Zobrazeno 1 - 10
of 39
pro vyhledávání: '"G, Quadro"'
Autor:
P Lissoni, S Barni, G Tancini, A Ardizzoia, G Ricci, R Aldeghi, F Brivio, E Tisi, F Rovelli, R Rescaldani, G Quadro, G Maestroni
Publikováno v:
British Journal of Cancer
Our previous experimental studies have shown that the best approach to increase the biological anti-tumour activity of interleukin 2 (IL-2) is not co-administration of another cytokine, but the association with immunomodulating neurohormones, in an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::670dccf833bf74fea2329b0f8dcfbc2f
https://pubmed.ncbi.nlm.nih.gov/8286206
https://pubmed.ncbi.nlm.nih.gov/8286206
Publikováno v:
Journal of Neurochemistry. 42:1762-1766
N-Pivaloyl-leucyl-gamma-aminobutyric acid (PLG) is a synthetic dipeptide with a partition coefficient of 1.67 in an ethyl acetate/water system that partially inhibits the synaptosomal uptake and activates the release of [U-14C]gamma-aminobutyric acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::466df06035a5e412a230c8e2343cc776
https://doi.org/10.1111/j.1471-4159.1984.tb12769.x
https://doi.org/10.1111/j.1471-4159.1984.tb12769.x
Pharmacokinetics and in vitro Effects of a 4-Aminobutyric Acid Derivative with Anticonvulsant Action
Publikováno v:
Pharmacology. 27:237-240
N-trimethyl-acetyl-4-aminobutyric acid, called PG2, is a new anticonvulsant acting as a 4-aminobutyric acid (GABA) pro-drug. The stimulatory effect of PG2 on synaptosomal 14C-GABA release and its inhibitory effect of synaptosomal 14C-GABA uptake were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa4ed8e09682c6b584965bd534fc6cd
https://doi.org/10.1159/000137876
https://doi.org/10.1159/000137876
Publikováno v:
Agressologie: revue internationale de physio-biologie et de pharmacologie appliquees aux effets de l'agression. 22(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::197fe1bbb363f90c48b9855adecc727e
https://pubmed.ncbi.nlm.nih.gov/7294295
https://pubmed.ncbi.nlm.nih.gov/7294295
Compound YS 035 [NN-bis-(3,4-dimethoxyphenethyl)-N-methylamine] is a new synthetic compound capable of inhibiting Ca2+ uptake by different cells. The inhibition of Ca2+ uptake by muscle cells isolated from chicken embryo is dose-dependent in the comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9285f6c10453a05ab72afe40eb956a4
https://europepmc.org/articles/PMC1153421/
https://europepmc.org/articles/PMC1153421/
Publikováno v:
Journal of chromatography. 343(1)
Analytical conditions that allow bencyclane, a vasodilator, to be evaluated in biological samples for pharmacokinetic and bioavailability investigations are reported. Two gas chromatographic methods were developed, one employing a flame-ionization de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde0818d8aa2159a81b98228e4c35d97
https://pubmed.ncbi.nlm.nih.gov/4066863
https://pubmed.ncbi.nlm.nih.gov/4066863
Publikováno v:
Arzneimittel-Forschung. 33(2)
2-(4-(2',4'-Difluorophenyl)-phenoxy)propionic acid (MR 714) is endowed with an interesting analgesic and antiinflammatory activity, while any remarkable gastro-ulcerogenic action is virtually absent. From a toxicological point of view, MR 714 orally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee74c461965c5b4ef9d4c44c5d7d5e75
https://pubmed.ncbi.nlm.nih.gov/6342626
https://pubmed.ncbi.nlm.nih.gov/6342626
Publikováno v:
Journal of chromatography. 272(1)
Extractive alkylation was carried out on fenquizone, a sulphonamide diuretic, in order to devise a suitable method for its determination in pharmacokinetic and bioavailability studies. After extraction as a tetramethyl derivative, fenquizone was eval
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e39632e81c60236daae5efd99f167b6c
https://pubmed.ncbi.nlm.nih.gov/6841550
https://pubmed.ncbi.nlm.nih.gov/6841550
Publikováno v:
Arzneimittel-Forschung. 31(10)
Apovincaminic acid (AVA) esters are eburnamenine derivatives with a vasodilating action that are mainly metabolized to AVA by enzymatic hydrolysis, in the rat in particular. In an organic solvent/water partition, AVA and AVA ester were quantitatively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30e92b6728fe6a9dc7c90c031395d897
https://pubmed.ncbi.nlm.nih.gov/7198444
https://pubmed.ncbi.nlm.nih.gov/7198444
Autor:
G. Quadro
Publikováno v:
Drugs of the Future. 7:114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f17ec5597c7c5abc2485aa676f5f6616
https://doi.org/10.1358/dof.1982.007.02.998228
https://doi.org/10.1358/dof.1982.007.02.998228