Conformational states of methylamides of N-acetyl α-amino acids and their N-methyl derivatives IV. Association in solutions

1973 ◽  
Vol 9 (3) ◽  
pp. 334-340
Author(s):  
E. S. Efremov ◽  
P. V. Kostetskii ◽  
V. T. Ivanov ◽  
E. M. Popov ◽  
Yu. A. Ovchinnikov
1973 ◽  
Vol 9 (3) ◽  
pp. 328-333
Author(s):  
E. S. Efremov ◽  
P. V. Kostetskii ◽  
V. T. Ivanov ◽  
E. M. Popov ◽  
Yu. A. Ovchinnikov

1973 ◽  
Vol 9 (3) ◽  
pp. 320-327
Author(s):  
V. T. Ivanov ◽  
P. V. Kostetskii ◽  
T. A. Balashova ◽  
S. L. Portnova ◽  
E. S. Efremov ◽  
...  

1973 ◽  
Vol 9 (3) ◽  
pp. 308-319 ◽  
Author(s):  
E. S. Efremov ◽  
L. B. Senyavina ◽  
V. N. Zheltova ◽  
A. G. Ivanova ◽  
P. V. Kostetskii ◽  
...  

2009 ◽  
Vol 23 (6) ◽  
pp. 581-587 ◽  
Author(s):  
Mara Tsesarskaia ◽  
Erika Galindo ◽  
Gyula Szókán ◽  
George Fisher

2018 ◽  
Vol 1 (3) ◽  
pp. e00070
Author(s):  
V.Yu. Grigorev ◽  
L.D. Grigoreva

A series of 20 proteinogenic amino acids was studied. Four types of fractal descriptors for 2 conformational states are calculated: α-helix and 1-strand β-sheet. Based on the analysis of the results obtained, it is established that when the conformational state of the amino acids (α-helix→β-sheet) changes, significant changes in the fractal descriptor Dtot, in the calculation of which all the atoms of the molecule are used, are not observed. However, the more specific descriptors Dval, Dvdw and Dunb, which reflect the aggregate of valence-coupled, van der Waals contact and unbound atoms, respectively, are more sensitive to the conformational transition. The increase Dval, Dvdw and the decrease Dunb values were established for a series of 7 amino acids.


2004 ◽  
Vol 22 (SI - Chem. Reactions in Foods V) ◽  
pp. S109-S112
Author(s):  
R. Kubec ◽  
M. Hrbáčová ◽  
R. A Musah ◽  
J. Velíšek

Precursors involved in the formation of pink and green-blue pigments during onion and garlic processing, respectively, have been studied. It has been confirmed that the formation of both pigments is of a very similar nature, with (E)-S-(1-propenyl)cysteine sulfoxide (isoalliin) serving as the primary precursor. Upon disruption of the tissue, isoalliin and other S-alk(en)ylcysteine sulfoxides are enzymatically cleaved, yielding prop-1-enylcontaining thiosulfinates [CH<sub>3</sub>CH = CHS(O)SR; R = methyl, allyl, propyl, 1-propenyl], among others. The latter compounds subsequently react with amino acids to produce the pigments. Whereas the onion and leek-related propyl, prop-1-enyl and methyl derivatives can form pink, pink-red and magenta compounds, those containing the allyl group yield dark blue products after reacting with glycine at pH 5.0.


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