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H-E-boro-Pro-OH
Vue en 3D

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H-E-boro-Pro-OH

Ref. 3D-PP45317

Taille indéfinieÀ demander
Livraison estimée en/au États-Unis, le mardi 10 décembre 2024

Informations sur le produit

Nom :
H-E-boro-Pro-OH
Synonymes :
  • NH2-Glu-boro-Pro-OH
Description :

Peptide H-E-boro-Pro-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-E-boro-Pro-OH include the following: Temperature and pH effects on biophysical and morphological properties of self-assembling peptide RADA16-I Z Ye, H Zhang , H Luo, S Wang, Q Zhou - European Peptide , 2008 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.988 Crystal structure of the E. coli peptide transporter YbgH Y Zhao , G Mao , M Liu, L Zhang , X Wang, XC Zhang - Structure, 2014 - cell.comhttps://www.cell.com/structure/pdf/S0969-2126(14)00183-X.pdf Pro-peptide as an intermolecular chaperone: renaturation of denatured subtilisin E with a synthetic pro-peptide Y Ohta, H Hojo, S Aimoto , T Kobayashi - Molecular , 1991 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-2958.1991.tb00797.x Catalytic diversity in self-propagating peptide assemblies TO Omosun, MC Hsieh , WS Childers , D Das - Nature , 2017 - nature.comhttps://www.nature.com/articles/nchem.2738 The world of peptides: a brief history of peptide chemistry T Wieland, M Bodanszky - 2012 - books.google.comhttps://books.google.com/books?hl=en&lr=&id=babwCAAAQBAJ&oi=fnd&pg=PR13&dq=(%22H-E-boro-Pro-OH%22+OR+%22E%22+OR+%22NH2-Glu-boro-Pro-OH%22)+AND+peptide&ots=D7SVl4x-rg&sig=jWLOUImbQQ2GRnLuQMW1lTLUObo Attachment of osteoblastic cells to hydroxyapatite crystals by a synthetic peptide (Glu7-Pro-Arg-Gly-Asp-Thr) containing two functional sequences of bone sialoprotein R Fujisawa, M Mizuno, Y Nodasaka, K Yoshinori - Matrix biology, 1997 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0945053X9790113X The apolipoprotein E-mimetic peptide COG112 inhibits NF-κB signaling, proinflammatory cytokine expression, and disease activity in murine models of colitis K Singh, R Chaturvedi , DP Barry, LA Coburn - Journal of biological , 2011 - ASBMBhttps://www.jbc.org/article/S0021-9258(20)54085-4/abstract Engineering of peptide beta-sheet nanotapes JN Keen, TCB McLeish - Journal of Materials Chemistry, 1997 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/1997/jm/a701088e A mitogenic peptide amide encoded within the E peptide domain of the insulin-like growth factor IB prohormone. JM Siegfried, PG Kasprzyk - Proceedings of the , 1992 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.89.17.8107 Structure-biological activity relationships of 11-residue highly basic peptide segment of bovine lactoferrin JH Kang, MK Lee, KL Kim - journal of peptide and , 1996 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-3011.1996.tb00852.x Electrostatic versus Steric Effects in Peptidomimicry: Synthesis and Secondary Structure Analysis of Gramicidin S Analogues with (E)-Alkene Peptide Isosteres J Xiao, B Weisblum , P Wipf - Journal of the American Chemical , 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja051002s An apolipoprotein E-derived peptide mediates uptake of sterically stabilized liposomes into brain capillary endothelial cells I Sauer, IR Dunay , K Weisgraber, M Bienert - Biochemistry, 2005 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi048080x Design, synthesis and characterization of a new anionic cell-penetrating peptide: SAP (E) I Martaca­n, M Teixido, E Giralt - ChemBioChem, 2011 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.201000679 Apolipoprotein E mimetic Peptide dramatically lowers plasma cholesterol and restores endothelial function in watanabe heritable hyperlipidemic rabbits H Gupta , CR White, S Handattu, DW Garber, G Datta - Circulation, 2005 - Am Heart Assochttps://www.ahajournals.org/doi/abs/10.1161/circulationaha.104.497107 Botulinum neurotoxins serotypes A and E cleave SNAP-25 at distinct COOH-terminal peptide bonds G Schiavo , A Santucci, BR Dasgupta, PP Mehta - FEBS letters, 1993 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0014579393804484 Identification of crucial residues for the antibacterial activity of the proline-rich peptide, pyrrhocoricin G Kragol , R Hoffmann , MA Chattergoon - European journal of , 2002 - Wiley Online Libraryhttps://febs.onlinelibrary.wiley.com/doi/abs/10.1046/j.1432-1033.2002.03119.x Allylic Amines as Key Building Blocks in the Synthesis of (E)-Alkene Peptide Isosteres EM Skoda, GC Davis, P Wipf - Organic process research & , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/op2002613 COG1410, a novel apolipoprotein E-based peptide, improves functional recovery in a murine model of traumatic brain injury DT Laskowitz , SE McKenna, P Song, H Wang - Journal of , 2007 - liebertpub.comhttps://www.liebertpub.com/doi/abs/10.1089/neu.2006.0192 A cleavage method which minimizes side reactions following Fmoc solid phase peptide synthesis DS King, CG FIELDS, GB FIELDS - journal of peptide and , 1990 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-3011.1990.tb00976.x Fast conventional Fmoc solid-phase peptide synthesis with HCTU CA Hood, G Fuentes, H Patel, K Page - European Peptide , 2008 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.921 Peptide Therapeutics 2.0 BG de la Torre , F Albericio - Molecules, 2020 - mdpi.comhttps://www.mdpi.com/1420-3049/25/10/2293 Peptide-based molecular shuttles AS Lane, DA Leigh , A Murphy - Journal of the American Chemical , 1997 - ACS Publicationshttps://pubs.acs.org/doi/full/10.1021/ja971224t Peptide bond mimicry by (E)-alkene and (Z)-fluoroalkene peptide isosteres: synthesis and bioevaluation of alpha-helical anti-HIV peptide analogues , K Tomita, H Ohno, T Naito, E Kodama - Organic & , 2009 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2009/ob/b907983a

Avis:
Nos produits sont destinés uniquement à un usage en laboratoire. Pour tout autre usage, veuillez nous contacter.
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Biosynth
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Propriétés chimiques

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Informations sur les risques

Numéro ONU :
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