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PHLOROGLUCINOL

  • Phloroglucinol
  • Chemical compound

    Phloroglucinol is an organic compound with the formula C6H3(OH)3. It is a colorless solid. It is used in the synthesis of pharmaceuticals and explosives

    Phloroglucinol

    Phloroglucinol

    Phloroglucinol

  • Phloroglucinol synthase
  • Phloroglucinol synthase is an acetyltransferase enzyme involved in the synthesis of phloroglucinol (also known as 1,3,5-trihydroxybenzene or cyclohexane-1

    Phloroglucinol synthase

    Phloroglucinol synthase

    Phloroglucinol_synthase

  • Phloroglucinol reductase
  • Class of enzymes

    In enzymology, phloroglucinol reductase (EC 1.3.1.57) is an enzyme that catalyzes the chemical reaction (1) + NADP+       H+   H+   (2) + NADPH   The two

    Phloroglucinol reductase

    Phloroglucinol reductase

    Phloroglucinol_reductase

  • Phloroglucinol carboxylic acid
  • Chemical compound

    Phloroglucinol carboxylic acid, also called ‘Phloroglucinic acid’ or simply ‘PGCA’, is a trihydroxybenzoic acid, a type of phenolic acid. It can be encountered

    Phloroglucinol carboxylic acid

    Phloroglucinol carboxylic acid

    Phloroglucinol_carboxylic_acid

  • 2,4,6-Trinitrobenzoic acid
  • Impact-resistant high explosive

    Reduction with tin gives 2,4,6-triaminobenzenoic acid, a precursor to phloroglucinol (1,3,5-trihydroxybenzene). "2,4,6-Trinitrobenzoic acid". pubchem.ncbi

    2,4,6-Trinitrobenzoic acid

    2,4,6-Trinitrobenzoic acid

    2,4,6-Trinitrobenzoic_acid

  • Dihydrophloroglucinol
  • Chemical compound

    of phloroglucinol and other phenolic compounds. The enzyme phloroglucinol reductase uses dihydrophloroglucinol and NADP+ to produce phloroglucinol, NADPH

    Dihydrophloroglucinol

    Dihydrophloroglucinol

    Dihydrophloroglucinol

  • Tannin
  • Class of astringent, bitter plant polyphenolic chemical compounds

    Base unit / scaffold Gallic acid Phloroglucinol Flavan-3-ol Polymer class Hydrolyzable tannins Phlorotannins Condensed tannins Phlobatannins (C-ring isomerized

    Tannin

    Tannin

    Tannin

  • Herbchronology
  • μm) of Penstemon venustus. Lignified tissue is stained reddish using Phloroglucinol/HCL. Black markers denote annual ring borders. Individual collected

    Herbchronology

    Herbchronology

    Herbchronology

  • Catechin
  • Secondary metabolite

    protocatechuic acid (PCA) and phloroglucinol carboxylic acid (PGCA). It is also degraded by Bradyrhizobium japonicum. Phloroglucinol carboxylic acid is further

    Catechin

    Catechin

    Catechin

  • Trihydroxybenzenes
  • Index of chemical compounds with the same name

    transforms benzene-1,2,3-triol (pyrogallol) into benzene-1,3,5-triol (phloroglucinol) and vice versa. It uses benzene-1,2,3,5-tetrol as a cosubstrate, thanks

    Trihydroxybenzenes

    Trihydroxybenzenes

    Trihydroxybenzenes

  • Pyrogallol hydroxytransferase
  • enzyme that catalyzes a chemical reaction that converts pyrogallol to phloroglucinol by formation of the intermediate 1,2,3,5-tetrahydroxybenzene. Pyrogallol

    Pyrogallol hydroxytransferase

    Pyrogallol hydroxytransferase

    Pyrogallol_hydroxytransferase

  • Eucalyptus
  • Genus of flowering plants

    correlation of these oils with other more potent toxins called formylated phloroglucinol compounds (euglobals, macrocarpals and sideroxylonals) allows koalas

    Eucalyptus

    Eucalyptus

    Eucalyptus

  • 1,3,5-Trinitrobenzene
  • Chemical compound

    of 1,3,5-trinitrobenzene gives 1,3,5-triaminobenzene, a precursor to phloroglucinol. Trinitrobenzene is more explosive than TNT, but more expensive. It

    1,3,5-Trinitrobenzene

    1,3,5-Trinitrobenzene

    1,3,5-Trinitrobenzene

  • Phenol
  • Chemical compound

    Benzeneselenol Benzenetellurol Sodium phenoxide Catechol Resorcinol Hydroquinone Phloroglucinol Pyrogallol Hydroxyquinol 1,2,3,5-Tetrahydroxybenzene Pentahydroxybenzene

    Phenol

    Phenol

    Phenol

  • Flopropione
  • Spasmolytic or antispasmodic agent

    to be a serotonin 5-HT1A receptor antagonist. It is synthesized from phloroglucinol in a Hoesch reaction.[citation needed] 2,4,6-Trihydroxyacetophenone

    Flopropione

    Flopropione

    Flopropione

  • Diphlorethol
  • Chemical compound

    class of phlorotannins due to the ether bond that connects its two phloroglucinol units. Sailler, Birgit; Glombitza, Karl-Werner (1999-03-10). "Phlorethols

    Diphlorethol

    Diphlorethol

    Diphlorethol

  • Hoesch reaction
  • Chemical reaction

    catalyst. The synthesis of 2,4,6-Trihydroxyacetophenone (THAP) from phloroglucinol is representative: If two-equivalents are added, 2,4-Diacetylphloroglucinol

    Hoesch reaction

    Hoesch_reaction

  • Enol
  • Organic compound with a C=C–OH group

    tautomer plays an important role. Many of the reactions of resorcinol and phloroglucinol involve the keto tautomers, for example. Naphthalene-1,4-diol exists

    Enol

    Enol

    Enol

  • Antispasmodic
  • Class of medications

    dantrolene have been used. Muscarinic antagonist Parasympatholytic Phloroglucinol Spasticity Propantheline bromide "Antispasmodic". thefreedictionary

    Antispasmodic

    Antispasmodic

  • Hypericum
  • Genus of flowering plants known as St. John's worts

    intracellular space lined with flattened cells that secrete oils and phloroglucinol derivates, including hyperforin. The distribution of these hypericin

    Hypericum

    Hypericum

    Hypericum

  • Flavaspidic acid
  • Index of chemical compounds with the same name

    Flavaspidic acid AB is a polyphenol that is a phloroglucinol derivative isolated from the rhizomes of Dryopteris Crassirhizoma and has been shown to exhibit

    Flavaspidic acid

    Flavaspidic_acid

  • Mallotophenone
  • Chemical compound

    Mallotophenone is a dimeric phloroglucinol found in Mallotus oppositifolius or in Mallotus japonicus. The bioassay-guided fractionation of an ethanol extract

    Mallotophenone

    Mallotophenone

    Mallotophenone

  • Pentacarbon dioxide
  • Chemical compound

    5-trione (C6N6O3). Diazo transfer can produce the latter compound from phloroglucinol. It is stable at room temperature in solution. The pure compound is

    Pentacarbon dioxide

    Pentacarbon dioxide

    Pentacarbon_dioxide

  • Hypericum perforatum
  • Flowering plant in the St John's wort family

    hypericin and pseudohypericin (naphthodianthrones), and hyperforin (a phloroglucinol derivative). The species contains a host of essential oils, the bulk

    Hypericum perforatum

    Hypericum perforatum

    Hypericum_perforatum

  • Gluconic acid
  • Chemical compound

    knowledge of some types of sugars: glucose, sucrose, fructose, sorbin, phloroglucinol]. Berichte der Deutschen Chemischen Gesellschaft (in German). 3 (1):

    Gluconic acid

    Gluconic acid

    Gluconic_acid

  • Griseofulvin
  • Antifungal medication used for dermatophytoses

    biosynthesis I. Some possible routes to derivatives of orcinol and phloroglucinol". Australian Journal of Chemistry. 6 (4): 360. Bibcode:1953AJCh....6

    Griseofulvin

    Griseofulvin

    Griseofulvin

  • Filicin
  • Chemical compound

    Isao (1972). "Pharmaceutical studies on Japanese ferns containing phloroglucinol derivatives. 9 Constituents of Dryopteris dickinsii". Yakugaku Zasshi

    Filicin

    Filicin

    Filicin

  • Simeticone
  • Anti-foaming agent used to reduce bloating, discomfort or pain caused by excessive gas

    Pladuet, Planex with pipenzolate bromide as Cadinol, Gasorbol Gotas with phloroglucinol as Meteoxane with trimebutine as Eumotil-S, Eumotrix Plus, Libertrim

    Simeticone

    Simeticone

    Simeticone

  • Hyperforin
  • Chemical compound

    species contain low amounts of hyperforin. Hyperforin is a prenylated phloroglucinol derivative and is a member of the polycyclic polyprenylated acylphloroglucinol

    Hyperforin

    Hyperforin

    Hyperforin

  • Polyphenol
  • Class of chemical compounds

    repeating phenolic moieties of pyrocatechol, resorcinol, pyrogallol, and phloroglucinol connected by esters (hydrolyzable tannins) or more stable C-C bonds

    Polyphenol

    Polyphenol

    Polyphenol

  • Eubacterium oxidoreducens
  • Species of bacterium

    by E. oxidoreducens. The enzyme phloroglucinol reductase uses dihydrophloroglucinol and NADP+ to produce phloroglucinol, NADPH, and H+. It is found in

    Eubacterium oxidoreducens

    Eubacterium_oxidoreducens

  • 2,4,6-Trihydroxyacetophenone
  • Chemical compound

    6-Trihydroxyacetophenone (THAP) is a chemical compound that is a derivative of phloroglucinol. In an animal model, THAP was reported to enhance cholesterol 7 alpha-hydroxylase

    2,4,6-Trihydroxyacetophenone

    2,4,6-Trihydroxyacetophenone

    2,4,6-Trihydroxyacetophenone

  • Phlorotannin
  • Class of chemical compounds

    hydrolysable or condensed tannins, these compounds are oligomers of phloroglucinol (polyphloroglucinols). As they are called tannins, they have the ability

    Phlorotannin

    Phlorotannin

    Phlorotannin

  • Tollens' reagent
  • Chemical reagent used to distinguish between aldehydes and ketones

    in this case. Another test relies on reaction of the furfural with phloroglucinol to produce a colored compound with high molar absorptivity. It also

    Tollens' reagent

    Tollens' reagent

    Tollens'_reagent

  • List of poisonous plants
  • ferns Dryopteridaceae The rhizomes of this family are known to contain phloroglucinol derived compounds, previously used to treat nematode infections. Dryopteris

    List of poisonous plants

    List of poisonous plants

    List_of_poisonous_plants

  • Lignin
  • Structural phenolic polymer in plant cell walls

    (furfural and 5-hydroxymethylfurfural). A solution of hydrochloric acid and phloroglucinol is used for the detection of lignin (Wiesner test). A brilliant red

    Lignin

    Lignin

    Lignin

  • 1,2,3,5-Tetrahydroxybenzene
  • Chemical compound

    (pyrogallol), whereas its two products are 1,3,5-trihydroxybenzene (phloroglucinol) and 1,2,3,5-tetrahydroxybenzene. 1,2,3,5-Tetrahydroxybenzene, also

    1,2,3,5-Tetrahydroxybenzene

    1,2,3,5-Tetrahydroxybenzene

    1,2,3,5-Tetrahydroxybenzene

  • Endodermis
  • Inner layer of cortex in vascular plant roots

    a starch sheath. Endodermis is often made visible with stains like phloroglucinol due to the phenolic and lipid nature of the Casparian strips or by the

    Endodermis

    Endodermis

    Endodermis

  • Pelobacter acidigallici
  • Species of bacterium

    (pyrogallol), whereas its two products are 1,3,5-trihydroxybenzene (phloroglucinol) and 1,2,3,5-tetrahydroxybenzene. This enzyme can be found in P. acidigallici

    Pelobacter acidigallici

    Pelobacter_acidigallici

  • Trihydroxybenzoic acid
  • Index of chemical compounds with the same name

    following phenolic acids: Gallic acid (3,4,5-trihydroxybenzoic acid) Phloroglucinol carboxylic acid (2,4,6-trihydroxybenzoic acid) O-methylated trihydroxybenzoic

    Trihydroxybenzoic acid

    Trihydroxybenzoic acid

    Trihydroxybenzoic_acid

  • Bradyrhizobium japonicum
  • Species of bacterium

    to degrade catechin with formation of phloroglucinol carboxylic acid, further decarboxylated to phloroglucinol, which is dehydroxylated to resorcinol

    Bradyrhizobium japonicum

    Bradyrhizobium japonicum

    Bradyrhizobium_japonicum

  • Proanthocyanidin
  • Class of polyphenols found in many plants

    undergo acid-catalyzed cleavage in the presence of a nucleophile like phloroglucinol (reaction called phloroglucinolysis), thioglycolic acid (thioglycolysis)

    Proanthocyanidin

    Proanthocyanidin

  • Eckol
  • Chemical compound

    possesses a dibenzo-p-dioxin skeleton and a phloroglucinol component. The molecule can also be viewed as a phloroglucinol trimer. It exhibits an antiplasmin inhibitory

    Eckol

    Eckol

    Eckol

  • Molecular symmetry
  • Symmetry of molecules of chemical compounds

    tetrafluoride Dichloromethane C3h E C3 C32 σh S3 S35 propeller boric acid phloroglucinol (1,3,5-trihydroxybenzene) benzotrifuroxan C3v E 2C3 3σv trigonal pyramidal

    Molecular symmetry

    Molecular_symmetry

  • Leptospermone
  • Chemical compound

    inhibitor herbicides on the market. Leptospermone can be synthesized from phloroglucinol by a reaction with 3-methylbutanenitrile (isovaleronitrile) in the presence

    Leptospermone

    Leptospermone

    Leptospermone

  • Phloretin hydrolase
  • Class of enzymes

    phloretate + phloroglucinol Thus, the two substrates of this enzyme are phloretin and H2O, whereas its two products are phloretate and phloroglucinol. This enzyme

    Phloretin hydrolase

    Phloretin_hydrolase

  • Phloretin
  • Chemical compound

    intestine. Phloretin hydrolase hydrolyses phloretin into phloretic acid and phloroglucinol. In an animal model, phloretin inhibited active transport of glucose

    Phloretin

    Phloretin

    Phloretin

  • C6H6O3
  • Index of chemical compounds with the same molecular formula

    Hydroxymethylfurfural Hydroxyquinol Isomaltol Levoglucosenone Maltol Phloroglucinol Pyrogallol Triacetic acid lactone This set index page lists chemical

    C6H6O3

    C6H6O3

  • Pentose
  • 5-Carbon simple sugar

    silver-mirror test for reducing sugars), the furfural ring reacts with phloroglucinol to produce a colored compound; in the aniline acetate test with aniline

    Pentose

    Pentose

  • TATB
  • Chemical compound

    switched over to a process involving the nitration and transamination of phloroglucinol, since this process is milder, cheaper, and reduces the amount of ammonium

    TATB

    TATB

    TATB

  • Gunzberg's test
  • Chemical test detecting hydrochloric acid

    hydrochloric acid. Gunzberg's reagent is made by dissolving two grams of phloroglucinol and one gram of vanillin in 100 millilitres of 95% ethanol. Hydrochloric

    Gunzberg's test

    Gunzberg's_test

  • Toluidine blue
  • Chemical compound

    turn from blue to blue-green. A similar test can be performed with phloroglucinol-HCl solution, which turns red. Toluidine blue is a basic phenothiazine

    Toluidine blue

    Toluidine blue

    Toluidine_blue

  • Phenolic content in wine
  • Wine chemistry

    Petunidin-3-O-acetylglucoside-4-vinyl(epi)catechin Phloroglucinol carboxylic acid Piceatannol Piceids Pinotin A Oligomeric procyanidins :

    Phenolic content in wine

    Phenolic content in wine

    Phenolic_content_in_wine

  • Phlobaphene
  • Chemical compound

    precipitation) can be minimized in using strong nucleophiles, such as phloroglucinol, m-phenylenediamine and urea, during pine tannins extraction. The use

    Phlobaphene

    Phlobaphene

    Phlobaphene

  • List of EC numbers (EC 1)
  • 3.1.56: cis-2,3-dihydrobiphenyl-2,3-diol dehydrogenase EC 1.3.1.57: phloroglucinol reductase EC 1.3.1.58: 2,3-dihydroxy-2,3-dihydro-p-cumate dehydrogenase

    List of EC numbers (EC 1)

    List_of_EC_numbers_(EC_1)

  • Procyanidin
  • Group of chemical compounds

    undergo acid-catalyzed cleavage in the presence of a nucleophile like phloroglucinol (reaction called phloroglucinolysis), thioglycolic acid (thioglycolysis)

    Procyanidin

    Procyanidin

    Procyanidin

  • ATC code A03
  • Pharmaceutical drug classification

    A03AX09 Trepibutone A03AX10 Isometheptene A03AX11 Caroverine A03AX12 Phloroglucinol A03AX13 Silicones A03AX14 Valethamate A03AX15 Menthae piperitae aetheroleum

    ATC code A03

    ATC_code_A03

  • Zonaria (alga)
  • Genus of algae

    Australian species Z. turneriana, Z. crenata and Z. angustata produce phloroglucinol derivatives. Zonaria are mostly found in Australasia, but can also be

    Zonaria (alga)

    Zonaria (alga)

    Zonaria_(alga)

  • Adamantane
  • Molecule with three connected cyclohexane rings arranged in the "armchair" configuration

    [page needed] Other researchers attempted to synthesize adamantane using phloroglucinol and derivatives of cyclohexanone, but also failed. Adamantane was first

    Adamantane

    Adamantane

    Adamantane

  • Mallotus oppositifolius
  • Species of flowering plant

    in Madagascar led to the isolation of the two new bioactive dimeric phloroglucinols mallotojaponins B and C, together with mallotophenone. These compounds

    Mallotus oppositifolius

    Mallotus oppositifolius

    Mallotus_oppositifolius

  • Linderatin
  • Skin whitening agent

    hydrocinnamonitrile (2-phenylethylcyanide; 1) with phloroglucinol (2) gives 3-phenylpropanoyl-phloroglucinol (3). Treatment with menthadiene (alpha-phellandrene;

    Linderatin

    Linderatin

    Linderatin

  • Hexachlorobenzene
  • Chemical compound

    seed dressing but is now banned in many countries. A minor industrial phloroglucinol synthesis nucleophilically substitutes hexachlorobenzene with alkoxides

    Hexachlorobenzene

    Hexachlorobenzene

  • Condensed tannin
  • Polymers formed by the condensation of flavans

    acid-catalyzed cleavage in the presence of (an excess of) a nucleophile like phloroglucinol (reaction called phloroglucinolysis), benzyl mercaptan (reaction called

    Condensed tannin

    Condensed tannin

    Condensed_tannin

  • Helichrysum petiolare
  • Species of flowering plant

    mixture of flavonoids, volatile oils, sesquiterpenoids and acylated phloroglucinols seem to mimic the effects of alkaloid compounds on the central nervous

    Helichrysum petiolare

    Helichrysum petiolare

    Helichrysum_petiolare

  • Ecklonia
  • Genus of seaweeds

    Retrieved January 27, 2022. Protective effect of phlorotannin components phloroglucinol and eckol on radiation-induced intestinal injury in mice. Changjong

    Ecklonia

    Ecklonia

    Ecklonia

  • Ecklonia stolonifera
  • Species of seaweed

    2-phloroeckol, phlorofucofuroeckol B, 6,6'-bieckol, triphlorethol-A, phloroglucinol and 7-phloroeckol. Those phlorotannins are responsible for the potent

    Ecklonia stolonifera

    Ecklonia_stolonifera

  • Naturally occurring phenols
  • Group of chemical compounds

    chemical. The proteobacterium Pseudomonas fluorescens produces phloroglucinol, phloroglucinol carboxylic acid and diacetylphloroglucinol. Another example

    Naturally occurring phenols

    Naturally occurring phenols

    Naturally_occurring_phenols

  • Mallotojaponin B
  • Chemical compound

    Mallotojaponin B is a dimeric phloroglucinol found in Mallotus oppositifolius. The bioassay-guided fractionation of an ethanol extract of the leaves and

    Mallotojaponin B

    Mallotojaponin B

    Mallotojaponin_B

  • Hypericum calycinum
  • Species of flowering plant in the St John's wort family

    such as mites and aphids. One type of DIP (dearomatized isoprenylated phloroglucinols), a category of pigments alongside flavonoids, was found to be toxic

    Hypericum calycinum

    Hypericum calycinum

    Hypericum_calycinum

  • Cystophora retroflexa
  • Species of seaweed

    contains phlorotannins of the classes of phlorethols and fucophlorethols (phloroglucinol, difucol, tetraphlorethol-E, pentaphlorethol-B, hexaphlorethol-A, fucotriphlorethol-G

    Cystophora retroflexa

    Cystophora retroflexa

    Cystophora_retroflexa

  • List of EC numbers (EC 2)
  • palmitoyltransferase EC 2.3.1.252: mycolipanoate synthase EC 2.3.1.253: phloroglucinol synthase EC 2.3.1.254: N-terminal methionine Nα-acetyltransferase NatB

    List of EC numbers (EC 2)

    List_of_EC_numbers_(EC_2)

  • Serotonin–norepinephrine–dopamine reuptake inhibitor
  • Class of drugs

    Costentin, J; von Poser, G. L.; Rates, S. M. (2012). "Uliginosin B, a phloroglucinol derivative from Hypericum polyanthemum: A promising new molecular pattern

    Serotonin–norepinephrine–dopamine reuptake inhibitor

    Serotonin–norepinephrine–dopamine_reuptake_inhibitor

  • Phloretic acid
  • Chemical compound

    reduction of the unsaturated side chain of p-coumaric acid. Together with phloroglucinol, it is produced by the action of the enzyme phloretin hydrolase on phloretin

    Phloretic acid

    Phloretic acid

    Phloretic_acid

  • Dryopteris crassirhizoma
  • Species of fern

    Jin Cheol; Lee, Sang Myung (2009). "Antibacterial activity of two phloroglucinols, flavaspidic acids AB and PB, from Dryopteris crassirhizoma". Archives

    Dryopteris crassirhizoma

    Dryopteris crassirhizoma

    Dryopteris_crassirhizoma

  • Heinrich Hlasiwetz
  • Austrian chemist (1825–1875)

    compounds. Hlasiwetz is remembered for his chemical analysis of quercitrin, phloroglucinol, resorcinol and creosote. Über das Quercitrin, 1859 Über eine neue Säure

    Heinrich Hlasiwetz

    Heinrich Hlasiwetz

    Heinrich_Hlasiwetz

  • Acinetobacter calcoaceticus
  • Species of bacterium

    It is also present in Tiger mosquito (Aedes albopictus) microflora. Phloroglucinol carboxylic acid is a degradation product excreted by A. calcoaceticus

    Acinetobacter calcoaceticus

    Acinetobacter_calcoaceticus

  • Rottlerin
  • Chemical compound

    Rottlerin (mallotoxin) is a polyphenol natural product isolated from the Asian tree Mallotus philippensis. Rottlerin displays a complex spectrum of pharmacology

    Rottlerin

    Rottlerin

    Rottlerin

  • Mallotojaponin C
  • Chemical compound

    Mallotojaponin C is a dimeric phloroglucinol found in Mallotus oppositifolius. The bioassay-guided fractionation of an ethanol extract of the leaves and

    Mallotojaponin C

    Mallotojaponin C

    Mallotojaponin_C

  • 2,4-Diacetylphloroglucinol
  • Chemical compound

    Achkar, J; Xian, M; Zhao, H; Frost, JW (April 2005). "Biosynthesis of phloroglucinol". Journal of the American Chemical Society. 127 (15): 5332–5333. doi:10

    2,4-Diacetylphloroglucinol

    2,4-Diacetylphloroglucinol

    2,4-Diacetylphloroglucinol

  • Trifucol
  • Chemical compound

    1016/0031-9422(76)85094-7. Pal Singh, Inder; Bharate, Sandip B. (2006). "Phloroglucinol compounds of natural origin". Natural Product Reports. 23 (4): 558–591

    Trifucol

    Trifucol

    Trifucol

  • 6,6'-Bieckol
  • Chemical compound

    Lee, S. H.; Kim, M. M.; Kim, S. K. (2008). "Anti-HIV-1 activity of phloroglucinol derivative, 6,6′-bieckol, from Ecklonia cava". Bioorganic & Medicinal

    6,6'-Bieckol

    6,6'-Bieckol

    6,6'-Bieckol

  • Crofelemer
  • Pharmaceutical drug

    polymerization for the oligomers ranges between 5 and 7.5, as determined by phloroglucinol degradation. The substance is a purified oligomeric proanthocyanidin

    Crofelemer

    Crofelemer

    Crofelemer

  • C7H6O5
  • Index of chemical compounds with the same molecular formula

    mass: 170.021523 u) may refer to: Gallic acid, a phenolic compound Phloroglucinol carboxylic acid, a phenolic compound This set index page lists chemical

    C7H6O5

    C7H6O5

  • Homoisoflavonoid
  • Type of phenolic compound

    synthesized from 3,5-methoxy phenols via chroman-4-one in three steps or from phloroglucinol. Conversion Homoisoflavanes can be obtained from the conversion of homoisoflavonoids

    Homoisoflavonoid

    Homoisoflavonoid

    Homoisoflavonoid

  • Castor oil glycidyl ether
  • Chemical compound

    (March 2020). "Bio-Based Epoxy Shape-Memory Thermosets from Triglycidyl Phloroglucinol". Polymers. 12 (3): 542. doi:10.3390/polym12030542. ISSN 2073-4360.

    Castor oil glycidyl ether

    Castor oil glycidyl ether

    Castor_oil_glycidyl_ether

  • Arachidonate 5-lipoxygenase inhibitor
  • Drug class

    Sciences in Moscow) and published in 1975. Hyperforin is a prenylated phloroglucinol derivative. Total synthesis of hyperforin has not yet been accomplished

    Arachidonate 5-lipoxygenase inhibitor

    Arachidonate_5-lipoxygenase_inhibitor

  • Pseudomonas fluorescens
  • Species of bacterium

    Jihane; Xian, Mo; Zhao, Huimin; Frost, J. W. (2005). "Biosynthesis of Phloroglucinol". J. Am. Chem. Soc. 127 (15): 5332–5333. Bibcode:2005JAChS.127.5332A

    Pseudomonas fluorescens

    Pseudomonas fluorescens

    Pseudomonas_fluorescens

  • Humulone
  • Chemical compound

    characteristic bitter flavor. In terms of structure, humulone is a phloroglucinol derivative with three isoprenoid side-chains. Two side-chains are prenyl

    Humulone

    Humulone

    Humulone

  • Trimethylolpropane triglycidyl ether
  • Chemical compound

    (March 2020). "Bio-Based Epoxy Shape-Memory Thermosets from Triglycidyl Phloroglucinol". Polymers. 12 (3): 542. doi:10.3390/polym12030542. ISSN 2073-4360.

    Trimethylolpropane triglycidyl ether

    Trimethylolpropane triglycidyl ether

    Trimethylolpropane_triglycidyl_ether

  • Bergapten
  • Chemical compound

    insure regiochemical integrity and convergence. As shown in the diagram, phloroglucinol (compound 1) was the starting material. Mono-methylation was conducted

    Bergapten

    Bergapten

    Bergapten

  • Mallotochromene
  • Chemical compound

    Mallotochromene is a phloroglucinol derivative found in the pericarp of the fruits of Mallotus japonicus. Arisawa, Munehisa; Fujita, Akio; Suzuki, Rieko;

    Mallotochromene

    Mallotochromene

    Mallotochromene

  • Lichexanthone
  • Chemical compound found in some lichens

    The earliest syntheses of lichexanthone used orsellinic aldehyde and phloroglucinol as starting reactants in the Tanase method. This method, one of six

    Lichexanthone

    Lichexanthone

    Lichexanthone

  • Mallotus japonicus
  • Species of flowering plant

    Hiroshi; Morita, Naokata (1990). "Cytotoxic and antiherpetic activity of phloroglucinol derivatives from Mallotus japonicus (Euphorbiaceae)". Chemical & Pharmaceutical

    Mallotus japonicus

    Mallotus japonicus

    Mallotus_japonicus

  • Agrimol B
  • Pharmaceutical compound

    Agrimol B is a natural product which is found in the plant Agrimonia pilosa, which is used in traditional herbal medicine in various countries in East

    Agrimol B

    Agrimol B

    Agrimol_B

  • Smooth Island (Tasmania)
  • Island close to the south-eastern coast of Tasmania

    April 2015. Blackman, Adrian J; Matthews, David J (1982). "Halogenated phloroglucinols from Rhabdonia verticillata". Phytochemistry. 21 (8): 2141–2142. Bibcode:1982PChem

    Smooth Island (Tasmania)

    Smooth Island (Tasmania)

    Smooth_Island_(Tasmania)

  • List of MeSH codes (D02)
  • The following is a partial list of the "D" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM)

    List of MeSH codes (D02)

    List_of_MeSH_codes_(D02)

  • Hypericum annulatum
  • Species of flowering plant in the St John's wort family

    anticancer compound found in the species is hyperatomarin, a prenylated phloroglucinol, which has a relatively high concentration of about 3% in extracts from

    Hypericum annulatum

    Hypericum annulatum

    Hypericum_annulatum

  • Leprocaulon
  • Genus of lichens

    thin-layer chromatography reveals an array of depsides, depsidones, phloroglucinol pigments, triterpenoids and fatty acids, although the exact profile

    Leprocaulon

    Leprocaulon

    Leprocaulon

  • Thiophanic acid
  • Chemical compound found in some lichens

    starting with dichloroeverninic acid. This compound was reacted with phloroglucinol (a type of phenol) in the presence of zinc chloride and phosphorus oxychloride

    Thiophanic acid

    Thiophanic acid

    Thiophanic_acid

  • Transition metal catalytic asymmetric dearomatization reactions
  • Category of organic chemical reactions

    Ji; Porco, John A. (2007-10-01). "Rapid Access to Polyprenylated Phloroglucinols via Alkylative Dearomatization−Annulation: Total Synthesis of (±)-Clusianone"

    Transition metal catalytic asymmetric dearomatization reactions

    Transition_metal_catalytic_asymmetric_dearomatization_reactions

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