نتایج جستجو برای: antibacterial products

تعداد نتایج: 329787  

2015
Ana C. S. Gonçalves Telma Franco Gianmaria Califano Scot E. Dowd Georg Pohnert Rodrigo Costa

We report here the draft genome sequence of Vibrio sp. Vb278, a biofilm-producing strain isolated from the marine sponge Sarcotragus spinosulus, showing in vitro antibacterial activity. The annotated genome displays a range of symbiotic factors and the potential for the biosynthesis of several biologically active natural products.

Journal: :Angewandte Chemie 2009
Chao Wang Chaoqun Li Xiaofeng Wu Alan Pettman Jianliang Xiao

1,2,3,4-Tetrahydroquinolines exist as key structural elements in many natural products and have found broad commercial application. In particular, optically pure tetrahydroquinolines are commonly present in alkaloids and are required in pharmaceutical and agrochemical synthesis. Representative examples include the bioactive alkaloids (+)-galipinine and ( )-augustureine, and the antibacterial dr...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2002
Moacir G Pizzolatti Andreia F Venson Artur Smânia Elza de F A Smânia Raimundo Braz-Filho

A mixture of flavalignan cinchonains Ia and Ib was isolated from the bark of Trichilia catigua. The structures were established on the basis of spectroscopic data of the natural products and their methylated derivatives including 2D NMR experiments, and compared with data in the literature. These flavalignans exhibited antibacterial activity against Bacillus

Journal: :iranian journal of catalysis 2013
somnath s. gholap umesh p. deshmukh macchindra s. tambe

an efficient synthesis of some novel coumarin derivatives via 1, 4- michael addition of indole to coumarin chalcones catalyzed by cellulose sulphonic acid (csa) under solvent free conditions is described. the corresponding michael addition products were obtained in good to excellent yield. the synthesized compounds were screened for their antibacterial activity against e. coli, s. aureus and an...

Journal: :iranian journal of catalysis 2013
ayoob bazgir seyyedeh cobra azimi

a simple, novel, efficient and three-component procedure for the synthesis of pyrimido[4,5-d]pyrimidine-2,4-dione derivatives by the reaction of 6-amino-1,3-dimethyluracil, aldehyde and 2-benzylisothiourea hydrochloride promoted by ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]br) under solvent-free conditions is reported. the presented method is benefited from operational simplicity,...

Aromatic plants have subscribed to the belief that they can be used in food, perfumery, pharmaceutical and cosmetic products due to their nutritional and biological properties. The present study was designed to examine the chemical composition and antibacterial and analgesic properties of Lavandula stoechas flowers originating Amol, north of Iran for the first time. The essential oil o...

Journal: :The Journal of antibiotics 1998
M Daferner T Anke V Hellwig W Steglich O Sterner

The antifungal and cytostatic compound strobilurin M (1) is a new variant of the strobilurins produced by Mycena sp. 96097, a tropical basidiomycete. The same fungus was found to produce tetrachloropyrocatechol (3a) and tetrachloropyrocatechol methyl ether (3b), new natural products, which exhibit antifungal, antibacterial and cytotoxic activities.

Journal: :Organic & biomolecular chemistry 2011
Thomas J K Findley David Sucunza Laura C Miller Matthew D Helm Madeleine Helliwell David T Davies David J Procter

The cis-hydrindane motif is found in a number of natural products that display important biological activity. A flexible, stereoselective approach to the framework has been developed that features highly diastereoselective, SmI(2)-mediated cyclisations. The strategy has been exploited in the first synthesis of the proposed structure of faurinone and an approach to the skeleton of the antibacter...

Journal: :Organic & biomolecular chemistry 2016
Kalpana Mishra Ashok Kumar Pandey Jay Bahadur Singh Radhey M Singh

A metal-free, TBHP-promoted economical route is developed via the sp(2) C-H bond functionalization strategy for the synthesis of indenoquinolinones, 4-azafluorenones and fluorenones. Reactions provided excellent yield of the products under mild conditions. We have successfully synthesized 11H-indeno[1,2-b]quinolin-11-one, an antibacterial agent, in excellent yields.

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید