Visions on Iboga/Ine from the International Community
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(12) United States Patent (10) Patent No.: US 8,859,764 B2 Mash Et Al
US008859764B2 (12) United States Patent (10) Patent No.: US 8,859,764 B2 Mash et al. (45) Date of Patent: Oct. 14, 2014 (54) METHODS AND COMPOSITIONS FOR 4,464,378 A 8, 1984 Hussain PREPARING NORIBOGAINE FROM 1999 A 5. E. E.ea. tal VOACANGINE 4,587,243 A 5/1986 LotSof 4,604,365. A 8, 1986 O'Neill et al. (75) Inventors: Deborah C. Mash, Miami, CA (US); 4,620,977 A 1 1/1986 Strahilevitz Robert M. Moriarty, Michiana Shores, 4,626,539 A 12/1986 Aungst et al. IN (US); Richard D. Gless, Jr., 2.s sy s: A : 3. E.OCS ca.t Oakland, CA (US) 4,737,586 A 4, 1988 Potier et al. 4,806,341 A 2f1989 Chien et al. (73) Assignee: DemeRx, Inc., Ft. Lauderdale, FL (US) 4,857,523 A 8, 1989 LotSof 5,026,697 A 6, 1991 LotSof (*) Notice: Subject to any disclaimer, the term of this 5,075,341. A 12, 1991 Mendelson et al. patent is extended or adjusted under 35 Sigi A 3. 3: E. al. U.S.C. 154(b) by 0 days. 5,152.994.J. I.- A 10/1992 Lotsofranger et al. 5,283,247 A 2f1994 Dwivedi et al. (21) Appl. No.: 13/496,185 5,290,784. A 3/1994 Quet al. 5,316,759 A 5/1994 Rose et al. (22) PCT Filed: Jan. 23, 2012 5,382,657 A 1/1995 Karasiewicz et al. 5,426,112 A 6/1995 Zagon et al. (86). PCT No.: PCT/US2012/022255 5,574,0525,552,406 A 1 9,1/1996 1996 MendelsonRose et al. -
Effect of Various Extracts of Tabernaemontana Divaricata on Haloperidol Induced Catalepsy in Rats
Raj et al., International Current Pharmaceutical Journal, February 2014, 3(3): 240-242 International Current http://www.icpjonline.com/documents/Vol3Issue3/02.pdf Pharmaceutical Journal ORIGINAL RESEARCH ARTICLE OPEN ACCESS Effect of various extracts of Tabernaemontana divaricata on haloperidol induced catalepsy in rats *Chanchal N. Raj1, A. Balasubramaniam2, Sayyed Nadeem2 1Department of Pharmacy, Karpagam University,Coimbatore, Tamilnadu, – 641021, India 2Technocrats Institute of Technology- Pharmacy, Bhopal, M.P.-462021, India ABSTRACT Parkinson’s disease (PD) is one of the neurodegenerative diseases with selective loss of dopamine neurons of the substantia n igra pars compacta. In the present study, anti-cataleptic activity of Tabernaemontana divaricata leaves extracts viz. aqueous and ethanolic at different doses (50, 100 and 150 mg/kg i.p.) were studied using haloperidol (1 mg/kg, i.p.) induced catalepsy in rats which is a useful animal model for screening drugs for Parkinson’s disease. Both the extracts were found to reduce catalepsy significantly (P<0.001) as compared to the haloperidol treated rats showing greater effect at 150 mg/kg i.p. dose. Thus the present study reveals the anti- cataleptic activity of Tabernaemontana divaricata evaluating the traditional folklore medicinal use of the plant. Key Words: Tabernaemontana divaricata, Parkinson’s disease (PD), catalepsy, haloperidol, bar test. INTRODUCTIONINTRODUCTION by the increase of the lipid peroxidation product, Neurological disorders include brain injuries, neuro- malonaldehyde. -
A Review on Tabernaemontana Spp.: Multipotential Medicinal Plant
Online - 2455-3891 Vol 11, Issue 5, 2018 Print - 0974-2441 Review Article A REVIEW ON TABERNAEMONTANA SPP.: MULTIPOTENTIAL MEDICINAL PLANT ANAN ATHIPORNCHAI* Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Burapha University, Bangsaen, Chonburi 20131 Thailand. Email: [email protected] Received: 01 March 2016, Revised and Accepted: 29 January 2018 ABSTRACT Plants in the genus Tabernaemontana have been using in Thai and Chinese traditional medicine for the treatment several diseases. The great majority constituents of Tabernaemontana species have already been subjected to isolation and identification of monoterpene indole alkaloids present in their several parts. Many of monoterpene indole alkaloids exhibited a wide array of several activities. The biogenesis, classification, and biological activities of these alkaloids which found in Tabernaemontana plants were discussed in this review and its brings the research up-to-date on the bioactive compounds produced by Tabernaemontana species, directly or indirectly related to human health. Keywords: Tabernaemontana plants, Phytochemistry, Biogenesis, Terpene indole alkaloids, Biological activities. © 2018 The Authors. Published by Innovare Academic Sciences Pvt Ltd. This is an open access article under the CC BY license (http://creativecommons. org/licenses/by/4. 0/) DOI: http://dx.doi.org/10.22159/ajpcr.2018.v11i5.11478 INTRODUCTION alkaloids are investigated. All monoterpene indole alkaloids are derived from aromatic amino acid tryptophan and the iridoid terpene Several already drugs were discovered from the natural products. secologanin (Scheme 1). Tryptophan converts to tryptamine using Especially, the treatments of infectious diseases and oncology have tryptophan decarboxylase which is a pyridoxal-dependent enzyme. benefited from numerous drugs which were found in natural product The specific iridoid precursor was subsequently identified as sources. -
UPS-QT11443.Pdf
UNIVERSIDAD POLITÉCNICA SALESIANA SEDE QUITO CARRERA: INGENIERÍA EN BIOTECNOLOGÍA DE LOS RECURSOS NATURALES Trabajo de titulación previo a la obtención del título de: INGENIERA EN BIOTECNOLOGÍA DE LOS RECURSOS NATURALES TEMA: INHIBICIÓN DE LA ACTIVIDAD HEMOLÍTICA DEL VENENO DE Bothrops atrox POR LOS EXTRACTOS DE Tabernaemontana sananho Ruiz & Pav. Y Mucuna cf. elliptica (Ruiz&Pav.) DC. AUTORA: JENNY VERÓNICA CUEVA PUNGACHO TUTOR: WILSON FABIÁN TAPIA HERNÁNDEZ Quito, marzo 2017 Dedicatoria Mi tesis la dedico con todo mi amor a Dios por haberme dado la vida y permitirme haber llegado hasta este momento tan importante de mi formación profesional. A mis padres Cecilia e Iván, a mis hermanos Lorena e Iván Cueva y mi Sobrinita Amelia por ser el pilar más importante en mi vida, demostrándome siempre su cariño, apoyo incondicional y sobre todo su confianza para culminar esta etapa de mi vida. A la compañera de toda la vida Birkha que fue quien en las noches frías de angustia siempre estuvo demostrándome su lealtad y cariño hasta su último suspiro. Agradecimiento Sin duda alguna mi profundo agradecimiento a la UNIVERSIDAD POLITÉCNICA SALESIANA que me dio la oportunidad de realizar mis sueños en la formación profesional con la ayuda de los maestros formadores de jóvenes con inspiraciones para un mañana lleno de sueños y formar un futuro de promesas para una vida mejor. Este proyecto es el resultado del esfuerzo conjunto de todos los que formamos el grupo de trabajo. De manera especial mi agradecimiento a mi tutor Químico Farmacéutico Wilson Tapia quien con su esfuerzo, dedicación y sobretodo con su profesionalismo que nos impartió sus conocimientos e hizo posible la culminación del proyecto. -
The Iboga Alkaloids
The Iboga Alkaloids Catherine Lavaud and Georges Massiot Contents 1 Introduction ................................................................................. 90 2 Biosynthesis ................................................................................. 92 3 Structural Elucidation and Reactivity ...................................................... 93 4 New Molecules .............................................................................. 97 4.1 Monomers ............................................................................. 99 4.1.1 Ibogamine and Coronaridine Derivatives .................................... 99 4.1.2 3-Alkyl- or 3-Oxo-ibogamine/-coronaridine Derivatives . 102 4.1.3 5- and/or 6-Oxo-ibogamine/-coronaridine Derivatives ...................... 104 4.1.4 Rearranged Ibogamine/Coronaridine Alkaloids .. ........................... 105 4.1.5 Catharanthine and Pseudoeburnamonine Derivatives .. .. .. ... .. ... .. .. ... .. 106 4.1.6 Miscellaneous Representatives and Another Enigma . ..................... 107 4.2 Dimers ................................................................................. 108 4.2.1 Bisindoles with an Ibogamine Moiety ....................................... 110 4.2.2 Bisindoles with a Voacangine (10-Methoxy-coronaridine) Moiety ........ 111 4.2.3 Bisindoles with an Isovoacangine (11-Methoxy-coronaridine) Moiety . 111 4.2.4 Bisindoles with an Iboga-Indolenine or Rearranged Moiety ................ 116 4.2.5 Bisindoles with a Chippiine Moiety ... ..................................... -
Cartografiando Un Camino Para La Iboga
CARTOGRAFIANDO UN CAMINO PARA LA IBOGA Iboga Community Engagement Initiative CONCLUSIONES Y RECOMENDACIONES Marzo 2021 Un proyecto de International Center for Ethnobotanical Education, Research and Service (ICEERS) Dirección del proyecto Ricard Faura, PhD Andrea Langlois Asesoramiento científico, legal y técnico en ICEERS Benjamin De Loenen, Dr. José Carlos Bouso, Genís Ona Edición Igor Domsac Fotografía Ricard Faura Diseño gráfico Àlex Verdaguer Marzo de 2021 Para más información o consultas, por favor envíe un correo electrónico a: [email protected] www.iceers.org CARTOGRAFIANDO UN CAMINO PARA LA IBOGA Iboga Community Engagement Initiative CONCLUSIONES Y RECOMENDACIONES CONTENIDOS Conclusiones y recomendaciones 5 Introducción 7 Breve contexto: de África al mundo 9 La Iniciativa de Compromiso 10 Cómo abordar este informe 11 Agradecimientos 11 A: Comunidad, reciprocidad y curación global 14 Conclusiones 14 Recomendaciones 16 B: Regeneración biocultural y sostenibilidad 23 Conclusiones 23 Recomendaciones 27 C: Reconocimiento y evolución de los enfoques curativos tradicionales y nuevos 31 Conclusiones 31 Recomendaciones 34 Notas 38 Conclusiones y recomendaciones 5 Conclusiones y recomendaciones A: Comunidad, reciprocidad y curación global Conclusiones » Las comunidades internacionales de la iboga y de la ibogaína se beneficiarían de una mayor interconexión, comunicación y colaboración para aumentar los esfuerzos de sostenibilidad y fomentar mayores oportunidades de curación humana y planetaria. » El actual ecosistema global de la iboga está -
Fall TNP Herbals.Pptx
8/18/14 Introduc?on to Objecves Herbal Medicine ● Discuss history and role of psychedelic herbs Part II: Psychedelics, in medicine and illness. Legal Highs, and ● List herbs used as emerging legal and illicit Herbal Poisons drugs of abuse. ● Associate main plant and fungal families with Jason Schoneman RN, MS, AGCNS-BC representave poisonous compounds. The University of Texas at Aus?n ● Discuss clinical management of main toxic Schultes et al., 1992 compounds. Psychedelics Sacraments: spiritual tools or sacred medicine by non-Western cultures vs. Dangerous drugs of abuse vs. Research and clinical tools for mental and physical http://waynesword.palomar.edu/ww0703.htm disorders History History ● Shamanic divinaon ○ S;mulus for spirituality/religion http://orderofthesacredspiral.blogspot.com/2012/06/t- mckenna-on-psilocybin.html http://www.cosmicelk.net/Chukchidirections.htm 1 8/18/14 History History http://www.10zenmonkeys.com/2007/01/10/hallucinogenic- weapons-the-other-chemical-warfare/ http://rebloggy.com/post/love-music-hippie-psychedelic- woodstock http://fineartamerica.com/featured/misterio-profundo-pablo- amaringo.html History ● Psychotherapy ○ 20th century: un;l 1971 ● Recreaonal ○ S;mulus of U.S. cultural revolu;on http://qsciences.digi-info-broker.com http://www.uspharmacist.com/content/d/feature/c/38031/ http://en.wikipedia.org/nervous_system 2 8/18/14 Main Groups Main Groups Tryptamines LSD, Psilocybin, DMT, Ibogaine Other Ayahuasca, Fly agaric Phenethylamines MDMA, Mescaline, Myristicin Pseudo-hallucinogen Cannabis Dissociative -
Brisbane Native Plants by Suburb
INDEX - BRISBANE SUBURBS SPECIES LIST Acacia Ridge. ...........15 Chelmer ...................14 Hamilton. .................10 Mayne. .................25 Pullenvale............... 22 Toowong ....................46 Albion .......................25 Chermside West .11 Hawthorne................. 7 McDowall. ..............6 Torwood .....................47 Alderley ....................45 Clayfield ..................14 Heathwood.... 34. Meeandah.............. 2 Queensport ............32 Trinder Park ...............32 Algester.................... 15 Coopers Plains........32 Hemmant. .................32 Merthyr .................7 Annerley ...................32 Coorparoo ................3 Hendra. .................10 Middle Park .........19 Rainworth. ..............47 Underwood. ................41 Anstead ....................17 Corinda. ..................14 Herston ....................5 Milton ...................46 Ransome. ................32 Upper Brookfield .......23 Archerfield ...............32 Highgate Hill. ........43 Mitchelton ...........45 Red Hill.................... 43 Upper Mt gravatt. .......15 Ascot. .......................36 Darra .......................33 Hill End ..................45 Moggill. .................20 Richlands ................34 Ashgrove. ................26 Deagon ....................2 Holland Park........... 3 Moorooka. ............32 River Hills................ 19 Virginia ........................31 Aspley ......................31 Doboy ......................2 Morningside. .........3 Robertson ................42 Auchenflower -
NJ Native Plants - USDA
NJ Native Plants - USDA Scientific Name Common Name N/I Family Category National Wetland Indicator Status Thermopsis villosa Aaron's rod N Fabaceae Dicot Rubus depavitus Aberdeen dewberry N Rosaceae Dicot Artemisia absinthium absinthium I Asteraceae Dicot Aplectrum hyemale Adam and Eve N Orchidaceae Monocot FAC-, FACW Yucca filamentosa Adam's needle N Agavaceae Monocot Gentianella quinquefolia agueweed N Gentianaceae Dicot FAC, FACW- Rhamnus alnifolia alderleaf buckthorn N Rhamnaceae Dicot FACU, OBL Medicago sativa alfalfa I Fabaceae Dicot Ranunculus cymbalaria alkali buttercup N Ranunculaceae Dicot OBL Rubus allegheniensis Allegheny blackberry N Rosaceae Dicot UPL, FACW Hieracium paniculatum Allegheny hawkweed N Asteraceae Dicot Mimulus ringens Allegheny monkeyflower N Scrophulariaceae Dicot OBL Ranunculus allegheniensis Allegheny Mountain buttercup N Ranunculaceae Dicot FACU, FAC Prunus alleghaniensis Allegheny plum N Rosaceae Dicot UPL, NI Amelanchier laevis Allegheny serviceberry N Rosaceae Dicot Hylotelephium telephioides Allegheny stonecrop N Crassulaceae Dicot Adlumia fungosa allegheny vine N Fumariaceae Dicot Centaurea transalpina alpine knapweed N Asteraceae Dicot Potamogeton alpinus alpine pondweed N Potamogetonaceae Monocot OBL Viola labradorica alpine violet N Violaceae Dicot FAC Trifolium hybridum alsike clover I Fabaceae Dicot FACU-, FAC Cornus alternifolia alternateleaf dogwood N Cornaceae Dicot Strophostyles helvola amberique-bean N Fabaceae Dicot Puccinellia americana American alkaligrass N Poaceae Monocot Heuchera americana -
Leishmanicidal Activity of a Supercritical Fluid Fraction Obtained from Tabernaemontana Catharinensis ⁎ Deivid Costa Soares A, Camila G
Parasitology International 56 (2007) 135–139 www.elsevier.com/locate/parint Leishmanicidal activity of a supercritical fluid fraction obtained from Tabernaemontana catharinensis ⁎ Deivid Costa Soares a, Camila G. Pereira b, Maria Ângela A. Meireles b, Elvira Maria Saraiva a, a Departamento de Imunologia, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, 21941-590, Brazil b LASEFI DEA/FEA, Universidade Estadual de Campinas, Campinas, São Paulo, Cx. Postal 6121, 13001-970, Brazil Received 28 August 2006; received in revised form 11 January 2007; accepted 15 January 2007 Available online 20 January 2007 Abstract The branches and leaves of Tabernaemontana catharinensis were extracted with supercritical fluid using a mixture of CO2 plus ethanol (SFE), and the indole alkaloid enriched fraction (AF3) was selected for anti-Leishmania activity studies. We found that AF3 exhibits a potent effect against intracellular amastigotes of Leishmania amazonensis, a causative agent of New World cutaneous leishmaniasis. AF3 inhibits Leishmania survival in a dose-dependent manner, and reached 88% inhibition of amastigote growth at 100 μg/mL. The anti-parasite effect was independent of nitric oxide (NO), since AF3 was able to inhibit NO production induced by IFN-γ plus LPS. In addition, AF3 inhibited TGF-β production, which could have facilitated AF3-mediated parasite killing. The AF3 fraction obtained from SFE was nontoxic for host macrophages, as assessed by plasma membrane integrity and mitochondrial activity. We conclude that SFE is an efficient method for obtaining bioactive indole alkaloids from plant extracts. Importantly, this method preserved the alkaloid properties associated with inhibition of Leishmania growth in macrophages without toxicity to host cells. -
BOARD MEETING AGENDA Meeting Location: Portland State Office Building 800 NE Oregon Street, Portland, OR 97232 June 6-7, 2018 Updated 6.4.18
Oregon Board of Pharmacy BOARD MEETING AGENDA Meeting Location: Portland State Office Building 800 NE Oregon Street, Portland, OR 97232 June 6-7, 2018 Updated 6.4.18 The mission of the Oregon State Board of Pharmacy is to promote, preserve and protect the public health, safety and welfare by ensuring high standards in the practice of pharmacy and by regulating the quality, manufacture, sale and distribution of drugs. Wednesday, June 6, 2018 @ 8:30AM – Conference Rm A Thursday, June 7, 2018 @ 8:30AM – Conference Room A ≈ If special accommodations are needed for you to attend or participate in this Board Meeting, please contact Loretta Glenn at: (971) 673-0001. ≈ WEDNESDAY, JUNE 6, 2018 I. 8:30AM OPEN SESSION, Penny Reher, R.Ph, Presiding A. Roll Call B. Agenda Review and Approval Action Necessary II. Contested Case Deliberation pursuant to ORS 192.690(1) - Not Open to the Public III. EXECUTIVE SESSION – NOT OPEN TO THE PUBLIC, pursuant to ORS 676.175, ORS 192.660 (1) (2) (f) (k). A. Items for Consideration and Discussion: 1. Deliberation on Disciplinary Cases and Investigations 2. Personal Appearances 3. Deficiency Notifications 4. Case Review B. Employee Performance Review pursuant to ORS 192.660(2)(i). IV. OPEN SESSION - PUBLIC MAY ATTEND - At the conclusion of Executive Session, the Board may convene Open Session to begin some of the following scheduled agenda items - time permitting at approximately 3:30PM. V. Approve Consent Agenda* Action Necessary *Items listed under the consent agenda are considered to be routine agency matters and will be approved by a single motion of the Board without separate discussion. -
Roth 04 Pharmther Plant Derived Psychoactive Compounds.Pdf
Pharmacology & Therapeutics 102 (2004) 99–110 www.elsevier.com/locate/pharmthera Screening the receptorome to discover the molecular targets for plant-derived psychoactive compounds: a novel approach for CNS drug discovery Bryan L. Rotha,b,c,d,*, Estela Lopezd, Scott Beischeld, Richard B. Westkaempere, Jon M. Evansd aDepartment of Biochemistry, Case Western Reserve University Medical School, Cleveland, OH, USA bDepartment of Neurosciences, Case Western Reserve University Medical School, Cleveland, OH, USA cDepartment of Psychiatry, Case Western Reserve University Medical School, Cleveland, OH, USA dNational Institute of Mental Health Psychoactive Drug Screening Program, Case Western Reserve University Medical School, Cleveland, OH, USA eDepartment of Medicinal Chemistry, Medical College of Virginia, Virginia Commonwealth University, Richmond, VA, USA Abstract Because psychoactive plants exert profound effects on human perception, emotion, and cognition, discovering the molecular mechanisms responsible for psychoactive plant actions will likely yield insights into the molecular underpinnings of human consciousness. Additionally, it is likely that elucidation of the molecular targets responsible for psychoactive drug actions will yield validated targets for CNS drug discovery. This review article focuses on an unbiased, discovery-based approach aimed at uncovering the molecular targets responsible for psychoactive drug actions wherein the main active ingredients of psychoactive plants are screened at the ‘‘receptorome’’ (that portion of the proteome encoding receptors). An overview of the receptorome is given and various in silico, public-domain resources are described. Newly developed tools for the in silico mining of data derived from the National Institute of Mental Health Psychoactive Drug Screening Program’s (NIMH-PDSP) Ki Database (Ki DB) are described in detail.