scholarly journals Totalsynthese von Thymosin /β4, 3[1,2] Klassische Synthese des Fragments [31 -43] von Thymosin ß4 / Total Synthesis of Thymosin β4, 3[1, 2] Conventional Synthesis of the Fragment [31-43] of Thymosin β4

1993 ◽  
Vol 48 (7) ◽  
pp. 1000-1008 ◽  
Author(s):  
Peter Link ◽  
Wolfgang Voelter

As part of our total synthesis of thymosin β4 an optimized synthesis of the C-terminal part of thymosin β4 is described. Side chain functional residues of the tridecapeptide are masked by tert-butyl and the α-amino residues are protected by Z groups. The fully protected peptide derivative was obtained by WSCI/HOBt coupling of three fragments representing the segments [31-35], [36-37] and [38-43].

2019 ◽  
Author(s):  
Huaimin Wang ◽  
Zhaoqianqi Feng ◽  
Weiyi Tan ◽  
Bing Xu

<p>Selectively targeting cell nucleolus remains a challenge. Here we report the first case that D-peptides form membraneless molecular condensates with RNA for targeting cell nucleolus. A D-peptide derivative, enriched with lysine and hydrophobic residues, self-assembles to form nanoparticles, which enter cells through clathrin dependent endocytosis and mainly accumulate at cell nucleolus. Structural analogue of the D-peptide reveals that particle morphology of the assemblies, which depends on the side chain modification, favors the cellular uptake. Contrasting to those of the D-peptide, the assemblies of the corresponding L-enantiomer largely localize in cell lysosomes. Preliminary mechanism study suggests that the D-peptide nanoparticles interact with RNA to form membraneless condensates in the nucleolus, which further induces DNA damage and results in cell death. This work illustrates a new strategy for rationally designing supramolecular assemblies of D-peptides for targeting subcellular organelles.</p>


ChemInform ◽  
2000 ◽  
Vol 31 (49) ◽  
pp. no-no
Author(s):  
Young S. Rho ◽  
Hyun Kyoung Ko ◽  
Wan-Joong Kim ◽  
Dong Jin Yoo ◽  
Heun Soo Kang
Keyword(s):  

2018 ◽  
Vol 151 ◽  
pp. 110-120 ◽  
Author(s):  
Ahmed Kotb ◽  
Nader S. Abutaleb ◽  
Mohamed A. Seleem ◽  
Mohamed Hagras ◽  
Haroon Mohammad ◽  
...  
Keyword(s):  

1980 ◽  
Vol 28 (1) ◽  
pp. 62-69 ◽  
Author(s):  
TAIICHIRO WATANABE ◽  
YOICHI KAWANO ◽  
TERUO TANAKA ◽  
TOSHIHIKO HASHIMOTO ◽  
TETSUO MIYADERA
Keyword(s):  

Synlett ◽  
2020 ◽  
Vol 32 (01) ◽  
pp. 45-50
Author(s):  
Udo Nubbemeyer ◽  
Analuisa Nava ◽  
Lukas Trippe ◽  
Andrea Frank ◽  
Lars Andernach ◽  
...  

AbstractStarting from methyl cycloheptatrienyl-1-carboxylate, 6-acylation was successfully achieved employing glutaryl chloride in the presence of AlCl3 under controlled reaction conditions to furnish keto carboxylic acid product. After protection of this keto carboxylic acid as tert-butyl ester, reagent-controlled enantioselective reductions delivered configuration-defined methyl-6-hydroxylalkyl cycloheptatriene-1-carboxylates with up to 80% ee. Whereas simple NaBH4 reduction of the keto carboxylic acid and subsequent lactonization afforded a methyl-6-tetrahydropyranonyl cycloheptatriene-1-carboxylate. Resolution using chiral HPLC delivered the product enantiomers with up to >99% ee Finally, ECD analyses enabled structure elucidation. The products are used as key intermediates in enantioselective 6,11-methylene-lipoxin B4 syntheses.


2009 ◽  
Vol 26 (2) ◽  
pp. 130-148 ◽  
Author(s):  
ARTHUR M. FELIX ◽  
EDGAR P. HEIMER ◽  
CHING-TSO WANG ◽  
THEODORE J. LAMBROS ◽  
JOSEPH SWISTOK ◽  
...  

2013 ◽  
Vol 15 (9) ◽  
pp. 2246-2249 ◽  
Author(s):  
O. Roy ◽  
C. Caumes ◽  
Y. Esvan ◽  
C. Didierjean ◽  
S. Faure ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document