H-DRV^YIHPF-OH

Ref. 3D-PP48746

Información del producto

• Nombre: H-DRV^YIHPF-OH

Descripción

Peptide H-DRV^YIHPF-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-DRV^YIHPF-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 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 Reactions of angiotensin ions with hydroiodic acid TG Schaaff, JL Stephenson Jr, SA McLuckey - International Journal of Mass , 2000 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1387380600002554 New free radical-initiated peptide sequencing (FRIPS) mass spectrometry reagent with high conjugation efficiency enabling single-step peptide sequencing ST Lee, H Park, I Jang, CS Lee, B Moon , HB Oh - Scientific Reports, 2022 - nature.comhttps://www.nature.com/articles/s41598-022-13624-0 Use of Designed Peptide Linkers and Recombinant Hemoglobin Mutants for Drug Delivery: In Vitro Release of an Angiotensin II Analog and Kinetic Modeling of SP Trimble, D Marquardt, DC Anderson - Bioconjugate chemistry, 1997 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bc970037h 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 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 Fragmentation of doubly-protonated peptide ion populations labeled by H/D exchange with CD3OD KA Herrmann, K Kuppannan, VH Wysocki - International journal of mass , 2006 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1387380606000170 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 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=(%22H-DRVYIHPF-OH%22+OR+%22DRVYIHPF%22+OR+%22DRV%5EYIHPF%22+OR+%22H-DRV%5EYIHPF-OH%22)+AND+peptide&ots=9_qVAwW84F&sig=t85uAf_CNjT6Aqeb-81rrbN4Zzo 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 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

• Marca: Biosynth