نتایج جستجو برای: triazene derivatives

تعداد نتایج: 105028  

Journal: :Acta Crystallographica Section E Structure Reports Online 2008

Journal: :The Journal of pharmacology and experimental therapeutics 1999
E Alvino R Pepponi E Pagani P M Lacal C Nunziata E Bonmassar S D'Atri

Temozolomide (TMZ) is a new cytotoxic triazene compound of clinical interest that is able to generate methyl adducts at the O(6)-guanine of DNA, which can be repaired by O(6)-alkylguanine-DNA alkyltransferase (OGAT). It was previously found that triazene compounds are highly immunosuppressive in mice. In the present study, we investigate whether TMZ could affect immune functions of human compet...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2014
mahmood payehghadr homa shafiekhani ali reza sabouri abdoll mohammad attaran mohammad kazem rofouei

a facile and highly efficient method have been developed for the preconcentration of the mercury content in crude oil and gasoline samples after digestion with microwave-assisted digestion. octadecyl silica membrane disk has been modified by the recently synthesized triazene ligand, (e)-1-(2-ethoxyphenyl)-3-(4-nitrophenyl) triaz-1-ene (ent), then the modified membrane was used for the preconcen...

2017
Ornella Franzese Francesco Torino Maria Pia Fuggetta Angelo Aquino Mario Roselli Enzo Bonmassar Anna Giuliani Stefania D’Atri

More than 40 years ago, we discovered that novel transplantation antigens can be induced in vivo or in vitro by treating murine leukemia with dacarbazine. Years later, this phenomenon that we called "Chemical Xenogenization" (CX) and more recently, "Drug-Induced Xenogenization" (DIX), was reproduced by Thierry Boon with a mutagenic/carcinogenic compound (i.e. N-methyl-N'-nitro-N-nitrosoguanidin...

Journal: :Biological & pharmaceutical bulletin 2000
H Takahashi T Ishioka Y Koiso M Sodeoka Y Hashimoto

Substituted phenylazo and phenylazoxy compounds were systematically prepared and their anti-androgenic activity was measured in terms of (1) the growth-inhibiting effect on an androgen-dependent cell line, SC-3, and (2) the binding affinity to nuclear androgen receptor. Generally, azo/azoxy compounds showed cell toxicity, and the growth-inhibiting effects on SC-3 cells correlated with the toxic...

2006
Dheeraj Singaraju René Vidal

We propose a closed form solution for segmenting mixtures of 2-D translational and 2-D affine motion models directly from the image intensities. Our approach exploits the fact that the spatial-temporal image derivatives generated by a mixture of these motion models must satisfy a bi-homogeneous polynomial called the multibody brightness constancy constraint (MBCC). We show that the degrees of t...

2010
Karel G. von Eschwege Annemarie Kuhn

The crystal structure of the title compound, (C(6)F(5))(2)N(3)H, is stabilized by N-H⋯N hydrogen bonding, forming centrosymmetric dimers organized in a herringbone motif. Important geometrical parameters are N-N = 1.272 (2) and 1.330 (2) Å and N-N-N = 112.56 (15)°. The dihedral angle between C(6)F(5) groups is 21.22 (9)°. The room temperature structure was reported by Leman et al. (1993). Inorg...

2015
José A. Romero Gerardo Aguirre Hernández Sylvain Bernès

The title trihalogenated nitro-benzene derivatives, C6H2Br3NO2 and C6H2Br2INO2, crystallize in triclinic and monoclinic cells, respectively, with two mol-ecules per asymmetric unit in each case. The asymmetric unit of the tri-bromo compound features a polarized Br(δ+)⋯Br(δ-) inter-molecular halogen bond. After substitution of the Br atom in the para position with respect to the nitro group, the...

Journal: :IEEE Trans. Pattern Anal. Mach. Intell. 1997
César Silva José Santos-Victor

We address the problem of egomotion estimation for a monocular observer moving under arbitrary translation and rotation, in an unknown environment. The method we propose is uniquely based on the spatio-temporal image derivatives, or the normal ow. We introduce a search paradigm which is based on geometric properties of the normal ow eld, and consists in considering a family of search subspaces ...

Journal: :journal of arthropod-borne diseases 0
viviane barros silva medicinal chemistry laboratory, pharmacy department, federal university of sergipe, são cristóvão, brazil daniele lima travassos medicinal chemistry laboratory, pharmacy department, federal university of sergipe, são cristóvão, brazil angelita nepel nuclear magnetic resonance laboratory, chemistry department, federal university of paraná, curitiba, brazil andersson barison nuclear magnetic resonance laboratory, chemistry department, federal university of paraná, curitiba, brazil emmanoel vilaça costa chemistry department, institute of sciences, federal university of amazonas, manaus, brazil luciana scotti biotechnology center, federal university of paraíba, campus i, joão pessoa, brazil

background : thymol and carvacrol have previously demonstrated larvicidal activity against aedes aegypti (diptera: culicidae). in view of this fact, it was of our interest to obtain synthetic derivatives and evaluate their larvicidal ac­tivity on ae. aegypti larvae. methods : structural modifications were performed on thymol and carvacrol in an effort to understand the functional groups necessa...

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