Zobrazeno 1 - 10
of 13
pro vyhledávání: '"F C, Pizzimenti"'
Autor:
C. Zappala, Gabbrielli G, Maria Gabriella Vigorita, Rosanna Maccari, Rosaria Ottanà, F. C. Pizzimenti
Publikováno v:
ChemInform. 26
Autor:
Maria Gabriella Vigorita, Rosanna Maccari, Rosaria Ottanà, C. Zappala, Gabbrielli G, F. C. Pizzimenti
Publikováno v:
ChemInform. 27
Publikováno v:
The new microbiologica. 26(1)
The antiherpes virus-1 and genotoxic activities of diethyl ether extract from flowering tops of Helichrysum italicum (Compositae) were investigated. The extract showed significant antiviral activity at concentrations ranging from 400 to 100 microg/ml
Publikováno v:
The new microbiologica. 22(2)
Wild, pigmented strains of Serratia marcescens and their non-pigmented mutants were compared on the basis of fatty acid profiles and lipid content. Classic biochemical tests show only minor differences, as well as fatty acid ratio C18:C16. The total
Publikováno v:
Bollettino chimico farmaceutico. 137(7)
Various kinds of lipophilic analogues of isonicotinic acid hydrazide (Isoniazid) were synthesized and in vitro explored in a search for antimycobacterial agents with extended activity spectrum against pathogens responsible for the AIDS-associated dis
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 50(11)
The 5-aryl-4-methyl-2-(4-pyridyl)-delta 2-1,3,4-oxadiazolines 3, previously synthesized along with isomer 4-aryl-1-methoxy-1-(4-pyridyl)-2,3-diaza-1,3-butadienes 2 from benzaldehyde isonicotinoylhydrazones and diazomethane, were tested for in vitro a
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 49(12)
As part of a research directed to the synthesis of novel isoniazid derivatives with potential activity on mycobacteria and HIV virus, the acetophenone-isonicotinoylhydrazones 3 and the 4-aryl-1-methoxy-1-(4-pyridyl)- 2,3-diaza-1,3-butadienes 5, obtai
Publikováno v:
Il Farmaco; edizione scientifica. 42(10)
The synthesis, antimicrobial and antitumor activities of new N,N'-substituted-2,5-dioxopiperazine derivatives are reported. The biological investigation showed that only the compounds containing the 5-nitrofurylidene moiety were active against some b
Publikováno v:
Chemischer Informationsdienst. 17