Search results for "Activity"

3-(1H-Indol-3-yl)-4-(3,4,5-trimethoxyphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione

2005

The crystal structure of the title compound, C21H18N2O5, was determined in order to study the electrocyclic reactivity of 3,4-di­aryl-1H-pyrrole-2,5-dione derivatives. Intermolecular hydrogen bonds form sheets.

Application of Molecular Topology to the Prediction of the Reaction Yield and Anticancer Activity of Imidazole and Guanidine Derivatives

2013

In this study molecular topology based QSAR has been applied to predict the reaction yield and anticancer activity of 18 imidazole and guanidine derivatives. Four properties were evaluated, namely reaction yield, anti prostatic-cancer activity, anti breast-cancer activity and anti lung-cancer activity. The four models have been validated by both internal and cross validation, and also by randomness tests. The results obtained are in full agreement with the experimental results and confirm the precision, accuracy and robustness of the method followed. After carrying out a virtual screening upon such models, new imidazole and guanidine derivatives with potential anticancer activity are propos…

From One-Pot NH-Sulfoximidations of Thiophene Derivatives to Dithienylethene-Type Photoswitches

2019

Thiophene NH-sulfoximines have been synthesized using a one-pot NH-sulfoximidation reaction of thiophenes. The reactivity of the products was investigated, and the developed protocols were used for the synthesis of a new class of dithienylethene-type photoswitches containing a sulfoximidoyl group.

Über die copolymerisation des acroleins und des methacroleins in homogener lösung. Polymere acroleine. 25. Mitt.

1962

Die Copolymerisation des Acroleins und des Methacroleins in Dimethylformamid sowie in Dioxan wird beschrieben. Die Parameter folgender Systeme wurden bestimmt: Acrolein/Acrylnitril (r1 = 1,60; r2 = 0,52); Acrolein/Acrylamid (r1 = 1,69; r2 = 0,21); Acrolein/Methacrylnitril (r1 = 0,72; r2 = 1,20); Acrolein/2-Vinylpyridin (r1 = 4; r2 = 0) und Methacrolein/Methacrylnitril (r1 = 1,78; r2 = 0,40). Die Berechnung der Q-und e-Werte bzw. der q- und ϵ-Werte ergab fur Acrolein: Q = 0,64; e = 0,61; q = -2,8 kcal/Mol; ϵ = 0,19 = 10−10 elektrostatische Einheiten und fur Methacrolein: Q = 1,59; e = 0,36; q = −3,4 kcal/Mol; ϵ = 0,11 = 10−10 elektrostatische Einheiten. The copolymerisation of acrolein and m…

Darstellung, Kristallstruktur und Wirkung von 2-Methyl-3-(4-oxo-3-phenyl-thiazolidin-2-ylidenamino)-4-(3H)-chinazolinon

1984

Quinazolinones. 1. Preparation, crystal structure and action of 2-methyl-3-(4-oxo-3-phenyl-thiazolidine-2-ylidenamino)-4-(3H)- quinazolinone.

Reaktivitäut und reaktionswege von methylsubstituierten bisindolylcarbenium-ionen

1987

Methyl substituted bisindolylcarbenium ions 1 react with some O- and C-nucleophiles regioselectively. The cations 1b, 1c yield with hydroxide ions the tetraindolyldimethyl ether 4 and with methoxide ions the bisin-dolylmethoxymethanes 5. Compounds 1a, 1b, 1c react with several methylindoles to isomeric bis- and trisin-dolylmethanes. An electrophilic reactivity order of cations 1 can be derived supporting on the experimental results.

Retinoid acid and analogs as potent inducers of differentiation and apoptosis. New promising chemopreventive and chemotherapeutic agents in oncology

2001

Abstract In this report we will describe the preparation and the biological activity of a novel class of heterocyclic arotinoids endowed with potent cytotoxic and apoptotic acitivity. Structure­activity relationship studies revealed that the different stereochemistry at the C9 double bond of retinoids seems associated with a different biological activity: potent apoptotic activity for the cis-isomers, whereas differentiating activity for the trans structures. An interesting modified Wittig procedure that allows easily to arotinoids will also be described. The substitution of the alkenyl portion with a more flexible oxymethyl or aminomethyl moiety gave compounds with poor activity, whereas i…

Preparation, reactivity and tautomeric preferences of novel (1H-quinolin-2-ylidene)propan-2-ones

2006

1,1-Difluoro-3-(1H-quinolin-2-ylidene)propan-2-one 1a, 1,1,1-trifluoro-3-(1H-quinolin-2-ylidene)propan-2-one 1b, 1,1,1-trifluoro-3-(4-chloro-1H-quinolin-2-ylidene)propan-2-one 1c and 1,3-dibromo-1,1-difluoro-3-(2-quinolyl)propan-2-one 2 are prepared and characterized by various spectroscopic techniques. The crystal structure of 1a is determined by X-ray diffraction. Furthermore, a series of previously known non-halogenated (1H-quinolin-2-ylidene)propan-2-ones 1d-1h are oxidized with AgBrO3 in the presence of AlCl3. In all cases, 2-(1-bromo-1-chloromethyl)quinoline 3 is obtained in high yield. The bromination order and sites of 1a are analyzed based on ab initio MP2 and DFT calculations for …

1983

The kinetics of the electrophilic bromination of 17 oligonuclear phenolic compounds with molecular bromine in acetic acid were studied at 22°C. Some of these compounds, consisting of up to 6 phenolic units, which are linked in ortho-position by methylene bridges, and having only one (or two) reactive ortho-position(s) at the end of the molecule, were synthesized for the first time. It could be shown, even for hexanuclear compounds, that the variation of substituents at one end of the molecule leads to a change in the reactivity at the other end, that means over a distance of 22 nonconjugated covalent links. So far, this can be explained only by a chain of intramolecular hydrogen bonds betwe…

1972