Results 1 - 10 of 144

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Philip Prathipati, Ngai Ling Ma* and Thomas H. Keller. Global Bayesian Models for the Prioritization of Antitubercular Agents, J. Chem. Inf. Model., 2008, 48 (12), pp 2362–2370
[DOI: 10.1021/ci800143n]
Xiaoyu Zhang and Zhongjun Ma. A new fluorescein isothiocyanate-based screening method for the rapid discovery of electrophilic compounds, Anal. Methods, 2010, 2, 1472.
[DOI: 10.1039/c0ay00305k]
Gold et al.. Identification of a copper-binding metallothionein in pathogenic mycobacteria, Nature Chemical Biology, 2008
[DOI: 10.1038/nchembio.109]
Bruce R. Lichtenstein, José F. CerdaCurrent address: Department of Chemistry, St. Joseph’s University, Philadelphia, PA 19131, USA. Tel: +1 (1) 610-660-1787., Ronald L. KoderCurrent address: Department of Physics, The City College of New York, New York, NY 10031, USA. Fax: +1 (1) 212-650-6940; Tel: +1 (1) 212-650-5502. and P. Leslie Dutton. Reversible proton coupled electron transfer in a peptide-incorporated naphthoquinoneamino acid, Chem. Commun., 2009, 168.
[DOI: 10.1039/b815915g]
Olivier Schaetzle, Frédéric Barrière and Keith Baronian. Bacteria and yeasts as catalysts in microbial fuelcells: electron transfer from micro-organisms to electrodes for green electricity, Energy Environ. Sci., 2008, 1, 607.
[DOI: 10.1039/b810642h]
Christophe Morin, Tatiana Besset, Jean-Claude Moutet, Martine Fayolle, Margit Brückner, Danièle Limosin, Katja Becker and Elisabeth Davioud-CharvetDelegate (E.D.C.) of Centre National de la Recherche Scientifique, France in the frame of a French–German cooperation with Heidelberg University, Germany.. The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyteglutathione reductase, Org. Biomol. Chem., 2008, 6, 2731.
[DOI: 10.1039/b802649c]
Olga V. Zalomaeva, Irina D. Ivanchikova, Oxana A. Kholdeeva and Alexander B. Sorokin. Kinetics and mechanism of the oxidation of alkyl substituted phenols and naphthols with tBuOOH in the presence of supported iron phthalocyanine, New J. Chem., 2009, 33, 1031.
[DOI: 10.1039/b821534k]
Akimitsu Okamoto. Chemical approach toward efficient DNA methylation analysis, Org. Biomol. Chem., 2009, 7, 21.
[DOI: 10.1039/b813595a]
P Nagaraja, R A Vasantha and H S Yathirajan. Spectrophotometric methods for the rapid determination of menadione and menadione sodium bisulphite and their application in pharmaceutical preparations., J Pharm Biomed Anal 28(1):161-168 (2002)
[PubMed: 11861]
Two simple, rapid and sensitive spectrophotometric determination of menadione and its sodium bisulphite derivative (MSB) have been carried out. The first method involves the reaction of menadione and its sodium bisulphite derivative with 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) is sodium hydroxide medium to give blue coloured product having maximum absorption at 625 nm and the coloured species is stable for more than 1 h. The Beer's law is obeyed in the range 0.4-16 microg ml(-1). The second method proposes the reaction of menadione and its sodium bisulphite derivative with resorcinol in concentrated sulphuric acid medium to give red coloured product having maximum absorption at 520 nm and is stable for 3 h. The Beer's law was obeyed in the range of 1-24 microg ml(-1). Molar absorptivity for the above two methods were found to be 7.6 x 10(3) and 4.5 x 10(3) l mol(-1) cm(-1), respectively. All the measurements were carried out at room temperature. These two methods have been successfully applied for menadione and its sodium bisulphite derivatives in injections and tablets of pharmaceutical formulations. The results compare favourably with official method.
Tohru Dairi, Tomohisa Kuzuyama, Makoto Nishiyama and Isao Fujii. Convergent strategies in biosynthesis, Nat. Prod. Rep., 2011, 28, 1054.
[DOI: 10.1039/c0np00047g]