Zobrazeno 1 - 10
of 274
pro vyhledávání: '"D, Vedaldi"'
Publikováno v:
Photochemistry and photobiology. 68(4)
We describe the synthesis of a novel psoralen peroxide 1 that generates on irradiation (350 nm) alkoxyl radicals, namely tert-butoxyl radicals, as confirmed by electron spin resonance studies with the spin trap 5,5-dimethyl-pyrroline-N-oxide. The rad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2af27a0a13647fa49d672a2bcf402c8
https://pubmed.ncbi.nlm.nih.gov/9796433
https://pubmed.ncbi.nlm.nih.gov/9796433
Psoralen was found to form an inclusion complex with beta-cyclodextrin (beta CD), heptakis(2,6-di-O-methyl)-beta-cyclodextrin (DM beta CD) and hepatakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TM beta CD). Phase solubility studies revealed the formati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f47dc7c5c144508090751df381214311
http://hdl.handle.net/11577/2512463
http://hdl.handle.net/11577/2512463
Autor:
D, Vedaldi, S, Frank, A, Pozzan, G, Miolo, F, Dall'Acqua, S, Caffieri, P, Rodighiero, A, Guiotto
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 49(10)
Pyrroloquinolinones, furocoumarin analogues, contain a divinilbenzene moiety, suggesting possible photoreactivity. Quantum mechanics calculations indicate that the pyrrole-side double bond exhibits strong photoreactivity, while the pyridone-side doub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e296583be12a4c7105c306f861816598
https://pubmed.ncbi.nlm.nih.gov/7826467
https://pubmed.ncbi.nlm.nih.gov/7826467
Autor:
D, Vedaldi, S, Caffieri, G, Miolo, F, Dall'Acqua, F, Baccichetti, A, Guiotto, F, Benetollo, G, Bombieri, G, Recchia, M, Cristofolini
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 46(12)
New bioisoters of psoralen, obtained by replacing carbon 8 of the central benzene ring with a nitrogen, were studied from the photochemical, photobiological and phototherapeutic points of view. In particular, 4,4'-, 4',5'-dimetyl, 4,4',5'-trimethyl a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d30f772f5baecd0d0aa0434ff1542324
https://pubmed.ncbi.nlm.nih.gov/1821628
https://pubmed.ncbi.nlm.nih.gov/1821628
Autor:
D, Vedaldi, F, Dall'Acqua, F, Baccichetti, F, Carlassare, F, Bordin, P, Rodighiero, P, Manzini, A, Guiotto
The effect of the introduction of one, two or three methyl groups at the level of 3,4 or 4',5' photoreactive site of angelicin, in terms of extent of intercalation and DNA-photobinding, was studied. The introduction of one methyl group both in the 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::12578b4494c465eba800d8690d43ce63
http://hdl.handle.net/11577/2512411
http://hdl.handle.net/11577/2512411
Publikováno v:
Toxicology Letters. 95:45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::299e6725391d2d34ee31e4f7b7ac9cfe
https://doi.org/10.1016/s0378-4274(98)80178-1
https://doi.org/10.1016/s0378-4274(98)80178-1
Publikováno v:
Melanoma Research. 4:34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac8a2dedeac6494276a70e908c01805a
https://doi.org/10.1097/00008390-199409001-00067
https://doi.org/10.1097/00008390-199409001-00067
Publikováno v:
Photochemistry and Photobiology. 33:261-264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::621904a1a665a9058ac38c16adaf8c45
https://doi.org/10.1111/j.1751-1097.1981.tb05335.x
https://doi.org/10.1111/j.1751-1097.1981.tb05335.x
Autor:
F, Dall'Acqua, D, Vedaldi, F, Bordin, F, Baccichetti, F, Carlassare, M, Tamaro, P, Rodighiero, G, Pastorini, A, Guiotto, G, Recchia, M, Cristofolini
Publikováno v:
Journal of Medicinal Chemistry. 26:870-876
Three derivatives of angelicin (1) [4'-methyl-, 4,4'-dimethyl-, and 4',5-dimethylangelicin (2a-c)] have been prepared with the aim of obtaining new agents for the photochemotherapy of psoriasis. These compounds form a complex in the dark with DNA tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ca73c3c2cf95f43bde607923e06906
https://doi.org/10.1021/jm00360a016
https://doi.org/10.1021/jm00360a016
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 44:1475-1478
C13H10ClO2NS, Mr = 279.75, monoclinic, P2(1)/a, a = 14.490 (3), b = 22.598 (5), c = 7.336 (2) A, beta = 92.4 (1) degree, U = 2400 (1) A3, Z = 8, D chi = 1.548 g cm-3, lambda(Mo K alpha) = 0.71069 A, mu = 2.07 cm-1, F(000) = 1152, room temperature, R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0aeb216c99124b996517d734817da54
https://doi.org/10.1107/s0108270188004457
https://doi.org/10.1107/s0108270188004457