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Index Vol. 12-15
353 INDEX VOL. 12-15 Die Stichworte des Sachregisters sind in der jeweiligen Sprache der einzelnen Beitrage aufgefiihrt. Les termes repris dans la Table des matieres sont donnes selon la langue dans laquelle l'ouvrage est ecrit. The references of the Subject Index are given in the language of the respective contribution. 14 AAG (Alpha-acid glycoprotein) 120 14 Adenosine 108 12 Abortion 151 12 Adenosine-phosphate 311 13 Abscisin 12, 46, 66 13 Adenosine-5'-phosphosulfate 148 14 Absorbierbarkeit 317 13 Adenosine triphosphate 358 14 Absorption 309, 350 15 S-Adenosylmethionine 261 13 Absorption of drugs 139 13 Adipaenin (Spasmolytin) 318 14 - 15 12 Adrenal atrophy 96 14 Absorptionsgeschwindigkeit 300, 306 14 - 163, 164 14 Absorptionsquote 324 13 Adrenal gland 362 14 ACAI (Anticorticocatabolic activity in 12 Adrenalin(e) 319 dex) 145 14 - 209, 210 12 Acalo 197 15 - 161 13 Aceclidine (3-Acetoxyquinuclidine) 307, 13 {i-Adrenergic blockers 119 308, 310, 311, 330, 332 13 Adrenergic-blocking activity 56 13 Acedapsone 193,195,197 14 O(-Adrenergic blocking drugs 36, 37, 43 13 Aceperone (Acetabutone) 121 14 {i-Adrenergic blocking drugs 38 12 Acepromazin (Plegizil) 200 14 Adrenergic drugs 90 15 Acetanilid 156 12 Adrenocorticosteroids 14, 30 15 Acetazolamide 219 12 Adrenocorticotropic hormone (ACTH) 13 Acetoacetyl-coenzyme A 258 16,30,155 12 Acetohexamide 16 14 - 149,153,163,165,167,171 15 1-Acetoxy-8-aminooctahydroindolizin 15 Adrenocorticotropin (ACTH) 216 (Slaframin) 168 14 Adrenosterone 153 13 4-Acetoxy-1-azabicyclo(3, 2, 2)-nonane 12 Adreson 252 -
Β-Phenylethylamines and the Isoquinoline Alkaloids
-Phenylethylamines and the isoquinoline alkaloids Kenneth W. Bentley Marrview, Tillybirloch, Midmar, Aberdeenshire, UK AB51 7PS Received (in Cambridge, UK) 28th November 2000 First published as an Advance Article on the web 7th February 2001 Covering: July 1999 to June 2000. Previous review: Nat. Prod. Rep., 2000, 17, 247. 1 Introduction 2 -Phenylethylamines 3 Isoquinolines 4 Naphthylisoquinolines 5 Benzylisoquinolines 6 Bisbenzylisoquinolines 7 Pavines and isopavines 8 Berberines and tetrahydoberberines 9 Protopines 10 Phthalide-isoquinolines 11 Other modified berberines 12 Emetine and related alkaloids 13 Benzophenanthridines 14 Aporphinoid alkaloids 14.1 Proaporphines 14.2 Aporphines 14.3 Aporphine–benzylisoquinoline dimers 14.4 Phenanthrenes 14.5 Oxoaporphines 14.6 Dioxoaporphines 14.7 Aristolochic acids and aristolactams 14.8 Oxoisoaporphines 15 Alkaloids of the morphine group 16 Colchicine and related alkaloids 17 Erythrina alkaloids 17.1 Erythrinanes 17.2 Cephalotaxine and related alkaloids 18 Other isoquinolines 19 References 1 Introduction Reviews of the occurrence of isoquinoline alkaloids in some plant species 1,2 and of recent developments in the chemistry and synthesis of alkaloids of these groups 3–6 have been published. 2 -Phenylethylamines β-Phenylethylamine, tyramine, N-methyltyramine, hordenine, mescaline, N-methylmescaline and N,N-dimethylmescaline 1, which is reported as an alkaloid for the first time, have been isolated from an unspecified species of Turbinocarpus 7 and N-trans-feruloyltyramine has been isolated from Cananga odorata.8 The N-oxides of the known alkaloid culantraramine 2 and the unknown culantraraminol 3, together with the related avicennamine 4 have been isolated as new alkaloids from Zanthoxylum avicennae.9 Three novel amides of dehydrotyr- leucine and proline respectively. -
Umbilicariaceae Phylogeny TAXON 66 (6) • December 2017: 1282–1303
Davydov & al. • Umbilicariaceae phylogeny TAXON 66 (6) • December 2017: 1282–1303 Umbilicariaceae (lichenized Ascomycota) – Trait evolution and a new generic concept Evgeny A. Davydov,1 Derek Peršoh2 & Gerhard Rambold3 1 Altai State University, Lenin Ave. 61, Barnaul, 656049 Russia 2 Ruhr-Universität Bochum, AG Geobotanik, Gebäude ND 03/170, Universitätsstraße 150, 44801 Bochum, Germany 3 University of Bayreuth, Plant Systematics, Mycology Dept., Universitätsstraße 30, NW I, 95445 Bayreuth, Germany Author for correspondence: Evgeny A. Davydov, [email protected] ORCID EAD, http://orcid.org/0000-0002-2316-8506; DP, http://orcid.org/0000-0001-5561-0189 DOI https://doi.org/10.12705/666.2 Abstract To reconstruct hypotheses on the evolution of Umbilicariaceae, 644 sequences from three independent DNA regions were used, 433 of which were newly produced. The study includes a representative fraction (presumably about 80%) of the known species diversity of the Umbilicariaceae s.str. and is based on the phylograms obtained using maximum likelihood and a Bayesian phylogenetic inference framework. The analyses resulted in the recognition of eight well-supported clades, delimited by a combination of morphological and chemical features. None of the previous classifications within Umbilicariaceae s.str. were supported by the phylogenetic analyses. The distribution of the diagnostic morphological and chemical traits against the molecular phylogenetic topology revealed the following patterns of evolution: (1) Rhizinomorphs were gained at least four times independently and are lacking in most clades grouping in the proximity of Lasallia. (2) Asexual reproductive structures, i.e., thalloconidia and lichenized dispersal units, appear more or less mutually exclusive, being restricted to different clades. -
A New Species of Lecanora S. Lat., Growing on Lasallia Pustulata
The Lichenologist 40(2): 111–118 (2008) 2008 British Lichen Society doi:10.1017/S0024282908007469 Printed in the United Kingdom A new species of Lecanora s. lat., growing on Lasallia pustulata Sergio PEuREZ-ORTEGA and Javier ETAYO Abstract: The new species Lecanora lasalliae Pe´rez-Ortega & Etayo is described from Spain. It is included provisionally in Lecanora s. lat as characters such as Lecanora-type ascus, exciple composed of thick radiating hyphae and the usual presence of algal cells in the excipulum or its lichenicolous habitus on Lasallia pustulata, do not fit well within any known genus of lichenicolous or lichenized fungi. Its taxonomic affinities with several taxa are discussed, including the parasitic Lecanora gyrophorina. Key words: Carbonea, Lecidea, lichenicolous fungi, Nesolechia, Phacopsis, Protoparmelia, Ramboldia, Scoliciosporum, Spain Introduction and compare it to other genera with licheni- The umbilicate genus Lasallia Me´rat does colous species with Lecanora-type ascus with not host many species of fungi; so we were which the species could be related or surprised to find several healthy thalli of confused. Lasallia pustulata (L.) Me´rat. with small patches of apothecia growing on the thallus Material and Methods margins, mainly mixed with clusters of isidia. Because of the frequent presence of The material was examined using standard micro- scopical techniques. Photographs were taken with a dispersed algae in the exciple, thick excipu- Leica Mz75 stereomicroscope and a Zeiss Axioskop2 lar hyphae, the nature of the pigments in Plus microscope equipped with differential contrast. paraphyses and excipulum, and the Amyloid reactions were tested with Lugol’s reagent, Lecanora-type ascus, we hesitated to include either without or with a pre-treatment with KOH (I and K/I respectively). -
A Systematic Review on Main Chemical Constituents of Papaver Bracteatum
Journal of Medicinal Plants A Systematic Review on Main Chemical Constituents of Papaver bracteatum Soleymankhani M (Ph.D. student), Khalighi-Sigaroodi F (Ph.D.)*, Hajiaghaee R (Ph.D.), Naghdi Badi H (Ph.D.), Mehrafarin A (Ph.D.), Ghorbani Nohooji M (Ph.D.) Medicinal Plants Research Center, Institute of Medicinal Plants, ACECR, Karaj, Iran * Corresponding author: Medicinal Plants Research Center, Institute of Medicinal Plants, ACECR, P.O.Box: 33651/66571, Karaj, Iran Tel: +98 - 26 - 34764010-9, Fax: +98 - 26-34764021 E-mail: [email protected] Received: 17 April 2013 Accepted: 12 Oct. 2014 Abstract Papaver bracteatum Lindly (Papaveraceae) is an endemic species of Iran which has economic importance in drug industries. The main alkaloid of the plant is thebaine which is used as a precursor of the semi-synthetic and synthetic compounds including codeine and naloxone, respectively. This systematic review focuses on main component of Papaver bracteatum and methods used to determine thebaine. All studies which assessed the potential effect of the whole plant or its extract on clinical or preclinical studies were reviewed. In addition, methods for determination of the main components, especially thebaine, which have been published from 1948 to March 2013, were included. Exclusion criteria were agricultural studies that did not assess. This study has listed alkaloids identified in P. bracteatum which reported since 1948 to 2013. Also, the biological activities of main compounds of Papaver bracteatum including thebaine, isothebaine, (-)-nuciferine have been reviewed. As thebaine has many medicinal and industrial values, determination methods of thebaine in P. bracteatum were summarized. The methods have being used for determination of thebaine include chromatographic (HPLC, GC and TLC) and non chromatographic methods. -
Towards Resolving Lamiales Relationships
Schäferhoff et al. BMC Evolutionary Biology 2010, 10:352 http://www.biomedcentral.com/1471-2148/10/352 RESEARCH ARTICLE Open Access Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Bastian Schäferhoff1*, Andreas Fleischmann2, Eberhard Fischer3, Dirk C Albach4, Thomas Borsch5, Günther Heubl2, Kai F Müller1 Abstract Background: In the large angiosperm order Lamiales, a diverse array of highly specialized life strategies such as carnivory, parasitism, epiphytism, and desiccation tolerance occur, and some lineages possess drastically accelerated DNA substitutional rates or miniaturized genomes. However, understanding the evolution of these phenomena in the order, and clarifying borders of and relationships among lamialean families, has been hindered by largely unresolved trees in the past. Results: Our analysis of the rapidly evolving trnK/matK, trnL-F and rps16 chloroplast regions enabled us to infer more precise phylogenetic hypotheses for the Lamiales. Relationships among the nine first-branching families in the Lamiales tree are now resolved with very strong support. Subsequent to Plocospermataceae, a clade consisting of Carlemanniaceae plus Oleaceae branches, followed by Tetrachondraceae and a newly inferred clade composed of Gesneriaceae plus Calceolariaceae, which is also supported by morphological characters. Plantaginaceae (incl. Gratioleae) and Scrophulariaceae are well separated in the backbone grade; Lamiaceae and Verbenaceae appear in distant clades, while the recently described Linderniaceae are confirmed to be monophyletic and in an isolated position. Conclusions: Confidence about deep nodes of the Lamiales tree is an important step towards understanding the evolutionary diversification of a major clade of flowering plants. The degree of resolution obtained here now provides a first opportunity to discuss the evolution of morphological and biochemical traits in Lamiales. -
An in Silico Study of the Ligand Binding to Human Cytochrome P450 2D6
AN IN SILICO STUDY OF THE LIGAND BINDING TO HUMAN CYTOCHROME P450 2D6 Sui-Lin Mo (Doctor of Philosophy) Discipline of Chinese Medicine School of Health Sciences RMIT University, Victoria, Australia January 2011 i Declaration I hereby declare that this submission is my own work and to the best of my knowledge it contains no materials previously published or written by another person, or substantial proportions of material which have been accepted for the award of any other degree or diploma at RMIT university or any other educational institution, except where due acknowledgment is made in the thesis. Any contribution made to the research by others, with whom I have worked at RMIT university or elsewhere, is explicitly acknowledged in the thesis. I also declare that the intellectual content of this thesis is the product of my own work, except to the extent that assistance from others in the project‘s design and conception or in style, presentation and linguistic expression is acknowledged. PhD Candidate: Sui-Lin Mo Date: January 2011 ii Acknowledgements I would like to take this opportunity to express my gratitude to my supervisor, Professor Shu-Feng Zhou, for his excellent supervision. I thank him for his kindness, encouragement, patience, enthusiasm, ideas, and comments and for the opportunity that he has given me. I thank my co-supervisor, A/Prof. Chun-Guang Li, for his valuable support, suggestions, comments, which have contributed towards the success of this thesis. I express my great respect to Prof. Min Huang, Dean of School of Pharmaceutical Sciences at Sun Yat-sen University in P.R.China, for his valuable support. -
EVALUATION of ACETYLCHOLINESTERASE INHIBITORY ACTIVITY and MODULATORY EFFECT on NICOTINIC ACETYLCHOLINE RECEPTORS of ALKALOIDS ISOLATED from Rhodolirium Andicola
UNIVERSIDAD DE LA FRONTERA Facultad de Ingeniería y Ciencias Doctorado en Ciencias de Recursos Naturales EVALUATION OF ACETYLCHOLINESTERASE INHIBITORY ACTIVITY AND MODULATORY EFFECT ON NICOTINIC ACETYLCHOLINE RECEPTORS OF ALKALOIDS ISOLATED FROM Rhodolirium andicola DOCTORAL THESIS IN FULFILLMENT OF THE REQUERIMENTS FOR THE DEGREE DOCTOR OF SCIENCES IN NATURAL RESOURCES FELIPE EDUARDO MORAGA NICOLÁS TEMUCO-CHILE 2018 Evaluation of acetylcholinesterase inhibitory activity and modulatory effect on nicotinic acetylcholine receptors of alkaloids isolated from Rhodolirium andicola Esta tesis fue realizada bajo la supervisión del director de Tesis Dra. ANA MUTIS TEJOS, y bajo la co-tutela del Dr. EMILIO HORMAZÁBAL URIBE, pertenecientes al Departamento de Ciencias Químicas y Recursos Naturales de la Universidad de La Frontera, y es presentada para su revisión por los miembros de la comisión examinadora. FELIPE EDUARDO MORAGA NICOLÁS Dr. Andrés Quiroz Director programa de Doctorado en Dra. Ana Mutis T. Ciencias de Recursos Naturales Dr. Emilio Hormazábal U. Dr. Patricio Iturriaga V. Dra. Mónica Rubilar Directora Académica de Postgrado Universidad de La Frontera Dr. Andrés Quiroz C. Dr. Alejandro Urzúa M. Dr. Leonardo Guzmán G. Dedico esta tesis a mi Madre por su apoyo amor y confianza Agradecimientos/Acknowledgments Este escrito no solo refleja los resultados de una investigación, sino también, interés y aprecio por los productos naturales. El desarrollo de este trabajo no habría sido posible sin el apoyo de todas aquellas personas, que directa o indirectamente, me han permitido llevar a cabo los objetivos propuestos en esta investigación. De este modo, las siguientes líneas expresan mis agradecimientos más sinceros a quienes colaboraron en hacer esto una realidad. -
Dr. Duke's Phytochemical and Ethnobotanical Databases Chemicals Found in Papaver Somniferum
Dr. Duke's Phytochemical and Ethnobotanical Databases Chemicals found in Papaver somniferum Activities Count Chemical Plant Part Low PPM High PPM StdDev Refernce Citation 0 (+)-LAUDANIDINE Fruit -- 0 (+)-RETICULINE Fruit -- 0 (+)-RETICULINE Latex Exudate -- 0 (-)-ALPHA-NARCOTINE Inflorescence -- 0 (-)-NARCOTOLINE Inflorescence -- 0 (-)-SCOULERINE Latex Exudate -- 0 (-)-SCOULERINE Plant -- 0 10-HYDROXYCODEINE Latex Exudate -- 0 10-NONACOSANOL Latex Exudate Chemical Constituents of Oriental Herbs (3 diff. books) 0 13-OXOCRYPTOPINE Plant -- 0 16-HYDROXYTHEBAINE Plant -- 0 20-HYDROXY- Fruit 36.0 -- TRICOSANYLCYCLOHEXA NE 0 4-HYDROXY-BENZOIC- Pericarp -- ACID 0 4-METHYL-NONACOSANE Fruit 3.2 -- 0 5'-O- Plant -- DEMETHYLNARCOTINE 0 5-HYDROXY-3,7- Latex Exudate -- DIMETHOXYPHENANTHRE NE 0 6- Plant -- ACTEONLYDIHYDROSANG UINARINE 0 6-METHYL-CODEINE Plant Father Nature's Farmacy: The aggregate of all these three-letter citations. 0 6-METHYL-CODEINE Fruit -- 0 ACONITASE Latex Exudate -- 32 AESCULETIN Pericarp -- 3 ALANINE Seed 11780.0 12637.0 0.5273634907250652 -- Activities Count Chemical Plant Part Low PPM High PPM StdDev Refernce Citation 0 ALKALOIDS Latex Exudate 50000.0 250000.0 ANON. 1948-1976. The Wealth of India raw materials. Publications and Information Directorate, CSIR, New Delhi. 11 volumes. 5 ALLOCRYPTOPINE Plant Father Nature's Farmacy: The aggregate of all these three-letter citations. 15 ALPHA-LINOLENIC-ACID Seed 1400.0 5564.0 -0.22115561650586155 -- 2 ALPHA-NARCOTINE Plant Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp. 17 APOMORPHINE Plant Father Nature's Farmacy: The aggregate of all these three-letter citations. 0 APOREINE Fruit -- 0 ARABINOSE Fruit ANON. -
The Orchid Flora of the Colombian Department of Valle Del Cauca Revista Mexicana De Biodiversidad, Vol
Revista Mexicana de Biodiversidad ISSN: 1870-3453 [email protected] Universidad Nacional Autónoma de México México Kolanowska, Marta The orchid flora of the Colombian Department of Valle del Cauca Revista Mexicana de Biodiversidad, vol. 85, núm. 2, 2014, pp. 445-462 Universidad Nacional Autónoma de México Distrito Federal, México Available in: http://www.redalyc.org/articulo.oa?id=42531364003 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Revista Mexicana de Biodiversidad 85: 445-462, 2014 Revista Mexicana de Biodiversidad 85: 445-462, 2014 DOI: 10.7550/rmb.32511 DOI: 10.7550/rmb.32511445 The orchid flora of the Colombian Department of Valle del Cauca La orquideoflora del departamento colombiano de Valle del Cauca Marta Kolanowska Department of Plant Taxonomy and Nature Conservation, University of Gdańsk. Wita Stwosza 59, 80-308 Gdańsk, Poland. [email protected] Abstract. The floristic, geographical and ecological analysis of the orchid flora of the department of Valle del Cauca are presented. The study area is located in the southwestern Colombia and it covers about 22 140 km2 of land across 4 physiographic units. All analysis are based on the fieldwork and on the revision of the herbarium material. A list of 572 orchid species occurring in the department of Valle del Cauca is presented. Two species, Arundina graminifolia and Vanilla planifolia, are non-native elements of the studied orchid flora. The greatest species diversity is observed in the montane regions of the study area, especially in wet montane forest. -
Root Fungal Associations in Some Non-Orchidaceous Vascular Lithophytes
Acta Botanica Brasilica - 30(3): 407-421. July-September 2016. doi: 10.1590/0102-33062016abb0074 Root fungal associations in some non-orchidaceous vascular lithophytes Thangavelu Muthukumar1*, Marimuthu Chinnathambi1 and Perumalsamy Priyadharsini1 Received: March 7, 2016 Accepted: July 11, 2016 . ABSTRACT Plant roots in natural ecosystems are colonized by a diverse group of fungi among which the most common and widespread are arbuscular mycorrhizal (AM) and dark septate endophyte (DSE) fungi. Th ough AM and DSE fungal associations are well reported for terricolous plant species, they are rather poorly known for lithophytic plant species. In this study, we examined AM and DSE fungal association in 72 non-orchidaceous vascular plant species growing as lithophytes in Siruvani Hills, Western Ghats of Tamilnadu, India. Sixty-nine plant species had AM and 58 species had DSE fungal associations. To our knowledge, we report AM fungal association in 42 and DSE fungal association in 53 plant species for the fi rst time. Th ere were signifi cant diff erences in total root length colonization and root length colonized by diff erent AM and DSE fungal structures among plant species. In contrast, the diff erences in AM and DSE fungal colonization among plants in various life-forms and lifecycles were not signifi cant. AM morphology reported for the fi rst time in 56 plant species was dominated by intermediate type AM morphology. A signifi cant negative relationship existed between total root length colonized by AM and DSE fungi. Th ese results clearly -
Estudos Das Potencialidades Farmacológicas De Plantas Endémicas /Medicinais De Cabo Verde: Campylanthus Glaber Benth Ssp Glaber E Da Globularia Amygdalifolia Webb
UNIVERSIDADE DA BEIRA INTERIOR Ciências Estudos das Potencialidades farmacológicas de plantas endémicas /medicinais de Cabo Verde: Campylanthus glaber Benth ssp glaber e da Globularia amygdalifolia Webb Versão final após defesa Nadir Alves Cardoso Dissertação para obtenção do Grau de Mestre em Química Medicinal (2º ciclo de estudos) Orientador: Prof. Doutor Jesús Miguel López Rodilla Covilhã, março de 2018 Dedicatória Ao meu pai João e à minha mãe Rosa “Os nossos pais amam-nos porque somos seus filhos, é um fato inalterável. Nos momentos de sucesso, isso pode parecer irrelevante, mas nas ocasiões de fracasso, oferecem um consolo e uma segurança que não se encontram em qualquer outro lugar.” Bertrand Russell ii Agradecimentos Ao Pai celestial Senhor Jeová pela vida e pelas bênçãos derramadas nessa caminhada, graças a Ele consegui suportar e ser bem sucedida em todas as dificuldades. Ao meu orientador, Prof. Doutor Jesús Miguel López Rodilla pelo apoio direto e incentivo desde o primeiro momento da minha chegada à Universidade, pelo tempo disponibilizado, e os conhecimentos transmitidos na orientação deste trabalho. Aqui exprimo a minha gratidão. À Faculdade de Ciências da Universidade da Beira Interior, particularmente o departamento de Química e todos os Professores e técnicos de laboratório pelo apoio na realização deste trabalho e a todos os professores que lecionaram unidades curriculares no Mestrado de Química Medicinal, obrigado pelos conhecimentos transmitido. À Universidade de Cabo Verde pela oportunidade e financiamento desse mestrado. Agradeço profundamente à Magnifica Reitora Judite Nascimento! À amiga e Professora Cláudia Beato, pelo incentivo, apoio emocional, pelo ombro emprestado nos momentos de desespero vividos aqui na Covilhã.