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Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies
Molecules 2010, 15, 7985-8005; doi:10.3390/molecules15117985 OPEN ACCESS molecules ISSN 1420-3049 www.mdpi.com/journal/molecules Review Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Shahriar Khadem * and Robin J. Marles Natural Health Products Directorate, Health Products and Food Branch, Health Canada, 2936 Baseline Road, Ottawa, Ontario K1A 0K9, Canada * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +1-613-954-7526; Fax: +1-613-954-1617. Received: 19 October 2010; in revised form: 3 November 2010 / Accepted: 4 November 2010 / Published: 8 November 2010 Abstract: Among the wide diversity of naturally occurring phenolic acids, at least 30 hydroxy- and polyhydroxybenzoic acids have been reported in the last 10 years to have biological activities. The chemical structures, natural occurrence throughout the plant, algal, bacterial, fungal and animal kingdoms, and recently described bioactivities of these phenolic and polyphenolic acids are reviewed to illustrate their wide distribution, biological and ecological importance, and potential as new leads for the development of pharmaceutical and agricultural products to improve human health and nutrition. Keywords: polyphenols; phenolic acids; hydroxybenzoic acids; natural occurrence; bioactivities 1. Introduction Phenolic compounds exist in most plant tissues as secondary metabolites, i.e. they are not essential for growth, development or reproduction but may play roles as antioxidants and in interactions between the plant and its biological environment. Phenolics are also important components of the human diet due to their potential antioxidant activity [1], their capacity to diminish oxidative stress- induced tissue damage resulted from chronic diseases [2], and their potentially important properties such as anticancer activities [3-5]. -
Chemical Composition, Cytotoxic and Antioxidative Activities of Ethanolic
CORE Metadata, citation and similar papers at core.ac.uk Provided by Cherry - Repository of the Faculty of Chemistry; University of Belgrade Chemical composition, cytotoxic and antioxidative activities of ethanolic extracts of propolis on HCT-116 cell line Jovana B Žižića,∗, Nenad L Vukovićb, Milka B Jadraninc, Boban D Anđelkovićd, Vele V Teševićd, Miroslava M Kacaniovae , Slobodan B Sukdolakb and Snežana D Markovića aDepartment of Biology and Ecology, Faculty of Science, University of Kragujevac, Radoja Domanovića 12, 34 000 Kragujevac, Serbia bDepartment of Chemistry, Faculty of Science, University of Kragujevac, Radoja Domanovića 12, 34 000 Kragujevac, Serbia cInstitute of Chemistry, Technology and Metallurgy, University of Belgrade, Njegoševa 12, 11000 Belgrade, Serbia dFaculty of Chemistry, University of Belgrade, Studentski trg 16, 11000 Belgrade, Serbia eDepartment of Microbiology, Faculty of Biotechnology and Food Science, Slovak University of Agriculture in Nitra, Tr. A. Hlinku 2, 949 76 Nitra, Slovak Republic This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1002/jsfa.6132 © 2013 Society of Chemical Industry *Correspondence to: Jovana B Žižić, Department of Biology and Ecology, Faculty of Science, University of Kragujevac, Radoja Domanovića 12, 34 000 Kragujevac, Serbia E-mail: [email protected] Abstract BACKGROUND: Propolis is a complex resinous sticky substance that honeybees collect from buds and exudates of various plants. Due to propolis versatile biological and pharmacological activities, it is widely used in medicine, cosmetics and food industry. -
Use of Substituted Cinnamic Acid Polymers to Treat AIDS
Europaisches Patentamt European Patent Office © Publication number: 0 544 321 A1 Office europeen des brevets EUROPEAN PATENT APPLICATION © Application number: 92120293.3 mt . ci .5 :A61K 31/78 @ Date of filing: 27.11.92 ® Priority: 27.11.91 JP 337796/91 © Inventor: Konno, Kunio 1-33-3, Kakinokizaka, Meguro-ku © Date of publication of application: Tokyo(JP) 02.06.93 Bulletin 93/22 Inventor: Sakagami, Hiroshi Chigusadai Danchi 246, 33, Chigusadai, @ Designated Contracting States: Midori-ku CH DE FR GB IT LI NL SE Yokohama-shi, Kanagawa-ken(JP) Inventor: Kawazoe, Yutaka © Applicant: Konno, Kunio 5-14-14, Shimomeguro, Meguro-ku 1-33-3, Kakinokizaka, Meguro-ku Tokyo(JP) Tokyo(JP) Inventor: Yamamoto, Naoki Applicant: Sakagami, Hiroshi Haramachi Jutaka 501, 3-11, Ebisu Minami, Chigusadai Danchi 246, 33, Chigusadai, Midori-ku Shibuya-ku Yokohama-shi, Kanagawa-ken(JP) Tokyo(JP) Applicant: Kawazoe, Yutaka 5-14-14, Shimomeguro, Meguro-ku Tokyo(JP) 0 Representative: Hansen, Bernd, Dr.rer.nat. et Applicant: Yamamoto, Naoki al Haramachi Jutaka 501, 3-11, Ebisu Minami, Hoffmann, Eitle & Partner Patentanwalte Shibuya-ku Arabellastrasse 4 Postfach 81 04 20 Tokyo(JP) W-8000 Munchen 81 (DE) © Use of substituted cinnamic acid polymers to treat AIDS. © AIDS therapeutic agents are provided which are less toxic, have a strong anti-AIDS virus activity and comprise as an effective ingredient a dehydrogenation polymer of a cinnamic acid derivative having a phenyl group substituted with at least one hydroxyl group or a pharmaceutically acceptable salt thereof. CM 00 Rank Xerox (UK) Business Services (3. 10/3.6/3.3. 1) EP 0 544 321 A1 BACKGROUND OF THE INVENTION Field of the Invention 5 The present invention relates to AIDS therapeutic agents containing a dehydrogenation polymer of a substituted cinnamic acid as an effective ingredient. -
Xanthones. Part I V.* a New Synthesis of Hydroxyxanthones and Hydrozybenzophenones
3982 Grover, Shah, agad Shah : Xanthones. Part I V.* A New Synthesis of Hydroxyxanthones and Hydrozybenzophenones. By P. I<. GROVER,G. D. SHAH,and R. C. SHAH. [Reprint Order No. 6470.1 Hydroxy-santhones and -benzophenones are conveniently obtained from hydroxybenzoic acids and phenols in presence of zinc chloride and phosphorus oxychloride. DISTILLATIONof a mixture of a phenol, a phenolic acid, and acetic anhydride is the earliest and simplest method for the synthesis of hydroxyxanthones (Michael, Amer. Chsm. J., 1883, 5, 81; Kostanecki and his co-workers, Ber., 1891, 24, 1896, 3981, etc.; Lund, Robertson, and Whalley, J., 1953, 2438), but yields are often poor, experimental conditions are rather drastic, and there is a possibility of decarboxylation, autocondensation, and other side reactions (Lespegnol, Bertrand, and Dupas, BUZZ. SOC.chim. France, 1939, 6, 1925; Lund et aZ., Zoc. cit.). There are numerous other routes, but none is of general application and some require uncommon starting materials or involve a number of steps. In continuation of the work on naturally occurring xanthones (J. Indian Chem. SOC., 1953,30,457,463; J. Sci. Id.Res., India, 1954,13, B, 175; 1955,14, B, 153) the known methods for the synthesis of 1 : 3 : 7 : 8-tetrahydroxyxanthone or its tetramethyl ether * Part 111, J. Sci. Ind. Res., India, 1954, 13, B, 175. [ 19551 Xanthones. Part IV. 3953 were found unsuitable. Condensation under mild conditions of a phenolcarboxylic acid with a reactive phenol in presence of condensing agents such as anhydrous aluminium chloride, phosphorus oxychloride, phosphoric oxide, or sulphuric acid was not promising ; but a mixture of phosphorus oxychloride and fused zinc chloride, which had previously been found effective for the preparation of 2 : 4dihydroxybenzophenone (Shah and Mehta, J. -
Medicinal Herbs Used in Traditional Management of Breast Cancer: Mechanisms of Action
medicines Review Medicinal Herbs Used in Traditional Management of Breast Cancer: Mechanisms of Action Donovan A. McGrowder 1,*, Fabian G. Miller 2,3, Chukwuemeka R. Nwokocha 4 , Melisa S. Anderson 5, Cameil Wilson-Clarke 4 , Kurt Vaz 1, Lennox Anderson-Jackson 1 and Jabari Brown 1 1 Department of Pathology, Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica; [email protected] (K.V.); [email protected] (L.A.-J.); [email protected] (J.B.) 2 Department of Physical Education, Faculty of Education, The Mico University College, 1A Marescaux Road, Kingston 5, Jamaica; [email protected] 3 Department of Biotechnology, Faculty of Science and Technology, The University of the West Indies, Kingston 7, Jamaica 4 Department of Basic Medical Sciences, Faculty of Medical Sciences, The University of the West Indies, Kingston 7, Jamaica; [email protected] (C.R.N.); [email protected] (C.W.-C.) 5 School of Allied Health and Wellness, College of Health Sciences, University of Technology, Kingston 7, Jamaica; [email protected] * Correspondence: [email protected] Received: 1 July 2020; Accepted: 9 August 2020; Published: 14 August 2020 Abstract: Background: Breast cancer is one of the principal causes of death among women and there is a pressing need to develop novel and effective anti-cancer agents. Natural plant products have shown promising results as anti-cancer agents. Their effectiveness is reported as decreased toxicity in usage, along with safety and less recurrent resistances compared with hormonal targeting anti-cancer agents. Methods: A literature search was conducted for all English-language literature published prior to June 2020. -
Downloads/ Drugs/Guidances/Ucm070107.Pdf (Accessed on 12 April 2020)
molecules Article Characterization of Free and Bound Phenolic Acids and Flavonoid Aglycones in Rosa rugosa Thunb. Leaves and Achenes Using LC–ESI–MS/MS–MRM Methods Marta Olech * , Wioleta Pietrzak and Renata Nowak Chair and Department of Pharmaceutical Botany, Medical University, 1 Chod´zkiStreet, 20-093 Lublin, Poland; [email protected] (W.P.); [email protected] (R.N.) * Correspondence: [email protected]; Tel.: +48-81448-7060 Academic Editor: Monika Waksmundzka-Hajnos Received: 20 March 2020; Accepted: 10 April 2020; Published: 15 April 2020 Abstract: Fast and reliable determination of polyphenols is a quite common goal during investigation of new plant materials and herbal products, their standardization, quality control, or chemo-taxonomical studies. The aim of this study was to develop and validate methods based on the application of reversed phase liquid chromatography/electrospray ionization triple quadrupole mass spectrometry (LC-ESI-MS/MS) using multiple reaction monitoring (MRM) for comprehensive quantitative and qualitative analysis of phenolic acids and flavonoid aglycones. LC-MS/MS-MRM protocols were applied for the determination of free and bound phenolics in a series of plant samples prepared from leaves and achenes (true fruits) of Japanese rose (Rosa rugosa Thunb.). The presence of large amount of phenolic compounds was detected in rose leaves (786.44 µg/g and 14.46 µg/g of phenolic acids and flavonoid aglycones, respectively). Isoferulic acid and five aglycones were revealed for the first time in this plant material. Moreover, 15 phenolic acids and six aglycones were found in the rose achenes, including eight phenolic acids and four aglycones that had not been previously reported in this rose organ. -
Glycosylation of Caffeic Acid and Structural Analogues Catalyzed by Novel Glucansucrases from Leuconostoc and Weissella Species
Biocatalysis and Agricultural Biotechnology 19 (2019) 101114 Contents lists available at ScienceDirect Biocatalysis and Agricultural Biotechnology journal homepage: www.elsevier.com/locate/bab Glycosylation of caffeic acid and structural analogues catalyzed by novel T glucansucrases from Leuconostoc and Weissella species ∗ Johannes Nolte, Alexander Kempa, Arne Schlockermann, Matthias Hochgürtel, Ulrich Schörken Faculty of Applied Natural Sciences, TH Köln-Campus Leverkusen, Chempark Leverkusen E39, Kaiser-Wilhelm-Allee, 51368, Leverkusen, Germany ARTICLE INFO ABSTRACT Keywords: Twelve Leuconostoc and seven Weissella strains with extracellular glucansucrase activity were obtained from an Caffeic acid analysis of 41 lactic acid bacteria. Culture supernatants of all glucansucrase positive strains catalyzed the gly- Glucansucrase cosylation of caffeic acid with sucrose as donor substrate. Eighteen enzymes produced one major peak, which Leuconostoc was identified as caffeic acid-4′-O-α-D-monoglucoside by LC-MS and NMR spectroscopy. Only W. beninensis DSM Weissella 22752 formed significant amounts of the corresponding 3´-O-α-D-monoglucoside. The Weissella strain and five Acceptor reaction Leuconostoc strains with high glycosylation activity were selected for further studies. All glucansucrases cata- Transglycosylation lyzed the glycosylation of the catechol protocatechuic acid, a side-chain truncated analogue of caffeic acid. The Leuconostoc enzymes displayed a preference for the 4′-O-α-D isomer, while the DSM 22752 glucansucrase also produced the protocatechuic acid-3′-O-α-D-monoglucoside. Lower activities with non-catecholic caffeic acid derivatives and no activity with mono-methylated caffeic acid were observed with all glucansucrases. Time- course analyses confirmed that glucansucrase from L. citreum DSM 5577 was the most efficient biocatalyst for catechol glucosylation with yields of up to 74% caffeic acid glucosides after 24 h. -
Frankland, and of Kolbe, 1849-1850. the Former Claimed To
1170 EMIL FISCHER. Frankland, and of Kolbe, 1849-1850. The former claimed to have isolated the radicals-methyl, ethyl, etc.-by the action of zinc upon the corresponding iodides, while Kolbe obtained the same radicals by the hydrolysis of the sodium salts of acetic, propionic and such acids. In vain did Gerhard and Laurent insist that the molecular formulas of all these so-called free radicals must be doubled, in accordance with Avogadro’s hypothesis. The existence of free radicals was generally accepted as late as 1865, fifty years after Gay Lussac’s introduction of this idea into chemistry. Even Kekul6 for a time considered Frankland’s “methyl” as distinct from ethane. But in 1864 Schorlemmer showed by experimental evidence that Frankland’s and Kolbe’s methyl and ethyl were nothing else than ethane and butane. From that time on, the question relative to the existence of free radicals was never seriously raised until the discovery of triphenylmethyl. How parallel these two periods in the history of chemistry are! Now, as then, a methyl was prepared by the abstraction of halogen from the corresponding alkyl-halide. Now, as then, it was found that the molec- ular weight of the product must be doubled. But now, unlike as in the period of fifty years ago, it was possible to show, by physical and chemicaI evidence, that the product which results from the coupling of the radicals is at best unstable. It was possible to show that it does not retain its individuality, but tends to break down again and is in equilibrium with the truly free radicals. -
Propolis Ethanolic Extracts Reduce Adenosine Diphosphate Induced
Bojić et al. Nutrition Journal (2018) 17:52 https://doi.org/10.1186/s12937-018-0361-y RESEARCH Open Access Propolis ethanolic extracts reduce adenosine diphosphate induced platelet aggregation determined on whole blood Mirza Bojić1* , Andrea Antolić2, Maja Tomičić3, Željko Debeljak4,5 and Željan Maleš6 Abstract Background: Propolis is a well-known bee product containing more than 2000 identified compounds. It has many beneficial effects on human health that include antibacterial, antiviral, anticancer and hepatoprotective justifying its use as a dietary supplement. Platelet aggregation plays crucial role in thrombus formation that can cause stroke or heart attacks. As cardiovascular diseases, including those caused by thrombus formation, are related to 50% of deaths of Western population, the objective of this study was to determine antiaggregatory activity of propolis on platelet aggregation on the whole blood samples. Methods: Twenty one propolis samples from Southeast Europe were characterized by spectrophotometric methods to determine content of the total flavonoids and phenolic acids. High performance liquid chromatography coupled with diode array detection was used to identify and quantify individual polyphenols. Platelet aggregation was tested by impedance aggregometry on the whole blood samples of ten healthy volunteers. Results: The mean content of total polyphenols was 136.14 mg/g and ranged from 59.23 to 277.39 mg/g. Content of total flavonoids ranged between 6.83 and 55.44 mg/g with the mean value of 19.28 mg/g. Percentage of total phenolic acids was in the range 8.79 to 45.67% (mean 26.63%). Minimal antiaggregatory concentration, representing the lowest concentration of propolis extract sample that can cause statistically significant reduction of aggregation, ranged from 5 μM to 10.4 mM. -
Fungal Endophytes As Efficient Sources of Plant-Derived Bioactive
microorganisms Review Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Archana Singh 1,2, Dheeraj K. Singh 3,* , Ravindra N. Kharwar 2,* , James F. White 4,* and Surendra K. Gond 1,* 1 Department of Botany, MMV, Banaras Hindu University, Varanasi 221005, India; [email protected] 2 Department of Botany, Institute of Science, Banaras Hindu University, Varanasi 221005, India 3 Department of Botany, Harish Chandra Post Graduate College, Varanasi 221001, India 4 Department of Plant Biology, Rutgers University, New Brunswick, NJ 08901, USA * Correspondence: [email protected] (D.K.S.); [email protected] (R.N.K.); [email protected] (J.F.W.); [email protected] (S.K.G.) Abstract: Fungal endophytes are well-established sources of biologically active natural compounds with many producing pharmacologically valuable specific plant-derived products. This review details typical plant-derived medicinal compounds of several classes, including alkaloids, coumarins, flavonoids, glycosides, lignans, phenylpropanoids, quinones, saponins, terpenoids, and xanthones that are produced by endophytic fungi. This review covers the studies carried out since the first report of taxol biosynthesis by endophytic Taxomyces andreanae in 1993 up to mid-2020. The article also highlights the prospects of endophyte-dependent biosynthesis of such plant-derived pharma- cologically active compounds and the bottlenecks in the commercialization of this novel approach Citation: Singh, A.; Singh, D.K.; Kharwar, R.N.; White, J.F.; Gond, S.K. in the area of drug discovery. After recent updates in the field of ‘omics’ and ‘one strain many Fungal Endophytes as Efficient compounds’ (OSMAC) approach, fungal endophytes have emerged as strong unconventional source Sources of Plant-Derived Bioactive of such prized products. -
The Pharmacodynamics, Pharmacokinetics and Clinical Use of Echinacea Purpurea by Kevin Spelman, Phd
CONTINUING EDUCATION The Pharmacodynamics, Pharmacokinetics and Clinical Use of Echinacea purpurea By Kevin Spelman, PhD pon successful completion of this these preparations account for 80 percent of commercial article, the pharmacist should be production. In addition, E. angustifolia and E. pallida are also able to: utilized in commerce but much less than E. purpurea. 1. List the main Echinacea species in use today. CHEMISTRY U2. Identify four active constituents in E. pur- All three species of Echinacea seen in commercial prepara- purea extracts. tions have undergone chemical and pharmacological stud- 3. Contrast doses used for acute infections ies. However, there are several other species of Echinacea versus doses used for chronic conditions. that have little to no research on their chemistry and phar- 4. Identify a strategy for converting adult doses macology. Due to the confusion between Echinacea spe- to children’s doses. cies the current body of scientific literature on Echinacea can be confusing due to the three species in use – namely Upon successful completion of this article, the E. purpurea, E. pallida and E. angustifolia. These three have pharmacy technician should be able to: phytochemical similarities but have notable differences, 1. List the main Echinacea species in use today particularly around the identity and concentration of key 2. Identify four active constituents in E. pur- constituents. A number of German studies in the 1980s purea extracts. were called into question when it was discovered that the 3. Contrast doses used for acute infections vs. species they intended to study was the wrong Echinacea doses used for chronic conditions. -
Cosmetic Composition Containing Polyorganosiloxane-Containing Epsilon-Polylysine Polymer, and Polyhydric Alcohol, and Production Thereof
Europäisches Patentamt *EP001604647A1* (19) European Patent Office Office européen des brevets (11) EP 1 604 647 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.7: A61K 7/48, A61K 7/06, 14.12.2005 Bulletin 2005/50 A61K 7/02, C08G 81/00, C08G 77/452, C08G 77/455, (21) Application number: 05010234.2 C08L 83/10 (22) Date of filing: 11.05.2005 (84) Designated Contracting States: (72) Inventors: AT BE BG CH CY CZ DE DK EE ES FI FR GB GR • Kawasaki, Yuji HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR Ibi-gun Gifu 501-0521 (JP) Designated Extension States: • Hori, Michimasa AL BA HR LV MK YU Gifu-shi Gifu 500-8286 (JP) • Yamamoto, Yuichi (30) Priority: 12.05.2004 JP 2004141778 5-1 Goikaigan Ichiharashi Chiba 290-8551 (JP) • Hiraki, Jun (71) Applicants: Tokyo 104-8555 (JP) • Ichimaru Pharcos Co., Ltd. Motosu-shi, Gifu 501-0475 (JP) (74) Representative: HOFFMANN EITLE • Chisso Corporation Patent- und Rechtsanwälte Osaka-shi, Osaka-fu 530-0005 (JP) Arabellastrasse 4 81925 München (DE) (54) Cosmetic composition containing polyorganosiloxane-containing epsilon-polylysine polymer, and polyhydric alcohol, and production thereof (57) It has been desired to develop a highly preserv- by reducing the amount of antibacterial preservative ative and antibacterial cosmetic composition that can agent to be used. easily be applied to both emulsion and non-emulsion There is provided a cosmetic composition compris- type cosmetics. It has also been desired to develop a ing one or a combination of two or more of polyorganosi- method of improving a preservative and/or antibacterial loxane-containing epsilon-polylysine compounds ob- effect(s) of a cosmetic composition comprising polyor- tained by reacting epsilon-polylysine with polyorganosi- ganosiloxane-containing epsilon-polylysine and there- loxane or a physiologically acceptable salt thereof, and polyhydric alcohol.