Biotin−Amino Acid Conjugates:  An Approach Toward Self-Assembled Hydrogelation

2005 ◽  
Vol 7 (9) ◽  
pp. 1741-1744 ◽  
Author(s):  
Sankarprasad Bhuniya ◽  
Sun Min Park ◽  
Byeang Hyean Kim
RSC Advances ◽  
2018 ◽  
Vol 8 (37) ◽  
pp. 20922-20927 ◽  
Author(s):  
Nien-Tzu Chu ◽  
Rajan Deepan Chakravarthy ◽  
Nai-Chia Shih ◽  
Yen-Hsu Lin ◽  
Yen-Chu Liu ◽  
...  

TPE-Ser molecules exhibit non-covalent interactions necessary for hydrogelation under physiological pH conditions.


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 ◽  
...  

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


2020 ◽  
Vol 17 (1) ◽  
pp. 71-84
Author(s):  
Riham M. Bokhtia ◽  
Siva S. Panda ◽  
Adel S. Girgis ◽  
Hitesh H. Honkanadavar ◽  
Tarek S. Ibrahim ◽  
...  

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.


2020 ◽  
Vol 18 (15) ◽  
pp. 2877-2885
Author(s):  
Faisal Hayat ◽  
Marie E. Migaud

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


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

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

2015 ◽  
Vol 51 (20) ◽  
pp. 4234-4236 ◽  
Author(s):  
Li Zhang ◽  
Qingxian Jin ◽  
Kai Lv ◽  
Long Qin ◽  
Minghua Liu

Self-assembled chiral nanostructures formed by a pyridylpyrazole-conjugated l-glutamide showed enantioselectivity for a fluorescence labeled chiral amino acid.


2001 ◽  
pp. 493-534 ◽  
Author(s):  
Jacquelyn Gervay-Hague ◽  
Thomas Weathers Jr

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