Application of Black Salve to a Thin Melanoma That Subsequently Progressed to Metastatic Melanoma: a Case Study
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Effects of Berberine, Chelerythrine, and Sanguinarine on Proliferation in Four Human Immortalized Cell Lines
Journal of the Iowa Academy of Science: JIAS Volume 119 Number 1-4 Article 6 2012 Effects of Berberine, Chelerythrine, and Sanguinarine on Proliferation in Four Human Immortalized Cell Lines David S. Senchina Drake University Nisarg B. Shah Drake University Marc G. Busch Drake University Let us know how access to this document benefits ouy Copyright © Copyright 2014 by the Iowa Academy of Science, Inc. Follow this and additional works at: https://scholarworks.uni.edu/jias Part of the Anthropology Commons, Life Sciences Commons, Physical Sciences and Mathematics Commons, and the Science and Mathematics Education Commons Recommended Citation Senchina, David S.; Shah, Nisarg B.; and Busch, Marc G. (2012) "Effects of Berberine, Chelerythrine, and Sanguinarine on Proliferation in Four Human Immortalized Cell Lines," Journal of the Iowa Academy of Science: JIAS, 119(1-4), 22-27. Available at: https://scholarworks.uni.edu/jias/vol119/iss1/6 This Research is brought to you for free and open access by the Iowa Academy of Science at UNI ScholarWorks. It has been accepted for inclusion in Journal of the Iowa Academy of Science: JIAS by an authorized editor of UNI ScholarWorks. For more information, please contact [email protected]. Jour. Iowa Acad. Sci. 119(1--4):22-27, 2012 Effects of Berberine, Chelerythrine, and Sanguinarine on Proliferation in Four Human Immortalized Cell Lines DAVIDS. SENCHINA1·*, NISARG B. SHAH2 and MARC G. BUSCH 1 1Deparcmenc of Biology, Drake University, Des Moines, IA 2Pharmacy Program, Drake University, Des Moines, IA Bloodroot (Sanguinaria canadensis L., Papaveraceae) is a plane rich in benzophenanchridine (isoquinoline) alkaloids ~uch_ as sanguinarine and chelerychrine. -
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. -
Crude Drugs Containing Quinoline, Isoquinoline, And
CRUDE DRUGS CONTAINING QUINOLINE, ISOQUINOLINE, AND PHENANTHRENE ALKALOIDS Content 1. MACROMORPHOLOGICAL EVAULATION Cinchonae cortex Ipecacuanhae radix Chelidonii herba Papaveris maturi fructus Opium crudum Fumariae herba 2. MICROSCOPICAL TESTS Cross section: Cinchonae cortex Ipecacuanhae radix Powder preparation: Cinchonae cortex 3. PHYSICO-CHEMICAL AND CHEMICAL TESTS Specific alkaloid reactions 3.1. Grahe test (Cinchonae cortex) 3.2. Emetine test (Ipecacuanhae radix) 3.3. Marquis test (Papaveris maturi fructus) 3.4. Meconic acid test (Papaveris maturi fructus) 3.5. Chelidonii herba tests (Chelidonii herba) 3.5.1. Chelidonic acid test (Chelidonii herba) 3.5.2. Quaternary amine test (Chelidonii herba) 3.5.3. Chromotropic acid test (Chelidonii herba) 3.5.4. Chelidonii herba alkaloid investigation with TLC 4. QUANTITATIVE DETERMNATIONS 4.1. Determination of alkaloid content in Cinchonae cortex (Ph.Eur.) 4.2 Quantitative determination of morphine in ripped capsules of poppy by TLC 1 1. MACROMORPHOLOGICAL EVALUATION Cinchonae cortex Cinchona bark Cinchona pubescens Vahl. Rubiaceae (Cinchona succirubra Pavon) C. calisaya (Weddell) C. ledgeriana (Moens ex Trimen) Ph. Eur. Whole or cut, dried bark of Cinchona species. Content: minimum 6.5 per cent of total alkaloids, of which 30 %- 60 % consists of quinine type alkaloids (dried drug). Ipecacuanhae radix Ipecacuanha root Cephaelis ipecacuanha (Brot.) A.Rich. Rubiaceae Cephaelis acuminata Karsten Ph. Eur. Karlten Ipecacuanha root consists of the fragmented and dried underground organs of Cephaelis species. It contains not less than 2.0 per cent of total alkaloids, calculated as emetine. The principal alkaloids are emetine and cephaeline. Chelidonii herba Greater Celandine Chelidonium majus L. Papaveraceae Ph.Eur. Dried, whole or cut aerial parts of Chelidonium majus L collected during flowering. -
Identification and Determination of Alkaloids in Fumaria Species from Romania
Digest Journal of Nanomaterials and Biostructures Vol. 8, No. 2, April - June 2013, p. 817 - 824 IDENTIFICATION AND DETERMINATION OF ALKALOIDS IN FUMARIA SPECIES FROM ROMANIA R. PĂLTINEANa, A. TOIUb* , J. N. WAUTERSc, M. FRÉDÉRICHc, M. TITSc, L. ANGENOTc, M. TĂMAŞa , G. CRIŞANa a Department of Pharmaceutical Botany, Faculty of Pharmacy, "Iuliu Hatieganu" University of Medicine and Pharmacy, 12 Ion Creanga Street, 400010 Cluj- Napoca, Romania bDepartment of Pharmacognosy, Faculty of Pharmacy, "Iuliu Hatieganu" University of Medicine and Pharmacy, 12 Ion Creanga Street, 400010 Cluj- Napoca, Romania cDepartment of Pharmacognosy, Drug Research Center (CIRM), Faculty of Medicine, University of Liège, 1, Avenue de l' Hôpital Street, B-4000- Liege, Belgium Four Fumaria species (F. vaillantii Loisel, F. parviflora Lam., F. rostellata Knaf and F. jankae Hausskn.) were analysed in order to determine the presence of the isoquinoline alkaloids allocryptopine, chelidonine, protopine, bicuculline, sanguinarine, cheleritrine, stylopine, and hydrastine through an HPLC-DAD method. Protopine and sanguinarine were present in all extracts. Bicuculline and stylopine were found in F. vaillantii and F. parviflora, whilst chelidonine was identified only in F. vaillantii and hydrastine in F. jankae, so they represent potential taxonomic markers that differentiate the four plants. The richest species in isoquinoline alkaloids was F. parviflora. Our study showed significant differences between the four Fumaria species, both qualitative and quantitative. (Received March 4, 2013; Accepted May 15, 2013) Keywords: Fumaria species; isoquinoline alkaloids; HPLC-DAD 1. Introduction The families Fumariaceae and Papaveraceae are closely related and are both very rich in isoquinoline alkaloids, especially of the aporphine, benzophenanthridine, protoberberine and protopine types. -
Hot Topics in Pharmacognosy: Opiates from Modified Microbes
Hot Topics in Pharmacognosy: Opiates from Modified Microbes Dr. David J. Newman Subsequent conversion into heroin (2) was first reported in s known by all pharmacognosists, throughout the ages 1874 by Wright in the United Kingdom as a result of boiling mor- humans and other animals relied on nature for their ba- phine acetate. It was commercialized by Bayer AG in 1898 and sic needs. Plants, in particular, formed the basis of so- sold as a “tonic” by then Smith Kline and French laboratories phisticated traditional medicine systems, with the earli- (precursor of GlaxoSmithKline) in the United States around the Aest records dating from around 2900-2600 BCE,1 documenting turn of the 20th Century. The use and abuse of these compounds the uses of approximately 1,000 plant-derived substances in is much too complex to discuss here, but in 1973, Pert and Syn- Mesopotamia2 and the active transportation of medicinal plants der reported the identification of opioid receptors in brain tis- and oils around what is now known as Southwest Asia. These sue,9 and this report was closely followed in 1975 by Kosterlitz included oils of Cedrus species (cedar) and Cupressus sempervi- and Hughes.10 This identification of “endogenous morphine-like rens (cypress), Glycyrrhiza glabra (licorice), Commiphora species substances” over the next few years led to the discovery of en- (myrrh), and the star of this story, Papaver somniferum (poppy kephalins, endorphins, and dynorphins, all of which had the com- juice). It should be noted that all are still used today for the treat- mon N-terminal sequence of Tyr-Gly-Gly-Phe-(Met/Leu), leading to ment of ailments ranging from coughs, colds, and analgesia to the concept that morphine actually mimics this sequence.11 parasitic infections and inflammation. -
Introduction (Pdf)
Dictionary of Natural Products on CD-ROM This introduction screen gives access to (a) a general introduction to the scope and content of DNP on CD-ROM, followed by (b) an extensive review of the different types of natural product and the way in which they are organised and categorised in DNP. You may access the section of your choice by clicking on the appropriate line below, or you may scroll through the text forwards or backwards from any point. Introduction to the DNP database page 3 Data presentation and organisation 3 Derivatives and variants 3 Chemical names and synonyms 4 CAS Registry Numbers 6 Diagrams 7 Stereochemical conventions 7 Molecular formula and molecular weight 8 Source 9 Importance/use 9 Type of Compound 9 Physical Data 9 Hazard and toxicity information 10 Bibliographic References 11 Journal abbreviations 12 Entry under review 12 Description of Natural Product Structures 13 Aliphatic natural products 15 Semiochemicals 15 Lipids 22 Polyketides 29 Carbohydrates 35 Oxygen heterocycles 44 Simple aromatic natural products 45 Benzofuranoids 48 Benzopyranoids 49 1 Flavonoids page 51 Tannins 60 Lignans 64 Polycyclic aromatic natural products 68 Terpenoids 72 Monoterpenoids 73 Sesquiterpenoids 77 Diterpenoids 101 Sesterterpenoids 118 Triterpenoids 121 Tetraterpenoids 131 Miscellaneous terpenoids 133 Meroterpenoids 133 Steroids 135 The sterols 140 Aminoacids and peptides 148 Aminoacids 148 Peptides 150 β-Lactams 151 Glycopeptides 153 Alkaloids 154 Alkaloids derived from ornithine 154 Alkaloids derived from lysine 156 Alkaloids -
The Alkaloids
The Alkaloids Alkaloids in the skin glands of poison frogs: A chemical defense against predation What are Alkaloids? • Low molecular weight Nitrogenous compounds • 20% of plant species have been found to contain them • Mainly involved in plant defense against herbivores and pathogens • Utilization by human 3000 Year History of Alkaloids use by Humans • In most human history, alkaloids from plant extracts have been used as ingredients in potions (liquid medicine) and poisons • Ancient people used plant extracts containing alkaloids for treating a large number of ailments including: snakebite, fever and insanity 3000 Year History of Alkaloids use by Humans In the middle east- the latex of Opium Poppy (Papaver) was already used at 1200 B.C. Alkaloids of Opium Poppy Opium Poppy capsule (Papaver) •Capsule Maturing capsule releasing latex when wounded • Latex contains the alkaloids morphine and related alkaloids such as codeine 1200 BC in Greece Alkaloids of Opium Poppy (Papaver) Bufo marinus frog accumulates high amount of morphine in its skin Later the use of Alkaloids Spread to the West Jacques Louis David painting (1787) - The piperidine alkaloid coniine (the first alkaloid to be synthesized) - Coniine is extremely toxic, causing paralysis of motor nerve endings - "The death of Socrates"- the philosopher Socrates drank and extract of coniine-containing hemlock (339 B.C.) In Egypt- Queen Cleopatra used extracts of henbane (Hyoscymus) to expand her pupils and appear more attractive to her male political competitors Alkaloids of Opium Poppy -
Sanguinaria Canadensis: Traditional Medicine, Phytochemical Composition, Biological Activities and Current Uses
International Journal of Molecular Sciences Review Sanguinaria canadensis: Traditional Medicine, Phytochemical Composition, Biological Activities and Current Uses Andrew Croaker 1,*, Graham J. King 1, John H. Pyne 2, Shailendra Anoopkumar-Dukie 3 and Lei Liu 1,* 1 Southern Cross Plant Science, Southern Cross University, Lismore, NSW 2480, Australia; [email protected] 2 School of Medicine, The University of Queensland, St. Lucia, QLD 4072, Australia; [email protected] 3 School of Pharmacy, Griffith University, Gold Coast Campus, Gold Coast, QLD 4222, Australia; s.dukie@griffith.edu.au * Correspondence: [email protected] (A.C.); [email protected] (L.L.); Tel.: +61-04-2959-4932 (A.C.); +61-02-6622-3211 (L.L.) Academic Editor: Chang Won Choi Received: 22 July 2016; Accepted: 12 August 2016; Published: 27 August 2016 Abstract: Sanguinaria canadensis, also known as bloodroot, is a traditional medicine used by Native Americans to treat a diverse range of clinical conditions. The plants rhizome contains several alkaloids that individually target multiple molecular processes. These bioactive compounds, mechanistically correlate with the plant’s history of ethnobotanical use. Despite their identification over 50 years ago, the alkaloids of S. canadensis have not been developed into successful therapeutic agents. Instead, they have been associated with clinical toxicities ranging from mouthwash induced leukoplakia to cancer salve necrosis and treatment failure. This review explores the historical use of S. canadensis, the molecular actions of the benzophenanthridine and protopin alkaloids it contains, and explores natural alkaloid variation as a possible rationale for the inconsistent efficacy and toxicities encountered by S. -
ARGEMONE OIL, SANGUINARINE, and EPIDEMIC-DROPSY GLAUCOMA*T by SOHRAB A
Br J Ophthalmol: first published as 10.1136/bjo.38.4.193 on 1 April 1954. Downloaded from Brit. J. Ophthal. (1954) 38, 193. COMMUNICATIONS ARGEMONE OIL, SANGUINARINE, AND EPIDEMIC-DROPSY GLAUCOMA*t BY SOHRAB A. E. HAKIM From the University Departments ofPhysiology and Pharmacology, Oxford Argemone mexicana Linn. (Linnaeus, 1753; Tournefort, 1694), is a herb of the Papaveraceae (poppy family) indigenous to the West Indies (Fig. 1). The study of this herb and its active principles is important, first to circumvent the serious epidemics of dropsy and glaucoma resulting from the unintentional ingestion of its seed oil in tropical countries; secondly to find a method of producing in _ laboratoryanimals conditions similar to, if not identical with, glaucoma; and thirdly to examine the possibility that other simiilar pla-nts, by indirect ingestion, may play an insidious role in the caus- ation of primary endemic copyright. ...... ..... .. ~...: glaucoma. ::? Argemone mexicana (or Prickly yellow poppy), being one of the most accommodat- ing of weeds, has spread by zonal distribution and-become naturalized during the last http://bjo.bmj.com/ 350 years in all eastern tropi- cal and sub-tropical countries, cluding Africa, India, South- East Asia, Australia and the Philippines, although it is rare along the American on September 26, 2021 by guest. Protected aific coasts (Pramn, 1895). F-o 1. - Argemone The dispersal of this pois- mexicana (after Curtis, onous weed across half the * 0 .1794).g t globe reveals a fascinating ....... story of man-induced follow- ed by natural spread; but one which is also sad in that suffering and blindness has been caused to masses of the poor populations in the East and especially in India. -
Molecular Geometry of Alkaloids Present in Seeds of Mexican Prickly Poppy
MOLECULAR GEOMETRY OF ALKALOIDS PRESENT IN SEEDS OF MEXICAN PRICKLY POPPY Ricardo Gobato [[email protected]] Secretaria de Estado da Educação do Paraná (SEED/PR) Av. Maringá, 290, Jardim Dom Bosco, Londrina/PR, 86060-000, Brasil. Desire Francine Gobato Fedrigo [[email protected]] Panoramic Residence, Rua Uruguai, 1380, ap. 405, Parque Jardim America, Centro, Londrina/PR, 86010-210, Brasil Alekssander Gobato [[email protected]] Faculdade Pitágoras Londrina Rua Edwy Taques de Araújo, 1100, Gleba Palhano, Londrina/PR, 86047-500, Brasil. ABSTRACT The work is a study of the geometry of the molecules via molecular mechanics of the main alkaloids found in the seeds of Argemone Mexicana Linn, a prickly poppy, which is considered one of the most important species of plants in traditional Mexican and Indian medicine system. The seeds have toxic properties as well as bactericide, hallucinogenic, fungicide, insecticide, in isoquinolines and sanguinarine alkaloids such as berberine. A computational study of the molecular geometry of the molecules through molecular mechanics of the main alkaloids compounds present in plant seeds is described in a computer simulation. The plant has active ingredients compounds: allocryptopine, berberine, chelerythrine, copsitine, dihydrosanguinarine, protopine and sanguinarine. The studied alkaloids form two groups having similar charge distribution among themselves, which have dipole moments of these two times higher than in the other group. Keywords: Alkaloids, Argemone Mexicana Linn, Bactericidal, Fungicide, Hallucinogenic, Insecticide, Molecular Geometry, Prickly Poppy, Toxic. Contents 3.5 Dihydrosanguinarine . 6 3.6 Protopine . 6 Introduction 1 3.7 Sanguinarine . 6 1 The plant 2 4 Discussion and conclusions 6 1.1 Argemone Mexicana Linn . -
<I>Glaucium Flavum</I>
ORIGINAL ARTICLES Department of Pharmacognosy1, Faculty of Pharmacy; Department of Genetics2, Faculty of Agriculture, University of Zagazig, Zagazig, Egypt; Department of Pharmaceutical Sciences3, School of Clinical Pharmacy, University of King Faisal, Ahsaa, Kingdom of Saudi Arabia Plant germination and production of callus from the yellow hornpoppy (Glaucium flavum): the first stage of micropropagation M. E. Mohamed 1,3,A.M.Arafa1, S. S. Soliman 2, S. I. Eldahmy 1 Received December 30, 2013, accepted January 30, 2014 Maged El-Sayed Mohamed, Department of Pharmaceutical Sciences, School of Clinical Pharmacy, University of King Faisal, P.P. 380, Ahsaa 31982, Kingdom of Saudi Arabia [email protected] Pharmazie 69: 715–720 (2014) doi: 10.1691/ph.2014.3992 The yellow hornpoppy, Glaucium flavum Cr. (Fam. Papaveraceae) is a perennial herb, distributed in the Mediterranean region, including Egypt. The plant contains many benzyl isoquinoline alkaloids from the aporphine type such as glaucine, isoboldine, l-chelidonine, l-norchelidonine and 3-O-methylarterenol, mak- ing it to display various medicinal activities including antitussive, anticancer, antioxidant, antimicrobial, antiviral, hypoglycemic, analgesic, antipyretic, bronchodilator and anti-inflammatory effects. The plant is now rare and endangered in the Egyptian flora due to urban sprawl. The present study looks into Glaucium flavum seeds’ in vitro germination as well as the ability of the explants taken from the growing seedlings to form stable callus lines in order to enable micropropagation as a way to save the rare plant. The study also scans the production of different medicinally valuable alkaloids, particularly glaucine, in produced callus. 1. Introduction (Kapai et al. 2010; Sarasan 2006). -
Antiviral and Antimicrobial Profiles of Selected Isoquinoline Alkaloids
Antiviral and Antimicrobial Profiles of Selected Isoquinoline Alkaloids from Fumaria and Corydalis Species Ilkay Orhana, Berrin Özc¸elikb, Taner Karaog˘luc, and Bilge S¸ enera,* a Department of Pharmacognosy, Faculty of Pharmacy, Gazi University, 06330 Ankara, Turkey. E-mail: [email protected] b Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Gazi University, 06330 Ankara, Turkey c Department of Virology, Faculty of Veterinary, Ankara University, 06110 Ankara, Turkey * Author for correspondence and reprint requests Z. Naturforsch. 62c,19Ð26 (2007); received July 28, 2006 In the current study, 33 isoquinoline alkaloids belonging to protopine-, benzylisoquinoline-, benzophenanthridine-, spirobenzylisoquinoline-, phthalideisoquinoline-, aporphine-, proto- berberine-, cularine-, and isoquinolone-types as well as 7 derivatives of them obtained from some Fumaria and Corydalis species growing in Turkey have been evaluated for their in vitro antiviral and antimicrobial activities. Both DNA virus Herpes simplex (HSV) and RNA virus Parainfluenza (PI-3) were employed for antiviral assessment of the compounds using Mad- ine-Darby bovine kidney and Vero cell lines and their maximum non-toxic concentrations (MNTC) and cytopathogenic effects (CPE) were determined using acyclovir and oseltamivir as the references. Antibacterial and antifungal activities of the alkaloids were tested against Escherichia coli, Pseudomonas aeruginosa, Proteus mirabilis, Klebsiella pneumoniae, Acineto- bacter baumannii, Staphylococcus aureus, Bacillus subtilis, and Candida albicans by the mi- crodilution method and compared to ampicilline, ofloxacine, and ketocanazole as the referen- ces. The alkaloids did not present any notable antibacterial effect, while they had significant antifungal activity at 8 μg/ml concentration. On the other hand, the alkaloids were found to have selective inhibition against the PI-3 virus ranging between 0.5 and 64 μg/ml as minimum and maximum CPE inhibitory concentrations, whereas they were completely inactive to- wards HSV.