Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Adriano Guiotto"'
Publikováno v:
Clinical chemistry and laboratory medicine. 54(11)
Background: The quality performance and the comparability between results of pharmacies point-of-care-testing (POCT) and institutional laboratories have been evaluated. Methods: Eight pharmacies participated in the project: a capillary specimen colle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6085fe1e8b635c26fb63ae65cbecc43a
https://pubmed.ncbi.nlm.nih.gov/27197133
https://pubmed.ncbi.nlm.nih.gov/27197133
Publikováno v:
Arzneimittelforschung. 56:707-713
1,4,6,8-Tetramethyl-2H-furo[2,3-h]quinolin-2-one (FQ) belongs to a series of furocoumarin isosters, designed to obtain new drugs for photochemotherapy. The objective of this study was to characterize the disposition of orally administered 3 H-FQ in n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed0d61f19231bc2fedf5e852a8443141
https://doi.org/10.1055/s-0031-1296777
https://doi.org/10.1055/s-0031-1296777
Publikováno v:
ChemMedChem. 6:996-1000
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e2e4725b3576d37188dbd78fd345c03
https://doi.org/10.1002/cmdc.201100041
https://doi.org/10.1002/cmdc.201100041
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:1197-1204
A new series of benzo[h]quinazoline and benzo[f]quinazoline derivatives was prepared and studied for the biological activity. The compounds carrying a dimethylaminoethyl side chain (6c, 8c and 12) inhibit cell growth. The ability to form a molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::545649a1d86f4377ebed72c237fc3011
https://doi.org/10.1016/j.bmc.2010.12.037
https://doi.org/10.1016/j.bmc.2010.12.037
Autor:
Adriano Guiotto, Vera Barbieri, P. Manzini, Giovanni Pastorini, Giovanni Marzaro, Adriana Chilin, Samuele Zanatta
Publikováno v:
Tetrahedron. 62:12351-12356
A new synthetic pathway to quinazolines is described. This new method uses hexamethylenetetramine in TFA and potassium ferricyanide in aqueous ethanolic KOH, starting from simple N-protected anilines. The method affords substituted quinazolines with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::138c71b3f1a6c214b5d11031560db22a
https://doi.org/10.1016/j.tet.2006.09.103
https://doi.org/10.1016/j.tet.2006.09.103
Publikováno v:
Bioorganic & Medicinal Chemistry. 11:1311-1318
4-Hydroxymethyl-1,6,8-trimethylfuro[2,3-h]quinolin-2(1H)-one (HOFQ) was prepared by a new profitable way, which allowed to synthesize also 4-methoxymethyl-1,6,8-trimethylfuro[2,3-h]quinolin-2(1H)-one (MOFQ), and 4-hydroxymethyl-6,8-dimethylfuro[2,3-h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f90900f3dbe9e1f9c7f104bd002adc0
https://doi.org/10.1016/s0968-0896(02)00618-1
https://doi.org/10.1016/s0968-0896(02)00618-1
Publikováno v:
Scopus-Elsevier
RCM. Rapid communications in mass spectrometry 17 (2003): 2781–2787.
info:cnr-pdr/source/autori:Basso E., Chilin A., Guiotto A., Traldi P./titolo:Electrospray Mass Spectrometry in the Differentiation of Some Isomeric Trimethylfurocoumarins/doi:/rivista:RCM. Rapid communications in mass spectrometry/anno:2003/pagina_da:2781/pagina_a:2787/intervallo_pagine:2781–2787/volume:17
RCM. Rapid communications in mass spectrometry 17 (2003): 2781–2787.
info:cnr-pdr/source/autori:Basso E., Chilin A., Guiotto A., Traldi P./titolo:Electrospray Mass Spectrometry in the Differentiation of Some Isomeric Trimethylfurocoumarins/doi:/rivista:RCM. Rapid communications in mass spectrometry/anno:2003/pagina_da:2781/pagina_a:2787/intervallo_pagine:2781–2787/volume:17
Electrospray mass spectrometry (ES-MS) was successfully employed for the structural differentiation of six isomeric trimethylfurocoumarins of possible pharmaceutical interest. Two different approaches were employed. The first was based on MSn experim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9179e4fd8ccbb0aae29199270e63c780
https://doi.org/10.1002/rcm.1260
https://doi.org/10.1002/rcm.1260
Publikováno v:
Rapid Communications in Mass Spectrometry. 12:1827-1830
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e00c9defbf12ac6bb6a1f9d57a470c5
https://doi.org/10.1002/(sici)1097-0231(19981130)12:22<1827::aid-rcm382>3.0.co
https://doi.org/10.1002/(sici)1097-0231(19981130)12:22<1827::aid-rcm382>3.0.co
Publikováno v:
Photochemistry and Photobiology. 67:628-634
A study of dark interaction and photoreaction between 4,6-dimethyltetrahydrobenzoangelicin (THBA) and DNA is described. 4,6-Dimethyltetrahydrobenzoangelicin is a furocoumarin derivative in which 4' and 5' carbons are linked by a four-methylene bridge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::111ca63f0891f8be64812d06e25ce0cd
https://doi.org/10.1111/j.1751-1097.1998.tb09104.x
https://doi.org/10.1111/j.1751-1097.1998.tb09104.x
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87fd9215e7880bc0360e6f3a965e77c5
https://doi.org/10.1055/s-1998-2024
https://doi.org/10.1055/s-1998-2024