Das Produkt wurde korrekt in den Warenkorb gelegt.

discount label
H-E-boro-Pro-OH
3D-Ansicht

Biosynth logo

H-E-boro-Pro-OH

Ref. 3D-PP45317

Unbestimmte GrößeNachfragen
Voraussichtliche Lieferung in Vereinigte Staaten, am Dienstag 10. Dezember 2024

Produktinformation

Name:
H-E-boro-Pro-OH
Synonyme:
  • NH2-Glu-boro-Pro-OH
Beschreibung:

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

Hinweis:
Unsere Produkte sind nur für Laborzwecke. Für jede andere Verwendung, bitte melden sie sich bei uns.
Marke:
Biosynth
Langzeitlagerung:
Hinweise:

Chemische Eigenschaften

MDL:
Schmelzpunkt:
Siedepunkt:
Flammpunkt:
Dichte:
Konzentration:
EINECS:
Merck:
HS-Code:

Gefahrenhinweise

UN-Nummer:
EQ:
Klasse:
H-Sätze:
P-Sätze:
Flugverbot:
Gefahrenhinweis:
Verpackungsgruppe:
LQ:

Technische Anfrage zu: 3D-PP45317 H-E-boro-Pro-OH

Bitte verwenden Sie stattdessen den Warenkorb, um ein Angebot oder eine Bestellung anzufordern

Wenn Sie ein Angebot anfordern oder eine Bestellung aufgeben möchten, legen Sie stattdessen die gewünschten Produkte in Ihren Warenkorb und fordern Sie dann ein Angebot oder eine Bestellung an aus dem Warenkorb. Es ist schneller, billiger und Sie können von den verfügbaren Rabatten und anderen Vorteilen profitieren.

* Obligatorische felder
Willkommen bei CymitQuimica!Wir verwenden Cookies, um Ihren Besuch zu verbessern. Wir schließen Werbung nicht ein.

Bitte beachten Sie unsere Cookie-Richtlinie  für weitere Details oder passen Sie Ihre Einstellungen unter “Konfigurieren” an.