Enzymatic and spectroscopic studies on the activation or inhibition effects by substituted phenolic compounds in the oxidation of aryldiamines and catechols catalyzed by Rhus vernicifera laccase

2006 ◽  
Vol 100 (12) ◽  
pp. 2127-2139 ◽  
Author(s):  
Luigi Casella ◽  
Michele Gullotti ◽  
Enrico Monzani ◽  
Laura Santagostini ◽  
Giorgio Zoppellaro ◽  
...  
FEBS Letters ◽  
1981 ◽  
Vol 136 (1) ◽  
pp. 80-84 ◽  
Author(s):  
L. Avigliano ◽  
J.L. Davis ◽  
M.T. Graziani ◽  
A. Marchesini ◽  
W.B. Mims ◽  
...  

Biochemistry ◽  
1997 ◽  
Vol 36 (16) ◽  
pp. 4852-4859 ◽  
Author(s):  
Sarra Gaspard ◽  
Enrico Monzani ◽  
Luigi Casella ◽  
Michele Gullotti ◽  
Silvana Maritano ◽  
...  

1976 ◽  
Vol 31 (4) ◽  
pp. 495-499 ◽  
Author(s):  
Farid S. G. Soliman ◽  
Thomas Kappe

Condensation of β-aminocrotononitrile (2 a) with 4-hydroxycoumarin (1 a, X = O, R = R2 = H, R1 = OH) afforded the tricyclic compound 7 and the bicyclic compound 11a from 4-hydroxy-6-methyl-2-pyrone (4). Analogous compounds could not be obtained from 4-hydroxy-6-methyl-2-pyridone (5) or 4-hydroxycarbostyril (6) due to the failure of the resulting condensation products 12a and 13, respectively to undergo intramolecular cyclization. The structures assigned to 7, 11a, 12a, 18, as well as to 5-cyano-4,6-dimethyl-2-pyridone (14), obtained by self-condensation of β-aminocrotononitrile, were substantiated by spectroscopic studies.


1979 ◽  
Vol 101 (17) ◽  
pp. 5038-5046 ◽  
Author(s):  
David M. Dooley ◽  
Jill Rawlings ◽  
John H. Dawson ◽  
Philip J. Stephens ◽  
Lars-Erik Andreasson ◽  
...  

Biochemistry ◽  
1984 ◽  
Vol 23 (2) ◽  
pp. 241-247 ◽  
Author(s):  
R. Max Wynn ◽  
David B. Knaff ◽  
Robert A. Holwerda

Author(s):  
Sulieman Ahmed Gasim El Said ◽  
Hatil Hashim EL-Kamali ◽  
Yousra Omer EL-Desogi

Two Ficus species that are commonly used in Sudanese Traditional Medicine for the management of various ailments were screened for their phytochemical groups using chemical reagent and Thin Layer Chromatography. Qualitative phytochemical tests were used to detect the presence of flavonoids, saponins, tannins, alkaloids, phenolic compounds and anthraquinones. Six compounds from F. benegalensis and seven from F. sycomorus quenching were reported from the various parts of these two plants. However , more number of compounds were found in the leaves. The data generated from this study have provided the chemical basis for wide use of F. sycomorus as therapeutic agent for treating various ailments. However, there is need to further carry out advanced hyphenated spectroscopic studies in order to elucidate the structure of these compounds. Furthermore, this data may be handy in probing of biochemistry of this plant in the future.


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