ChemInform Abstract: Fluorine Containing Amino Acids. Part 4. Synthesis and Biological Activity of β-(Polyfluoromethyl)-Substituted Aromatic Amino Acids.

ChemInform ◽  
1988 ◽  
Vol 19 (34) ◽  
Author(s):  
M. T. KOLYCHEVA ◽  
YU. L. YAGUPOL'SKII ◽  
L. M. ZAITSEV ◽  
I. I. GERUS ◽  
V. P. KUKHAR' ◽  
...  
1988 ◽  
Vol 22 (2) ◽  
pp. 110-114 ◽  
Author(s):  
M. T. Kolycheva ◽  
Yu. L. Yagupol'skii ◽  
L. M. Zaitsev ◽  
I. J. Gerus ◽  
V. P. Kukhar' ◽  
...  

2018 ◽  
Vol 20 (31) ◽  
pp. 20371-20381 ◽  
Author(s):  
Manuel M. Neidhardt ◽  
Katharina Schmitt ◽  
Angelika Baro ◽  
Carmen Schneider ◽  
Ursula Bilitewski ◽  
...  

Does the mesomorphic behaviour of l-amino acid-based ILCs correlate with biological activity?


2010 ◽  
Vol 2 (2) ◽  
pp. 344-350 ◽  
Author(s):  
Puja Ohri ◽  
Satinder Kaur Pannu

The term, phenolics has been used to describe a group of structurally diverse plant secondary metabolites. This group includes metabolites derived from the condensation of acetate units (terpenoids), those produced by the modification of aromatic amino acids (phenylpropanoids, cinnamic acid, lignin precursor, catechols and coumarins), flavonoids, isoflavonoids, and tannins. The occurrence and metabolism of phenolic substances in plants, in response to injury or invasion by pathogens, such as fungi, bacteria and viruses have already been studied. Oxidised compounds produced in plants after invasion by pathogens often show considerable biological activity and are a common mechanism of resistance to plant pathogens. The present review gives information regarding the effects of different phenolic compounds on nematode system. It is found that these compounds are involved in plant defense and hence provide resistance against nematode attack.


2019 ◽  
Author(s):  
A Craig ◽  
N Kolks ◽  
E Urusova ◽  
BD Zlatopolskiy ◽  
B Neumaier

2018 ◽  
Author(s):  
Golaleh Asghari ◽  
Emad Yuzbashian ◽  
Maryam Zarkesh ◽  
Parvin Mirmiran ◽  
Mehdi Hedayati ◽  
...  

2018 ◽  
Author(s):  
Nidhi Gour ◽  
Bharti Koshti ◽  
Chandra Kanth P. ◽  
Dhruvi Shah ◽  
Vivek Shinh Kshatriya ◽  
...  

We report for the very first time self-assembly of Cysteine and Methionine to discrenible strucutres under neutral condition. To get insights into the structure formation, thioflavin T and Congo red binding assays were done which revealed that aggregates may not have amyloid like characteristics. The nature of interactions which lead to such self-assemblies was purported by coincubating assemblies in urea and mercaptoethanol. Further interaction of aggregates with short amyloidogenic dipeptide diphenylalanine (FF) was assessed. While cysteine aggregates completely disrupted FF fibres, methionine albeit triggered fibrillation. The cytotoxicity assays of cysteine and methionine structures were performed on Human Neuroblastoma IMR-32 cells which suggested that aggregates are not cytotoxic in nature and thus, may not have amyloid like etiology. The results presented in the manuscript are striking, since to the best of our knowledge,this is the first report which demonstrates that even non-aromatic amino acids (cysteine and methionine) can undergo spontaneous self-assembly to form ordered aggregates.


Sign in / Sign up

Export Citation Format

Share Document