نتایج جستجو برای: triazines

تعداد نتایج: 1203  

2007
Lorentz JÄNTSCHI Sorana Daniela BOLBOACĂ

Correlation coefficients and associated squared values are used as assessment parameters in validation of structure-activity relationships. Seven correlation coefficients were calculated for models that characterized the relationship between chemical structure the herbicidal activity of a triazine analogues series. Three previously reported models were compared by using Pearson (rPrs), Spearman...

2014
R. A. González-Fuenzalida Y. Moliner-Martínez Helena Prima-Garcia Antonio Ribera P. Campins-Falcó Ramon J. Zaragozá

The use of magnetic nanomaterials for analytical applications has increased in the recent years. In particular, magnetic nanomaterials have shown great potential as adsorbent phase in several extraction procedures due to the significant advantages over the conventional methods. In the present work, the influence of magnetic forces over the extraction efficiency of triazines using superparamagne...

2006
L Jäntschi

Herbicidal activity of a set of thirty 1,3,5-substituted-triazines were studied using an original structure-activity relationships approach. The cross-validation leave-one-out correlation score, the training vs. test analysis, and the model stability sustained the prediction ability of the best performing multi-varied model with four variables. The comparison with the previous reported model wa...

Journal: :YAKUGAKU ZASSHI 1994

Journal: :ACS chemical neuroscience 2014
Ana Vázquez-Romero Manuel Criado Angel Messeguer Miquel Vidal-Mosquera José Mulet Francisco Sala Salvador Sala

We have characterized the effect of triazine derivatives on neuronal nicotinic receptors expressed in Xenopus oocytes. All triazines investigated inhibit the current of α7 and α3β4 neuronal nicotinic receptors elicited by acetylcholine. The effect is concentration dependent, reversible, and noncompetitive. In contrast, some derivatives have a dual effect on α4β2 receptors, by potentiating the c...

Journal: :Environmental pollution 2004
T Dombek D Davis J Stine D Klarup

To help elucidate the mechanism of dechlorination of chlorinated triazines via metallic iron, terbutylazine (TBA: 2-chloro-4-ethylamino-6-terbutylamino-1,3,5-triazine), deisopropyl atrazine (DIA: 2-amino-4-chloro-6-ethylamino-1,3,5-triazine), and chlorinated dimethoxy triazine (CDMT: 2-chloro-4,6-dimethoxy-1,3,5-triazine) were degraded via zero valent iron under controlled pH conditions. The lo...

Journal: :Critical reviews in toxicology 1997
N Sathiakumar E Delzell

We evaluated epidemiologic evidence pertaining to the human carcinogenic potential of triazine herbicides in general and of atrazine, the most common triazine. Cancers for which data are available included non-Hodgkin's lymphoma, Hodgkin's disease, leukemia, multiple myeloma, soft tissue sarcoma, colon cancer, and ovarian cancer. The investigations had methodologic limitations, including lack o...

2017
Nadia A. Abdelriheem Yasser H. Zaki Abdou O. Abdelhamid

BACKGROUND Pyrazolo[1,5-a]pyrimidines are purine analogues. They have beneficial properties as antimetabolites in purine biochemical reactions. This division compounds have attracted wide pharmaceutical interest because of their antitrypanosomal activity. RESULTS The present work depicts an effective synthesis convention of pyrazolo[1,5-a]pyrimidines, pyrazolo[5,1-c]triazines, thieno[2,3-b]py...

2002
Mircea V. Diudea Lorentz Jäntschi Ljupčo Pejov

Motivation. Substituted 1,3,5-triazines are known as useful herbicidal substances. In view of reducing the cost of biological screening, computational methods are carried out for evaluating the biological activity of organic compounds. Often a class of bioactives differ only in the substituent attached to a basic skeleton. In such cases substituent descriptors will give the same prospecting res...

Journal: :Nucleosides, nucleotides & nucleic acids 2005
Frank Seela W Lin Z Kazimierczuk H Rosemeyer V Glaron X Peng Y He X Ming M Andrzejewska A Gorska X Zhang H Eickmeier P La Colla

The synthesis of base modified L-nucleosides is described with pyrrolo[2,3-d]pyrimidines, pyrazolo[3,4-d]pyrimidines, benzimidazoles, and imidazo[1,2-a]-s-triazines as nucleobases. The conformation of the nucleosides is studied and the antiviral activity is evaluated.

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