Selective inhibition of monoamine oxidase A by purpurin, an anthraquinone.
暂无分享,去创建一个
[1] Daeui Park,et al. Potent selective monoamine oxidase B inhibition by maackiain, a pterocarpan from the roots of Sophora flavescens. , 2016, Bioorganic & medicinal chemistry letters.
[2] R. Tripathi,et al. Exploration of a Library of 3,4‐(Methylenedioxy)aniline‐Derived Semicarbazones as Dual Inhibitors of Monoamine Oxidase and Acetylcholinesterase: Design, Synthesis, and Evaluation , 2016, ChemMedChem.
[3] G. Zengin,et al. Evaluation of antioxidant, enzyme inhibition, and cytotoxic activity of three anthraquinones (alizarin, purpurin, and quinizarin) , 2016, Human & experimental toxicology.
[4] S. Ignacimuthu,et al. Larvicidal and Pupicidal Activities of Alizarin Isolated from Roots of Rubia cordifolia Against Culex quinquefasciatus Say and Aedes aegypti (L.) (Diptera: Culicidae) , 2016, Neotropical Entomology.
[5] N. Denora,et al. Searching for Multi-Targeting Neurotherapeutics against Alzheimer’s: Discovery of Potent AChE-MAO B Inhibitors through the Decoration of the 2H-Chromen-2-one Structural Motif , 2016, Molecules.
[6] Jintae Lee,et al. Calcium-chelating alizarin and other anthraquinones inhibit biofilm formation and the hemolytic activity of Staphylococcus aureus , 2016, Scientific Reports.
[7] B. N. Sinha,et al. Monoamine Oxidase Inhibitory Activity of Novel Pyrazoline Analogues: Curcumin Based Design and Synthesis. , 2016, ACS medicinal chemistry letters.
[8] I. Orhan. Potential of Natural Products of Herbal Origin as Monoamine Oxidase Inhibitors. , 2015, Current pharmaceutical design.
[9] S. Nam,et al. Inhibition of Monoamine Oxidase by Anithiactins from Streptomyces sp. , 2015, Journal of microbiology and biotechnology.
[10] A. Ganesan,et al. cis‐cyclopropylamines as mechanism‐based inhibitors of monoamine oxidases , 2015, The FEBS journal.
[11] J. P. Petzer,et al. Indanones As High‐Potency Reversible Inhibitors of Monoamine Oxidase , 2015, ChemMedChem.
[12] T. Huh,et al. Purpurin inhibits adipocyte-derived leucine aminopeptidase and angiogenesis in a zebrafish model. , 2014, Biochemical and biophysical research communications.
[13] C. Sonesson,et al. A novel series of 6-substituted 3-(pyrrolidin-1-ylmethyl)chromen-2-ones as selective monoamine oxidase (MAO) A inhibitors. , 2014, European journal of medicinal chemistry.
[14] B. Harvey,et al. The interactions of azure B, a metabolite of methylene blue, with acetylcholinesterase and butyrylcholinesterase. , 2014, Toxicology and applied pharmacology.
[15] C. Parsons,et al. Memantine and Cholinesterase Inhibitors: Complementary Mechanisms in the Treatment of Alzheimer’s Disease , 2013, Neurotoxicity Research.
[16] R. Ramsay. Inhibitor design for monoamine oxidases. , 2013, Current pharmaceutical design.
[17] M. Rejžek,et al. Application of a Novel Microtitre Plate-Based Assay for the Discovery of New Inhibitors of DNA Gyrase and DNA Topoisomerase VI , 2013, PloS one.
[18] Hamed I. Ali,et al. Synthesis of new 7-oxycoumarin derivatives as potent and selective monoamine oxidase A inhibitors. , 2012, Journal of medicinal chemistry.
[19] R. Ramsay. Monoamine oxidases: the biochemistry of the proteins as targets in medicinal chemistry and drug discovery. , 2012, Current topics in medicinal chemistry.
[20] S. Vilar,et al. Monoamine oxidase inhibitors: ten years of docking studies. , 2012, Current topics in medicinal chemistry.
[21] S. Avnet,et al. The natural compound Alizarin as an osteotropic drug for the treatment of bone tumors , 2012, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[22] A. Clarke,et al. Identification of the First Known Inhibitors of O‐Acetylpeptidoglycan Esterase: A Potential New Antibacterial Target , 2012, Chembiochem : a European journal of chemical biology.
[23] Irene Bolea,et al. Synthesis, biological evaluation, and molecular modeling of donepezil and N-[(5-(benzyloxy)-1-methyl-1H-indol-2-yl)methyl]-N-methylprop-2-yn-1-amine hybrids as new multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimer's disease. , 2011, Journal of medicinal chemistry.
[24] K. Kang,et al. Novel antifungal activity of purpurin against Candida species in vitro. , 2010, Medical mycology.
[25] K. Hasumi,et al. Purpurin as a specific inhibitor of spermidine-induced autoactivation of the protease plasma hyaluronan-binding protein. , 2010, Biological & pharmaceutical bulletin.
[26] Gene-Jack Wang,et al. Reversible Inhibitors of Monoamine Oxidase-A (RIMAs): Robust, Reversible Inhibition of Human Brain MAO-A by CX157 , 2010, Neuropsychopharmacology.
[27] P. Renard,et al. 3-[5-(4,5-dihydro-1H-imidazol-2-yl)-furan-2-yl]phenylamine (Amifuraline), a promising reversible and selective peripheral MAO-A inhibitor. , 2006, Journal of medicinal chemistry.
[28] Keith F. Tipton,et al. The therapeutic potential of monoamine oxidase inhibitors , 2006, Nature Reviews Neuroscience.
[29] Conrad C. Huang,et al. UCSF Chimera—A visualization system for exploratory research and analysis , 2004, J. Comput. Chem..
[30] C. H. Cheng,et al. Inhibition of MAO A and B by some plant-derived alkaloids, phenols and anthraquinones. , 2004, Journal of ethnopharmacology.
[31] T. Gunnlaugsson,et al. Detecting microdamage in bone , 2003, Journal of anatomy.
[32] E. Takahashi,et al. Preventive effects of anthraquinone food pigments on the DNA damage induced by carcinogens in Drosophila. , 2001, Mutation research.
[33] M. Trivedi,et al. Meta-Analysis of the Reversible Inhibitors of Monoamine Oxidase Type A Moclobemide and Brofaromine for the Treatment of Depression , 1999, Neuropsychopharmacology.
[34] H. Chiang,et al. Inhibition of xanthine oxidase by hydroxylated anthraquinones and related compounds. , 1997, Anticancer research.
[35] Z. Rong-liang,et al. Phenolic compounds and an analog as superoxide anion scavengers and anti oxidants , 1991 .
[36] T. Hergueta,et al. Comparison of the monoamine oxidase inhibiting properties of two reversible and selective monoamine oxidase-A inhibitors moclobemide and toloxatone, and assessment of their effect on psychometric performance in healthy subjects. , 1990, British journal of clinical pharmacology.
[37] Lee Chi Hoon,et al. Antifungal Property of Dihydroxyanthraquinones Against Phytopathogenic Fungi , 2005 .
[38] R. Ramsay,et al. Inhibition of Monoamine Oxidase A by β-Carboline Derivatives , 1997 .
[39] D. Barnard,et al. Evaluation of the antiviral activity of anthraquinones, anthrones and anthraquinone derivatives against human cytomegalovirus. , 1992, Antiviral research.