H-VVIA-OH
Ref. 3D-PH00558
1mg
164.00€
10mg
183.00€
100mg
263.00€
Product Information
Name:H-VVIA-OH
Synonyms:
- H-Val-Val-Ile-Ala-acid MeOSuc-Val-Val-Ile-Ala-pNA
Brand:Biosynth
Description:Peptide H-VVIA-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-VVIA-OH include the following: Peptidotriazolamers Inhibit Aβ (1-42) Oligomerization and Cross a Blood-Brain-Barrier Model N Tonali, L Hericks, DC Schröder, O Kracker- ..., 2021 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cplu.202000814 Partitioning of Aβ Peptide Fragments into Blood-Brain Barrier Mimetic Bilayer CM Siwy, BM Delfing , C Lockhart - The Journal of ..., 2021 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jpcb.0c11253 Breaker peptides against amyloid-β aggregation: a potential therapeutic strategy for Alzheimer's disease N Ghosh, LM Kundu - Future Medicinal Chemistry, 2021 - Taylor & Francishttps://www.tandfonline.com/doi/abs/10.4155/fmc-2021-0184 Successive cleavage of β-amyloid precursor protein by gamma-secretase S Funamoto, S Tagami, M Okochi- Seminars in cell & ..., 2020 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1084952119302794 Improving the Sustainability of Peptide and Polymer Chemistry S Lawrenson - 2018 - etheses.whiterose.ac.ukhttps://etheses.whiterose.ac.uk/21397/ Identification of small peptides in human cerebrospinal fluid upon amyloid-β degradation N Mizuta, K Yanagida, T Kodama - Neurodegenerative ..., 2017 - karger.comhttps://karger.com/ndd/article/17/2-3/103/207526 Design of a molecular hybrid of dual peptide inhibitors coupled on AuNPs for enhanced inhibition of amyloid β-protein aggregation and cytotoxicity N Xiong, Y Zhao, X Dong, J Zheng , Y Sun - Small, 2017 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/smll.201601666 Peptide synthesis: ball-milling, in solution, or on solid support, what is the best strategy? O Maurin, P Verdié , G Subra , F Lamaty- Beilstein Journal of ..., 2017 - beilstein-journals.orghttps://www.beilstein-journals.org/bjoc/articles/13/206 Atomistic characterization of binding modes and affinity of peptide inhibitors to amyloid-β protein F Liu , W Du, Y Sun, J Zheng , X Dong - Frontiers of Chemical Science and ..., 2014 - Springerhttps://link.springer.com/article/10.1007/s11705-014-1454-6 gamma-Secretase associated with lipid rafts: multiple interactive pathways in the stepwise processing of β-carboxyl-terminal fragment N Matsumura, M Takami, M Okochi- Journal of Biological ..., 2014 - ASBMBhttps://www.jbc.org/article/S0021-9258(20)44149-3/pdf Molecular dynamics simulation and binding free energy calculation of the conformational transition of amyloid peptide 42 inhibited by peptide inhibitors X DONG, W DU, F LIU - Acta Physico-Chimica Sinica, 2012 - ingentaconnect.comhttps://www.ingentaconnect.com/content/apcs/apcs/2012/00000028/00000011/art00030 C-terminal tetrapeptides inhibit Aβ42-induced neurotoxicity primarily through specific interaction at the N-terminus of Aβ42 H Li, Z Du, DHJ Lopes , EA Fradinger- Journal of medicinal ..., 2011 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm200982p Multifunctional Oligopeptides as an Artificial Toolkit for Molecular Recognition Events PR Wich - 2009 - opus.bibliothek.uni-wuerzburg.dehttps://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/3159 gamma-Secretase: successive tripeptide and tetrapeptide release from the transmembrane domain of β-carboxyl terminal fragment M Takami, Y Nagashima, Y Sano- Journal of ..., 2009 - Soc Neurosciencehttps://www.jneurosci.org/content/29/41/13042.short Rapid Sequencing of Split-and-Mix Peptide Receptor Libraries-Identification of Binding Partners for Val-Val-Ile-Ala in Aqueous Solution J Shepherd, GJ Langley , JM Herniman, JD Kilburn - 2007 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.200601004 Combinatorial approaches to peptide receptors J Shepherd - 2005 - eprints.soton.ac.ukhttps://eprints.soton.ac.uk/466566/
Notice:Our products are intended for lab use only. For any other use, please contact us.
Chemical properties
Molecular weight:634.73 g/mol
Formula:C30H46N6O9
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