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H-FYY-OH
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H-FYY-OH

Rif. 3D-PP45399

1mg
172,00 €
10mg
196,00 €
100mg
303,00 €
Consegna stimata in Stati Uniti, il Venerdì 27 Dicembre 2024

Informazioni sul prodotto

Nome:
H-FYY-OH
Sinonimi:
  • NH2-Phe-Tyr-Tyr-OH
Descrizione:

Peptide H-FYY-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 H-FYY-OH include the following: The FcϵRIbeta immunoreceptor tyrosine-based activation motif exerts inhibitory control on MAPK and IκB kinase phosphorylation and mast cell cytokine production Y Furumoto, S Nunomura , T Terada, J Rivera - Journal of Biological , 2004 - ASBMBhttps://www.jbc.org/article/S0021-9258(19)32309-9/abstract Nanopore stochastic sensing based on non-covalent interactions X Chen , Y Zhang , P Arora, X Guan - Analytical Chemistry, 2021 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.1c02102 Occurrence of isopenicillin-N-synthase homologs in bioluminescent ctenophores and implications for coelenterazine biosynthesis WR Francis, NC Shaner , LM Christianson, ML Powers - PLoS , 2015 - journals.plos.orghttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0128742 Emerging roles of bioactive peptides on brain health promotion S Katayama , S Nakamura - International journal of food science , 2019 - Wiley Online Libraryhttps://ifst.onlinelibrary.wiley.com/doi/abs/10.1111/ijfs.14076 Naturally occurring and synthetic peptides: Efficient tyrosinase inhibitors R Hariri, M Saeedi , T Akbarzadeh - Journal of Peptide Science, 2021 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.3329 Tripeptides conjugated with thiosemicarbazones: new inhibitors of tyrosinase for cosmeceutical use P Ledwoà „ , W Goldeman, K Haà ‚dys - Journal of Enzyme , 2023 - Taylor & Francishttps://www.tandfonline.com/doi/abs/10.1080/14756366.2023.2193676 Mushroom Tyrosinase Oxidizes Tyrosine-Rich Sequences to Allow Selective Protein Functionalization MJC Long , L Hedstrom - ChemBioChem, 2012 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.201100792 De novo designed library of linear helical peptides: An exploratory tool in the discovery of protein-protein interaction modulators Maca Bonache de Marcos, B Balsera, B Lopez-Mendez - 2014 - digital.csic.eshttps://digital.csic.es/handle/10261/97782 De novo designed library of linear helical peptides: an exploratory tool in the discovery of protein-protein interaction modulators MA Bonache, B Balsera, B López-Méndez - ACS Combinatorial , 2014 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/co500005x Phosphorylation of tyrosines 1158, 1162 and 1163 on a synthetic dodecapeptide by the insulin receptor protein-tyrosine kinase M Dickens, JM Tavare, B Clack, L Ellis - and biophysical research , 1991 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0006291X9191484T Identification of the major autophosphorylation sites of Nyk/Mer, an NCAM-related receptor tyrosine kinase L Ling, D Templeton, HJ Kung - Journal of Biological Chemistry, 1996 - ASBMBhttps://www.jbc.org/article/S0021-9258(18)31989-6/abstract Food-derived Peptides as Promising Neuroprotective Agents: Mechanism and Therapeutic Potential K Patel , A Mani - Current Topics in Medicinal Chemistry, 2024 - ingentaconnect.comhttps://www.ingentaconnect.com/content/ben/ctmc/2024/00000024/00000014/art00003 Structural and functional properties of food protein-derived antioxidant peptides ID Nwachukwu , RE Aluko - Journal of food biochemistry, 2019 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/jfbc.12761 Walnut-derived peptide activates PINK1 via the NRF2/KEAP1/HO-1 pathway, promotes mitophagy, and alleviates learning and memory impairments in a mice model F Zhao, C Liu, L Fang, H Lu, J Wang - Journal of Agricultural , 2021 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jafc.0c07546 Fluorescence properties of the three tyrosine residues in the ribose-binding protein DY Kim, CY Park - Biochemical and biophysical research communications, 1993 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0006291X83721777 Engineered tyrosine residues serve as the local probes to detect a kinetic intermediate in the folding of ribose-binding protein D Kim, C Kim , C Park - Journal of molecular biology, 1994 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0022283684714525 Regulation of the wild-type and Y1235D mutant Met kinase activation C Cristiani, L Rusconi, R Perego, N Schiering - Biochemistry, 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi051242k A soluble insulin receptor kinase catalyzes ordered phosphorylation at multiple tyrosines of dodecapeptide substrates BA Levine, B Clack, L Ellis - Journal of Biological Chemistry, 1991 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0021925819678324 Disrupting VEGF-VEGFR1 Interaction: De Novo Designed Linear Helical Peptides to Mimic the VEGF13-25 Fragment B Balsera, Maca Bonache, M Reille-Seroussi - Molecules, 2017 - mdpi.comhttps://www.mdpi.com/1420-3049/22/11/1846 Unique substrate specificity of anaplastic lymphoma kinase (ALK): development of phosphoacceptor peptides for the assay of ALK activity A Donella-Deana, O Marin, L Cesaro, RH Gunby - Biochemistry, 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi0472954

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I nostri prodotti sono destinati esclusivamente ad uso di laboratorio. Per qualsiasi altro utilizzo, vi preghiamo di contattarci.
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Biosynth
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EINECS:
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