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Type of compounds
For the parent molecule 9,10-anthraquinone, see anthraquinone Anthraquinones (also known as anthraquinonoids) are a class of naturally occurring phenolic
Anthraquinones
Yellow chemical compound: building block of many dyes
substituted anthraquinones, the enzyme encoded by the gene UGT1A8 has glucuronidase activity with many substrates including anthraquinones. Benzoquinone
Anthraquinone
Process for the production of hydrogen peroxide
The anthraquinone process, also called the Riedl–Pfleiderer process, is a process for the production of hydrogen peroxide, which was developed by IG Farben
Anthraquinone_process
Compounds having a fully conjugated cyclic dione structure
examples are 1,2-benzoquinone (ortho-quinone), 1,4-naphthoquinone and 9,10-anthraquinone. The name is derived from that of quinic acid (with the suffix "-one"
Quinone
Class of chemical compounds
Anthraquinone dyes are an abundant group of dyes comprising a anthraquinone unit as the shared structural element. Anthraquinone itself is colourless,
Anthraquinone_dyes
Species of plant
throughout the tropics and is widely naturalised. The plant contains anthraquinones, which can be harmful to human health. Although the fresh fruit is edible
Morinda_citrifolia
Dye for synthetic polymers
polar molecules containing anthraquinone or azo groups. It is estimated that 85% of disperse dyes are azos or anthraquinone dyes. The history of disperse
Disperse_dye
Species of herbaceous perennial plant with fleshy, sour edible stalks
anthraquinones have been separated from powdered rhubarb root for purposes in traditional medicine, although long-term consumption of anthraquinones has
Rhubarb
Genus of plants
a rich source of anthraquinones. Zhou, Zhu; Jiang, Shan-Hao; Zhu, Da-Yuan; Lin, Long-Ze; A Cordell, Geoffrey (1994). "Anthraquinones from Knoxia valerianoides"
Knoxia
Chemical compound
10-anthraquinone (AQ). It formed when AQ is hydrogenated. It is easily dissolved in alkaline solutions and is often called soluble anthraquinone (SAQ)
9,10-Dihydroxyanthracene
Chemical compound
Hawas, U. W.; El-Beih, A. A.; El-Halawany, A. M. (2012). "Bioactive anthraquinones from endophytic fungus Aspergillus versicolor isolated from red sea
Arugosin_C
Chemical element with atomic number 13 (Al)
industrial uses involving this reaction, such as in the manufacture of anthraquinones and styrene. Aluminium trichloride is also often used as the precursor
Aluminium
Constipation and surgery medication
is considered contraindicated in people with a documented allergy to anthraquinones. Such allergies are rare and typically limited to dermatological reactions
Senna_glycoside
Intermediate Chemical in H2O2 Synthesis
industrially by the anthraquinone process which involves using 2-alkyl-9,10-anthraquinones for hydrogenation. Many derivatives of anthraquinone are used but
2-Ethylanthraquinone
Chemical compound
Brishammar S, Svensson C, Bengtsson M, Andersson R (March 1, 1993). "Anthraquinones from some Drechslera species and Bipolaris sorokiniana". Mycological
Catenarin
Chemical compound
Quinizarin Blue, Disperse Blue 72, and C.I. 60725, is a synthetic anthraquinone dye with bright bluish violet hue. It is a solid insoluble in water
Solvent_Violet_13
Agents that relax and loosen the bowels and stools
(casanthranol) Anthraquinone colon 36–8 hours Buckthorn Anthraquinone colon 36–8 hours Senna extract (senna glycoside) Anthraquinone colon 36–8 hours
Laxative
Chemical compound
monochlorinated anthraquinone isomers. The compound is prepared by diacylation of chlorobenzene with phthalic anhydride, a standard route to anthraquinones. Heating
2-Chloroanthraquinone
Genus of lichens
presence of anthraquinones in the apothecial disc and true exciple, with the exception of Kuettlingeria diphyodes, which entirely lacks anthraquinones. First
Kuettlingeria
Chemical compound found in some lichens
is an organic compound in the structural class of chemicals known as anthraquinones. It is found in some lichens, particularly in the family Teloschistaceae
Fallacinol
Chemical compound
of coal tar. Anthracene is used as a precursor in the production of anthraquinone and its derivatives such as the red dye alizarin, and as a scintillator
Anthracene
many dihydroxy derivatives of other anthraquinones, such as 1,2-anthraquinone, 1,4-anthraquinone, and 2,6-anthraquinone. Hydroxyquinone Hydroxybenzoquinone
Dihydroxyanthraquinone
Chemical compound
(AMS) is a water-soluble anthraquinone derivative. In the laboratory it can be prepared by sulfonation of anthraquinone. AMS is used as a catalyst in
Sodium 2-anthraquinonesulfonate
Sodium_2-anthraquinonesulfonate
Species of plant
polyphenols, acetylated mannans, polymannans, anthraquinones C-glycosides, anthrones, and other anthraquinones, such as emodin and various lectins. The flowers
Aloe_vera
Index of chemical compounds with the same molecular formula
4'-Trihydroxyflavone Aloe emodin, an anthraquinone Emodin, a purgative resin Genistein, an isoflavone Morindone, an anthraquinone dye Thunberginol A, an isocoumarin
C15H10O5
Species of flowering plant
phenolics such as phenolic acid; and anthraquinone derivatives such as the aldehyde nordamnacanthal (1,3-dihydroxy-anthraquinone-2-al). The species is native
Galium_aparine
Chemical compound
Disperse Red 9, or 1-(methylamino)anthraquinone, is a red dye derived from anthraquinone. Disperse Red 9 is used in some older red and violet-red colored
Disperse_Red_9
Class of plant and fungus secondary metabolites
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Flavonoid
Species of bacterium
lupini is an endophytic actinomycete notable for producing antitumour anthraquinones: lupinacidins A (1), B (2) and C. Its genome has been sequenced. Igarashi
Micromonospora_lupini
Class of chemical compounds
of any quinone (such as 1,2-benzoquinone, 1,4-naphthoquinone or 9,10-anthraquinone), where any number n of hydrogens have been replaced by n hydroxyls
Hydroxyquinone
dithionite promoted reaction of a phenolic anthraquinone with an aldehyde to yield a substituted phenolic anthraquinone after the addition of acid. The mechanism
Marschalk_reaction
Soluble chemical substance or natural material which can impart color to other materials
water-soluble hydroquinone, allowing anthraquinone dyes to be used as vat dyes. With appropriate substituents, anthraquinone dyes can also be used as disperse
Dye
Chemical compound
monochlorinated anthraquinone isomers. The compound is prepared by direct chlorination of anthraquinone. It can also be prepared by chlorination of anthraquinone-1-sulfonic
1-Chloroanthraquinone
Species of bacterium
galvaquinone B, galvaquinone C, spithioneine A, spithioneine B and anthraquinones. List of Streptomyces species LPSN bacterio.net Straininfo of Streptomyces
Streptomyces_spinoverrucosus
Chemical compound
Aloe emodin (1,8-dihydroxy-3-(hydroxymethyl)anthraquinone) is an anthraquinone and an isomer of emodin present in aloe latex, an exudate from the aloe
Aloe_emodin
Species of flowering plant
gallic acid, pfaffic acid, glomeric acid, oleanolic acid, saponins, anthraquinones, tannins, flavonoids, rubrosterone, and ecdysterone, in addition to
Pfaffia_glomerata
Class of chemical compounds
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Phenolic_acid
Genus of lichen-forming fungi
Lichens in the genus Psora generally have a squamulose thallus and anthraquinones in the hymenium. Photobiont partners of Psora lichens include members
Psora
Chemical compound
Damnacanthal is an anthraquinone isolated from the root of Morinda citrifolia, using water or organic solvents. In a 1995 in vitro study, damnacanthal
Damnacanthal
Species of plant
Australia, Queensland and New South Wales. Senna occidentalis seeds contain anthraquinones (AQs) such as Rhein, Emodin, Aloe-emodin, Chrysophanol, and Physcion
Senna_occidentalis
Class of phenolic chemical compounds
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Xanthonoid
Chemical compounds produced by plants
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Phytochemical
Chemical compound
Aloin is an anthraquinone glycosyl, meaning that its anthraquinone skeleton has been modified by the addition of a sugar molecule. Anthraquinones are a common
Aloin
Chemical compound
Hawas, U. W.; El-Beih, A. A.; El-Halawany, A. M. (2012). "Bioactive anthraquinones from endophytic fungus Aspergillus versicolor isolated from red sea
Siderin
Genus of lichens
particular, its non-carbonised ascomata and the presence of a vivid orange anthraquinone compound. The type species of the genus, Neosergipea aurata, was found
Neosergipea
Class of chemicals found in plants
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Diarylheptanoid
Chemical compound
C. H.; Niederländer, H. A. G.; van Beek, T. A. (2002). "Analysis of Anthraquinones in Rubia tinctorum L. by Liquid Chromatography Coupled with Diode-Array
1,4-Dihydroxyanthraquinone
Any organic aromatic compound with a structure based on a phenylpropane skeleton
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Phenylpropanoid
Species of true bug
water-soluble polyhydroxy-anthraquinones, collectively called lac dye. Apart from their usage in food and cosmetics, these anthraquinones also exhibit many pharmaceutical
Kerria_lacca
Chemical compound
tectoquinone, is an organic compound which is a methylated derivative of anthraquinone. An off-white solid, it is an important precursor to many dyes. It is
2-Methylanthraquinone
Chemical compound
Usama W.; El-Beih, Ahmed Atef; El-Halawany, Ali M. (2012). "Bioactive anthraquinones from endophytic fungus Aspergillus versicolor isolated from red sea
Evariquinone
Chemical compound
is a scarlet or orange-red-hue synthetic organic colourant. It is an anthraquinone derivative, first synthesized in 1913 as a vat dye, C.I. Vat Orange
Dibromoanthanthrone
Chemical compound
J.; Hagen, G. (1967). "Chemical Studies on Lichens. 9. Chlorinated Anthraquinones from Nephroma laevigatum". Acta Chemica Scandinavica. 21: 2889–2890
Fragilin
15711 azo 5610-64-0 Acid Blue AS Weak Acid Blue Acid Blue 25 62055 anthraquinone 6408-78-2 Acid fuchsin Acid Magenta Acid Rubin Acid Violet 19 42685
List_of_dyes
Pungent chemical compound in chili peppers
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Capsaicin
Chemical compound
exclusively by the anthraquinone process, which was originally developed by BASF in 1939. It begins with the reduction of an anthraquinone (such as 2-ethylanthraquinone
Hydrogen_peroxide
Chemical compound
Morindone is an anthraquinone compound obtained from various Morinda species, especially M. tinctoria, but also M. citrifolia. Its principal use is as
Morindone
Chemical compound
Laccaic acids or laccainic acids are a group of five anthraquinone derivatives, designated A through E, which are components of the red shellac obtained
Laccaic_acid
extensively in the preparation of chlorinated anthraquinones such as 1-chloroanthraquinone and 2-anthraquinones. 1,5-Dichloroanthraquinone [wd] forms from
Fischer_reaction
Species of fungus
The red color is caused by the production of rubellin, a photodynamic anthraquinone-derived phytotoxin. R. rubella was originally described from Rumex aquaticus
Ramularia_rubella
Chemical compound
Rubiadin is a bioactive anthraquinone dye that occurs naturally in several plant species, including Morinda citrifolia. Although rubiadin was first isolated
Rubiadin
Genus of lichens
smooth or slightly lobed. Chemically, it contains compounds called anthraquinones. Its outer protective layer, or cortex, has a paraplectenchymatous tissue
Orientophila
Species of legume
as a laxative. It also serves as a fungicide. Senna products contain anthraquinones, which if ingested can cause liver disease. The active ingredients are
Senna_alexandrina
Class of enzymes
{\displaystyle \rightleftharpoons } UDP + 1-hydroxy-2-(beta-D-glucosyloxy)-9,10-anthraquinone Thus, the two substrates of this enzyme are UDP-glucose and alizarin
Alizarin 2-beta-glucosyltransferase
Alizarin_2-beta-glucosyltransferase
Index of chemical compounds with the same molecular formula
24 g/mol, exact mass: 282.052823 u) may refer to: Damnacanthal, an anthraquinone Pseudobaptigenin, an isoflavone This set index page lists chemical structure
C16H10O5
Topics referred to by the same term
Corporation) Saky, a city in Crimea also romanized as "Saq" Soluble anthraquinone the Self Assessment Questionnaire for the Payment Card Industry Data
SAQ
Class of chemical compounds
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Polyphenol
Chemical compound
water-soluble and anionic and used for adsorption research. The structure is an anthraquinone. Acid Blue 25 is powder-like and poorly soluble in water. The dye is
Acid_Blue_25
Index of chemical compounds with the same molecular formula
Kaempferol, a flavonol Isoscutellarein, a tetrahydroxyflavone Lunatin, an anthraquinone Luteolin, a tetrahydroxyflavone Norartocarpetin, a tetrahydroxyflavone
C15H10O6
Molecule in which a sugar is bound to another functional group
These glycosides contain an aglycone group that is a derivative of anthraquinone. They have a laxative effect. They are mainly found in dicot plants
Glycoside
Chemical compound
while atorvastatin decreases cholesterol production in the liver. Anthraquinones, chrysophanol derivatives among them, have been shown to be hepatotoxic
Chrysophanol
Chemical compound
Anthraquinone-1-sulfonic acid is an organic compound with the formula C14H7O2SO3H. It is one of two of monosulfonated anthraquinone isomers. The compound
Anthraquinone-1-sulfonic_acid
including sitosterol and scopoletin.[citation needed] 2,700 BCE Rhubarb Anthraquinones, (e.g. emodin) which are cathartic and laxative. Stilbenoids (e.g. rhaponticin)
List of drugs by year of discovery
List_of_drugs_by_year_of_discovery
Chemical compound
Oil Blue 35 is a blue anthraquinone dye used for colouring alcoholic and hydrocarbon based solvents, including oils, fats, and waxes. It is used also
Oil_Blue_35
Species of succulent flowering plant in the spurge family
identified the presence of flavonoids, alkaloids, tannins, glycosides, anthraquinones, triterpenoids, and phytosterols. The species was named Euphorbia heptagona
Euphorbia_heptagona
Species of fungus
been reported to produce sterigmatocystin, versicolorins, and some anthraquinones. Apsergillus bicolor has been cultivated on both Czapek yeast extract
Aspergillus_bicolor
with formula (C12H4(OH)4)(CO)2, almost invariably derived from 9,10-anthraquinone by replacing four hydrogen atoms by hydroxyl groups. Only a few of these
Tetrahydroxyanthraquinone
Chemical compound
4-diamino-2-methoxyanthraquinone, is a red disperse dye derived from anthraquinone. It is water insoluble. Disperse Red 11 can be used in plastics and
Disperse_Red_11
Chemical compounds used to color plastic
Colorant Chemical class Type Diarylide pigment azo dye pigment Sudan stain azo dye dye Oil Blue A anthraquinone dye Disperse Red 11 anthraquinone dye
Plastic_colorant
Glycoside that is derived from glucose
k-strophanthin from Stroph. kombé. These are generally substituted anthraquinones; many have medicinal applications, being used as purgatives, while one
Glucoside
are dyes which comprise at least two conjugated carbonyl groups. Both anthraquinone dyes and indigo dyes belong to the group of carbonyl dyes. The most
Carbonyl_dyes
Chemical compound
Rhein, also known as cassic acid, is a substance in the anthraquinone group obtained from rhubarb. Like all such substances, rhein is a cathartic, which
Rhein_(molecule)
Chemical compound
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
Isocoumarin
Topics referred to by the same term
college sports 8-Aminoquinoline (AQ), a heterocyclic bidentate ligand Anthraquinone (AQ), an aromatic organic compound Aqueous solution (aq), dissolved
AQ
Chemical compound
one of many tetrahydroxyanthraquinone isomers, formally derived from anthraquinone by replacement of four hydrogen atoms by hydroxyl (OH) groups at the
Quinalizarin
Subfamily of flowering plants, in monocot family Asphodelaceae
aloe). The Asphodeloideae are distinguished by a general presence of anthraquinones, simultaneous microsporogenesis, atypical ovules morphology, and the
Asphodeloideae
Chemical compound
Aromatics with o-Phthaloyl Dichlorides: Regioselective Synthesis of Anthraquinones". The Journal of Organic Chemistry. 60 (20): 6588–6591. doi:10.1021/jo00125a054
Phthaloyl_chloride
Chemical compound
Dioxamycin is a benz[a]anthraquinone antibiotic and kinase inhibitor with the molecular formula C38H40O15. Dioxamycin is produced by the bacterium Streptomyces
Dioxamycin
Species of lichen-forming fungus
non-chlorinated anthraquinones (e.g., parietin series) and lacks chlorinated anthraquinones; the thallus itself is usually without anthraquinones. Cinereorufa-green
Blastenia_hungarica
Class of enzymes
hydroxyanthraquinone and UDP-glucose. Its products are the corresponding glucosylated anthraquinone and uridine diphosphate (UDP). For example, emodin, an active component
Hydroxyanthraquinone glucosyltransferase
Hydroxyanthraquinone_glucosyltransferase
Chemical compound
called purpurin, is an anthraquinone. It is a naturally occurring red/yellow dye. It is formally derived from 9,10-anthraquinone by replacement of three
1,2,4-Trihydroxyanthraquinone
Index of chemical compounds with the same molecular formula
molecular formula C14H8O2 (molar mass: 208.216 g/mol) may refer to: Anthraquinone, also known as anthracenedione or dioxoanthracene Phenanthrenequinone
C14H8O2
Pinosylvin Curcuminoids Curcumin Tannins Others Diarylheptanoids (C6-C7-C6) Anthraquinones Chalconoids (C6-C3-C6) Kavalactones Naphthoquinones (C6-C4) Phenylpropanoids
List of phytochemicals in food
List_of_phytochemicals_in_food
Solvent Yellow 124, Solvent Blue 35, etc. Red and yellow solvent dyes are often azo dyes, green and blue ones tend to be anthraquinone dyes. Solvent Dye
Solvent_dye
Class of chemical compounds
where n ≥ 1. Almost all hydroxyanthraquinones are derivative of 9,10-anthraquinone. One peculiarity of the hydroxyanthraquinones is the relative obscurity
Hydroxyanthraquinone
Juice of the fruit of the species Morinda citrifolia
been issued for the same types of violations. Research has pointed to anthraquinones found in noni roots, leaves and fruit as potentially toxic to the liver
Noni_juice
Chemical compound found in some lichens
is an organic compound in the structural class of chemicals known as anthraquinones. It is found in many species of the lichen family Teloschistaceae. In
Fallacinal
Mineral
geologist Adolf Hoel (1879–1964). Its chemical formula is C14H8O2 (9,10-anthraquinone). It is a very rare organic mineral which occurs in coal fire environments
Hoelite
Chemical compound
Quinizarine Green SS, also called Solvent Green 3 is an anthraquinone derivative. It is a black powder that is soluble in polar organic solvents, but
Quinizarine_Green_SS
Species of lichen
roccellic/angardianic acids. It may also contain from two to four unidentified anthraquinone compounds. When tested with common lichen chemical spot tests, it is
Lepraria_achariana
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