5TAMRA-R-OH

Ref. 3D-PP44499

Produktinformation

• Name: 5TAMRA-R-OH
• Synonyme: 5Thr-Ala-Met-Arg-Ala-Arg-OH

Beschreibung

Peptide 5TAMRA-R-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 5TAMRA-R-OH include the following: Quantitative structure-activity relationship study of antioxidative peptide by using different sets of amino acids descriptors YW Li , B Li, J He, P Qian - Journal of Molecular Structure, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S002228601100384X Conjugation of a photosensitizer to an oligoarginine-based cell-penetrating peptide increases the efficacy of photodynamic therapy Y Choi , JR McCarthy, R Weissleder - ChemMedChem , 2006 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cmdc.200500036 Role of peptide hydrophobicity in the mechanism of action of alpha-helical antimicrobial peptides Y Chen , MT Guarnieri , AI Vasil, ML Vasil - Antimicrobial agents , 2007 - Am Soc Microbiolhttps://journals.asm.org/doi/abs/10.1128/aac.00925-06 Peptide modifications differentially alter G protein-coupled receptor internalization and signaling bias V Made, S Babilon, N Jolly, L Wanka - Angewandte Chemie , 2014 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201403750 Systemic in vivo distribution of activatable cell penetrating peptides is superior to that of cell penetrating peptides TA Aguilera , ES Olson, MM Timmers, T Jiang - Integrative , 2009 - academic.oup.comhttps://academic.oup.com/ib/article-abstract/1/5-6/371/5211408 C-end rule peptides mediate neuropilin-1-dependent cell, vascular, and tissue penetration T Teesalu , KN Sugahara - Proceedings of the , 2009 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.0908201106 Concomitant Occurrence of Peptide 310- and alpha-Helices Probed by NMR S Mammi, M Rainaldi, M Bellanda - Journal of the , 2000 - ACS Publicationshttps://pubs.acs.org/doi/full/10.1021/ja002710a Stearylated arginine-rich peptides: a new class of transfection systems S Futaki, W Ohashi, T Suzuki, M Niwa - Bioconjugate , 2001 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bc015508l Arginine-rich peptides: an abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery S Futaki, T Suzuki, W Ohashi, T Yagami - Journal of Biological , 2001 - ASBMBhttps://www.jbc.org/article/S0021-9258(19)46333-3/abstract Translocation of branched-chain arginine peptides through cell membranes: flexibility in the spatial disposition of positive charges in membrane-permeable peptides S Futaki, I Nakase, T Suzuki, Zhang , Y Sugiura - Biochemistry, 2002 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi0256173 Cell-surface interactions on arginine-rich cell-penetrating peptides allow for multiplex modes of internalization S Futaki, I Nakase - Accounts of chemical research, 2017 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.accounts.7b00221 Arginine-rich peptides: potential for intracellular delivery of macromolecules and the mystery of the translocation mechanisms S Futaki - International journal of pharmaceutics, 2002 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S037851730200337X Arginine-rich cell penetrating peptides: Design, structure-activity, and applications to alter pre-mRNA splicing by steric-block oligonucleotides R Abes, A Arzumanov, H Moulton - European Peptide , 2008 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.979 Exploring the sequence space for (tri-) peptide self-assembly to design and discover new hydrogels PWJM Frederix , GG Scott, YM Abul-Haija - Nature , 2015 - nature.comhttps://www.nature.com/articles/nchem.2122 Design, synthesis, and evaluation of amphiphilic cyclic and linear peptides composed of hydrophobic and positively-charged amino acids as antibacterial agents N Riahifard, S Mozaffari , T Aldakhil, F Nunez - Molecules, 2018 - mdpi.comhttps://www.mdpi.com/1420-3049/23/10/2722 Selective amino acid substitution reduces cytotoxicity of the antimicrobial peptide mastoparan LN Irazazabal, WF Porto , SM Ribeiro , S Casale - et Biophysica Acta (BBA , 2016 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0005273616302449 Synthesis and application of unprotected cyclic peptides as building blocks for peptide dendrimers L Zhang, JP Tam - Journal of the American Chemical Society, 1997 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja9621105 Molecular transporters for peptides: delivery of a cardioprotective ϵPKC agonist peptide into cells and intact ischemic heart using a transport system, R7 L Chen, LR Wright, CH Chen, SF Oliver, PA Wender - Chemistry & biology, 2001 - cell.comhttps://www.cell.com/ccbio/pdf/S1074-5521(01)00076-X.pdf Antibacterial activities of ferrocenoyl-and cobaltocenium-peptide bioconjugates JT Chantson, MVV Falzacappa, S Crovella - Journal of , 2005 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0022328X05005243 Effects of cargo molecules on the cellular uptake of arginine-rich cell-penetrating peptides JR Maiolo, M Ferrer , EA Ottinger - Biochimica et Biophysica Acta (BBAhttps://www.sciencedirect.com/science/article/pii/S0005273605001094 Peptide synthesis using unprotected peptides through orthogonal coupling methods. JP Tam , YIAN Lu, CFA Liu - Proceedings of the , 1995 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.92.26.12485 ω-Amino acids in peptide design. Crystal structures and solution conformations of peptide helices containing a beta-alanyl-γ-aminobutyryl segment IL Karle, A Pramanik , A Banerjee - Journal of the , 1997 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja970566w A helix-stabilized cell-penetrating peptide as an intracellular delivery tool H Yamashita, M Oba , T Misawa, M Tanaka - , 2016 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.201500468 Sequence-specific Ni (II)-dependent peptide bond hydrolysis for protein engineering: reaction conditions and molecular mechanism E Kopera, A Krezel , AM Protas, A Belczyk - Inorganic , 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ic1005709 Neuroprotective peptides fused to arginine-rich cell penetrating peptides: Neuroprotective mechanism likely mediated by peptide endocytic properties BP Meloni , D Milani, AB Edwards , RS Anderton - Pharmacology & , 2015 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0163725815001175 Selective peptide bond hydrolysis of cysteine peptides in the presence of Ni (II) ions AM Protas, A Bonna , E Kopera, W Bal - Journal of inorganic biochemistry, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0162013410002175 Prediction of peptide retention at different HPLC conditions from multiple linear regression models , M Marszaà ‚à ‚ , YV Heyden , R Kaliszan - Journal of Proteome , 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/pr049780r

• Marke: Biosynth