Effect of hydrolipophilic equilibrium of the muramyl dipeptide derivatives on their internalization and interactions in biological membranes

1996 ◽  
Vol 122 (6) ◽  
pp. 1219-1221
Author(s):  
O. V. Kalyuzhin ◽  
B. B. Fuks

1992 ◽  
Vol 114 (6) ◽  
pp. 1838-1841
Author(s):  
A. �. Medvedev ◽  
B. B. Fuks ◽  
N. V. Bovin ◽  
A. E. Zemlyakov


1981 ◽  
Vol 12 (4) ◽  
Author(s):  
S. KOBAYASHI ◽  
T. FUKUDA ◽  
H. YUKIMASA ◽  
I. IMADA ◽  
M. FUJINO ◽  
...  


1982 ◽  
Vol 13 (10) ◽  
Author(s):  
T. FUKUDA ◽  
S. KOBAYASHI ◽  
H. YUKIMASA ◽  
S. TERAO ◽  
M. FUJINO ◽  
...  


1994 ◽  
Vol 49 (5) ◽  
pp. 702-716 ◽  
Author(s):  
Jochen Tschakert ◽  
Wolfgang Voelter

New muramyl dipeptide derivatives with exchanged carbohydrate residues are described. Each derivative is synthesized via a solid phase synthesis using an aminomethyl anchor resin. All synthetic products can be isolated in good yields. Their biological activities are tested by the luminol-dependent chemiluminescence associated with the phagocytosis of opsonized zymosan by granulocytes.



1981 ◽  
Vol 29 (8) ◽  
pp. 2215-2221 ◽  
Author(s):  
TSUNEHIKO FUKUDA ◽  
SHIGERU KOBAYASHI ◽  
HIDEFUMI YUKIMASA ◽  
ISUKE IMADA ◽  
MASAHIKO FUJINO ◽  
...  


1985 ◽  
Vol 47 (3) ◽  
pp. 665-669 ◽  
Author(s):  
K Nishimura ◽  
H Okumura ◽  
I Saiki ◽  
H Okuyama ◽  
I Azuma


Author(s):  
Magdalena Wysocka ◽  
Krystyna Dzierzbicka ◽  
Beata Krawczyk

Search for new and efficient antibiotic is crucial because of microbial drug resistance and problems with side effects of the administered medication. In this study, we evaluate the in vitro microbiological activity of muramyl dipeptide derivatives, retro-tuftsin derivatives (i.e., tuftsin with reversed amino acid sequences), and combinations of retro-tuftsin derivatives with substituted anthraquinones. The potency of the investigated derivatives towards methicillin-sensitive Staphylococcus aureus (MSSA), methicillin-resistant Staphylococcus aureus (MRSA), Pseudomonas aeruginosa, Escherichia coli, and Klebsiella pneumoniae ESBL (extended-spectrum β-lactamases) was compared based on the spectroscopically-measured minimal inhibitory concentrations (MIC values). The bacterial growth have also been studied with different concentrations of compounds. Statistical analysis of the results revealed that certain modifications lead to promising activity against S. aureus (anthraquinone analogue – 3c and retro-tuftsin derivative – 2b), while other derivatives exhibit activity against P. aeruginosa (muramyl dipeptide derivative – 1d and retro-tuftsin derivative – 2b). The obtained results of microbiological activity indicate that the structure of the tested compounds may be the basis for further modifications.



1994 ◽  
Vol 117 (5) ◽  
pp. 508-512 ◽  
Author(s):  
O. V. Kalyuzhin ◽  
B. B. Fuks ◽  
N. V. Bovin ◽  
A. E. Zemlyakov ◽  
V. Ya. Chirva


1979 ◽  
Vol 76 (12) ◽  
pp. 6557-6561 ◽  
Author(s):  
L. Chedid ◽  
M. Parant ◽  
F. Parant ◽  
F. Audibert ◽  
F. Lefrancier ◽  
...  


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