A New Approach to the Neoglycopeptides:  Synthesis of Urea- and Carbamate-TetheredN-Acetyl-d-glucosamine Amino Acid Conjugates

2006 ◽  
Vol 8 (22) ◽  
pp. 5009-5012 ◽  
Author(s):  
Yoshiyasu Ichikawa ◽  
Fumiyo Ohara ◽  
Hiyoshizo Kotsuki ◽  
Keiji Nakano
Keyword(s):  
Amino Acid ◽  
New Approach ◽  
Amino Acid Conjugates

Nanofibrous hydrogels self-assembled from naphthalene diimide (NDI)/amino acid conjugates

RSC Advances ◽  
2015 ◽  
Vol 5 (26) ◽  
pp. 20410-20413 ◽  
Author(s):  
Ling-Huang Hsu ◽  
Shu-Min Hsu ◽  
Fang-Yi Wu ◽  
Yu-Hao Liu ◽  
Srinivasa Rao Nelli ◽  
...  
Keyword(s):  
Amino Acid ◽  
New Approach ◽  
Amino Acid Conjugates ◽  
Naphthalene Diimide ◽  
Self Assembled

A new approach is proposed for the design of NDI-capped supramolecular hydrogels.

scholarly journals A New Approach to the Neoglycopeptides: Synthesis of Urea- and Carbamate-Tethered N-Acetyl-D-glucosamine Amino Acid Conjugates.

ChemInform ◽  
2007 ◽  
Vol 38 (9) ◽  
Author(s):  
Yoshiyasu Ichikawa ◽  
Fumiyo Ohara ◽  
Hiyoshizo Kotsuki ◽  
Keiji Nakano
Keyword(s):  
Amino Acid ◽  
New Approach ◽  
Amino Acid Conjugates

Fluoroquinolone-3-carboxamide Amino Acid Conjugates: Synthesis, Antibacterial Properties And Molecular Modeling Studies

2020 ◽  
Vol 17 (1) ◽  
pp. 71-84
Author(s):  
Riham M. Bokhtia ◽  
Siva S. Panda ◽  
Adel S. Girgis ◽  
Hitesh H. Honkanadavar ◽  
Tarek S. Ibrahim ◽  
...  
Keyword(s):  
Experimental Data ◽  
Antibacterial Activity ◽  
Amino Acid ◽  
Bacterial Infections ◽  
Antibacterial Agents ◽  
Antibacterial Properties ◽  
Computational Studies ◽  
Protecting Group ◽  
Amino Acid Conjugates ◽  
Molecular Modeling Studies

Background: Bacterial infections are considered as one of the major global health threats, so it is very essential to design and develop new antibacterial agents to overcome the drawbacks of existing antibacterial agents. Method: The aim of this work is to synthesize a series of new fluoroquinolone-3-carboxamide amino acid conjugates by molecular hybridization. We utilized benzotriazole chemistry to synthesize the desired hybrid conjugates. Result: All the conjugates were synthesized in good yields, characterized, evaluated for their antibacterial activity. The compounds were screened for their antibacterial activity using methods adapted from the Clinical and Laboratory Standards Institute. Synthesized conjugates were tested for activity against medically relevant pathogens; Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27856) Staphylococcus aureus (ATCC 25923) and Enterococcus faecalis (ATCC 19433). Conclusion: The observed antibacterial experimental data indicates the selectivity of our synthesized conjugates against E.Coli. The protecting group on amino acids decreases the antibacterial activity. The synthesized conjugates are non-toxic to the normal cell lines. The experimental data were supported by computational studies.

scholarly journals Avoided motifs: short amino acid strings missing from protein datasets

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Pablo Mier ◽  
Miguel A. Andrade-Navarro
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Protein Function ◽  
Large Protein ◽  
New Approach ◽  
Cellular Context ◽  
Human Proteins ◽  
Context Specific ◽  
Protein Datasets

Abstract According to the amino acid composition of natural proteins, it could be expected that all possible sequences of three or four amino acids will occur at least once in large protein datasets purely by chance. However, in some species or cellular context, specific short amino acid motifs are missing due to unknown reasons. We describe these as Avoided Motifs, short amino acid combinations missing from biological sequences. Here we identify 209 human and 154 bacterial Avoided Motifs of length four amino acids, and discuss their possible functionality according to their presence in other species. Furthermore, we determine two Avoided Motifs of length three amino acids in human proteins specifically located in the cytoplasm, and two more in secreted proteins. Our results support the hypothesis that the characterization of Avoided Motifs in particular contexts can provide us with information about functional motifs, pointing to a new approach in the use of molecular sequences for the discovery of protein function.

scholarly journals Nicotinamide riboside–amino acid conjugates that are stable to purine nucleoside phosphorylase

2020 ◽  
Vol 18 (15) ◽  
pp. 2877-2885
Author(s):  
Faisal Hayat ◽  
Marie E. Migaud
Keyword(s):  
Amino Acid ◽  
Acid Ester ◽  
Purine Nucleoside Phosphorylase ◽  
Amino Acid Ester ◽  
Purine Nucleoside ◽  
Nucleoside Phosphorylase ◽  
Amino Acid Conjugates ◽  
Nicotinamide Riboside

O5′ amino acid ester conjugates of nicotinamide riboside, generated via a reduced intermediate, are stable to purine nucleoside phosphorylase.

Synthesis and anti-phlogistic potency of some new non-proteinogenic amino acid conjugates of ?Diclofenac?

Amino Acids ◽  
1999 ◽  
Vol 16 (3-4) ◽  
pp. 425-440 ◽  
Author(s):  
M. H. Abo-Ghalia ◽  
A. M. Shalaby ◽  
W. I. El-Eraqi ◽  
H. M. Awad
Keyword(s):  
Amino Acid ◽  
Amino Acid Conjugates ◽  
Proteinogenic Amino Acid

Synthesis and evaluation of some amino acid conjugates of pirprofen

2013 ◽  
Vol 3 (3) ◽  
pp. 241-246 ◽  
Author(s):  
S.K. Sharma ◽  
C. Karthikeyan ◽  
N.S. Hari Narayana Moorthy ◽  
D.K. Jain ◽  
P. Trivedi
Keyword(s):  
Amino Acid ◽  
Amino Acid Conjugates

New Approach to the Coupling of γ-Amino β-Hydroxy Acids and β,γ-Dihydroxy Acids with α-Amino Acid Esters

1996 ◽  
Vol 61 (26) ◽  
pp. 9196-9201 ◽  
Author(s):  
Claudio Palomo ◽  
José I. Miranda ◽  
Anthony Linden
Keyword(s):  
Amino Acid ◽  
Amino Acid Esters ◽  
Hydroxy Acids ◽  
New Approach ◽  
Acid Esters
Sign in / Sign up

Export Citation Format

Share Document