5Fam-DRVYIHPF-OH

Ref. 3D-PP44223

Product Information

• Name: 5Fam-DRVYIHPF-OH
• Synonyms: 5Fam-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-OH

Description

Peptide 5Fam-DRVYIHPF-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 5Fam-DRVYIHPF-OH include the following: The effect of the secondary structure on dissociation of peptide radical cations: Fragmentation of angiotensin III and its analogues Z Yang , C Lam, IK Chu , J Laskin - The Journal of Physical , 2008 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jp805226x The ornithine effect in peptide cation dissociation WM McGee, SA McLuckey - Journal of Mass Spectrometry, 2013 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/jms.3233 New Substrates for Enteropeptidase: I. Biologically Active Hepta-, Octa-, and Nonapeptides VV Likhareva, BV Vas' kovskii, NE Shepel' - Russian Journal of , 2003 - Springerhttps://link.springer.com/article/10.1023/A:1023200230022 Synthetic model and bioactive peptides as potential substrates for enteropeptidase VV Likhareva, AG Mikhailova, BV Vaskovsky - Letters in Peptide , 2002 - Springerhttps://link.springer.com/article/10.1023/A:1024146528313 Mass spectrometry analysis of synthetically myristoylated peptides TS Chen, JD Yoder, DE Hruby - European Journal of Mass , 2004 - journals.sagepub.comhttps://journals.sagepub.com/doi/abs/10.1255/ejms.652 Design of substrate-type ACE inhibitory pentapeptides with an antepenultimate C-terminal proline for efficient release of inhibitory activity S Rao, S Liu, T Ju, W Xu, G Mei, Y Xu - Biochemical engineering , 2012 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1369703X11002634 Novel copoly (styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method S EG Souza, L Malavolta , EM Cilli - Protein and Peptide , 2015 - ingentaconnect.comhttps://www.ingentaconnect.com/content/ben/ppl/2015/00000022/00000005/art00003 Department zyxwvutsrqponmlkjihgfed QUM GU, GD PRESTWICH - academia.eduhttps://www.academia.edu/download/71325798/j.1399-3011.1997.tb01155.x20211004-14905-ztg6w4.pdf Photochemical conjugation of peptides to carrier proteins using 1,2,3-thiadiazole-4-carboxylic acid Immunoreactivity of free C-terminal epitope with specific PR HANSEN , H FLYGE, A HOLM - Journal of Peptide , 1996 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-3011.1996.tb01092.x HIV Fusion Peptides Significantly Soften Lipid Bilayers P Shchelokovskyy , S Tristram-Nagle , R Lipowsky - Biophysical , 2010 - cell.comhttps://www.cell.com/biophysj/pdf/S0006-3495(09)03330-X.pdf Spectroscopic Studies of the Interaction of Native and TOAC-Labeled Peptide Hormones with Model Membranes: Angiotensin II N Maraca­n , E Poletti , CR Nakaie , S Schreier - Biophysical Journal, 2010 - cell.comhttps://www.cell.com/biophysj/pdf/S0006-3495(09)03327-X.pdf )-2, 2, 5, 5-tetramethylpyrrolidine-N-oxyl-3-amino-4-carboxylic acid]: A novel protected spin labeled beta-amino acid for peptide and protein chemistry M Tominaga, SR Barbosa, EF Poletti - Chemical and , 2001 - jstage.jst.go.jphttps://www.jstage.jst.go.jp/article/cpb/49/8/49_8_1027/_article/-char/ja/ Screening for silver nanoparticle-binding peptides by using a peptide array M Kuboyama, R Kato , M Okochi, H Honda - Biochemical engineering , 2012 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1369703X12001180 Tools for the Identification of Receptor Dimmers: Synthesis and Biological Evaluation of On-Resin Dimerized, Photosensitive Analogues of Angiotensin II KA Therrien, M Deraaca«t, A Dubois, L Rihakova - Peptides: The Wave of , 2001 - Springerhttps://link.springer.com/chapter/10.1007/978-94-010-0464-0_414 Energetics and dynamics of dissociation of deprotonated peptides: Fragmentation of angiotensin analogs J Laskin , Z Yang - International Journal of Mass Spectrometry, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1387380611002570 Fragmentation energetics for angiotensin II and its analogs from time-and energy-resolved surface-induced dissociation studies J Laskin , TH Bailey, JH Futrell - International Journal of Mass Spectrometry, 2004 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1387380604001174 Comparative Investigation of the Cleavage Step in the Synthesis of Model Peptide Resins: Implications for Nalpha-9-Fluorenylmethyloxycarbonyl-Solid Phase Peptide GN Jubilut, EM Cilli , E Crusca Jr , EH Silva - Chemical and , 2007 - jstage.jst.go.jphttps://www.jstage.jst.go.jp/article/cpb/55/3/55_3_468/_article/-char/ja/ Use of the same polymer for synthesis and purification of peptides EH Silva, A Etchegaray , RSH Carvalho - Journal of the Brazilian , 2005 - SciELO Brasilhttps://www.scielo.br/j/jbchs/a/jjp9dx7pbsZSwQS64xHBmkm/?lang=en&format=html Gamma ray irradiation of the vasoactive peptide bradykinin reveals a residue-and position-dependent structural modification DT Nardi, JC Rosa , GN Jubilut, A Miranda - Journal of Peptide , 2010 - Springerhttps://link.springer.com/article/10.1007/s10989-010-9205-0 Antiplasmodial Activity of Angiotensin II Analogs DM de Freitas, VXO Junior - of the 24 th American Peptide , 2015 - researchgate.nethttps://www.researchgate.net/profile/Vani-Junior/publication/299917946_Antiplasmodial_Activity_of_Angiotensin_II_Analogs/links/573df8a408ae9f741b2fff1e/Antiplasmodial-Activity-of-Angiotensin-II-Analogs.pdf Comparison of methods to examine the endogenous peptides of fetal calf serum D Williams, P Zhu, P Bowden , C Stacey, M McDonell - Clinical Proteomics, 2006 - Springerhttps://link.springer.com/article/10.1385/CP:2:1:67 A Photolabile Thiol Protecting Group for Cellular Studies D Abate-Pella, N Zeliadt, D Mullen - Peptides: Breaking - books.google.comhttps://books.google.com/books?hl=en&lr=&id=sl1PAgAAQBAJ&oi=fnd&pg=PA362&dq=(%22DRVYIHPF%22+OR+%225Fam-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-OH%22+OR+%225Fam-DRVYIHPF-OH%22)+AND+peptide&ots=9_qVAwUb6F&sig=VEhy6PPhcw0NEgXcAxRZvjUvsdQ Intermolecular condensation products formed during the pyrolysis of peptides C Liu, F Basile - Journal of analytical and applied pyrolysis, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0165237011001045 Characterization of the dehydration products due to thermal decomposition of peptides by liquid chromatography-tandem mass spectrometry C Liu, E Topchiy , T Lehmann - Journal of Mass , 2015 - Wiley Online Libraryhttps://analyticalsciencejournals.onlinelibrary.wiley.com/doi/abs/10.1002/jms.3570 Structural and activity changes in three bioactive anuran peptides when Asp is replaced by isoAsp AN Calabrese , K Markulic, IF Musgrave , H Guo - Peptides, 2012 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0196978112004329 Linear Peptides Related to Angiotensin II with Antiplasmodial Activity AF Silva , MDT Torres, LS Silva , FL Alves , AAS Pinheiro - researchgate.nethttps://www.researchgate.net/profile/Margareth-Capurro/publication/299917711_Linear_Peptides_Related_to_Angiotensin_II_with_Antiplasmodial_Activity/links/573b1e1708ae9f741b2d7701/Linear-Peptides-Related-to-Angiotensin-II-with-Antiplasmodial-Activity.pdf

• Brand: Biosynth