry 2011
Eduard Dolušić Pierre Larrieu Sébastien Blanc Frédéric Sapunaric Bernadette Norberg Laurence Moineaux Delphine Colette Vincent Stroobant Luc Pilotte Didier Colau Thierry Ferain Graeme Fraser Moreno Galleni Jean-Marie Frère Bernard Masereel Benoît Van den Eynde Johan Wouters Raphaël Frédérick

Indoleamine 2,3-dioxygenase (IDO) is a heme dioxygenase which has been shown to be involved in the pathological immune escape of diseases such as cancer. The synthesis and structure-activity relationships (SAR) of a novel series of IDO inhibitors based on the indol-2-yl ethanone scaffold is described. In vitro and in vivo biological activities have been evaluated, leading to compounds with IC(5...

Journal: :The Cancer Journal 2010

Journal: :Cancer research 2011
Rikke Bæk Sørensen Tania Køllgaard Rikke Sick Andersen Joost Huibert van den Berg Inge Marie Svane Per thor Straten Mads Hald Andersen

Several lines of data have suggested a possible link between the indoleamine 2,3-dioxygenase (IDO)-like protein IDO2 and cancer. First, IDO2 expression has been described in human tumors, including renal, gastric, colon, and pancreatic tumors. Second, the apparent selective inhibition of IDO2 by the D stereoisomer of the IDO blocker 1-methyl-tryptophan (1MT), which tends to be more active than ...

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