H-DRVYI^HPF-OH

Ref. 3D-PP43843

Produktinformation

• Name: H-DRVYI^HPF-OH
• Synonyme: NH2-Asp-Arg-Val-Tyr-Ile^His-Pro-Phe-OH

Beschreibung

Peptide H-DRVYI^HPF-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-DRVYI^HPF-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 Distinct multisite synergistic interactions determine substrate specificities of human chymase and rat chymase-1 for angiotensin II formation and degradation S Sanker , UM Chandrasekharan, D Wilk - Journal of Biological , 1997 - ASBMBhttps://www.jbc.org/article/S0021-9258(19)67399-0/abstract 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 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 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 The specificity of lysosomal tripeptidyl peptidase-I determined by its action on angiotensin-II analogues MJ Warburton, F Bernardini - FEBS letters, 2001 - Wiley Online Libraryhttps://febs.onlinelibrary.wiley.com/doi/abs/10.1016/S0014-5793(01)02608-4 )-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/ 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 Lactoferricin-related peptides with inhibitory effects on ACE-dependent vasoconstriction JM Centeno, MC Burguete - Journal of agricultural , 2006 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jf060482j Peptide ozonolysis: Product structures and relative reactivities for oxidation of tyrosine and histidine residues JA Lloyd, JM Spraggins , MV Johnston - Journal of the American , 2006 - Springerhttps://link.springer.com/article/10.1016/j.jasms.2006.05.009 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 The active site specificity of angiotensin II converting enzyme 2 investigated through single and multiple residue changes and beta-amino acid substrate analogs. D Clayton , I Hanchapola, P Perlmutter, AI Smith - Peptides for Youth: The , 2009 - Springerhttps://link.springer.com/chapter/10.1007/978-0-387-73657-0_245 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+%22DRVYI%5EHPF%22+OR+%22H-DRVYIHPF-OH%22+OR+%22NH2-Asp-Arg-Val-Tyr-Ile%5EHis-Pro-Phe-OH%22+OR+%22H-DRVYI%5EHPF-OH%22)+AND+peptide&ots=9_qVAwU96A&sig=qwDcPWYPMNKPcpvgWsAgccUtdYM 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 Factors regulating tachyphylaxis triggered by N-terminal-modified angiotensin II analogs AJ Barros, CM Ito, EN Makino, FAM Cembranelli - 2009 - degruyter.comhttps://www.degruyter.com/document/doi/10.1515/BC.2009.143/html 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

• Marke: Biosynth