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Registros recuperados: 8
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Improvement in the Properties of 3-Phenyl-3-trifluoromethyldiazirine Based Photoreactive Bis-Glucose Probes for GLUT4 Following Substitution on the Phenyl Ring OAK
Hashimoto, Makoto; Yang, Jing; Hatanaka, Yasumaru; Sadakane, Yutaka; Nakagomi, Kazuya; Holman, Geoffrey David.
日本薬学会Chemical & pharmaceutical bulletin 50(7) p.1004-1006より転載
Palavras-chave: Photoaffinity label; Diazirine; Glucose transporter.
Ano: 2002 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/332
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Selective Hydrogenation of Alkene in (3-Trifluoromethyl) Phenyldiazirine Photophor with Wilkinson’s Catalyst for Photoaffinity Labeling OAK
HASHIMOTO, Makoto; KATO, Yuh-hi; HATANAKA, Yasumaru; 橋本, 誠.
Selective hydrogenation of carbon–carbon double bond in the presence of nitrogen–nitrogen double bond in (3-trifluoromethyl) phenyldiazirine achieved with Wilkinson's catalyst.
Palavras-chave: Photoaffinity labeling; Diazirine; Hydrogenation; Wilkinson’s catalyst.
Ano: 2007 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/3611
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Positively coded photoaffinity label for altering isoelectric points of proteins OAK
Hashimoto, Makoto; Hatanaka, Yasumaru.
Novel diazirinyl photoaffinity ligand, which contains (3-trifluoromethyl) phenyldiazirine and penta(epsilon-Boc-Lys) as a photoreactive code, allows the introduction of a positive cascade to alter the pI value of labeled components, facilitating the isolation of photolabeled biocomponents with isoelectric focusing techniques. (c) 2006 Elsevier Ltd. All rights reserved.
Palavras-chave: Photoaffinity labeling; Diazirine; Isoelectric focusing; Biotin.
Ano: 2006 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/1321
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Simple synthesis of deuterium and 13C labeled trifluoromethyl phenyldiazirine derivatives as stable isotope tags for mass spectrometry OAK
Hatanaka, Yasumaru; Hashimoto, Makoto.
日本薬学会Chemical & pharmaceutical bulletin 52(11)p.185-1386より転載
Palavras-chave: Diazirine; Photoaffinity label; Stable isotope.
Ano: 2004 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/127
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Recent progress in diazirine based photoaffinity labeling OAK
Hashimoto, Makoto; Hatanaka, Yasumaru; 橋本, 誠.
Based on the recent development of molecular biology, the investigation of biofunctional machinery at their ligand accepting interface has become one of the challenging and important subject of post-genome field. The technique of photoaffinity labeling has become increasingly appreciated as a powerful methodology for the purpose. This micro review focused synthesis of trifluoromethylphenyldiazirine, which is one of the most promising photophore, and its application to the biomolecules.
Palavras-chave: Photoaffinity labeling; Chemical biology; Bioorganic chemistry; Structure-activity relationships; Diazirine.
Ano: 2008 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/2700
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Post-biotinylation of Photocrosslinking by Staudinger-Bertozzi Ligation of Preinstalled Alkylazide Tag OAK
Hashimoto, Makoto; Hatanaka, Yasumaru.
Post-biotinylation of the alkyl azide derivative of trifluoromethyl phenyldiazirine (TPD) was elucidated to apply a photoaffinity biotinylation technique. A photo-modified polyvinilidene difluoride (PVDF) membrane was used as a photolabeled component and we introduced biotin by Staudinger-Bertozzi ligation. The 15 pmol amount of biotinylated reagent was still effective for the visualization of cross-linked product on the matrix. The results show the potential utility of alkyl azide carrying TPD derivatives in the application of photoaffinity biotinylation, which could be useful for the ligands with tight structural requirements.
Palavras-chave: Diazirine; Photoaffinity label; Chemical biology; Staudinger reaction; Avidin-biotin.
Ano: 2005 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/832
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Stereoselective synthesis of (E)- and (Z)-β-bromostyrene containing trifluoromethyldiazirine for photoaffinity labeling OAK
Hashimoto, Makoto; Komano, Tomoko; Nabeta, Kensuke; Hatanaka, Yasumaru.
日本薬学会 Chemical & pharmaceutical bulletin 53(1)p.140-142より転載
Palavras-chave: Diazirine; Photoaffinity label; Stable isotope; Hydrogenolysis.
Ano: 2005 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/128
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Enzyme cleavable and biotinylated photoaffinity ligand with diazirine OAK
Hashimoto, Makoto; Okamoto, Shun’ji; Nabeta, Kensuke; Hatanaka, Yasumaru.
The efficient synthesis of an enzyme cleavable biotinylated diazirinyl photoaffinity ligand is described to allow the effective manipulation of the photolabeled biocomponents. The compound contains a glutamic acid gamma-methyl ester, which is a precursor of the substrate for V8 protease, between the diazirinyl photophor and biotin moiety. After alkaline hydrolysis of the ester, the compound can be proteolyzed at the Glu moiety by V8 protease. The photophore was introduced to L-Phe p-nitroanilide and the ligand was applied to photolabel of chymotrypsin to manipulate the application of the concept.
Palavras-chave: Photoaffinity labeling; Diazirine; Avidin-biotin; V8 protease; Chymotrypsin.
Ano: 2004 URL: http://ir.obihiro.ac.jp/dspace/handle/10322/738
Registros recuperados: 8
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