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α-BOC-di-ε-Z-lysyllysine is a complex peptide compound consisting of two lysine molecules connected through their ε-amino groups, with one lysine molecule being N-terminally protected by a benzyloxycarbonyl (Z) group and the other C-terminally protected by a tert-butyloxycarbonyl (BOC) group. This specific arrangement allows for controlled peptide synthesis, as the BOC and Z groups can be selectively removed under mild conditions to facilitate further reactions. The compound plays a crucial role in the synthesis of larger peptides and proteins, as it enables chemists to build up complex structures in a stepwise manner while maintaining the integrity of the individual amino acid residues.

27317-71-1

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27317-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27317-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,1 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27317-71:
(7*2)+(6*7)+(5*3)+(4*1)+(3*7)+(2*7)+(1*1)=111
111 % 10 = 1
So 27317-71-1 is a valid CAS Registry Number.

27317-71-1Relevant academic research and scientific papers

CO2 in supramolecular chemistry: Preparation of switchable supramolecular polymers

Xu, Heng,Rudkevich, Dmitry M.

, p. 5432 - 5442 (2004)

CO2 gas was used to construct novel types of supramolecular polymers. Self-assembling nanostructures 11 and 13 were prepared, which employ both hydrogen bonding and dynamic, thermally reversible carbamate bonds. As precursors, calixarene ureas

Pillar[5]arene-Based Polycationic Glyco[2]rotaxanes Designed as Pseudomonas aeruginosa Antibiofilm Agents

Coenye, Tom,De Winter, Julien,Diaconu, Andrei,Fransolet, Maude,Gillon, Emilie,Imberty, Anne,Jimmidi, Ravikumar,Michiels, Carine,Mohy El Dine, Tharwat,Vincent, Stéphane P.

, p. 14728 - 14744 (2021/10/12)

Pseudomonas aeruginosa (P.A.) is a human pathogen belonging to the top priorities for the discovery of new therapeutic solutions. Its propensity to generate biofilms strongly complicates the treatments required to cure P.A. infections. Herein, we describe the synthesis of a series of novel rotaxanes composed of a central galactosylated pillar[5]arene, a tetrafucosylated dendron, and a tetraguanidinium subunit. Besides the high affinity of the final glycorotaxanes for the two P.A. lectins LecA and LecB, potent inhibition levels of biofilm growth were evidenced, showing that their three subunits work synergistically. An antibiofilm assay using a double δlecAδlecB mutant compared to the wild type demonstrated that the antibiofilm activity of the best glycorotaxane is lectin-mediated. Such antibiofilm potency had rarely been reached in the literature. Importantly, none of the final rotaxanes was bactericidal, showing that their antibiofilm activity does not depend on bacteria killing, which is a rare feature for antibiofilm agents.

Peptidic molecular brushes with enhanced chirality

Li, Wen,Zhang, Xiuqiang,Wang, Jue,Qiao, Xiao,Liu, Kun,Zhang, Afang

, p. 4063 - 4072 (2012/10/30)

Tethering oligopeptides through one end densely packed onto a linear polymer main chain will greatly reduce freedom of the peptide chains, which affords an easy access to investigate the secondary structure of peptides under constrained condition. Herein,

Supramolecular structures from lysine peptides and carbon dioxide

Stastny, Vaclav,Anderson, Anjenique,Rudkevich, Dmitry M.

, p. 8696 - 8705 (2007/10/03)

The design, synthesis, and characterization of novel linear and cross-linked supramolecular polymers that are easily available from biologically friendly lysine peptides and carbon dioxide (CO2) are reported here. Polymeric structures 5, 6, and

PROLINE DERIVATIVES

-

, (2008/06/13)

Proline derivatives of the formulae: STR1 wherein R 1 through R 11 have defined values, and acid-and base-addition salts thereof, and equilibrium addition compounds of the aldehyde group thereof; processes for their preparation; pharmaceutical compositions; and intermediates for preparing said proline derivatives. The proline derivatives are human leukocyte elastase inhibitors which are useful, for example, in treating pulmonary emphysema.

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