A Abalone, 1428 Abamectine, 1727 Abdelazim, 544 Abdominal Pain

Total Page:16

File Type:pdf, Size:1020Kb

A Abalone, 1428 Abamectine, 1727 Abdelazim, 544 Abdominal Pain Index A Actinomucor, 247 Abalone, 1428 Activation energy, 1970, 1971 Abamectine, 1727 Activation transcription factor 3, 617 Abdelazim, 544 Active components, 2213 Abdominal pain, 1902 Active ingredient, 1718 Aberrant crypt foci (ACF), 952 Activity retention, 2043–2044 Ability to fecundation, 1195 Acute reference dose (ARfD), 1739 Abiotic stress, 2209 Acute risk, 1748 Abnormal bleeding, 1198 Acylation, 869, 871, 875, 876, 879 Absorption, distribution, metabolism, excretion Added-value, 1389 (ADME), 1931, 1933, 1951 Adducts, 255 absorption, 121, 124, 126–128, 130, 1146, Adenocarcinomas, 1202 1383, 1391, 1902, 1933 Adherence, 31, 32, 34–36, 43–46 excretion, 1932, 1933 Adhesion, 1537 metabolism, 1193, 1382, 1391, 1392, 1877, molecules, 1238 1931–1934, 1936, 1943, 1951, 1952 Adhesiveness, 745 Acarbose, 1304 Adipocytokine genes expression, 168–169 Acaricide, 1722 Adipokines, 1243 Acceleration of menarche, 1196 Adiponectin, 732, 1022, 1062 Acceptability, 1383, 1385, 1389, 1675 Adipose tissue, 1058 Acceptable daily intake (ADI), 1739 Adiposity, 691, 1242 Accumulation, 114, 115 Adolescents, 32, 43–46, 734 Aceramic jars, 227 Adoxaceae, 2264 Acetamiprid, 2152, 2154, 2155 Adulterants, 2121 Acetate, 473, 728 Adulteration, 2133 α-Acetolactate decarboxylase, 2049 of foods, 2121 Acetonitrile, 1740 Advanced glycation end products (AGEs), Acetyl-β-glucoside, 270 1285–1290, 1292 Acetylcholinesterase (AChE), 2192 formation of, 1286–1288, 1295, 1296, inhibiting activity, 1613 1303, 1304 Acetyl-CoA carboxylase (ACC), 1024 inhibition of, 1293, 1299, 1304 Acheta domesticus, 420 pathological conditions, 1286 Acidification, 828 role of, 1286 Acid ratio, 1685 Aerogels, 2054 Acid tolerance, 1536 AF-1 domain, 1204 Acidulant, 1296 AF-2 transactivation factors, 1204 Acne, 1269 Aflatoxins, 422, 2121, 2123 Actinidin, 444, 445, 453–455, 457 African diets, 1529 © Springer Nature Switzerland AG 2019 2317 J.-M. Mérillon, K. G. Ramawat (eds.), Bioactive Molecules in Food, Reference Series in Phytochemistry, https://doi.org/10.1007/978-3-319-78030-6 2318 Index African traditional cereal fermented Alzheimer’s disease, 58, 66, 592, 611–612, foods, 1538 1263, 1589, 1613 Agaricus, 1823 Mediterranean diet (MD), 1075 A. bisporus, 1819 Amadori product, 1286, 1291, 1298 Age plus five rule, 706 Amanita muscaria, 1820 Aggregation, 59, 1962, 1965 Amaranth, 707, 851–852, 1472, 1473, 1488, Agidi, 1541 1696, 1698–1707 Aging, 337–338, 592 Amaranthus Aglycone, 1146, 1581 A. caudatus, 852 Agrochemicals, 2121 A. cruentus, 851 residue, 2123 Ambigels, 2054 Agro-climatic regions, 2241 Amino acids, 357, 681, 735, 1402, 1826, 1877, Agrocybin, 1834 2252 Agro industrial by-products, 302 model, 407 Agro-industries, 1381, 1383 seafood items, 1403–1404 Agronomic conditions, 115 Aminoguanidine, 1286, 1288, 1290, 1291, Agro-residues, 1820 1295–1304 AIDS, 1632 Aminotransferase, 1032 Air-drying method, 1879 Ammonia, 1824 Air layering, 1504 5’AMP-activated protein kinase (AMPK), 309, Albatrellus ovinus, 1835 730, 1013 Albumins, 233, 1937–1941, 1943, Amphiphilic molecules, 2167 1946, 1951 Amphiphilic properties, 242 Alcohol(s), 2212 α-Amylase, 827, 984, 985 consumption, 570, 571 activity, 1063 Alcoholic beverages, 1539 β-Amylase, 827 Aldose reductase, 1304 Amylase activity, 1549 Aldrin, 1796, 1808, 1809 Amyloglucosidase, 827 Aleurone, 297, 302, 305–307, 708 Amyloid-β, 598 Alfa-amylase, 1580 β-Amyloid cleaving enzyme 1 (BACE1), 590, Alfalfa, 1162, 1175, 1181, 1191 594 Alginates, 705, 768, 776 Amyloid precursor protein (APP), 1263 Alkalinization process, 1056 β-Amyloid proteins, 611 Alkaloids, 1513, 1612–1614, 1877–1878 Amylopectin, 818, 1962, 1966 Alkanes, 2212 retrogradation products, 822 Alkylglycerol, 487 starch, 827 Alkylphenols, 491 Amylose, 712, 818 Alkyl radical, 531 digestion of, 820 Allahabad Safeda, 1502 retrogradation, 822 All-E configuration, 880 Amylose-amylopectin ratio, 823 Allergens, 421 Amylose-lipid complexes, 823 Allergic reactions, 241 Anabolic agents, 1184 Allergic skin reactions, 1316 Anacardic acids, 493 Allergy(ies), 371, 1300 Anaemia, 1631 All-Food-Seq (AFS) software pipeline, 2077 Analysis, of bioactive compounds, 1878–1880 All-trans-β-carotene, 2243 Analysis of variance (ANOVA), 2128, 2131, Allylic hydroperoxide, 533 2132 Aloe vera, 1570 non-parametric analysis of variance, 2130 Alpha-foetoprotein, 1199 Analytical (measurement) uncertainty, 2128 Alpha-linolenic acid, 470, 1256 Andean grains, see Pseudocereals Alternaria, 1726 Andes, 228 Alternative nutritional approaches, 395 Andmorin, 66 Alternative protein, 426 Anemia, 736 Index 2319 Anethum graveolens, 1319 diet, 1113 Angelica archangelica, 1319–1320 digestion, 1101 Angiogenesis, 63, 942, 943, 950, 954, 1034, dysbiosis, 1114 1236, 2249 dysbiotic state, 1113 Angiotensin converting enzyme (ACE) enterohepatic recirculation, 1113 inhibitory, 276, 363, 374, 378, 985 equilibrium forms, 1101 activity, 412 factors, 872 peptides, 326, 330, 374 fibroblasts, 1120 Angiotensin I-converting enzyme (ACE), 309, flavonoid, 1101 1017, 1416 flavylium, 1100, 1101, 1106 Animal feed, 426 in food, 1103–1104 Animal foods, 39, 44 food industry, 1126 Animal livestock, 420 foodstuff, 1101 Anise, 1325 formulation, 1123 Annealing, 825 in fruits and vegetables, 1104 Annual growth, 1820 functional food, 1111 Ano-genital distance, 1187–1188 gastric absorption mechanism, 1108 Anorexia, 1302 GI absorption, 1101 Anthelmintics, 1266 glucose absorption, 1105 Anthesis, 300 gut-brain axis, 1114, 1116 Anthocyanidins, 146 gut microbiota, 1112 Anthocyanin(s), 55, 57, 60, 62, 68, 69, 146, gut microbiota modulation, 1113–1114 149, 1056, 1142, 1227, 1586, 1757, HaCat cells, 1120 1854, 1934, 1935, 1948, 1990, 2120, high-fat, 1116 2166, 2211, 2268, 2298, 2300, 2303 hypercholesterolemic, 1112 alterations during processing, 873 intestinal tract, 1111 anthocyanin-rich foods, 1112 membrane interactions, 1106 antioxidant, 1101 metabolic syndromes, 1111–1113, 1126 antioxidant enzymes, 1122 metabolism, 1107–1111 antiproliferative, 1107 metabolites, 1111 bacteria, 1113 metabolization, 1104 bioaccessibility, 1103–1104 microbiota, 1108 bioactives, 1118 milligrams per person, 1125 bioavailability, 1107–1111 natural compounds, 1118 biological targets, 1099 neuroinflammation, 1116 biomembranes, 1106 neurologic disorders, 1113 in blood, 1107 neuroprotective effects, 1117 carbohydrate, 1105 obesity, 1111–1113 catabolites, 1110 occurrence, 1098–1103 chemical structures, properties and oral, 1104 occurrence, 868–871 pH, 1101 chemistry, 1098–1103 pharmacokinetics, 1104 collagen, 1118, 1121 phase II conjugates, 1110 color, 869, 1125 photoaging, 1118 composition, 871 physiological conditions, 1107 conjugates, 1109 plants, functions in, 1101 co-pigmentation, 1101 pro-inflammatory markers, 1122 cosmeceuticals, 1124–1126 proteins, 1104 cosmetic formulations, 1120 pyranoanthocyanins, 1101, 1103, 1109 crossover trial, 1110 ROS formation, 1119 deglycosylation, 1108 salivary, 1104 dermatological applications, 1124 skin aging, 1118–1122 diabetes, 1125 and skin diseases, 1122–1124 2320 Index Anthocyanin(s) (cont.) Antiglycation agents skin health, 1117–1124 apples, 1291 stability, 1098–1103 bael, 1292 stability and alterations, processing and banana, 1288–1290 storage of food, 871 bitter melon, 1292 stomach, 1108–1110 black nightshade, 1300 transport, 1109 black tea, 1296 tryptophan, 1116 buckwheat, 1299 in urine, 1107 clove, 1304 UV protection, 1118–1122 common juniper, 1292–1293 wound healing agents, 1119 cornelian cherry, 1290 Anthocyans, 62 cumin, 1303–1304 Anthracene, 2006 dendrobii, 1298 Anthracnose, 1732 ginger, 1302–1303 Anthropogenic endocrine disruptors, 1197 grape vine, 1293 Anti-allergic agents, 1884 green tea, 1296–1297 Anti-allergic effect, 2310 guava, 1291 Anti angiogenic, 1830 kokum, 1296 Anti-apoptotic effects, 60 lingonberry, 1293–1294 Antiapoptotic Bcl2 gene, 616 longan, 1294 Anti-apoptotic proteins, 1352 lotus, 1302 Anti-aromatase, 1203 luobuma tea, 1297–1298 Antibacterial activity, 1533, 1761, 1884, 2190 mung bean, 1298 Antibiotics, 1832, 1897 passion fruit, 1294 in agriculture, 1782 pomegranate, 1294–1295 consumption of, 1776 rambutan, 1295 in environmental samples, 1777, 1781 sangwhang, 1300–1301 monitoring, manure/sludge, 1780 saucer berry, 1293 plants, absorption of, 1780 shaddock fruit, 1295 residues, 1776, 1781 sickle senna, 1300 in soil, mud and manure samples, turmeric, 1301–1302 1778–1779 water apple, 1295–1296 toxic effects, plants, 1780 yerba mate, 1297–1298 veterinary, 1776 Anti-Helicobacter pylori activity, 1766 in water samples, 1783–1785 Anti-HIV-1, 1607 Anti-caking agent, 1565 Antihyperglycemic activity, 1515, 1765 Anticancer, 1141, 1866, 1883 Anti-hyperglycemic property, 1512 action, 63 Antihyperlipidemic, 2025 activity, 887 Anti-hypertensive effect, 309 Anti-cancerous phenolics, 87 Antihypertensive peptides, 323 Anticarcinogenic effect, 1905–1907 as functional food ingredients, 328–330 dietary fiber, 771 from meat proteins, 330–342 Anticarcinogenic properties, 1537 mechanism of, 323–326 Anti-caries effects, 1570 production of, 326–328 Anti-diabetic, 1830 Antihypertensive properties, 402 activity, 2308 Anti-infective activity, S. nigra, 2271–2273 effect, 1885 Anti-inflammatory, 60, 373, 413, 562, 569, 570, properties, 887 573, 574, 1614, 1830, 2309 Antidiabetogenic, 1765 action, 58, 59 Anti-estrogens, 1203 peptides, 372 Anti-fertility agents, 1162 role, 574 Anti-FSH effect, 1200 Anti-insecticide movement, 1794, 1805 Antifungal, 413, 1830 Antileukoproteinase, 1234 Index 2321 Antimicrobial(s), 413, 455, 1182, 1561, Antiviral effects, 2273 1566, 1570 Anxiety, 1264
Recommended publications
  • Chemoprotective Effects of Flaxseed Lignans Enterodiol And
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Texas A&M Repository CHEMOPROTECTIVE EFFECTS OF FLAXSEED LIGNANS ENTERODIOL AND ENTEROLACTONE IN NON-TRANSFORMED COLONOCYTES A Thesis by CHRISTINA ALISON CURRY Submitted to the Office of Graduate and Professional Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Chair of Committee, Clinton Allred Committee Members, Joseph Awika Jenna Anding Head of Department, Boon Chew December 2015 Major Subject: Nutrition Copyright 2015 Christina Alison Curry ABSTRACT Previous epidemiological studies have shown that colon cancer incidence is correlated to diet and estrogen status. Phytoestrogens are molecules with similar structures to estrogen that occur naturally in plants. There is in vitro and in vivo evidence that phytoestrogens in the diet can inhibit carcinogenesis. The phytoestrogenic mammalian lignans enterolactone (EL) and enterodiol (ED) in flaxseed have been shown to be effective in decreasing tumor incidence in carcinogenic models, but there is little data regarding their effects in non-malignant cells. The following studies used a non- transformed cell line of young adult mouse colonocytes (YAMC) to determine the protective effects of ED and EL in chemoprevention. Our results demonstrate that low levels of EL (1µM) and ED (5µM) are effective at significantly reducing cell growth and increasing apoptosis. These treatments also regulated transcription via significant differences in gene levels related to apoptosis and cell cycle progression. The data collected demonstrate some of the physiological effects of EL and ED on the cellular and molecular level.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. N0.: US 2014/0221426 A1 Gerk Et Al
    US 20140221426A1 (19) United States (12) Patent Application Publication (10) Pub. N0.: US 2014/0221426 A1 Gerk et al. (43) Pub. Date: Aug. 7, 2014 (54) SELECTIVE METABOLIC APPROACH TO A61K 31/216 (2006.01) INCREASING ORAL BIOAVAILABILITY OF A61K 31/09 (2006.01) PHENYLEPHRINE AND OTHER PHENOLIC A61K 31/05 (2006.01) BIOACTIVITIES A61K 31/353 (2006.01) A61K 31/4525 (2006.01) (71) Applicant: VIRGINIA COMMONWEALTH A61 K 31/3 75 (2006.01) UNIVERSITY, Richmond, VA (US) A61K 31/121 (2006.01) _ _ _ (52) US. Cl. (72) Inventorsl Ph_lll_lP M- Gerk’ Rthmond, VA (Us); CPC ........... .. A61K 31/137 (2013.01); A61K 31/3 75 Wllllam H- Fa", R10hm°nda VA (Us); (2013.01); A61K 31/235 (2013.01); A61K J"sellh K- thter’ Rlchmond, VA (Us) 31/11 (2013.01); A61K 31/085 (2013.01); _ A61K 31/121 (2013.01); A61K 31/09 (21) APP1~ NO" 14/345,689 (2013.01); A61K31/05 (2013.01); A61K . _ 31/353 (2013.01);A61K31/4525 (2013.01); (22) PCT Filed. Sep. 27, 2012 A61K31/216 (201301) USPC ......... .. 514/321' 514/653' 514/474' 514/544' ( 86 ) PCT N 0 .: PCT/U52012/057588 ’ ’ 514/456;’ 514/532’ § 371 (0X1), Related US“ Application Data Presystemic metabolism in intestine of bioactives such as (60) Provisional application No. 61/539,530, ?led on Sep. phenylephrine 1? avoided by administering a Sllbject (human 27, 2011, provisional application No. 61/544,396, 0r 21111111211) the bloactlve(e-g-,Pheny1ephr1ne)1n comblnatlon ?led on Oct 7, 201 1_ With one or more inhibitors of sulfation (e.g., sulfotransferase enzymes aka SULTs).
    [Show full text]
  • The Mycological Society of San Francisco • Jan. 2016, Vol. 67:05
    The Mycological Society of San Francisco • Jan. 2016, vol. 67:05 Table of Contents JANUARY 19 General Meeting Speaker Mushroom of the Month by K. Litchfield 1 President Post by B. Wenck-Reilly 2 Robert Dale Rogers Schizophyllum by D. Arora & W. So 4 Culinary Corner by H. Lunan 5 Hospitality by E. Multhaup 5 Holiday Dinner 2015 Report by E. Multhaup 6 Bizarre World of Fungi: 1965 by B. Sommer 7 Academic Quadrant by J. Shay 8 Announcements / Events 9 2015 Fungus Fair by J. Shay 10 David Arora’s talk by D. Tighe 11 Cultivation Quarters by K. Litchfield 12 Fungus Fair Species list by D. Nolan 13 Calendar 15 Mushroom of the Month: Chanterelle by Ken Litchfield Twenty-One Myths of Medicinal Mushrooms: Information on the use of medicinal mushrooms for This month’s profiled mushroom is the delectable Chan- preventive and therapeutic modalities has increased terelle, one of the most distinctive and easily recognized mush- on the internet in the past decade. Some is based on rooms in all its many colors and meaty forms. These golden, yellow, science and most on marketing. This talk will look white, rosy, scarlet, purple, blue, and black cornucopias of succu- at 21 common misconceptions, helping separate fact lent brawn belong to the genera Cantharellus, Craterellus, Gomphus, from fiction. Turbinellus, and Polyozellus. Rather than popping up quickly from quiescent primordial buttons that only need enough rain to expand About the speaker: the preformed babies, Robert Dale Rogers has been an herbalist for over forty these mushrooms re- years. He has a Bachelor of Science from the Univer- quire an extended period sity of Alberta, where he is an assistant clinical profes- of slower growth and sor in Family Medicine.
    [Show full text]
  • Database Code: TP109
    Database Code: TP109 Title:DEMO Fungi Data Abstract: none available Keywords:Fungi;Fungi populations;Green tree retention;Timber harvesting;populations;silviculture;resource management;timber harvest;fungi; Date data commenced:1993-10-01 Date data terminated:2001-05-24 Principal Investigator:Daniel L. Luoma List of Entities: 1. DEMO Mushroom collections 2. DEMO Truffle collections 1. DEMO Mushroom collections Attribute List: DATACODE N N char(5) enum FORMAT N N numeric(1,0) range 1.0000 1.0000 number BLOCK N N char(1) enum 1.0000 8.0000 TRT N Y char(1) enum 1.0000 6.0000 YEAR N N numeric(4,0) range 1993.00001998.0000 YYYY MONTH N Y numeric(2,0) range 5.0000 11.0000 month DAY N Y numeric(2,0) range 1.0000 31.0000 day SEASON N Y char(1) enum TRANS N Y char(3) freetext 1.0000 MMETER N Y numeric(3,0) range 1.0000 54.0000 m SRL N Y char(1) enum PLOT N Y numeric(3,0) range 1.0000 172.0000 number COLLNO N Y numeric(6,0) range 3278.000013488.0000 number MUSHSPEC N Y char(7) enum WEIGHT N Y numeric(6,2) range 0.0100 243.8000 g DUG N Y char(1) enum LOCATION N Y char(1) enum GENUS N Y char(12) enum 2. DEMO Truffle collections Attribute List: DATACODE N N char(5) enum FORMAT N N numeric(1,0) range 2.0000 2.0000 number BLOCK N N char(1) enum 1.0000 8.0000 TRT N Y char(1) enum 1.0000 6.0000 YEAR N N numeric(4,0) range 1993.00002001.0000 YYYY MONTH N Y numeric(2,0) range 5.0000 11.0000 month DAY N Y numeric(2,0) range 1.0000 31.0000 day SEASON N Y char(1) enum PLOT N N numeric(3,0) range 1.0000 300.0000 number CWD1 N Y numeric(3,1) range 0.0000 100.0000
    [Show full text]
  • Phytoestrogens : Daidzein, Enterodiol, Enterolactone, Equol, Geinstein, O-Desmethylangolensin Matrix: Urine Method: HPLC-ESI-MS/MS Method No: 4069.03
    Laboratory Procedure Manual Analyte: Phytoestrogens : Daidzein, Enterodiol, Enterolactone, Equol, Geinstein, O-Desmethylangolensin Matrix: Urine Method: HPLC-ESI-MS/MS Method No: 4069.03 Revised: March 2018 as performed by: Nutritional Biomarkers Branch (NBB) Division of Laboratory Sciences (DLS) National Center for Environmental Health (NCEH) contact: James L. Pirkle, M.D., Ph.D. Director, Division of Laboratory Sciences Important Information for Users CDC periodically refines these laboratory methods. It is the responsibility of the user to contact the person listed on the title page of each write-up before using the analytical method to find out whether any changes have been made and what revisions, if any, have been incorporated. Phytoestrogen NHANES 2013-2014 This document details the Lab Protocol for testing the items listed in the following table. This method file describes measurements of U1PHYTO_H_R and U2PHYTO_H_R. One method was used to measure both the 24 hour urine phytoestrogen, 1st urine collection and 24 hour urine phytoestrogen, 2nd urine collection. However, these results are released as 2 separate data files. Variable File Name SAS Label (and SI units) Name Daidzein, Urine 1st collection UR1DAZ (ng/mL) o-Desmethylangolensin, Urine 1st UR1DMA Collection (ng/mL) UR1EQU Equol, Urine 1st Collection (ng/mL) Enterodiol, Urine 1st Collection UR1ETD (ng/mL) Enterolactone, Urine 1st Collection UR1ETL (ng/mL) Genistein, Urine 1st Collection UR1GNS (ng/mL) U1PT_H_R Daidzein, Urine 2nd collection U2PT_H_R UR2DAZ (ng/mL) o-Desmethylangolensin, Urine 2nd UR2DMA Collection (ng/mL) UR2EQU Equol, Urine 2nd Collection (ng/mL) Enterodiol, Urine 2nd Collection UR2ETD (ng/mL) Enterolactone, Urine 2nd Collection UR2ETL (ng/mL) Genistein, Urine 2nd Collection UR2GNS (ng/mL) 2 of 54 Phytoestrogen NHANES 2013-2014 1.
    [Show full text]
  • Advances in Enzyme Biotechnology Advances in Enzyme Biotechnology
    Pratyoosh Shukla Brett I. Pletschke Editors Advances in Enzyme Biotechnology Advances in Enzyme Biotechnology Pratyoosh Shukla • Brett I. Pletschke Editors Advances in Enzyme Biotechnology Editors Pratyoosh Shukla Brett I. Pletschke Department of Microbiology Department of Biochemistry, Maharshi Dayanand University Microbiology and Biotechnology Rohtak, Haryana , India Rhodes University Grahamstown, South Africa ISBN 978-81-322-1093-1 ISBN 978-81-322-1094-8 (eBook) DOI 10.1007/978-81-322-1094-8 Springer New Delhi Heidelberg New York Dordrecht London Library of Congress Control Number: 2013945175 © Springer India 2013 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. Exempted from this legal reservation are brief excerpts in connection with reviews or scholarly analysis or material supplied specifi cally for the purpose of being entered and executed on a computer system, for exclusive use by the purchaser of the work. Duplication of this publication or parts thereof is permitted only under the provisions of the Copyright Law of the Publisher’s location, in its current version, and permission for use must always be obtained from Springer. Permissions for use may be obtained through RightsLink at the Copyright Clearance Center. Violations are liable to prosecution under the respective Copyright Law. The use of general descriptive names, registered names, trademarks, service marks, etc.
    [Show full text]
  • Highly Cytotoxic Kettapeptin, Bhimamycins Possessing Unusual Chromophores and Further New Secondary Metabolites from Terrestrial and Marine Bacteria
    Serge Fotso ___________________________________________________ Highly Cytotoxic Kettapeptin, Bhimamycins Possessing Unusual Chromophores and Further New Secondary Metabolites from Terrestrial and Marine Bacteria CH 3 O OH H C O CH 3 OH 3 CH CH CH O 3 3 3 NH HN CH3 N CH HO 3 O O O N O MeO O H CH N 3 O N N OH H3C HN O H3C H3C OH O O O CH3 O N O O CH OH O CH3 HO 3 OH Dissertation Highly Cytotoxic Kettapeptin, Bhimamycins Possessing Unusual Chromophores and Further New Secondary Metabolites from Terrestrial and Marine Bacteria Dissertation zur Erlangung des Doktorgrades der Mathematisch-Naturwissenschaftlichen Fakultäten der Georg-August-Universität zu Göttingen vorgelegt von Serge Fotso aus Yaoundé (Kamerun) Göttingen 2005 D7 Referent: Prof. Dr. H. Laatsch Korreferent: Prof. Dr. A. Zeeck Tag der mündlichen Prüfung: 02.11.2005 Die vorliegende Arbeit wurde in der Zeit von Oktober 2001 bis September 2005 im Institut für Organische Chemie der Georg-August-Universität zu Göttingen unter der Leitung von Herrn Prof. Dr. H. Laatsch angefertigt. Herrn Prof. Dr. H. Laatsch danke ich für die Möglichkeit zur Durchführung dieser Arbeit sowie die ständige Bereitschaft, auftretende Probleme zu diskutieren. Für meine Eltern und meine Verlobte I 1 Introduction...................................................................................................... 1 1.1 New drugs from the Sea............................................................................. 1 2 Aim of the present work................................................................................
    [Show full text]
  • Phenylpropanoids
    Phenylpropanoids The phenylpropanoids are a diverse family of organic compounds that are synthesized by plants from the amino acids phenylalanine and tyrosine. Their name is derived from the six-carbon, aromatic phenyl group and the three-carbon propene tail of cinnamic acid, which is synthesized from phenylalanine in the first step of phenylpropanoid biosynthesis. Phenylpropanoids are found throughout the plant kingdom, where they serve as essential components of a number of structural polymers, provide protection from ultraviolet light, defend against herbivores and pathogens, and mediate plant-pollinator interactions as floral pigments and scent compounds. Concentrations of phenylpropanoids within plants are also altered by changes in resource availability. www.MedChemExpress.com 1 Phenylpropanoids Inhibitors & Modulators (+)-Columbianetin (+)-Columbianetin acetate ((S)-Columbianetin) Cat. No.: HY-N0363 ((S)-Columbianetin acetate) Cat. No.: HY-N0363A (+)-Columbianetin is an isomer of Columbianetin. (S)-Columbianetin acetate is an isomer of Columbianetin is a phytoalexin associated with Columbianetin. Columbianetin is a phytoalexin celery (Apium graveolens) resistance to associated with celery (Apium graveolens) pathogens during storage. Columbianetin exhibits resistance to pathogens during storage. excellent anti-fungal and anti-inflammatory Columbianetin exhibits excellent anti-fungal and activity. anti-inflammatory activity. Purity: >98% Purity: >98% Clinical Data: No Development Reported Clinical Data: No Development Reported Size: 5 mg, 10 mg, 20 mg Size: 5 mg, 10 mg, 20 mg (+)-Guaiacin (+)-Peusedanol Cat. No.: HY-N2247A Cat. No.: HY-N6063 (+)-Guaiacin is a compound extracted of the bark (+)-Peusedanol is a coumarin isolated from of Machilus wangchiana Chun. (Lauraceae). Peucedanumjaponicum. (+)-Guaiacin shows potent in vitro activities against the release of β-glucuronidase in rat polymorphonuclear leukocytes (PMNs) induced by platelet-activating factor (PAF) .
    [Show full text]
  • Toxic Fungi of Western North America
    Toxic Fungi of Western North America by Thomas J. Duffy, MD Published by MykoWeb (www.mykoweb.com) March, 2008 (Web) August, 2008 (PDF) 2 Toxic Fungi of Western North America Copyright © 2008 by Thomas J. Duffy & Michael G. Wood Toxic Fungi of Western North America 3 Contents Introductory Material ........................................................................................... 7 Dedication ............................................................................................................... 7 Preface .................................................................................................................... 7 Acknowledgements ................................................................................................. 7 An Introduction to Mushrooms & Mushroom Poisoning .............................. 9 Introduction and collection of specimens .............................................................. 9 General overview of mushroom poisonings ......................................................... 10 Ecology and general anatomy of fungi ................................................................ 11 Description and habitat of Amanita phalloides and Amanita ocreata .............. 14 History of Amanita ocreata and Amanita phalloides in the West ..................... 18 The classical history of Amanita phalloides and related species ....................... 20 Mushroom poisoning case registry ...................................................................... 21 “Look-Alike” mushrooms .....................................................................................
    [Show full text]
  • Ramaria Lacteobrunnescens) Funnen För Första Gången I Nordeuropa I En Uppländsk Kalkbarrskog
    Svensk Mykologisk Tidskrift Volym 29 · nummer 3 · 2008 Svensk Mykologisk Tidskrift inkluderar tidigare: www.svampar.se Svensk Mykologisk Tidskrift Sveriges Mykologiska Förening Tidskriften publicerar originalartiklar med svamp- Föreningen verkar för anknytning och med svenskt och nordeuropeiskt - en bättre kännedom om Sveriges svampar och intresse. Tidskriften utkommer med fyra nummer svampars roll i naturen per år och ägs av Sveriges Mykologiska Förening. - skydd av naturen och att svampplockning och annat Instruktioner till författare finns på SMF:s hemsida uppträdande i skog och mark sker under iakttagande www.svampar.se Tidskrift erhålls genom medlem- av gällande lagar skap i SMF. - att kontakter mellan lokala svampföreningar och Detta nummer av Svensk Mykologisk Tidskrift svampintresserade i landet underlättas framställs med bidrag från Tore Nathorst-Windahls - att kontakt upprätthålls med mykologiska föreningar minnesfond, Skogsstyrelsen och Naturvårdsverket. i grannländer - en samverkan med mykologisk forskning och veten- Redaktion skap. Redaktör och ansvarig utgivare Mikael Jeppson Medlemskap erhålles genom insättning av medlems- Lilla Håjumsgatan 4, avgiften på föreningens bankgiro 461 35 TROLLHÄTTAN 5388-7733 eller plusgiro 443 92 02-5. 0520-82910 [email protected] Medlemsavgiften för 2009 är: • 250:- för medlemmar bosatta i Sverige Hjalmar Croneborg • 300:- för medlemmar bosatta utanför Sverige Mattsarve Gammelgarn • 125:- (halv avgift) för studerande medlemmar 620 16 LJUGARN bosatta i Sverige (maximalt under 5 år) 018-672557 • 50:- för familjemedlemmar (erhåller ej SMT) [email protected] Subscriptions from abroad are welcome. Payments Jan Nilsson for 2009 (SEK 300.-) can be made to our bank ac- Smeberg 2 count: 450 84 BULLAREN Swedbank AB (publ) 0525-20972 Berga Företag [email protected] Box 22181 SE 250 23 Helsingborg, Sweden Äldre nummer av Svensk Mykologisk Tidskrift (inkl.
    [Show full text]
  • November 2014
    MushRumors The Newsletter of the Northwest Mushroomers Association Volume 25, Issue 4 December 2014 After Arid Start, 2014 Mushroom Season Flourishes It All Came Together By Chuck Nafziger It all came together for the 2014 Wild Mushroom Show; an October with the perfect amount of rain for abundant mushrooms, an enthusiastic volunteer base, a Photo by Vince Biciunas great show publicity team, a warm sunny show day, and an increased public interest in foraging. Nadine Lihach, who took care of the admissions, reports that we blew away last year's record attendance by about 140 people. Add to that all the volunteers who put the show together, and we had well over 900 people involved. That's a huge event for our club. Nadine said, "... this was a record year at the entry gate: 862 attendees (includes children). Our previous high was in 2013: 723 attendees. Success is more measured in the happiness index of those attending, and many people stopped by on their way out to thank us for the wonderful show. Kids—and there were many—were especially delighted, and I'm sure there were some future mycophiles and mycologists in Sunday's crowd. The mushroom display A stunning entry display greets visitors arriving at the show. by the door was effective, as always, at luring people in. You could actually see the kids' eyes getting bigger as they surveyed the weird mushrooms, and twice during the day kids ran back to our table to tell us that they had spotted the mushroom fairy. There were many repeat adult visitors, too, often bearing mushrooms for identification.
    [Show full text]
  • Trans-Resveratrol [501-36-0]
    trans-Resveratrol [501-36-0] Review of Toxicological Literature March 2002 trans-Resveratrol [501-36-0] Review of Toxicological Literature Prepared for Scott Masten, Ph.D. National Institute of Environmental Health Sciences P.O. Box 12233 Research Triangle Park, North Carolina 27709 Contract No. N01-ES-65402 Submitted by Karen E. Haneke, M.S. Integrated Laboratory Systems P.O. Box 13501 Research Triangle Park, North Carolina 27709 March 2002 Toxicological Summary for trans-Resveratrol [501-36-0] 03/2002 Executive Summary Nomination trans-Resveratrol was nominated for toxicology studies by the National Institute of Environmental Health Sciences (NIEHS) based on the widespread human exposure to resveratrol through natural dietary sources and dietary supplement use, and concern that it has not been sufficiently evaluated for potential toxicological effects. Non-Toxicological Data General Description: trans-Resveratrol is a polyphenol that occurs naturally in grapes, peanuts, and a number of other plants. It is found in foods/drinks made from grapes and peanuts, and also in a number of herbal remedies, both alone and as part of plant extracts. Commercial Availability, Production, and Uses: trans-Resveratrol is produced commercially by several companies. A commercial extraction method involves using alcohol and water to produce trans­ resveratrol from Polygonum cuspidatum. Resveratrol compounds may be produced or extracted for research purposes by treating cell suspension cultures of grapes with a natural substance from a fungus. Resveratrol compounds have long been found in herbal medicines. Health claims of oral dietary supplements containing trans-resveratrol include protection from free-radical damage, inhibition of arthritic inflammation, inhibition of the cyclooxygenase-2 enzyme, protection of blood vessels, protection against cardiovascular disease and cancer, and alleviation of menopausal symptoms.
    [Show full text]