Search results for "Isoindole"
showing 10 items of 83 documents
The Reactivity of 4’-Substituted Spiro[Isoindole-1,3’-pyrazoles] Derivatives: Substitution/Elimination Reactions and Access to Biaryl Derivatives
2017
This paper describes aspects of the chemistry of 4’-substituted spiro [indole-1,3’-pyrazoles]. These compounds underwent substitution and/or elimination reactions to afford some new spiro- as well as biaryl derivatives of potential pharmaceutical relevance. Mechanistic considerations are discussed as well.
2-(2-Iodoethyl)isoindole-1,3-dione
2007
The title compound, C10H8INO2, is an N-substituted phthalimide derivative in which the crystallographic intermolecular contact pattern consists of I⋯I, C—H⋯I, C—H⋯O and aromatic π–π interactions.
A novel pro-apoptotic role of zinc octacarboxyphthalocyanine in melanoma me45 cancer cell's photodynamic therapy (PDT)
2018
Abstract Zn-based phthalocyanine acts as drug or photosensitizer in photodynamic therapy (PDT) for the treatment of cancer cells. The activated zinc octacarboxyphthalocyanine (ZnPcOC) reacts with oxygen, to generate reactive oxygen species for the damage of melanoma cancer cells, Me45. This in vitro study aimed at investigating the cytotoxic effects of different concentrations of ZnPcOC activated with a diode laser (λ = 685 nm) on Me45, and normal human fibroblast cells, NHDF. To perform this study 104 cells/ml were seeded in 96-well plates and allowed to attach overnight, after which cells were treated with different concentrations of ZnPcOC (10, 20 and 30 μM). After 4 h, cells were irradi…
Hypoxia-induced dysfunction of rat diaphragm
2004
Contains fulltext : 47331.pdf (Publisher’s version ) (Closed access) Oxidants may play a role in hypoxia-induced respiratory muscle dysfunction. In the present study we hypothesized that hypoxia-induced impairment in diaphragm contractility is associated with elevated peroxynitrite generation. In addition, we hypothesized that strenuous contractility of the diaphragm increases peroxynitrite formation. In vitro force-frequency relationship, isotonic fatigability, and nitrotyrosine levels were assessed under hypoxic (Po(2) approximately 6.5 kPa) and hyperoxic (Po(2) approximately 88.2 kPa) control conditions and also in the presence of authentic peroxynitrite (60 min), ebselen (60 min), and t…
Aza-isoindolo and isoindolo-azaquinoxaline derivatives with antiproliferative activity
2015
Abstract Three new ring systems, pyrido[2′,3′:3,4]pyrrolo[1,2- a ]quinoxalines, pyrido[3′,2′:3,4]pyrrolo[1,2- a ]quinoxalines and pyrido[2′,3′:5,6]pyrazino[2,1- a ]isoindoles, were synthesized through an aza-substitution on the already active isoindolo-quinoxaline system and in particular in the position 7 or 4 of the isoindole moiety and in position 5 of the quinoxaline portion. All new compounds were screened by the National Cancer Institute (Bethesda, MD) against a panel of 60 human tumor cell lines. Biological results of the most active derivatives, with pGI 50 values between 7.09 and 7.27, confirmed the importance of the presence of methoxy substituents for biological activity. The ant…
CCDC 263681: Experimental Crystal Structure Determination
2005
Related Article: D.Schollmeyer, R.Hoffmann, J.Mattay|2005|Acta Crystallogr.,Sect.E:Struct.Rep.Online|61|o290|doi:10.1107/S1600536805000140
CCDC 1547096: Experimental Crystal Structure Determination
2018
Related Article: Himadri Sekhar Sarkar, Sujoy Das, Kari Rissanen, Prithidipa Sahoo|2017|Anal.Chem.|89|13054|doi:10.1021/acs.analchem.7b04430
CCDC 831724: Experimental Crystal Structure Determination
2013
Related Article: B.Maggio, D.Raffa, M.V.Raimondi, F.Plescia, M.L.Trincavelli, C.Martini, F.Meneghetti, L.Basile, S.Guccione, G.Daidone|2012|Eur.J.Med.Chem.|54|709|doi:10.1016/j.ejmech.2012.06.028
CCDC 1969794: Experimental Crystal Structure Determination
2019
Related Article: L. Tapmeyer, M. Beske, J. Plackmeyer|2019|IUCrData|4|x191629|doi:10.1107/S2414314619016298
CCDC 930310: Experimental Crystal Structure Determination
2013
Related Article: Aaron Breivogel, Michael Meister, Christoph Förster, Frédéric Laquai, Katja Heinze|2013|Chem.-Eur.J.|19|13745|doi:10.1002/chem.201302231