نتایج جستجو برای: quinoline alkaloids

تعداد نتایج: 18029  

2012
R. Musiol A. Kurczyk

Drug design is a complex issue that still lack general approach with proven reliability. Combinatorial chemistry and HTS techniques did not appear to be effort-effective. As an alternative we have the fragment based design and more recently so called the privileged structures approach. We believe that some structural subunits are especially effective in design of bioeffectors. However it is not...

2006
Magnus Rueping Andrey P. Antonchick Thomas Theissmann David A. Evans

The enantioselective hydrogenation of olefins, ketones, and imines still represents an important topic in organic synthesis and catalysis. Although many highly enantioselective processes based on chiral Rh, Ru, and Ir complexes have been reported, most of these catalysts failed to give satisfactory results in the asymmetric hydrogenation of aromatic and heteroaromatic compounds. Examples of eff...

2014
M. Thenmozhi

Vitiligo is a depigmentation disorder; Reactive Oxygen Species (ROS) plays a major role in the development of depigmentation. Monoamine oxidase-A(MAO-A) enzyme is one of the reasons in producing ROS by metabolizing norepinephrine which found to be high level in vitiligo patients. Inhibiting MAO-A enzyme prevents further depigmentation. Clinical studies proved that the isoquinoline alkaloids hav...

Journal: :Scientific reports 2016
Wonhwa Lee JungIn Lee Roshan Kulkarni Mi-Ae Kim Jae Sam Hwang MinKyun Na Jong-Sup Bae

The aim of this study was to discover small-molecule anticoagulants from Scolopendra subspinipes mutilans (SSM). A new acylated polyamine (1) and a new sulfated quinoline alkaloid (2) were isolated from SSM. Treatment with the new alkaloids 1, 2, and indole acetic acid 4 prolonged the activated partial thromboplastin time and prothrombin time and inhibited the activity and production of thrombi...

Journal: :Cancer research 1989
S Kumar H C Sikka S K Dubey A Czech N Geddie C X Wang E J LaVoie

The mutagenic activities of benzo[f]quinoline, benzo[h]quinoline, and a number of their derivatives, including dihydrodiols, K-region oxides, diol epoxides, and tetrahydroepoxides, were assessed in strain TA 100 of Salmonella typhimurium. The dihydrodiol derivatives of benzo[f]quinoline and benzo[h]quinoline were also tested for tumorigenic activity in newborn mice. Benzo[f]quinoline was metabo...

Journal: :The Plant cell 2013
Keisuke Asada Vonny Salim Sayaka Masada-Atsumi Elizabeth Edmunds Mai Nagatoshi Kazuyoshi Terasaka Hajime Mizukami Vincenzo De Luca

Iridoids form a broad and versatile class of biologically active molecules found in thousands of plant species. In addition to the many hundreds of iridoids occurring in plants, some iridoids, such as secologanin, serve as key building blocks in the biosynthesis of thousands of monoterpene indole alkaloids (MIAs) and many quinoline alkaloids. This study describes the molecular cloning and funct...

2002
Maique W. Biavatti Paulo C. Vieira João B. Fernandes Sandra R. Victor Fernando C. Pagnocca Sérgio Albuquerque Ignez Caracelli Julio Zukerman-Schpector

Raulinoa is a monospecific genus and the species Raulinoa echinata Cowan (Rutaceae) is endemic in the Itajaí Valley, SC, Brazil. This perennial woody shrub is characterized by the presence of spines and has only been found in a short interval (1000 m) on the frequently inundated banks of Itajaí river in an approximate altitude of 100 m, showing a high degree of adaptation to the environment. We...

Journal: :The Journal of biological chemistry 2011
Mai Nagatoshi Kazuyoshi Terasaka Akito Nagatsu Hajime Mizukami

Iridoids are one of the most widely distributed secondary metabolites in higher plants. They are pharmacologically active principles in various medicinal plants and key intermediates in the biosynthesis of monoterpenoid indole alkaloids as well as quinoline alkaloids. Although most iridoids are present as 1-O-glucosides, the glucosylation step in the biosynthetic pathway has remained obscure. W...

2000
Maciej Kubicki Teresa Borowiak Krystyna Gawrońska Jacek Gawroński

Maciej Kubicki, Teresa Borowiak, Krystyna Gawrońska, and Jacek Gawroński Department of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznan, Poland Reprint requests to Dr M.Kubicki. Fax +48(0)-61-8658008. E-mail [email protected] Z. Naturforsch. 55 b, 1083-1088 (2000); received August 4, 2000 Cinchona Alkaloids, Association Modes, Hydrogen Bonds A series of (bis-2,3-naphth...

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