Home

Zingerone wiki

C 11 H 14 O 3: Molmasse: 194,22 g / mol Schmelzpunkt: 40 bis 41 ° C (104 bis 106 ° F; 313 bis 314 K) Siedepunkt: 187 bis 188 ° C (369 bis 370 ° F; 460 bis 461 K) bei 14 mmH Zingerone, also called vanillylacetone, is thought by some to be a key component of the pungency of ginger, but imparts the sweet flavor of cooked ginger. Zingerone is a crystalline solid that is sparingly soluble in water and soluble in ether. When synthesized and tasted does not have any pungency

zingerone (usually uncountable, plural zingerones) (organic chemistry) A crystalline solid organic compound that gives ginger its pungent taste Die Verbindung wurde 1917 erstmals von dem japanischen Chemiker Hiroshi Nomura aus der Ingwer isoliert. Es ist der Scharfstoff im Oleoresin des Ingwers Zingerone is a ketone that is 4-phenylbutan-2-one in which the phenyl ring is substituted at positions 3 and 4 by methoxy and hydroxy groups respectively. The major pungent component in ginger. It has a role as an antioxidant, an anti-inflammatory agent, a radiation protective agent, an antiemetic, a flavouring agent and a fragrance C 11 H 14 O 3 : Molar masse : 194,22 g / mol Smeltepunkt : 40 til 41 ° C (104 til 106 ° F, 313 til 314 K) Kogepunkt : 187 til 188 ° C (369 til 370 ° F; 460 til 461 K) ved 14 mmH

Le Gingembre fait-il Maigrir : Info ou Intox ? - Bruleur

Media in category Zingerone The following 2 files are in this category, out of 2 total Zingerone - Zingerone. De la Wikipedia, enciclopedia liberă . Zingerone Numele Numele IUPAC . 4- (4-hidroxi-3-metoxifenil) -butan-2-onă . Identificatori Numar CAS . 122-48-5 ; Model 3D ( JSmol ) Imagine interactivă ; ChEBI : CHEBI: 68657 ; ChEMBL : ChEMBL25894 ; ChemSpider : 28952 ; ECHA InfoCard : 100.004.136 : PubChem CID . 31211 ; UNII : 4MMW850892 ; Tablou de bord CompTox ( EPA. English: synthesis of Zingerone from Vanillin and Acetone. Datum: 10. Juli 2020: Quelle: Eigenes Werk: Urheber: NadirSH: Lizenz. Ich, der Urheber dieses Werkes, veröffentliche es unter der folgenden Lizenz: Diese Datei ist lizenziert unter der Creative-Commons-Lizenz Namensnennung - Weitergabe unter gleichen Bedingungen 4.0 international. Dieses Werk darf von dir verbreitet werden. Datei:Zingerone Structural Formula V.1.svg. Sprache; Beobachten; Bearbeiten; Datei; Dateiversionen; Dateiverwendung; Globale Dateiverwendung; Metadaten; Größe der PNG-Vorschau dieser SVG-Datei: 469 × 192 Pixel. Weitere Auflösungen: 320 × 131 Pixel | 640 × 262 Pixel | 800 × 328 Pixel | 1.024 × 419 Pixel | 1.280 × 524 Pixel. Originaldatei ‎ (SVG-Datei, Basisgröße: 469 × 192 Pixel.

Structure, properties, spectra, suppliers and links for: zingerone, 122-48-5 WikiZero Özgür Ansiklopedi - Wikipedia Okumanın En Kolay Yolu . Zingerone From Wikipedia the free encyclopedia. Zingerone ; Names ; IUPAC name. 4-(4-hydroxy-3-methoxyphenyl)-butan-2-one. Identifiers ; CAS Number. 122-48-5 3D model . Interactive image; ChEBI: CHEBI.

Wikipedia's Zingerone as translated by GramTrans. La ĉi-suba teksto estas aŭtomata traduko de la artikolo Zingerone article en la angla Vikipedio, farita per la sistemo GramTrans on 2016-07-06 14:01:25. Eventualaj ŝanĝoj en la angla originalo estos kaptitaj per regulaj retradukoj. Se vi volas enigi tiun artikolon en la originalan Esperanto-Vikipedion, vi povas uzi nian specialan redakt. Usage on en.wikipedia.org Zingerone; Usage on www.wikidata.org Q1064625; Metadata. This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file. Gingerenone A. 128700-97- (E)-1,7-bis(4-hydroxy-3-methoxyphenyl)hept-4-en-3-one. AS-HK014. CHEBI:535

zingerone: ChEBI ID CHEBI:68657: Definition A ketone that is 4-phenylbutan-2-one in which the phenyl ring is substituted at positions 3 and 4 by methoxy and hydroxy groups respectively. The major pungent component in ginger. Stars This entity has been manually annotated by the ChEBI Team.. La cottura trasforma lo gingerolo in zingerone, attraverso una reazione retro-aldolica. Note [ modifica | modifica wikitesto ] ^ ( EN ) P Monge, R Scheline e E Solheim, The metabolism of zingerone, a pungent principle of ginger , in Xenobiotica; the fate of foreign compounds in biological systems , vol. 6, n. 7, 1976, pp. 411-23, DOI : 10.3109/00498257609151654 , PMID 997589 Zingerone acts as antioxidants, recent evidence supports the idea that zingerone primarily acts on reactive oxygen species, free radicals, and also antioxidant sparing activity to elicit a positive, beneficial response from cells. Apart from the redox properties, zingerone has known pharmacological and biological activities including anti-inflammatory, anticancer, antimicrobial activity, and. French: ·(organic chemistry) zingerone Definition from Wiktionary, the free dictionar

Wikipedia Zingerone Clinical Trials Clinical Trials . Phase Status Purpose Conditions Count. Pharmacoeconomics Manufacturers. Not Available. Packagers. Not Available. Dosage Forms Not Available Prices Not Available Patents Not Available Properties State Not Available Experimental Properties Not Available Predicted Properties. Property Value Source ; Water Solubility: 0.567 mg/mL: ALOGPS: logP. Zingerone. Zingerone decreased the activities of aminotransferases, gamma glutamyl transpeptidase, and total bilirubin and increases the levels of total protein, albumin, and globulin, which could be attributed to the ability of zingerone to prevent ethanol-induced hepatic damage and dysfunction as well as improvement in the function/secretory mechanisms of the liver cells Zingeron je organsko jedinjenje, koje sadrži 11 atoma ugljenika i ima molekulsku masu od 194,227 Da File:zingerone.svg estas vektora versio de ĉi tiu bildo. Ĝi estu uzata anstataŭ ĉi tiu rastruma bildo, se ĝi ne estas malpli bonkvalita. File:Zingerone.png File:zingerone.svg. Pliajn informojn vidu ĉe Help:SVG. In other languages Priskribo: chemical structure of zingerone: Dato: la 15-a de novembro 2007: Fonto: Propra verko: Aŭtoro: Edgar181: Permeso (Reuzo de la dosiero) Public domain.

Disse Siet is över en mehrdüdigen Begreep un vertellt, wat disse Begreep allens bedüden kann. Disse Siet is sotoseggen en Gavelsiet, de Weg gavelt sik hier un du kannst di een Siet utsöken, üm mehr över dissen Begreep to lesen The entire wiki with photo and video galleries for each article. WikiVisually the entire wiki with photos and video WikiVisually People Places History Art Science the entire wiki with photos and video History top lists Rare Coins Featured Videos Celebrities World Banknotes Crown Jewels History by Country Greatest Museums Wars and Battles British Monarchs Recovered Treasures Kings of France. Definition from Wiktionary, the free dictionary. Jump to navigation Jump to search. English [] Noun []. zingerones. plural of zingerone zingerone natural : zingerone, natural : zingherone : zingiberone . Articles: PubMed:Synthesis and quorum sensing inhibitory activity of key phenolic compounds of ginger and their derivatives. PubMed:Ginger and its pungent constituents non-competitively inhibit serotonin currents on visceral afferent neurons. PubMed:Zingerone attenuates lipopolysaccharide-induced acute lung injury in mice.

Zingerone - Zingerone - qaz

Talk:Zingerone. Language; Watch; Edit; Active discussions. WikiProject Food and drink (Rated Stub-class) This article is within the scope of WikiProject Food and drink, a collaborative effort to improve the coverage of food and drink related articles on Wikipedia. If you would like to participate, please visit the project page, where you can join the discussion and see a list of open tasks. Zingerone, also called vanillylacetone, is a key component of the pungency of ginger. [1] Zingerone is a crystalline solid that is sparingly soluble in water, but soluble in ether. [2]Zingerone is similar in chemical structure to other flavor chemicals such as vanillin and eugenol.It is used as a flavor additive in spice oils and in perfumery to introduce spicy aromas Dehydrozingerone | C11H12O3 | CID 5354238 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities.

Zingerone - WikiMili, The Best Wikipedia Reade

  1. Category:Zingerone. Izvor: Wikimedia Commons. Idi na navigaciju Idi na pretrag
  2. ˈzinjəˌrōn noun ( s) Etymology: International Scientific Vocabulary zinger (irregular from New Latin Zingiber) + one : a pungent crystalline phenolic ketone C11H14O3 present in traces in ginger oil but made synthetically from vanillin an
  3. Curlone | C15H22O | CID 196216 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety.
  4. zingerone. Interpretation Translation  zingerone. noun. A crystalline solid organic compound that gives ginger its bad taste. Wikipedia foundation. cruddiness; tetraene; Look at other dictionaries: Zingérone.

zingerone - Wiktionar

  1. Zerumbone is a sesquiterpenoid and cyclic ketone that is (1E,4E,8E)-alpha-humulene which is substituted by an oxo group at the carbon atom attached to two double bonds. It is obtained by steam distillation from a type of edible ginger, Zingiber zerumbet Smith, grown particularly in southeast Asia
  2. Look at other dictionaries: Zingérone — Zingerone Zingerone Général Nom IUPAC 4 (4 hydroxy 3 méthoxyphényl)butan 2 one Synonymes Wikipédia en Français. Zingerone — Général Nom IUPAC 4 (4 hydroxy 3 méthoxyphényl)butan 2 one Synonymes Vanillylacétone; [ — Général Nom IUPAC 4 (4 hydroxy 3 méthoxyphényl)butan 2 one Synonyme
  3. zingerone. Interpretation Translation  zingerone ['zindʒәrәun] 姜油酮. β-(3-甲氧基-4-羥苯基)-2-丁酮. English-Chinese dictionary. 2013. zinger; zingiber; Look at other dictionaries: Zingérone — Zingerone Zingerone Général Nom IUPAC 4 (4 hydroxy 3 méthoxyphényl)butan 2 one Synonymes Wikipédia en Français.

Vanillylaceton - Wikipedi

  1. From Human Salivary Proteome Wiki. Jump to: navigation, search. Term Data Source Ontology Chemical Entities of Biological Interest Accession CHEBI:68657 Term Name zingerone Description A ketone that is 4-phenylbutan-2-one in which the phenyl ring is substituted at positions 3 and 4 by methoxy and hydroxy groups respectively. The major pungent component in ginger. Charge 0 Database Cross.
  2. Look at other dictionaries: Zingérone — Zingerone Zingerone Général Nom IUPAC 4 (4 hydroxy 3 méthoxyphényl)butan 2 one Synonymes Wikipédia en Français. Zingerone
  3. (organic chemistry, uncountable) A caustic, poisonous, white crystalline compound, C6H5OH, derived from benzene and used in resins, plastics, and pharmaceuticals and in dilute form as a disinfectant and antiseptic; once called carbolic acid.· (organic chemistry, countable) Any of a class of aromatic organic compounds having at least one.
  4. ZINGERONE 4MMW850892 Other Structure General Activity Publications Application Names 16: Classification 2: Identifiers 10: Related Substances 1: ZINGERONE 4MMW850892 Other Details Stereochemistry: ACHIRAL Molecular Formula.
  5. 122-48-5 - OJYLAHXKWMRDGS-UHFFFAOYSA-N - Zingerone - Similar structures search, synonyms, formulas, resource links, and other chemical information

Zingerone C11H14O3 - PubChe

Zingerone wikipedia. Zingerone, additionally referred to as vanillylacetone, is idea by some to be a key component of the pungency of ginger, however imparts the sweet taste of cooked ginger. Definitely. Girl residing on wateronly weight loss plan stops each day mail on line. Lady dwelling on wateronly weight loss program stops on day 47 after figuring out she can be encouraging others to. Pressemitteilung von Mk-Vital UG (haftungsbeschränkt) Klinische Studie zu Ingwer bei DNA-Schäden im Sperma veröffentlicht auf openP According to Dr. Keith Block (who has dealt with advanced cancers for over 32 years) in his thorough book Life Over Cancer, chronic inflammation is one of the biochemical conditions in the human body that can promote cancer establishment, and proliferation.. In this video, Dr. Michael Greger (nutritionfacts.org) describes an elegant experiment in which the blood of those eating different types.

In this video Dr. Greger talks about studies done on actual people and demonstrating the effectiveness of zingerone (a phytonutrient of ginger) in combating the effects of radiation exposure. One study compared it to the leading drug used for radiation sickness and found it 150 times more powerful. This is even more important for parents of children getting CT scans to know as children have an. I read that zingerone is produced by heating gingerol through a retro aldol reaction. Now, mind me if I say something stupefying as I do not have much practical lab experience, but would an aldol reaction of zingerone and what appears would be an aldehyde be at all feasible? If anyone could help out, I'd really appreciate it. I have a backup plan if I cannot figure something out with zingerone. Preiselbeere (Vaccinium vitis-idaea)Vanillylaceton kommt natürlich in Preiselbeeren und Ingwer vor. Die Verbindung wurde 1917 erstmals von dem japanischen Chemiker Hiroshi Nomura aus der Ingwer isoliert. Es ist der Scharfstoff im Oleoresin des Ingwers.. Gewinnung und Darstellung [Bearbeiten | Quelltext bearbeiten]. Vanillylaceton 4 kann durch eine Aldolkondensation von Vanillin 1 und Aceton 2. Från Wikipedia, den fria encyklopedin . Zingerone Namn IUPAC-namn . 4- (4-hydroxi-3-metoxifenyl) -butan-2-o

Category:Zingerone - Wikimedia Common

inchi = 1 / c11h14o3 / c1-8 (12) 3-4-9-5-6-10 (13) 11 (7-9) 14-2 / h5-7,13h, 3-4h2,1-2h3 . chave: ojylahxkwmrdgs-uhfffaoyan . sorriso Zingerone, also called vanillylacetone, is a key component of the pungency of ginger. Zingerone is a crystalline solid that is sparingly soluble in water, but soluble in ether. Zingerone is similar in chemical structure to other flavor chemicals such as vanillin and eugenol. It is used as a flavor additive in spice oils and in perfumery to introduce spicy aromas. Fresh ginger does not contain.

Datei:Synthesis Zingerone

About Wikipedia; Disclaimers; Search. Orchidaceae. Language; Watch; Edit; The Orchidaceae are a diverse and widespread family of or zingerone) to perform pollination. The flowers may produce attractive odours. Although absent in most species, nectar may be produced in a spur of the labellum (8 in the illustration above), or on the point of the sepals, or in the septa of the ovary, the most. Zingerone contains vanilloid (3-methoxy-4-hydroxy benzene) group in its structure. These phenolic hydroxyl groups provide the possibility to introduce a 4-ether-linked propanolamine side chain. Propanolamine derivatives were obtained by reacting zingerone with epichlorohydrin, and the obtained epoxide compounds were then reacted with isopropylamine, tert-butylamine or guaiacoxyethylamine. Wikipedia:Zingerone; Ontology: Chebi Relationships is a type of: ketone monomethoxybenzene phenols. has_role: anti-inflammatory agent antiemetic antioxidant flavouring agent fragrance... Show All 6 Terms.

Select categories you would like to watch. Updates to this gene will be send to {{ username } Ginger is a plant believed to have originated in South Asia.. Extracts of ginger have been found to be effective antiemetics, and ginger is believed to have at least one (likely more than one) pharmacologically active compound which inhibits activation of 5-HT 3 receptors. Lete and Allue (2016) noted that 6-shogaol, 6-gingerol, and zingerone could inhibit the 5-HT response in a concentration. Cooking ginger transforms gingerol into zingerone, which is less pungent and has a spicy-sweet aroma. When ginger is dried, gingerol undergoes a dehydration reaction forming shogaols, which are about twice as pungent as gingerol. This explains why dried ginger is more pungent than fresh ginger. Ginger also contains 8-gingerol, 10-gingerol, and 12-gingerol. Physiological effects [6]-Gingerol.

Datei:Zingerone Structural Formula V

zingerone C11H14O3 ChemSpide

Wikipedia English - The Free Encyclopedia Zingerone , also called vanillylacetone , is a key component of the pungency of ginger. Zingerone is a crystalline solid that is sparingly soluble in water, but soluble in ether Allerdings geht damit die einzigartige Kombination mit weiteren Inhaltsstoffen, wie etwa Zingerone verloren. Schon in den 80-er Jahren wiesen indische Forscher auf die ausbalancierte Wirkung von Ingwerextrakt hin, mit der sich unerwünschte Eigenschaften der Einzelteile in der Summe ausgleichen. 6 Wenn Du also die ganze Kraft des Ingwers nutzen willst, solltest Du auf ein ganzheitliches. Asked by Wiki User. See Answer. Top Answer. Wiki User Answered 2014-07-09 16:01:34. A zingerone is a crystalline organic compound - it gives ginger its distinctive taste. 0 0 1 0 0. Press release - Orian Research - Zingerone Global Market Future Scope, Opportunities with Strategic Growth and Top Players are Gogia Chemical Industries Pvt. Ltd, Harmonious Natural Biotechnology.

Zingerone‎ (4 F) Media in category Ketones The following 200 files are in this category, out of 384 total. (previous page) (-)-Dolabriferol.svg 562 × 246; 42 KB (2S,3S)-Iso E Super structure.svg 280 × 183; 14 KB (R. Zingeron, též nazývaný vanilylaceton -2-butanon) je organická sloučenina získávaná ze zázvoru. Jedná se o krystalickou pevnou látku špatně rozpustnou ve vodě, dobře rozpustnou v diethyletheru Zingerone is a food additive permitted for direct addition to food for human consumption as a synthetic flavoring substance and adjuvant in accordance with the following conditions: a) they are used in the minimum quantity required to produce their intended effect, and otherwise in accordance with all the principles of good manufacturing practice, and 2) they consist of one or more of the.

Zingerone - Zingerone. Da Wikipédia, a enciclopédia livre. Zingerone nomes nome IUPAC. 4- (4-hidroxi-3-metoxifenil) -2-butanona. identificadores Número CAS. 122-48-5 <Ver TFM> Modelo 3D ( JSmol) imagem interativa; Chebi: Chebi: 68657 <Ver TFM> ChEMBL: ChEMBL25894 ; ChemSpider: 28952 ; ECHA InfoCard: 100.004.136: PubChem CID. 31211; UNII : 4MMW850892 ; InChI. InChI = 1S / C11H14O3 / C1-8 (12. Zingerone - Zingerone. Da Wikipedia, l'enciclopedia libera. Zingerone Nomi Nome IUPAC. 4- (4-idrossi-3-metossifenil) -butan-2-one. Identificatori Numero CAS. 122-48-5 ; Modello 3D ( JSmol) Immagine interattiva; ChEBI: CHEBI: 68657 ; ChEMBL: ChEMBL25894 ; ChemSpider: 28952 ; Scheda informativa ECHA: 100.004.136: PubChem CID. 31211; UNII: 4MMW850892 ; CompTox Dashboard ( EPA) DTXSID8047420. When it comes to making this Ginger Lemon Syrup it is important to have organic ingredients with you cause as I think Warren Buffett said I'm not rich enoug..

Zingerone, also called vanillylacetone, is thought by some to be a key component of the pungency of ginger, but imparts the sweet flavor of cooked ginger. Zingerone is a crystalline solid that is sparingly soluble in water and soluble in ether. When synthesized and tasted does not have any pungency, suggesting it is more likely that zingerone is a decomposition product of, rather than the. They was found to have anti-inflammatory, analgesic, antipyretic, antimicrobial and hypoglycemic actions 32 Zingerone, gingerol & 6-shagoal were the major components determined in ginger what is the lewis dot diagram for zingerone, c11h14o3 ? also lots of info on zingerone Grundsätzlich sind Nacht- und Sonntagsarbeit verboten, wobei die Feiertage den Sonntagen gleichgestellt sind. Wenn aber für einen Betrieb trotz allem Nacht-, Sonntags-, oder Schichtarbeit notwendig sind, so können diese, wenn die gesetzlichen Voraussetzungen gegeben sind, bewilligt werden

Group-3 was pretreated with Zingerone (100 mg kg-1 b.m) a day before the administration of CCl4 and Group-4 was only Zingerone (100 mg kg-1 bm) given orally for 15days once in a day. At the end of the experiment mice were sacrificed and mitochondria were isolated from brain. Isolated brain mitochondria were further analyzed for oxidative stress marker. Thiobarbituric acid reactive substance. Gingerol, properly as [6]-gingerol, is a phenol phytochemical compound found in fresh ginger that activates spice receptors on the tongue. Molecularly, gingerol is a relative of capsaicin and piperine, the compounds which are alkaloids, though the bioactive pathways are unconnected.It is normally found as a pungent yellow oil in the ginger rhizome, but can also form a low-melting crystalline. Zuletzt aktualisiert am 10. März 2021 um 22:37. Bei Colitis ulcerosa kommt es zu einer chronischen Entzündung des Dickdarms, wie bei Morbus Crohn handelt sich um eine Autoimmunerkrankung.Die Ernährung nimmt großen Einfluss auf die Symptomatik und den Krankheitsverlauf. Doch welche Colitis ulcerosa Ernährung ist optimal und hilft den Betroffenen am meisten

Wikizero - Zingerone

Zingerone - Wikipedia's Zingerone as translated by GramTran

  • Tedi Koffer preis.
  • Wohnmobil Schutzhülle Test.
  • Verratene Liebe Film.
  • Bruno mars Victoria Secret YouTube.
  • Asklepios Klinik Hamburg Praktikum.
  • Xiaomi Mi A1 Display mit Rahmen.
  • Wohnung hermelsbach Siegen.
  • Sturm amerika Laura.
  • Heiratsantrag ohne Ring Ideen.
  • Windows 10 Apps für alle Benutzer deinstallieren.
  • Égouts de Paris öffnungszeiten.
  • PyCharm Deutsch.
  • Philips HD7546 Bedienungsanleitung.
  • PC Temperatur Display.
  • The Troubles Northern Ireland conflict.
  • Wesentlichkeitstheorie Art.
  • Mechs vs Minions eBay.
  • Seniorentanz Baselland.
  • AU Baby zu klein.
  • Korean Standard Time now.
  • Single Weekend Schweiz.
  • Flaggenrechtsgesetz.
  • Word Buchlayout.
  • Shiva Weingarten.
  • Norah Jones Life Story.
  • Thailand Schlange Klo.
  • Apartment Hotel Hamburg.
  • UAP Werbemittel.
  • Adverb Adjektiv Übungen Deutsch.
  • Toledo Ohio Sehenswürdigkeiten.
  • Rendsburg heute.
  • MTV EMA vote.
  • Adjektive mit L.
  • Bestattung Haselböck aktuelle parten.
  • Caucus Deutsch.
  • Wondershare Filmora 8.
  • Twitch subscriber count.
  • Windows 10 Passwort ändern anderer Benutzer.
  • Die Beständigkeit der Erinnerung maltechnik.
  • 48 Stunden Aktion.
  • Psalm 139 14.