Extraction of High Value Triterpenic Acids from Eucalyptus Globulus Biomass Using Hydrophobic Deep Eutectic Solvents
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Intestinal Anti-Inflammatory Activity of Terpenes in Experimental Models
molecules Review Intestinal Anti-Inflammatory Activity of Terpenes in Experimental Models (2010–2020): A Review Maria Elaine Araruna 1, Catarina Serafim 1, Edvaldo Alves Júnior 1, Clelia Hiruma-Lima 2, Margareth Diniz 1,3 and Leônia Batista 1,3,* 1 Postgraduate Program in Natural Products and Bioactive Synthetic, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051-900, PB, Brazil; [email protected] (M.E.A.); [email protected] (C.S.); [email protected] (E.A.J.); [email protected] (M.D.) 2 Department of Structural and Functional Biology (Physiology), Institute of Biosciences, São Paulo State University, Botucatu 18618-970, SP, Brazil; [email protected] 3 Department of Pharmacy, Health Sciences Center, Federal University of Paraíba, João Pessoa 58051-900, PB, Brazil * Correspondence: [email protected]; Tel.: +55-83-32167003; Fax: +55-83-32167502 Academic Editors: Maurizio Battino, Jesus Simal-Gandara and Esra Capanoglu Received: 8 September 2020; Accepted: 28 September 2020; Published: 20 November 2020 Abstract: Inflammatory bowel diseases (IBDs) refer to a group of disorders characterized by inflammation in the mucosa of the gastrointestinal tract, which mainly comprises Crohn’s disease (CD) and ulcerative colitis (UC). IBDs are characterized by inflammation of the intestinal mucosa, are highly debilitating, and are without a definitive cure. Their pathogenesis has not yet been fully elucidated; however, it is assumed that genetic, immunological, and environmental factors are involved. People affected by IBDs have relapses, and therapeutic regimens are not always able to keep symptoms in remission over the long term. Natural products emerge as an alternative for the development of new drugs; bioactive compounds are promising in the treatment of several disorders, among them those that affect the gastrointestinal tract, due to their wide structural diversity and biological activities. -
Betulinic Acid and Its Derivatives As Anti-Cancer Agent: a Review
Available online a t www.scholarsresearchlibrary.com Scholars Research Library Archives of Applied Science Research, 2014, 6 (3):47-58 (http://scholarsresearchlibrary.com/archive.html) ISSN 0975-508X CODEN (USA) AASRC9 Betulinic acid and its derivatives as anti-cancer agent: A review Gomathi Periasamy*, Girma Teketelew, Mebrahtom Gebrelibanos, Biruk Sintayehu, Michael Gebrehiwot, Aman Karim and Gereziher Geremedhin Department of Pharmacy, College of Health Sciences, Mekelle University, Mekelle, Ethiopia _____________________________________________________________________________________________ ABSTRACT Betulinic acid is a known natural product which has gained a lot of attention in the recent years since it exhibits a variety of biological and medicinal properties. This review provides the most important anticancer properties of betulinic acid and its derivatives. _____________________________________________________________________________________________ INTRODUCTION Cancer is a group of diseases that cause cells in the body to change and grow out of control[1]. Cancer cell growth is different from normal cell growth. Instead of dying, cancer cells keep on growing and form new cancer cells. These cancer cells can grow into (invade) other tissues, something that normal cells cannot do. In most cases the cancer cells form a tumor. But some cancers, like leukemia, rarely form tumors. Instead, these cancer cells are in the blood and bone marrow[2]. Cancer cell escape from many of the normal homeostatic mechanism that control proliferation. They invade surrounding tissues, gets into the body’s circulating system and set up areas of proliferation away from the site of their original appearance[3]. Cancer is the second most important disease leading to death in both the developing and developed countries nowadays. The global burden of cancer continues to increase largely because of the aging and growth of the world population alongside an increasing adoption of cancer-causing behaviors, particularly smoking, in economically developing countries[4]. -
Antiviral Activities of Oleanolic Acid and Its Analogues
molecules Review Antiviral Activities of Oleanolic Acid and Its Analogues Vuyolwethu Khwaza, Opeoluwa O. Oyedeji and Blessing A. Aderibigbe * Department of Chemistry, University of Fort Hare, Alice Campus, Alice 5700, Eastern Cape, South Africa; [email protected] (V.K.); [email protected] (O.O.O) * Correspondence: [email protected]; Tel.: +27-406022266; Fax: +08-67301846 Academic Editors: Patrizia Ciminiello, Alfonso Mangoni, Marialuisa Menna and Orazio Taglialatela-Scafati Received: 27 July 2018; Accepted: 5 September 2018; Published: 9 September 2018 Abstract: Viral diseases, such as human immune deficiency virus (HIV), influenza, hepatitis, and herpes, are the leading causes of human death in the world. The shortage of effective vaccines or therapeutics for the prevention and treatment of the numerous viral infections, and the great increase in the number of new drug-resistant viruses, indicate that there is a great need for the development of novel and potent antiviral drugs. Natural products are one of the most valuable sources for drug discovery. Most natural triterpenoids, such as oleanolic acid (OA), possess notable antiviral activity. Therefore, it is important to validate how plant isolates, such as OA and its analogues, can improve and produce potent drugs for the treatment of viral disease. This article reports a review of the analogues of oleanolic acid and their selected pathogenic antiviral activities, which include HIV, the influenza virus, hepatitis B and C viruses, and herpes viruses. Keywords: HIV; influenza virus; HBV/HCV; natural product; triterpenoids; medicinal plant 1. Introduction Viral diseases remain a major problem for humankind. It has been reported in some reviews that there is an increase in the number of viral diseases responsible for death and morbidity around the world [1,2]. -
Possible Fungistatic Implications of Betulin Presence in Betulaceae Plants and Their Hymenochaetaceae Parasitic Fungi Izabela Jasicka-Misiak*, Jacek Lipok, Izabela A
Possible Fungistatic Implications of Betulin Presence in Betulaceae Plants and their Hymenochaetaceae Parasitic Fungi Izabela Jasicka-Misiak*, Jacek Lipok, Izabela A. S´wider, and Paweł Kafarski Faculty of Chemistry, Opole University, Oleska 48, 45-052 Opole, Poland. Fax: +4 87 74 52 71 15. E-mail: [email protected] * Author for correspondence and reprint requests Z. Naturforsch. 65 c, 201 – 206 (2010); received September 23/October 26, 2009 Betulin and its derivatives (especially betulinic acid) are known to possess very interesting prospects for their application in medicine, cosmetics and as bioactive agents in pharmaceu- tical industry. Usually betulin is obtained by extraction from the outer layer of a birch bark. In this work we describe a simple method of betulin isolation from bark of various species of Betulaceae trees and parasitic Hymenochaetaceae fungi associated with these trees. The composition of the extracts was studied by GC-MS, whereas the structures of the isolated compounds were confi rmed by FTIR and 1H NMR. Additionally, the signifi cant fungistatic activity of betulin towards some fi lamentous fungi was determined. This activity was found to be strongly dependent on the formulation of this triterpene. A betulin-trimyristin emul- sion, in which nutmeg fat acts as emulsifi er and lipophilic carrier, inhibited the fungal growth even in micromolar concentrations – its EC50 values were established in the range of 15 up to 50 μM depending on the sensitivity of the fungal strain. Considering the lack of fungistatic effect of betulin applied alone, the application of ultrasonic emulsifi cation with the natural plant fat trimyristin appeared to be a new method of antifungal bioassay of water-insoluble substances, such as betulin. -
Assessment of Betulinic Acid Cytotoxicity and Mitochondrial Metabolism Impairment in a Human Melanoma Cell Line
International Journal of Molecular Sciences Article Assessment of Betulinic Acid Cytotoxicity and Mitochondrial Metabolism Impairment in a Human Melanoma Cell Line Dorina Coricovac 1,2,† , Cristina Adriana Dehelean 1,2,†, Iulia Pinzaru 1,2,* , Alexandra Mioc 1,2,*, Oana-Maria Aburel 3,4, Ioana Macasoi 1,2, George Andrei Draghici 1,2 , Crina Petean 1, Codruta Soica 1,2, Madalina Boruga 3, Brigitha Vlaicu 3 and Mirela Danina Muntean 3,4 1 Faculty of Pharmacy, “Victor Babes, ” University of Medicine and Pharmacy Timis, oara, Eftimie Murgu Square No. 2, RO-300041 Timis, oara, Romania; [email protected] (D.C.); [email protected] (C.A.D.); [email protected] (I.M.); [email protected] (G.A.D.); [email protected] (C.P.); [email protected] (C.S.) 2 Research Center for Pharmaco-toxicological Evaluations, Faculty of Pharmacy, “Victor Babes” University of Medicine and Pharmacy Timis, oara, Eftimie Murgu Square No. 2, RO-300041 Timis, oara, Romania 3 Faculty of Medicine “Victor Babes, ” University of Medicine and Pharmacy Timis, oara, Eftimie Murgu Square No. 2, RO-300041 Timis, oara, Romania; [email protected] (O.-M.A.); [email protected] (M.B.); [email protected] (B.V.); [email protected] (M.D.M.) 4 Center for Translational Research and Systems Medicine, Faculty of Medicine,” Victor Babes, ” University of Medicine and Pharmacy Timis, oara, Eftimie Murgu Sq. no. 2, RO-300041 Timis, oara, Romania * Correspondence: [email protected] (I.P.); [email protected] (A.M.); Tel.: +40-256-494-604 † Authors with equal contribution. Citation: Coricovac, D.; Dehelean, Abstract: Melanoma represents one of the most aggressive and drug resistant skin cancers with C.A.; Pinzaru, I.; Mioc, A.; Aburel, poor prognosis in its advanced stages. -
Download Product Insert (PDF)
Product Information Betulin Item No. 11041 CH2 CAS Registry No.: 473-98-3 H3C β Formal Name: lup-20(29)-ene-3 ,28-diol H Synonyms: NSC 4644, Trochol OH H MF: C30H50O2 CH CH FW: 442.7 3 3 Purity: ≥98% H CH3 Stability: ≥2 years at -20°C Supplied as: A crystalline solid OH H Laboratory Procedures For long term storage, we suggest that betulin be stored as supplied at -20°C. It should be stable for at least two years. Betulin is supplied as a crystalline solid. A stock solution may be made by dissolving the betulin in the solvent of choice. Betulin is soluble in dimethyl formamide (DMF), which should be purged with an inert gas. The solubility of betulin in DMF is approximately 2.5 mg/ml. Betulin is sparingly soluble in aqueous solutions. To enhance aqueous solubility, dilute the organic solvent solution into aqueous buffers or isotonic saline. If performing biological experiments, ensure the residual amount of organic solvent is insignificant, since organic solvents may have physiological effects at low concentrations. We do not recommend storing the aqueous solution for more than one day. Sterol regulatory element binding protein 2 (SREBP-2) regulates cholesterol synthesis by activating the transcription of genes for HMG-CoA reductase and other enzymes of the cholesterol synthetic pathway.1,2 When cellular sterol levels are high, SREBP is bound by SCAP and Insig to ER membranes as a glycosylated precursor protein. Upon cholesterol depletion, the protein is cleaved to its active form and translocated into the nucleus to stimulate transcription of genes involved in the uptake and synthesis of cholesterol.3 Betulin, the precursor of betulinic acid, is a pentacyclic triterpene found in the bark of birch trees. -
Review Article Small Molecules from Nature Targeting G-Protein Coupled Cannabinoid Receptors: Potential Leads for Drug Discovery and Development
Hindawi Publishing Corporation Evidence-Based Complementary and Alternative Medicine Volume 2015, Article ID 238482, 26 pages http://dx.doi.org/10.1155/2015/238482 Review Article Small Molecules from Nature Targeting G-Protein Coupled Cannabinoid Receptors: Potential Leads for Drug Discovery and Development Charu Sharma,1 Bassem Sadek,2 Sameer N. Goyal,3 Satyesh Sinha,4 Mohammad Amjad Kamal,5,6 and Shreesh Ojha2 1 Department of Internal Medicine, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE 2Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, Abu Dhabi, UAE 3DepartmentofPharmacology,R.C.PatelInstituteofPharmaceuticalEducation&Research,Shirpur,Mahrastra425405,India 4Department of Internal Medicine, College of Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, CA 90059, USA 5King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia 6Enzymoics, 7 Peterlee Place, Hebersham, NSW 2770, Australia Correspondence should be addressed to Shreesh Ojha; [email protected] Received 24 April 2015; Accepted 24 August 2015 Academic Editor: Ki-Wan Oh Copyright © 2015 Charu Sharma et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The cannabinoid molecules are derived from Cannabis sativa plant which acts on the cannabinoid receptors types 1 and 2 (CB1 and CB2) which have been explored as potential therapeutic targets for drug discovery and development. Currently, there are 9 numerous cannabinoid based synthetic drugs used in clinical practice like the popular ones such as nabilone, dronabinol, and Δ - tetrahydrocannabinol mediates its action through CB1/CB2 receptors. -
Integrated Metabolomics and Transcriptomics Study of Traditional Herb Astragalus Membranaceus Bge. Var. Mongolicus
Wu et al. BMC Genomics 2020, 21(Suppl 10):697 https://doi.org/10.1186/s12864-020-07005-y RESEARCH Open Access Integrated metabolomics and transcriptomics study of traditional herb Astragalus membranaceus Bge. var. mongolicus (Bge.) Hsiao reveals global metabolic profile and novel phytochemical ingredients Xueting Wu1†, Xuetong Li1,2†, Wei Wang3†, Yuanhong Shan1, Cuiting Wang1, Mulan Zhu1,4, Qiong La5, Yang Zhong3,5,YeXu6*, Peng Nan3* and Xuan Li1,2* From The 18th Asia Pacific Bioinformatics Conference Seoul, Korea. 18-20 August 2020 Abstract Background: Astragalus membranaceus Bge. var. mongolicus (Bge.) Hsiao is one of the most common herbs widely used in South and East Asia, to enhance people’s health and reinforce vital energy. Despite its prevalence, however, the knowledge about phytochemical compositions and metabolite biosynthesis in Astragalus membranaceus Bge. var. mongolicus (Bge.) Hsiao is very limited. (Continued on next page) * Correspondence: [email protected]; [email protected]; [email protected] †Xueting Wu, Xuetong Li and Wei Wang contributed equally to this work. 6Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China 3Ministry of Education Key Laboratory for Biodiversity Science and Ecological Engineering, School of Life Sciences, Fudan University, Shanghai 200438, China 1Key Laboratory of Synthetic Biology, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai 200032, China Full list of author information is available at the end of the article © The Author(s). 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. -
The Phytochemistry of Cherokee Aromatic Medicinal Plants
medicines Review The Phytochemistry of Cherokee Aromatic Medicinal Plants William N. Setzer 1,2 1 Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA; [email protected]; Tel.: +1-256-824-6519 2 Aromatic Plant Research Center, 230 N 1200 E, Suite 102, Lehi, UT 84043, USA Received: 25 October 2018; Accepted: 8 November 2018; Published: 12 November 2018 Abstract: Background: Native Americans have had a rich ethnobotanical heritage for treating diseases, ailments, and injuries. Cherokee traditional medicine has provided numerous aromatic and medicinal plants that not only were used by the Cherokee people, but were also adopted for use by European settlers in North America. Methods: The aim of this review was to examine the Cherokee ethnobotanical literature and the published phytochemical investigations on Cherokee medicinal plants and to correlate phytochemical constituents with traditional uses and biological activities. Results: Several Cherokee medicinal plants are still in use today as herbal medicines, including, for example, yarrow (Achillea millefolium), black cohosh (Cimicifuga racemosa), American ginseng (Panax quinquefolius), and blue skullcap (Scutellaria lateriflora). This review presents a summary of the traditional uses, phytochemical constituents, and biological activities of Cherokee aromatic and medicinal plants. Conclusions: The list is not complete, however, as there is still much work needed in phytochemical investigation and pharmacological evaluation of many traditional herbal medicines. Keywords: Cherokee; Native American; traditional herbal medicine; chemical constituents; pharmacology 1. Introduction Natural products have been an important source of medicinal agents throughout history and modern medicine continues to rely on traditional knowledge for treatment of human maladies [1]. Traditional medicines such as Traditional Chinese Medicine [2], Ayurvedic [3], and medicinal plants from Latin America [4] have proven to be rich resources of biologically active compounds and potential new drugs. -
TERPENES and FLAVONOIDS from SALVIA APIANA and THEIR AFFINITIES to CANNABINOID and OPIOID RECEPTORS By: Taylor Hayes a Thesis Su
TERPENES AND FLAVONOIDS FROM SALVIA APIANA AND THEIR AFFINITIES TO CANNABINOID AND OPIOID RECEPTORS By: Taylor Hayes A thesis submitted to the faculty of The University of Mississippi in partial fulfillment of the requirements of the Sally McDonnell Barksdale Honors College Oxford, MS May 2016 Approved by _________________________ Advisor: Dr. Samir A. Ross _________________________ Reader: Dr. Stephen J. Cutler _________________________ Reader: Dr. John M. Rimoldi © 2016 Taylor Josephine Hayes ALL RIGHTS RESERVED ii ACKNOWLEDGEMENTS I first want to thank my advisor, Dr. Samir A. Ross, and Dr. Sri Vedavyasa Sri Radhakrishnan for their guidance and encouragement. I am very thankful for Dr. Ross allowing me to work with in his lab in order to complete this process. I am extremely thankful for Dr. Radhakrishnan for the countless hours he has devoted to teaching me about the process of research and scientific writing. I would not have been able to finish this project without their support. Thank you to Dr. Stephen J. Cutler and Dr. John M. Rimoldi for serving as readers for this thesis. It would not have been possible without their input and willingness to help out. All of this Research was made possible by the Institutional Development Award (IDeA) Grant Number P20GM104932 from the National Institute of General Medical Sciences (NIGMS) and the Center of Research Excellence in Natural Products Neuroscience at the University of Mississippi. I would also like to thank the Sally McDonnell Barksdale Honors College for giving me the opportunity and the push that I needed take on a thesis. Dr. John Samonds was very helpful in answering all of my questions and concerns through this process. -
The Wound Healing Properties of Betulin from Birch Bark from Bench to Bedside
Published online: 2019-03-11 Reviews The Wound Healing Properties of Betulin from Birch Bark from Bench to Bedside Author Armin Scheffler Affiliation ABSTRACT Niefern-Öschelbronn, Germany, With central European approval in January 2016 for a betulin- oleogel (Episalvan), used to accelerate wound closure in par- Key words tial thickness wounds, the herbal active ingredient triterpene ‑ wound healing, split thickness skin graft, burn wounds, dry extract (betulin), from birch bark, was introduced into Betula pendula Betula pubescens Betulaceae, , ,betulin therapy for the first time. Clinical evidence of accelerated wound healing was provided in a new study design by means received October 30, 2018 of intraindividual comparison of split-thickness skin graft do- revised January 28, 2019 nor wounds and burn wounds. Clinical results of a phase II accepted January 29, 2019 study evidencing accelerated wound healing in the rare dis- Bibliography ease epidermolysis bullosa are also available, and a pivotal DOI https://doi.org/10.1055/a-0850-0224 multi-centre phase III study is currently being conducted. Published online March 11, 2019 | Planta Med 2019; 85: 524– The mode of action affects all three phases of wound healing 527 © Georg Thieme Verlag KG Stuttgart · New York | (inflammation, migration, and differentiation), and it has ISSN 0032‑0943 been possible, in some cases, to shed light on this down to the molecular level. After temporary stimulation of the in- Correspondence flammatory phase, the keratinocytes migrate more rapidly to Dr. Armin Scheffler the wound closure and, finally, epidermal differentiation is Bussardweg 15/1, 75223 Niefern-Öschelbronn, Germany stimulated. With this project, we have shown that scientifi- Phone: + 4972333580, Fax: + 497233974138 cally founded new developments in phytotherapy are possible [email protected] in Europe. -
Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: a Route to New Bioactive Compounds
Review Recent Developments in the Functionalization of Betulinic Acid and Its Natural Analogues: A Route to New Bioactive Compounds Joana L. C. Sousa 1,2,*, Carmen S. R. Freire 2, Armando J. D. Silvestre 2 and Artur M. S. Silva 1,* 1 QOPNA & LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal 2 CICECO, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal; [email protected] (C.S.R.F.); [email protected] (A.J.D.S.) * Correspondence: [email protected] (J.L.C.S.); [email protected] (A.M.S.S.); Tel.: +351-234-370-714 (A.M.S.S.) Received: 29 December 2018; Accepted: 17 January 2019; Published: 19 January 2019 Abstract: Betulinic acid (BA) and its natural analogues betulin (BN), betulonic (BoA), and 23- hydroxybetulinic (HBA) acids are lupane-type pentacyclic triterpenoids. They are present in many plants and display important biological activities. This review focuses on the chemical transformations used to functionalize BA/BN/BoA/HBA in order to obtain new derivatives with improved biological activity, covering the period since 2013 to 2018. It is divided by the main chemical transformations reported in the literature, including amination, esterification, alkylation, sulfonation, copper(I)-catalyzed alkyne-azide cycloaddition, palladium-catalyzed cross-coupling, hydroxylation, and aldol condensation reactions. In addition, the synthesis of heterocycle-fused BA/HBA derivatives and polymer‒BA conjugates are also addressed. The new derivatives are mainly used as antitumor agents, but there are other biological applications such as antimalarial activity, drug delivery, bioimaging, among others. Keywords: triterpenes; betulinic acid; betulin; betulonic acid; 23-hydroxybetulinic acid; synthesis; functionalization; derivatization 1.