About: Synthesis of Poly(amidoamine) Dendrimer with a Diphenyl Diselenide Core

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rdf:type	Item
description	article scientifique publié en 2010 (fr) наукова стаття, опублікована в грудні 2010 (uk) im Dezember 2010 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57575620-280FA0C8-1D97-4890-9C23-5041FE7EAD44
publication date	2010-12-30 00:00:00Z (xsd:dateTime)
cites work	wds:Q57575620-070C84E2-DBF7-4288-A7D2-C2ACF04D5697 wds:Q57575620-0C1EB44F-7EB4-4F55-BC3A-D7C5686C01A3 wds:Q57575620-16829E81-CD6B-4D10-987C-418176E074AE wds:Q57575620-16C1D167-730E-4079-89F5-4653C6934DA5 wds:Q57575620-2E18E932-E2DD-4BB9-964B-37A79C9AD96E wds:Q57575620-38162255-76E4-476A-A74C-C5682F105088 wds:Q57575620-3BC5B155-6A32-4670-819E-2CAFB3510112 wds:Q57575620-40F9DB8E-DB17-4914-B8E5-DC95C7EBF933 wds:Q57575620-41CAC324-BA16-4CF9-98C5-D473F374EB5B wds:Q57575620-4EBC202C-0179-429A-A60F-EFC234338DDF wds:Q57575620-52143FD0-417E-4EC8-BE77-F643ED253213 wds:Q57575620-557D35FD-B2F4-49D4-8274-9669167C801D wds:Q57575620-6769F2A3-3E86-4005-A526-9F7F6429ECE8 wds:Q57575620-7A47B04F-1662-4D30-91DF-09EA62026789 wds:Q57575620-8388A47E-C7A5-4A22-8D7E-60378A616BEE wds:Q57575620-85A4826E-B045-4A11-A5AA-03960F960DED wds:Q57575620-8A3AAE5A-05A8-4A98-B723-D3DDA7800129 wds:Q57575620-8DDCF86D-4E36-425B-8D81-0105BF4CF7F8 wds:Q57575620-9DFD00EB-7CB6-45C3-A054-78BEB30B171C wds:Q57575620-9E668435-BEF8-4041-938C-86F925C4FBCC wds:Q57575620-9FAF9FFE-EFD0-4633-A273-59138C4119C4 wds:Q57575620-BF82B172-3D6E-444E-A61D-965C000F93C4 wds:Q57575620-C5869CB4-84F2-4282-BBC9-E5F4668BD024 wds:Q57575620-DD3B6F10-7AE0-45F8-9103-F4C5C0F3EB9D wds:Q57575620-E0E8EE4C-F7C9-4D8F-904F-5E7C9B3B3C95 wds:Q57575620-E18A4E2F-28EB-4796-AFD3-570CEC3098BE wds:Q57575620-EC8F18C4-51E1-423F-B4CC-EF9933248164 wds:Q57575620-F41C851D-01E2-491C-A2A0-7000BD8E6825 wds:Q57575620-F5C63BB5-F8F6-415E-85D1-E24602D108C1 wds:Q57575620-F93671F1-E12A-4030-9734-4540EDC42D0A
cites work	Cloning of a cDNA for the type II iodothyronine deiodinase Hepatic iodothyronine 5'-deiodinase. The role of selenium Biochemistry, cellular and molecular biology, and physiological roles of the iodothyronine selenodeiodinases. Chemistry of biologically important synthetic organoselenium compounds. Novel selenoproteins identified in silico and in vivo by using a conserved RNA structural motif Thioredoxin reductase Molecular cloning and characterization of a mitochondrial selenocysteine-containing thioredoxin reductase from rat liver Glutathione peroxidase: a selenoenzyme. Selenium: Biochemical Role as a Component of Glutathione Peroxidase Purification and characterization of human plasma glutathione peroxidase: a selenoglycoprotein distinct from the known cellular enzyme Thioredoxin reductase two modes of catalysis have evolved A new selenoprotein from human lung adenocarcinoma cells: purification, properties, and thioredoxin reductase activity Mitochondrial thioredoxin reductase in bovine adrenal cortex its purification, properties, nucleotide/amino acid sequences, and identification of selenocysteine. Dendritic Encapsulation of Function: Applying Nature's Site Isolation Principle from Biomimetics to Materials Science Cloning and expression of a cDNA for a mammalian type III iodothyronine deiodinase Organoselenium and organotellurium compounds: toxicology and pharmacology Glutathione peroxidase-like antioxidant activity of diaryl diselenides: a mechanistic study Dendrimers as artificial enzymes Benzoselenazolinone derivatives designed to be glutathione peroxidase mimetics feature inhibition of cyclooxygenase/5-lipoxygenase pathways and anti-inflammatory activity. The deiodinase family of selenoproteins Iodothyronine deiodinases The Dendrimer Effect in Homogeneous Catalysis Reactivity at the interface of chiral amphiphilic dendrimers. High asymmetric reduction by NaBH(4) of various prochiral ketones Novel Photoreaction Using Diphenyl Disulfide Derivatives: Photoinduced Oxidation of Allyl Alcohol Highly efficient dendrimer-based mimic of glutathione peroxidase. Hyperbranched polyselenides as glutathione peroxidase mimics. Photoinduced isomerization of allyl alcohols to carbonyl compounds using dendrimer disulfide as catalyst Synthesis and Characterization of a Poly(amide amine) Dendrimer Disulfide Having Hydroxy Groups as the Terminals Synthesis and Characterization of a Poly(Benzyl Ether) Dendron Sulfenyl Iodide Synthesis, Characterization, and Controlling Morphology of an Aryl Ether Dendrimer Containing a Dichalcogenide Bond as the Core
author name string	wds:Q57575620-15966F54-2AE7-439D-846A-7EF50B79500A wds:Q57575620-325F6CD6-7D48-41F7-BBBB-3956A89B9416 wds:Q57575620-5DEB58DF-E2C1-4232-A21C-40170A7D9B44 wds:Q57575620-D56BA0A1-FDF3-475C-9D17-4DBA36BAE9A0
author name string	Tomoyuki Tajima Yukie Yamaguchi Yutaka Takaguchi Yo-hei Shiomoto
rdfs:label	Synthesis of Poly(amidoamine) Dendrimer with a Diphenyl Diselenide Core (en)
skos:prefLabel	Synthesis of Poly(amidoamine) Dendrimer with a Diphenyl Diselenide Core (en)
name	Synthesis of Poly(amidoamine) Dendrimer with a Diphenyl Diselenide Core (en)
title	wds:Q57575620-D501FEB2-DF53-4611-8512-A632F46DADA5
title	Synthesis of Poly(amidoamine) Dendrimer with a Diphenyl Diselenide Core (en)
page(s)	wds:Q57575620-60FD31CC-6F71-4443-9184-44D3B501AD15
page(s)	2-11
instance of	wds:Q57575620-1AAD0237-EC50-4579-814C-0E2BD71C1F10
instance of	scholarly article
published in	wds:Q57575620-FEF494F5-55BB-47B3-BD32-8C9A47198598
published in	Phosphorus, Sulfur, and Silicon and the Related Elements
issue	wds:Q57575620-8236575C-5783-484D-BF60-1C2748601CFB
volume	wds:Q57575620-1BA16E4D-0E43-4B9E-8CA0-8EDBA9404E37
issue	1
volume	186
DOI	wds:Q57575620-D7B595DE-F850-4527-9C54-B04C976D5F29
DOI	http://dx.doi.org/10.1080/10426501003767102
DOI	10.1080/10426501003767102
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57575620

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