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Fluor-YGG-OH
Vue en 3D

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Fluor-YGG-OH

Ref. 3D-PP45354

Taille indéfinieÀ demander
Livraison estimée en/au États-Unis, le mardi 3 décembre 2024

Informations sur le produit

Nom :
Fluor-YGG-OH
Synonymes :
  • Fluor-Tyr-Gly-Gly-OH
Description :

Peptide Fluor-YGG-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice. Recent citations using Fluor-YGG-OH include the following: Peptide fragmentation and surface structural analysis by means of ToF-SIMS using large cluster ion sources Y Yokoyama, S Aoyagi , M Fujii, J Matsuo - Analytical , 2016 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.5b04133 A comparison of the fragmentation pathways of [CuII(Ma)(Mb)]"¢2+ complexes where Ma and Mb are peptides containing either a tryptophan or a tyrosine residue Y Ke, HE Aribi, CK Siu , KWM Siu - in mass spectrometry, 2010 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/rcm.4783 Micellar electrokinetic chromatography of enkephalin-related peptides with laser-induced fluorescence detection Y Huang, J Duan, Q Chen, G Chen - Electrophoresis, 2004 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/elps.200405810 Quantitative Heterodimerization of Aromatic Peptides through Host-Enhanced Polar-Ï€ Interactions for On-Resin Recognition X Chen , Z Huang, G Wu, K Sokà ‚olowski, K King - 2021 - chemrxiv.orghttps://chemrxiv.org/engage/chemrxiv/article-details/60c7585ebdbb899437a3ad4f The effect of cyclodextrins on the stability of peptides in nasal enzymic systems WJ Irwin, AK Dwivedi, PA Holbrook, MJ Dey - Pharmaceutical research, 1994 - Springerhttps://link.springer.com/article/10.1023/A:1018946829225 Comprehensive conformational studies of five tripeptides and a deduced method for efficient determinations of peptide structures W Yu , Z Wu, H Chen, X Liu - The Journal of , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jp207807a Electron density and electrostatic properties of two peptide molecules: tyrosyl-glycyl-glycine monohydrate and glycyl-aspartic acid dihydrate V Pichon-Pesme, H Lachekar, M Souhassou - Section B: Structural , 2000 - scripts.iucr.orghttps://scripts.iucr.org/cgi-bin/paper?bs0010 Conformation-specific spectroscopy of peptide fragment ions in a low-temperature ion trap TN Wassermann, OV Boyarkin , B Paizs - Journal of the , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1007/s13361-012-0368-0 Protection against dynorphin-(1-8) hydrolysis in membrane preparations by the combination of amastatin, captopril and phosphoramidon T Hiranuma, K Kitamura, T Taniguchi, M Kanai - of Pharmacology and , 1998 - ASPEThttps://jpet.aspetjournals.org/content/286/2/863.short Almost complete protection from [Met5]-enkephalin-Arg6-Gly7-Leu8 (Met-enk-RGL) hydrolysis in membrane preparations by the combination of amastatin, captopril T Hiranuma, K Iwao, K Kitamura, T Matsumiya - Journal of Pharmacology , 1997 - ASPEThttps://jpet.aspetjournals.org/content/281/2/769.short Characterization and kinetic analysis of enzyme-substrate recognition by three recombinant lactococcal tripeptidases S Mori, S Nirasawa, S Komba, T Kasumi - Biochimica et Biophysica Acta , 2005 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S157096390400336X Nonspecific protease-catalyzed hydrolysis/synthesis of a mixture of peptides: Product diversity and ligand amplification by a molecular trap PG Swann, RA Casanova, A Desai - Peptide , 1996 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/(SICI)1097-0282(1996)40:6%3C617::AID-BIP3%3E3.0.CO;2-Z Cold denaturation of monomeric peptide helices NH Andersen, JR Cort , Z Liu, SJ Sjoberg - Journal of the American , 1996 - ACS Publicationshttps://pubs.acs.org/doi/full/10.1021/ja961143h Tyrosyl Rotamer Interconversion Rates and the Fluorescence Decays of N-Acetyltyrosinamide and Short Tyrosyl Peptides JR Unruh , MR Liyanage - The Journal of Physical , 2007 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jp0645059 Proteolytic conversion of [Met] enkephalin-Arg6-Gly7-Leu8 by brain synaptic membranes. Characterization of formed peptides and mechanism of proteolysis. JA Norman, JY Chang - Journal of Biological Chemistry, 1985 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0021925818894108 F/YGG-motif is an intrinsically disordered nucleic-acid binding motif J Van Lindt, T Lazar , D Pakravan, M Demulder - RNA biology, 2022 - Taylor & Francishttps://www.tandfonline.com/doi/abs/10.1080/15476286.2022.2066336 Electronic spectra of GYG peptide by laser desorption supersonic jet spectroscopy J Shinohara, WY Sohn, S Ishiuchi, M Fujii - molsci.center.ims.ac.jphttp://molsci.center.ims.ac.jp/area/2014/pdf/3P015_w.pdf The role of weakly polar and H-bonding interactions in the stabilization of the conformers of FGG, WGG, and YGG; An aqueous phase computational study J Csontos , RF Murphy, S Lovas - : Original Research on , 2008 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/bip.21049 Peroxidase-mediated cross-linking of a tyrosine-containing peptide with ferulic acid G Oudgenoeg, R Hilhorst, SR Piersma - Journal of Agricultural , 2001 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jf000906o Structure of isolated tyrosyl-glycyl-glycine tripeptide. A comparative conformational study with peptides containing an aromatic ring E Barrera Guisasola , M Masman , R Enriz - Open , 2010 - degruyter.comhttps://www.degruyter.com/document/doi/10.2478/s11532-010-0015-1/html Oral absorption of peptides: influence of pH and inhibitors on the intestinal hydrolysis of leu-enkephalin and analogues DI Friedman, GL Amidon - Pharmaceutical research, 1991 - Springerhttps://link.springer.com/article/10.1023/A:1015842609565 Detection of the tripeptide Tyr-Gly-Gly, a putative enkephalin metabolite in brain, using a sensitive radioimmunoassay C Llorens-Cortes , JC Schwartz, C Gros - FEBS letters, 1985 - Wiley Online Libraryhttps://febs.onlinelibrary.wiley.com/doi/abs/10.1016/0014-5793(85)81049-8 EVALUATION OF STRIATAL ENKEPHALIN RELEASE IN VIVO FROM STEADY AND TURNOVER RATES OF THE TRIPEPTIDE TYR-GLY-GLY STATE C Llorens-Cortes , C Gros - Progress in Opioid , 1986 - books.google.comhttps://books.google.com/books?hl=en&lr=&id=1KqJllN9ghQC&oi=fnd&pg=PA275&dq=(%22YGG%22+OR+%22Fluor-YGG-OH%22+OR+%22Fluor-Tyr-Gly-Gly-OH%22)+AND+peptide&ots=Be1yV57ydA&sig=_g-mKvQyzdL-tZVRr6IhkmxONe0 Steady-state level and turnover rate of the tripeptide Tyr-Gly-Gly as indexes of striatal enkephalin release in vivo and their reduction during pentobarbital anesthesia. C Llorens-Cortes , C Gros - Proceedings of the , 1986 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.83.16.6226 Study of endogenous Tyr-Gly-Gly, a putative enkephalin metabolite, in mouse brain: validation of a radioimmunoassay, localisation and effects of peptidase inhibitors C Llorens-Cortes , C Gros, JC Schwartz - European journal of pharmacology, 1985 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0014299985902948 The endogenous tripeptide Tyr-Gly-Gly as an extracellular metabolite of enkephalins in rat brain: origin and metabolism B Giros , C Llorens-Cortes , C Gros - Progress in Opioid , 1976 - books.google.comhttps://books.google.com/books?hl=en&lr=&id=HZJx5Yza02IC&oi=fnd&pg=PA271&dq=(%22YGG%22+OR+%22Fluor-YGG-OH%22+OR+%22Fluor-Tyr-Gly-Gly-OH%22)+AND+peptide&ots=0Nw1rwov8m&sig=PSJHvGcYCGpqmKxbQ1lvnyX3SFE The endogenous tripeptide Tyr-Gly-Gly as a possible metabolite of opioid peptides in rat brain: identification, regional distribution, effects of lesions and formation in B Giros , C Llorens-Cortes , C Gros, JC Schwartz - Peptides, 1986 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0196978186900434 Conformational structure of tyrosine, tyrosyl-glycine, and tyrosyl-glycyl-glycine by double resonance spectroscopy A Abo-Riziq, L Grace, B Crews - The Journal of , 2011 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jp110601w

Avis:
Nos produits sont destinés uniquement à un usage en laboratoire. Pour tout autre usage, veuillez nous contacter.
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Biosynth
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Propriétés chimiques

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Informations sur les risques

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