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GRANADA FEI Passport No: 104DK01/ITA
DECISION of the FEI TRIBUNAL dated 14 July 2017 Positive Anti-Doping Case No.: 2016/BS09 Horse: GRANADA FEI Passport No: 104DK01/ITA Person Responsible/NF/ID: Allegra Ieraci/ITA/10097333 Represented by: Studio Legale Avv. Claudio Brugnatelli, Strada Nuova n. 53, 27100 Pavia, Italy Event/ID: CSI3*-W – El Jadida (MAR) - 2016_CI_0722_S_S_01 Date: 13 – 16 October 2016 Prohibited Substances: Oripavine, Morphine and Codeine I. COMPOSITION OF PANEL Mr. Erik Elstad, one member panel II. SUMMARY OF THE FACTS 1. Memorandum of case: By Legal Department. 2. Summary information provided by Person Responsible (PR): The FEI Tribunal duly took into consideration all evidence, submissions and documents presented in the case file, as well as during the oral hearing, as also made available by and to the PR. 3. Oral hearing: 6 July 2017 – via telephone conference call. Present: The FEI Tribunal Panel Ms. Erika Riedl, FEI Tribunal Clerk For the PR: Mr. Claudio Brugnatelli, Legal Counsel Mr. Giovanni Ieraci, PR’s father Page 1 of 19 For the FEI: Ms. Anna Thorstenson, FEI Legal Counsel III. DESCRIPTION OF THE CASE FROM THE LEGAL VIEWPOINT 1. Articles of the Statutes/Regulations which are applicable: Statutes 23rd edition, effective 29 April 2015 (“Statutes”), Arts. 1.4, 38 and 39. General Regulations, 23rd edition, 1 January 2009, updates effective 1 January 2016, Arts. 118, 143.1, 161, 168 and 169 (“GRs”). Internal Regulations of the FEI Tribunal, 2nd edition, 1 January 2012 (“IRs”). FEI Equine Anti-Doping and Controlled Medication Regulations ("EADCMRs"), 2nd edition, effective 1 January 2016. FEI Equine Anti-Doping Rules ("EAD Rules"), 2nd edition, effective 1 January 2016. -
Seized Drugs Technical Manual, 12-08-2020
Seized Drugs Technical Manual Approval Date: 12/08/2020 Document Number: 4561 Approved By: David Gouldthorpe, Kim Murga, Cassandra Robertson Revision Number: 17 Date Published: 12/08/2020 Las Vegas Metropolitan Police Department Forensic Laboratory 5605 W. Badura Ave. Ste. 120B Las Vegas, NV 89118 Seized Drugs Technical Manual Uncontrolled Copy if not located in Qualtrax Page 1 of 166 Seized Drugs Technical Manual Approval Date: 12/08/2020 Document Number: 4561 Approved By: David Gouldthorpe, Kim Murga, Cassandra Robertson Revision Number: 17 Date Published: 12/08/2020 Table of Contents Chapter Title Introduction ANALYTICAL TECHNIQUES 1.1 Color Tests 1.2 Chromatography 1.3 Mass Spectrometry (MS) 1.4 Infrared Spectroscopy (IR) 1.5 X-Ray Fluorescence (XRF) 1.6 Raman Spectroscopy QUALITY CONTROL 2.1 Reference Materials and Supplies 2.2 Reference Material Inventory Audit 2.3 Color Test Reagent Quality Control 2.4 Quality Control Plan SEIZED DRUG ANALYSIS 3.1 Seized Drugs Analysis Quality Control 3.2 Sampling 3.3 Identification Criteria 3.4 Evidence Discrepancies and Preliminary Field Test Errors 3.5 Cannabis Analysis 3.6 Opium Analysis 3.7 Analysis of Fentanyl and Fentanyl Related Substances CLANDESTINE LABORATORIES 4.1 Clandestine Laboratory Response 4.2 Clandestine Laboratory Analysis REPORTING AND TECHNICAL REVIEW 5.1 Reporting 5.2 Technical Review 6 Retraining 7 Recipes and Derivatizing Agents PROCEDURES 8.1 Logging Reference Materials into LIMS 8.2 Verifying Reference Materials Uncontrolled Copy if not located in Qualtrax Page 2 of 166 -
Chemistry Exam - 2015
Scientific Officer Chemistry Exam - 2015 (Final Answer Key) Chemistry Q.No: 1 The major detoxification reaction involved in Phase - I are all except. A Oxidation B Hydrolysis C Acetylation D Hydroxylation Q.No: 2 Which of the endogenous substance is detoxified through glucuronidation reaction ? A Aspirin B Methanol C Bilirubin D Phenyl Acetate Q.No: 3 Which of the following is not a conjugating agent in drug metabolisim? A Active acetate B Active sulfate C Active glucuronate D Active Bicarbonate Q.No: 4 Which of the following statements is not true about receptors ? A Most receptors are proteins situated in the cell membrane B Receptors contain a cleft- known as binding site C Receptors catalyze reactions on chemical messengers D Receptors bind to chemical messengers e.g. neurotransmitters etc Q.No: 5 The mechanism behind pesticide poisoning is A Irreversible binding with Acetyl choline esterase B Reversible binding with Acetyl choline esterase C Irreversible binding with nicotinic receptors D Reversible binding with nicotinic receptors Q.No: 6 Which one of the following have binding affinity but no intrinsic activity? A Agonist B Antagonist C Partial Agonist D Inverse Agonist Q.No: 7 Which of the following is not a requirement for a drug to act as an agonist ? A Functional group B Metabolic stability C Pharmacophore D Size Q.No: 8 Polycyclic aromatic hydrocarbons (PAH) in cigarette smoke may cause - A Inhibition of cytochrome P-450 and delayed metabolism B Inhibition of cytochrome P-450 and enhanced metabolism C Induction of cytochrome -
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. -
Determination of Morphine Content in Turkish Type Poppy Seed by Hplc Method
DETERMINATION OF MORPHINE AND TOTAL PHENOLIC CONTENT IN POPPY SEED OF TURKISH ORIGIN A THESIS SUBMITTED TO THE GRADUATE SCHOOL OF NATURAL AND APPLIED SCIENCES OF MIDDLE EAST TECHNĠCAL UNIVERSITY BY ALĠ GEVENKĠRĠġ IN PARTIAL FULLFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE IN CHEMISTRY FEBRUARY 2011 DETERMINATION OF MORPHINE AND TOTAL PHENOLIC CONTENT IN POPPY SEED OF TURKISH ORIGIN Submitted by ALİ GEVENKİRİŞ in partial fulfillment of the requirements fort he degree of Master of Science in Chemistry Department, Middle East Technical University by, Prof. Dr. Canan Özgen -------------------- Dean, Graduate School of Natural and Applied Sciences Prof. Dr. Ġlker Özkan -------------------- Head of Department, Chemistry Assoc. Prof. Dr. Nursen ÇORUH -------------------- Supervisor, Chemistry Department, METU Examining Committe Members: Prof. Dr. Cihangir TANYELĠ -------------------- Chemistry Department, METU Assoc. Prof. Dr. Nursen ÇORUH -------------------- Supervisor, Chemistry Department, METU Prof. Dr. Ceyhan KAYRAN -------------------- Chemistry Department, METU Prof. Dr. Özdemir DOĞAN -------------------- Chemistry Department, METU Assoc. Prof. Dr. Hakan ULUKAN -------------------- Faculty of Agriculture, Field Crops Dept. Ankara University Date: / / ii I hereby declare that all information in this document has been obtained and presented in accordance with academic rules and ethical conduct. I also declare that, as required by these rules and conduct, I have fully cited and referenced all material and results that not original to the this work. Name, Last name: Ali GEVENKİRİŞ Signature: iii ABSTRACT DETERMINATION OF MORPHINE AND TOTAL PHENOLIC CONTENT IN POPPY SEED OF TURKISH ORIGIN GevenkiriĢ, Ali M.Sc.,Department of Chemistry Supervisor: Assoc. Prof. Dr. Nursen Çoruh February 2011, 51 Pages Turkey is important major licid opium poppy (Papaver Somniferum) producer for medicinal and scientific purposes in the world and one of the two traditional producer country. -
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. -
Seized Drugs SOP 09.09.2019
Seized Drugs Standard Operating Procedures Comparative and Analytical Division Seized Drugs Standard Operating Procedures Comparative and Analytical Division Table of Contents 1. Goals and Objectives ................................................................................................................................8 1.1. Goals.............................................................................................................................................8 1.2. Objectives.....................................................................................................................................8 2. Evidence Handling ..................................................................................................................................10 2.1 Scope..........................................................................................................................................10 2.2. Receiving and Documenting Evidence.............................................................................................10 2.3. Cases Containing Currency, Valuables, Large Items, and Bullets.....................................................12 2.4. Cases Requiring Examination for Latent Prints................................................................................12 2.5. Cases Containing Possible Biohazards .............................................................................................12 2.6. Return of Evidence to the Submitting Agency.................................................................................13 -
OPIUM Latest Revision: June 30, 2000
OPIUM Latest Revision: June 30, 2000 1. SYNONYMS CFR: Opium CAS #: Codeine Base: 76-57-3 Codeine Hydrochloride: 1422-07-7 Morphine Base: 57-27-2 Morphine Hydrochloride: 52-26-6 Thebaine Base: 115-37-7 Noscapine Base: 128-62-1 Noscapine Hydrochloride: 912-60-7 Papaverine Base: 58-74-2 Papaverine Hydrochloride: 61-25-6 Other Names: Oil poppy Opium poppy 2. CHEMICAL AND PHYSICAL DATA The immediate precursor of heroin is morphine, and morphine is obtained from opium. Opium is the dried milky juice (latex) obtained from the unripe seed pods of Papaver somniferum L., more commonly referred to as the opium poppy or oil poppy. Morphine has also been reported to be present in Papaver setigerum, and as a minor alkaloid in Papaver decaisnei and Papaver rhoeas. However, there is no known instance of these poppies being used for opium production, and work that is more recent has cast considerable doubt as to the presence of morphine in Papaver rhoeas. A major review by Kapoor on the botany and chemistry of the opium poppy is recommended additional reading. Opium latex is obtained from the seed capsule of the poppy while the capsule is still in the green stage, usually seven or more days after flowering and petal fall. Physically, the opium latex is contained within laticiferous vessels, which lie just beneath the epicarp of the seed capsule. The latex is harvested by making a series of shallow incisions through the epicarp, which allows the latex to "bleed" onto the surface of the seed capsule. Most commonly, the latex is allowed to partially dry on the capsule surface, and is then removed by scraping the capsule with specially designed hand tools. -
LXV.-On the Relation Bet Ween the Absorption Spectra and the Chemical Stmetwe of Corydaline, Ber- Berine, and Other Alkaloids
View Article Online / Journal Homepage / Table of Contents for this issue ABSORPTION SPECTRA OF ALKALOIDS. 605 Published on 01 January 1903. Downloaded by Rensselaer Polytechnic Institute 23/10/2014 03:49:06. LXV.-On the Relation bet ween the Absorption Spectra and the Chemical Stmetwe of Corydaline, Ber- berine, and other Alkaloids. By JAMESJ. DOBBIE,M.A., D.Sc., and ALEXANDERLAUDER, B.Sc. INa paper read before the Society in December, 1901 (Trans., 1902, 81, 145), we communicated the results of our investigation on the constitution of corydaline, and showed that this alkaloid is closely related to berberine. We have since been engaged in the spectroscopic View Article Online 606 DOBBIE AND LAUDER: ABSORPTION SPECTRA AND examination of these two alkaloids and their decomposition products, and me now propose to lay the results of this supplementary investi- gation before the Society, with the object mainly of showing that the spectroscopic method might, with advantage, be generally employed in such researches, In a paper communicated to the Royal Society eighteen years ago by Professor Hartley (PM,Frans., 1885, Part 11, 471), it is shown that the principal alkaloids give highly characteristic absorption spectra which can be used for their identification and for ascertaining their purity. It is further shown that alkaloids closely related to one another, like quinine and quinidine, cinchonine and cinchonidine, mor- phine and codeine, give very similar spectra. At the time at which this paper was published, however, little progress had been made with tho investigation of the alkaloids, and it was not possible, therefore, to trace any close connection between their structure and their spectra. -
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. -
Further Studies of Sequestration of Alkaloids in Papaver Somniferum L
Further Studies of Sequestration of Alkaloids in Papaver somniferum L. Latex Vacuoles Margaret F. Roberts, B. C. Homeyer, and Thi D. T. Pham The Department of Pharmacognosy, The School of Pharmacy, London University, 29/39 Brunswick Square, London WC 1 N 1 AX Z. Naturforsch. 46c, 377-388 (1991); received December 12, 1990 Papaver somniferum, Latex Vacuoles, Alkaloid, Sequestration The uptake and sequestration of alkaloids by latex vacuoles of P. somniferum sedimenting at 900 x g and 1100 x g were studied; both populations take up morphine effectively. Morphine uptake by the 1100 x g vacuoles was stimulated by exogenous ATP and, after uptake of large amounts of alkaloid, both populations were stimulated by exogenous ATP to take up further morphine; this effect was no longer present in 900 x g vacuoles isolated from the latex of more mature capsules. Uptake by 1100 x g vacuoles was more sensitive to temperature than that of 900 x g vacuoles. Determination of the proton gradient across the vacuolar membrane (ApH), controlled dissipation of ApH through the use of NH 4C1, and correlation with morphine up take demonstrated that morphine uptake was strongly dependant on the maintenance of ApH. Inhibitors designed to produce loss of protons from the vacuole had, however, little effect on the system. Nitrate, as an inhibitor of tonoplast ATPase, had an inhibitory effect on morphine uptake by the 1100 x g vacuoles. Uptake of meconate, [ 35S]sulphate and L-[Ul4C]malate, important acid constituents of the 900 x g vacuoles was investigated. Uptake of sulphate and malate was continuous and satura tion was not reached; the rate of uptake of sulphate and malate was much lower than that of morphine and other alkaloids, and uptake of meconate by these vacuoles was not detected. -
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