Zobrazeno 1 - 10
of 66
pro vyhledávání: '"C, Passarotti"'
Publikováno v:
IJCoL, Vol 10, Iss 1 (2024)
The article presents the process of linking the Dictionary of Medieval Latin in the Czech Lands to the LiLa Knowledge Base, which adopts the Linked Data paradigm to make linguistic resources for Latin interoperable. First, we provide an overview of t
Externí odkaz:
https://doaj.org/article/c39334c4fec043c1b40960038ca1f0f8
Publikováno v:
IJCoL, Vol 2, Iss 2, Pp 31-49 (2016)
Different lexical resources may pursue different views on lexical meaning. However, all of them deal with lexical items as common basic components, which are described according to criteria that may vary from one resource to another. In this paper, w
Externí odkaz:
https://doaj.org/article/ad8b89c336ed49ee99e6f4679f195db1
Autor:
C, Passarotti
Publikováno v:
Bollettino chimico farmaceutico. 143(4)
Publikováno v:
Bollettino chimico farmaceutico. 130(8)
Within a plan of researches concerning drugs with anti-ulcer activity, a series of 5-azaflavones has been prepared. In this first communication we report the relevant synthesis obtained by cyclization of appropriate beta-diketones in HCOOH at the boi
Publikováno v:
International journal of tissue reactions. 13(1)
In previous studies we have shown that ibuprofen, guaiacol and the guaiacol ester of ibuprofen (I.N.N. metoxibutropate) are able to inhibit in-vitro prostaglandin synthesis. In the present study we have evaluated the effect of ibuprofen, guaiacol and
Publikováno v:
Bollettino chimico farmaceutico. 130(1)
During a search on PG-like compounds as antiulcer drugs we synthetized some hetherocyclic derivatives. Some compounds of this series were found to be effective after oral administration in inhibiting restraint induced ulcers in the rat. Three of the
Publikováno v:
Bollettino chimico farmaceutico. 129(7-8)
We report the results of the in vitro-release of the active ingredients (flurbiprofen and ibuprofen) from dermal form obtained by the Sartorius Absorption simulator SM16750. The results show that the choice of the excipients is basic. Using NSAID, th
Publikováno v:
Bollettino chimico farmaceutico. 129(5)
Preparation of (15 S)-hydroxy derivative (1-b), a key intermediate in the synthesis of PG like compounds, by reduction the corresponding enone (2), is described. High yields in (S)-isomer was obtained by means of chiral phase-transfer catalyst: (-)-N
Autor:
Joaquim F.A. Claro, Katia R. M. Leite, Enrico F m Andrade, Mario Paranhos, Miguel Srougi, Carlo C. Passarotti, Valdemar Ortiz
Publikováno v:
Journal of Urology. 173:459-459
Autor:
G, Doria, C, Passarotti, R, Sala, R, Magrini, P, Sberze, M, Tibolla, A, Buttinoni, M, Ferrari, L, Tremolada
Publikováno v:
Il Farmaco; edizione scientifica. 40(11)
A series of 7-oxo-1H,7H-pyrazolo[1,5-a]pyrimidine-6-N-pyridylcarboxamides was synthesized and assayed in the carrageenin-induced paw oedema test in the rat. Some compounds showed moderate antiinflammatory activity.