Zobrazeno 1 - 10
of 45
pro vyhledávání: '"E, Manghisi"'
Autor:
G, Cascio, L, Lorenzi, D, Caglio, E, Manghisi, F, Arcamone, G, Guanti, G, Satta, G, Morandotti, R, Sperning
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 51(3)
New series of monobactam antibiotics, bearing thio-and dithiocarbamate derivatives as C-4 side chain, were synthesized. Some compounds were found to have good antibacterial activity against Gram-negative bacteria.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::419099e79115d198de96fe326f3df097
https://pubmed.ncbi.nlm.nih.gov/8688141
https://pubmed.ncbi.nlm.nih.gov/8688141
Publikováno v:
Il Farmaco; edizione scientifica. 31(6)
A series of new butyrophenones was synthesized, the aim being to reduce neuroleptic activity and enhance the hypotensive effects of this class of drugs. The compounds were screened for toxicity according to the Irwin scheme and tested in anaesthetize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0dd17a1b7a62fbeb87787ee4d5f7c45
https://pubmed.ncbi.nlm.nih.gov/945189
https://pubmed.ncbi.nlm.nih.gov/945189
Autor:
A. SALIMBENI, E. MANGHISI
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb1d2fa424d1788d132237fb84eb86e3
https://doi.org/10.1002/chin.198042186
https://doi.org/10.1002/chin.198042186
Autor:
E, Manghisi, A, Salimbeni
Publikováno v:
Bollettino chimico farmaceutico. 113(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1cee4c210a5c69378c2c6d304980fb3a
https://pubmed.ncbi.nlm.nih.gov/4464903
https://pubmed.ncbi.nlm.nih.gov/4464903
Publikováno v:
Il Farmaco; edizione scientifica. 36(11)
The synthesis and some pharmacological properties of five 2,3-dihydro-3-phenyl-1,4-behzodioxin derivatives (II d-h) are reported. The new compounds generally result more active as local anaesthetics, but less effective as anti-arrhythmic agents than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd5b9c110dba7a0264ad3f90610f9c64
https://pubmed.ncbi.nlm.nih.gov/7308460
https://pubmed.ncbi.nlm.nih.gov/7308460
Publikováno v:
Bollettino chimico farmaceutico. 114(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5197fd69901286f52990f8d83ff2ead
https://pubmed.ncbi.nlm.nih.gov/812540
https://pubmed.ncbi.nlm.nih.gov/812540
Publikováno v:
Il Farmaco; edizione scientifica. 38(8)
A few analogs of the isoxsuprine drug with the phenoxyethyl group incorporated into the heterocyclic 2,3-dihydro-1,4-benzodioxin or 1,3-benzodioxol ring have been synthesized. Among these compounds, the benzodioxol derivative (I e) has been found to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f29acbffd3ee479e2675cb268040e0c3
https://pubmed.ncbi.nlm.nih.gov/6617852
https://pubmed.ncbi.nlm.nih.gov/6617852
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2352b44dbe4bdad40ba82ca292908d9
https://doi.org/10.1002/chin.197532214
https://doi.org/10.1002/chin.197532214
Publikováno v:
Il Farmaco; edizione scientifica. 35(7)
A series of omega-amino-2-hydroxy-p-fluorobutyrophenones have been synthesized to evaluate the influence exerted by a hydroxyl group in alpha-position to the carbonyl on the persistence of their neuroleptic and collateral properties. The new compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d81058632a4d59e5d004415a81074c26
https://pubmed.ncbi.nlm.nih.gov/6108874
https://pubmed.ncbi.nlm.nih.gov/6108874
Publikováno v:
Il Farmaco; edizione scientifica. 30(4)
A series of acyloxy- and alkyloxymethyl esters of meclofenamic, flufenamic and mefenamic acids has been synthesized and its antiinflammatory, analgesic and antipyretic activities have been compared with those of the corresponding acids and the methyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::617717db84f73478b0235eb4d5be9be2
https://pubmed.ncbi.nlm.nih.gov/1183605
https://pubmed.ncbi.nlm.nih.gov/1183605