C. Galeffi
Istituto Superiore di Sanità
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Featured researches published by C. Galeffi.
Tetrahedron | 1982
G. B. Marini Bettolo; M. Patamia; M. Nicoletti; C. Galeffi; I. Messana
Abstract A new glycoside, hypoxoside, was isolated from rhizome of Hypoxis obtusa , a plant used in Mozambique in native medicine for the treatment of urinary diseases. The structure 1 of a diglycoside of 1-(3′,4′-dihydroxyphenyl)-5-(3″,4″-dihydroxyphenyl)-1-penten-4-yne was attributed to hypoxoside on the basis of physico-chemical determinations and chemical behaviour.
Journal of Chromatography A | 1981
G. B. Marini-Bettolo; M. Nicoletti; M. Patamia; C. Galeffi; I. Messana
Abstract The plant kingdom constitutes an invaluable source of new chemical products which may be important due to their biological properties and in particular because of their potential use in medicine. In many countries, mainly in the Tropics, systematic surveys of plants are currently in progress. It is therefore important to have a simple and universal method available for preliminary chemical screening of plants under field conditions. The procedure suggested here is based on the identification in raw plant extracts of some chemical groups of substances (alkaloids, quinones, saponins, polyphenols, anthranoids) by precipitation and colour reactions. To obtain more accurate results, a second stage, based on thin-layer chromatographic separation of extracts of plant material, can be applied. Solvent systems, specific spray reagents and reference substances are proposed. A number of groups of products, including flavonoids, coumarins, cardenolides and steroids can be rapidly identified in plants by this method.
Tetrahedron | 1982
G.B. Marini-Bettolo; M. Nicoletti; Irene Messana; M. Patamia; C. Galeffi; J.U. Oguakwa; G. Portalone; A. Vaciago
Abstract From the bark of Alstonia boonei De Wild (Apocynaceac) a new monoterpenoid δ-lactone 1, named boonein, was isolated. The structure was established by chemical and spectroscopical methods and by X-ray analysis.
Phytotherapy Research | 2001
David Ramanitrahasimbola; Philippe Rasoanaivo; S. Ratsimamanga-Urverg; Elena Federici; Giovanna Palazzino; C. Galeffi; Marcello Nicoletti
The in vivo antiplasmodial activity of voacamine was assessed in a 4‐day test. It was shown to exhibit in vivo activity with 25.4% and 43.4% inhibition of parasitaemia with 2.5 and 10 mg/kg, respectively. In synchronized cultures, it was found to act on trophozoite and schizont stages of Plasmodium falciparum. Using the FMC29 strain of Plasmodium falciparum as parasite and the isobologram curve as a method to assess interaction in drug combination, it was shown to lack any chloroquine‐enhancing activity and its in vitro antiplasmodial effect was not potentiated by the chemosensitizer malagashanine. Copyright
Tetrahedron | 1985
G. B. Marini-Bettolo; M. Nicoletti; Irene Messana; C. Galeffi; J. D. Msonthi; W. A. Chapya
Abstract From rhizome of Hypoxis nyasica two diglucosides were isolated: hypoxoside, (1), and a new one, the 0,0-β,β-di-D-glu- copyranoside of 1-(4 - hydroxyphenyl)-3-(4 - hydroxyphenyl)-1,4-pen- tadiene, (2), named nyasoside.
Phytochemistry | 1997
C. Galeffi; Philippe Rasoanaivo; Elena Federici; Giovanna Palazzino; Marcello Nicoletti; Benoît Rasolondratovo
Abstract From the root bark of Millettia pervilleana , which showed high cytotoxic activity, two prenylated isoflavanones were isolated. Their structures were determined by means of chemical and spectroscopic properties to be (3 R )-2′,7-dihydroxy-3′,4′-dimethoxy-5′- α , α -dimethylallylisoflavanone, named pervilleanone, and its 3′- O -demethyl derivative.
Phytochemistry | 2000
Giovanna Palazzino; C. Galeffi; Elena Federici; Franco Delle Monache; Maria Francesca Cometa; Maura Palmery
From the rhizomes of Curculigo pilosa, two benzylbenzoate diglucosides, piloside A and piloside B, and a glucosyl-fused norlignan, pilosidine, previously obtained only as the tetra-O-methyl derivative, were isolated. Pilosidine showed facilitating effect on adrenaline evoked contractions in rabbit aorta isolated preparations.
Phytochemistry | 1986
Hawa Abdullahi; E. Nyandat; C. Galeffi; I. Messana; M. Nicoletti; G. B. Marini Bettolo
Abstract From the stems of Halleria lucida a new 1,4-yclohexandiol, a tranS -1-(2′-hydroxyethyl)cyclohexan-1,4-diol named isorengyol, together with the known cis isomer rengyol, was isolated. The leaves of the same plant contain acteoside, rutin, luteolin-5- O -glucoside and a 4-hydroxy-4-(2′-hydroxyethyl)cyclohexanone, of which the hemiketalic tautomer has recently been described.
Phytochemistry | 1982
S. Woodhead; C. Galeffi; G. B. Marini Bettolo
Abstract p-Hydroxybenzaldehyde is present in concentrations up to 30% in the wax of Sorghum bicolor seedlings. It is highly deterrent to locusts, reducing their normal feeding by 90%.
Phytochemistry | 1980
G. B. Marini-Bettolo; C. Galeffi; Marcello Nicoletti; Irene Messana
Abstract A new corynantheine-type alkaloid, strychnorubigine, was identified from root bark of Strychnos rubiginosa D.C. 11-Methoxydiaboline and normacusine B were also isolated and the 13 C NMR spectral data of their O -acetyl derivatives are reported.