Das Produkt wurde korrekt in den Warenkorb gelegt.

discount label
norleucyl-piperidine
3D-Ansicht

Biosynth logo

norleucyl-piperidine

Ref. 3D-PP44671

Unbestimmte GrößeNachfragen
Voraussichtliche Lieferung in Vereinigte Staaten, am Freitag 25. Oktober 2024

Produktinformation

Name:
norleucyl-piperidine
Synonyme:
  • NORLEUCys-Tyr-Leu-Pro-Ile-Pro-Glu-Arg-Ile-Asp-Ile-Asn-Glu
Beschreibung:

Peptide norleucyl-piperidine 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 norleucyl-piperidine include the following: Synthesis, in vitro assay, and molecular modeling of new piperidine derivatives having dual inhibitory potency against acetylcholinesterase and Abeta1-42 aggregation YE Kwon, JY Park, KT No , JH Shin , SK Lee - Bioorganic & medicinal , 2007 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0968089607006190 )-dl-p-amidinophenylalanyl-piperidine (NAPAP) and (2R,4R)-4-methyl-1-[Nalpha-(3-methyl-1,2,3,4-tetrahydro-8-quinolinesulphonyl)-l-arginyl]-2-piperidine carboxylic acid (MQPA W Bode, D TURK , J Sturzebecher - European journal of , 1990 - Wiley Online Libraryhttps://febs.onlinelibrary.wiley.com/doi/abs/10.1111/j.1432-1033.1990.tb19320.x Piperidine carbamate peptidomimetic inhibitors of the serine proteases HGFA, matriptase and hepsin VC Damalanka , SA Wildman , JW Janetka - MedChemComm, 2019 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2019/md/c9md00234k Piperidine is preferred to morpholine for Fmoc cleavage in solid phase glycopeptide synthesis as exemplified by preparation of glycopeptides related to HIV gp120 T Vuljanic, KE Bergquist, H Clausen , S Roy, J Kihlberg - Tetrahedron, 1996 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0040402096003699 Green Solid-Phase Peptide Synthesis: Oxyma-Triggered Spectrophotometric Monitoring of Residual Piperidine SL Broman, M Rosenberg, F Wojcik - Process Research & , 2024 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.oprd.3c00339 Structure-based design and synthesis of macroheterocyclic peptidomimetic inhibitors of the aspartic protease beta-site amyloid precursor protein cleaving enzyme (BACE S Hanessian, G Yang, JM Rondeau - Journal of medicinal , 2006 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm060154a and Structural Investigation of beta-Peptidosulfonamides and beta-Peptidosulfonamide/beta-Peptide Hybrids: beta-Peptidosulfonamide and beta-Peptide Foldamers are Two of R de Jong, DTS Rijkers, RMJ Liskamp - Helvetica chimica acta, 2002 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/hlca.200290008 New t-butyl based aspartate protecting groups preventing aspartimide formation in Fmoc SPPS R Behrendt, S Huber, R Martaca­ - Journal of Peptide , 2015 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.2790 Deprotection reagents in Fmoc solid phase peptide synthesis: moving away from piperidine? OF Luna, J Gomez, C Cardenas , F Albericio - Molecules, 2016 - mdpi.comhttps://www.mdpi.com/1420-3049/21/11/1542 Rapid continuous peptide synthesis via FMOC amino acid chloride coupling and 4-(aminomethyl) piperidine deblocking M Beyermann, M Bienert, H Niedrich - The Journal of , 1990 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/jo00289a056 Microwave-assisted solid-phase peptide synthesis of neurosecretory protein GL composed of 80 amino acid residues K Masuda, H Ooyama, K Shikano - Journal of Peptide , 2015 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.2756 Synthesis and Biological Evaluation of Optimized Analogues of Benzyl Piperidine Based Neuropeptide FF Receptor Ligands K Galal - 2020 - search.proquest.comhttps://search.proquest.com/openview/b4870e34cc467ee7a6a88cd8a917ea01/1?pq-origsite=gscholar&cbl=18750&diss=y Design and Synthesis of Novel Biologically Active Thrombin Receptor Non-Peptide Mimetics Based on the Pharmacophoric Cluster Phe/Arg/NH2 of the Ser42-Phe-Leu-Leu K Alexopoulos, P Fatseas, E Melissari - Journal of medicinal , 2004 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm031080v Separation and identification of hydrophilic peptides in dairy products using FMOC derivatization JM Roturier, D Le Bars, JC Gripon - Journal of Chromatography A, 1995 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0021967394012346 Sequence dependence of aspartimide formation during 9-fluorenylmethoxycarbonyl solid-phase peptide synthesis JL Lauer , CG Fields, GB Fields - Letters in peptide science, 1995 - Springerhttps://link.springer.com/article/10.1007/BF00117955 Cymit Quimicaesis of the Central Piperidine Nitrogen Heterocycle in Series a Thiopeptides J Liu, Z Lin, H Chen, H Guo, J Tao - Chinese Journal of , 2019 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/cjoc.201800497 Association constants of pyridine and piperidine alkaloids to amyloid ss peptide determined by electrochemical impedance spectroscopy I Grabowska, H Radecka, A Burza - Current Alzheimer , 2010 - ingentaconnect.comhttps://www.ingentaconnect.com/content/ben/car/2010/00000007/00000002/art00008 Replacing piperidine in solid phase peptide synthesis: effective Fmoc removal by alternative bases G Martelli, P Cantelmi, C Palladino, A Mattellone - Green , 2021 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2021/gc/d1gc02634h The tea-bag protocol for comparison of Fmoc removal reagents in solid-phase peptide synthesis F Guzman, A Gauna, O Luna, T Roman, C acalvarez - Amino Acids, 2020 - Springerhttps://link.springer.com/article/10.1007/s00726-020-02883-8 Efficient synthesis of peptides with 4-methylpiperidine as Fmoc removal reagent by solid phase synthesis CF Vergel Galeano, ZJ Rivera Monroy - Journal of the Mexican , 2014 - scielo.org.mxhttps://www.scielo.org.mx/scielo.php?pid=S1870-249X2014000400004&script=sci_abstract&tlng=pt Orally Active Non-Peptide Fibrinogen Receptor (GpIIb/IIIa) Antagonists: Identification of 4-[4-[4-(Aminoimino methyl) phenyl]-1-piperazinyl]-1-piperidineacetic Acid as a CD Eldred, B Evans, S Hindley - Journal of medicinal , 1994 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/jm00049a006 Potent Cyclic Monomeric and Dimeric Peptide Inhibitors of VLA-4 (alpha4beta1 Integrin)-Mediated Cell Adhesion Based on the Ile-Leu-Asp-Val Tetrapeptide AS Dutta, M Crowther, JJ Gormley - Journal of Peptide , 2000 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/1099-1387(200007)6:7%3C321::AID-PSC259%3E3.0.CO;2-A Synthesis of novel fluorescent heterocyclic-derived alpha-amino acids and the total syntheses of piperidine natural products AH Harkiss - 2017 - theses.gla.ac.ukhttps://theses.gla.ac.uk/id/eprint/8629 Novel orally bioavailable piperidine derivatives as extracellular arginase inhibitors developed by a ring expansion A Gzik, B Borek, J Chrzanowski , K Jedrzejczak - European Journal of , 2024 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0223523423010000 New orally active non-peptide fibrinogen receptor (GpIIb-IIIa) antagonists: identification of ethyl 3-[N-[4-[4-[amino [(ethoxycarbonyl) imino] methyl] phenyl]-1, 3-thiazol-2 A Badorc, MF Bordes, P de Cointet, P Savi - Journal of medicinal , 1997 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/jm970240y

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-PP44671 norleucyl-piperidine

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.