Welcome to Iris Biotech
For better service please confirm your country and language we detected.
Währung
EUR
Schneller Kontakt
Bitte senden Sie mir mehr Informationen über
Neu
Fmoc-L-Lys(4-Thz, Boc)-OH
Chemischer Name: (2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-(tert-butoxycarbonyl)thiazolidin-5-yl)butanoic acid // Synonyme: Fmoc-Lys(4-Thz, Boc)-OH
- Art-Nr.:FAA9340
- CAS Nr.:1240666-28-7
- Formel:C27H32N2O6S
- Molare Masse:512,62 g/mol
Startet von auf Anfrage
description
Bicyclic peptides have high potential as next generation pharmaceuticals, e.g., to disrupt the difficult to target interactions between proteins. For controlled cyclization, selective reactivities are required. Our 1,2-aminothiol and 1,3-thiazole building blocks yield the ideal combination for this purpose, and, in addition, are compatible with SPPS. Besides, when used N-terminally, 1,2-aminothiols are useful for connecting peptide fragments by native chemical ligation (NCL).
references
Chemical synthesis of phosphorylated ubiquitin and diubiquitin exposes positional sensitivities of E1-E2 enzymes and deubiquitinases; S. Bondalapati, W. Mansour, M. A. Nakasone, S. K. Maity, M. H. Glickman, A. Brik; Chem. Eur. J. 2015; 21(20): 7360-7364. https://doi.org/10.1002/chem.201500540
Convergent Versus Sequential Protein Synthesis: The Case of Ubiquitinated and Glycosylated H2B; M. Seenaiah, M. Jbara, S. M. Mali, A. Brik; Angew. Chem. Int. Ed. 2015; 54(42): 12374-12378. https://doi.org/10.1002/anie.201503309
Chemical Synthesis of Ubiquitinated Peptides with Varying Lengths and Types of Ubiquitin Chains to Explore the Activity of Deubiquitinases; S. N. Bavikar, L. Spasser, M. Haj-Yahya, S. V. Karthikeyan, T. Moyal, K. S. A. Kumar, A. Brik; Angew. Chem. Int. Ed. 2012; 51(3): 758-763. https://doi.org/10.1002/anie.201106430
Segmental isotopic labeling of ubiquitin chains to unravel monomer-specific molecular behavior; C. A. Castaneda, L. Spasser, S. N. Bavikar, A. Brik, D. Fushman; Angew. Chem. Int. Ed. 2011; 50(47): 11210-11214. https://doi.org/10.1002/anie.201104649
Platform for Orthogonal N-Cysteine-Specific Protein Modification Enabled by Cyclopropenone Reagents; A. Istrate, M. Geeson, C. Navo, B. Sousa, M. Marques, R. Taylor, T. Journeaux, S. Oehler, M. Mortensen, M. Deery, A. Bond, F. Corzana, G. Jiménez-Osés, G. Bernardes; JAmChemSoc. 2022; 144: 10396-10406. https://doi.org/10.1021/jacs.2c02185
Recent advances in N- and C-terminus cysteine protein bioconjugation; R. Spears, V. Chudasama; CurrOpinChemBiol. 2023; 75: 102306. https://doi.org/10.1016/j.cbpa.2023.102306
Biocompatible and Selective Generation of Bicyclic Peptides; S. Ullrich, J. George, A. Coram, R. Morewood, C. Nitsche; AngewChemIntEd. 2022; 61: e202208400. https://doi.org/10.1002/anie.202208400
Bulk oder Großmengen-Bestellung?
Sie benötigen größere Mengen für Ihre Entwicklung oder Produktion?
Benötigen Sie weitere Informationen über dieses Produkt?
kontaktieren Sie uns
Verwandte Produkte
Related news
-
News Amino Acids Life Sciences Product FocusAminothiols for Versatile Side-Chain Modification
Beyond cysteines: Unlock targeted side-chain modifications of your peptides and proteins via the introduction of 1,2-amin
Details ansehen
Produkte, die Sie auch interessieren könnten!
![Structure image for Fmoc-L-Lys[C20-OtBu-L-Glu(OtBu)-AA-AA]-OH](https://www.iris-biotech.de/media/catalog/product/F/A/FAA9210.svg?width=216&height=140&store=de&image-type=small_image)
