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Index of chemical compounds with the same name
are: 2,3-Dihydroxybenzoic acid (2-Pyrocatechuic acid or hypogallic acid) 2,4-Dihydroxybenzoic acid (β-Resorcylic acid) 2,5-Dihydroxybenzoic acid (Gentisic
Dihydroxybenzoic_acid
Chemical compound
2,4-Dihydroxybenzoic acid (β-resorcylic acid) is a dihydroxybenzoic acid. As a resorcylic acid, it is one of the three isomeric crystalline acids that
2,4-Dihydroxybenzoic_acid
Chemical compound
3,5-Dihydroxybenzoic acid (α-resorcylic acid) is a dihydroxybenzoic acid. It is a colorless solid. It is prepared by disulfonation of benzoic acid followed
3,5-Dihydroxybenzoic_acid
Chemical compound
2,3-Dihydroxybenzoic acid is a dihydroxybenzoic acid, a type of organic compound. It occurs naturally in various plants, bacteria, and fungi. It is a potentially
2,3-Dihydroxybenzoic_acid
Chemical compound
2,6-Dihydroxybenzoic acid (γ-resorcylic acid) is a dihydroxybenzoic acid. Haynes, William M., ed. (2016). "3". CRC Handbook of Chemistry and Physics (PDF)
2,6-Dihydroxybenzoic_acid
Index of chemical compounds with the same name
Resorcylic acid, resorcinolic acid, or carboxyresorcinol are names for a type of dihydroxybenzoic acid structurally related to resorcinol. They may refer
Resorcylic_acid
Chemical compound
Protocatechuic acid (PCA) is a dihydroxybenzoic acid, a type of phenolic acid. Its name is derived from the catechu extract. It is a major metabolite of
Protocatechuic_acid
Chemical compound
Vanillic acid (4-hydroxy-3-methoxybenzoic acid) is a dihydroxybenzoic acid derivative used as a flavoring agent. It is an oxidized form of vanillin. It
Vanillic_acid
Index of chemical compounds with the same name
(3-hydroxysalicylic acid) 2,4-Dihydroxybenzoic acid (4-hydroxysalicylic acid) 2,5-Dihydroxybenzoic acid (5-hydroxysalicylic acid) 2,6-Dihydroxybenzoic acid (6-hydroxysalicylic
Hydroxysalicylic_acid
Nonsteroidal anti-inflammatory drug
salicyluric acid (75%), free salicylic acid (10%), salicylic phenol (10%), acyl glucuronides (5%), gentisic acid (< 1%), and 2,3-dihydroxybenzoic acid. When
Aspirin
Chemical compound
Gentisic acid is a dihydroxybenzoic acid. It is a derivative of benzoic acid and a minor (1%) product of the metabolic break down of aspirin, excreted
Gentisic_acid
Species of flowering plant
The flesh is crunchy but sour and acidic in taste. Its fruit is rich in an antimicrobial agent-2,3-Dihydroxybenzoic acid. The family Salicaceae includes
Flacourtia_inermis
Chemical compound
The aromatic amino acids phenylalanine, tryptophan, and tyrosine Indole, indole derivatives and tryptophan 2,3-Dihydroxybenzoic acid (DHB) used for enterobactin
Chorismic_acid
Ionization technique
commonly used are sinapinic acid, α-cyano-4-hydroxycinnamic acid (α-CHCA, alpha-cyano or alpha-matrix) and 2,5-dihydroxybenzoic acid (DHB). A solution of one
Matrix-assisted laser desorption/ionization
Matrix-assisted_laser_desorption/ionization
Index of chemical compounds with the same name
(m-hydroxybenzoic acid) 4-Hydroxybenzoic acid (p-hydroxybenzoic acid) Dihydroxybenzoic acids Trihydroxybenzoic acids Phenolic acid This set index article
Hydroxybenzoic_acid
Flavoprotein
catalyzes the regioselective hydroxylation of 4-hydroxybenzoic acid, giving 3,4-dihydroxybenzoic acid as the product. The mechanism consists of the following
4-hydroxybenzoate 3-monooxygenase
4-hydroxybenzoate_3-monooxygenase
Chemical compound
Cannabigerolic acid (CBGA) is the acidic form of cannabigerol (CBG). It is a dihydroxybenzoic acid and olivetolic acid in which the hydrogen at position
Cannabigerolic_acid
Index of chemical compounds with the same molecular formula
to: Dihydroxybenzoic acids, a type of phenolic acids 2,3-Dihydroxybenzoic acid (2-pyrocatechuic acid or hypogallic acid) 2,4-Dihydroxybenzoic acid (β-resorcylic
C7H6O4
Chemical compound
toxicity of free iron. Chorismic acid, an aromatic amino acid precursor, is converted to 2,3-dihydroxybenzoic acid (DHB) by a series of enzymes, EntA
Enterobactin
Largest stable synthetic molecule ever made
PG5 is the largest stable synthetic molecule ever made up to 2010. PG5 is a dendrimer designed by the organic chemistry research group working at the Federal
PG5
InterPro Family
3-dihydrobenzoic acid + NAD+ H+ H+ 2,3-Dihydroxybenzoic acid + NADH The two substrates of this enzyme are (2S,3S)-2,3-dihydroxy-2,3-dihydrobenzoic acid and
2,3-dihydro-2,3-dihydroxybenzoate dehydrogenase
2,3-dihydro-2,3-dihydroxybenzoate_dehydrogenase
Group of estrogenic compounds
β-zearalenol. Resorcylic acid lactones (RALs) are fungal polyketides that consist of a β-resorcylic acid residue (2,4-dihydroxybenzoic acid) embedded in a macrolactone
Resorcylic_acid_lactone
ISBN 978-3-527-30385-4. Arthur W. Weston, C. M. Suter (1941). "3,5-Dihydroxybenzoic Acid". Organic Syntheses. 21: 27. doi:10.15227/orgsyn.021.0027.
Desulfonation_reaction
Chemical reaction
through other methods for instance esters of the sensitive 2,4-dihydroxybenzoic acid. A characteristic is the formal uptake of water generated in the
Steglich_esterification
Class of enzymes
catalyzes the chemical reaction 3-Hydroxybenzoic acid + reduced acceptor O2 H2O 2,3-Dihydroxybenzoic acid + electron acceptor The three substrates
3-hydroxybenzoate 2-monooxygenase
3-hydroxybenzoate_2-monooxygenase
Chemical compound
Olivetolic acid is an organic compound with the formula C5H11C6H2(OH)2CO2H. Several isomers with this formula exist. Olivetolic acid can be viewed as
Olivetolic_acid
Class of enzymes
reaction 2,3-Dihydroxybenzoic acid O2 2-carboxy-cis,cis-muconic acid The two substrates of this enzyme are 2,3-dihydroxybenzoic acid and oxygen
2,3-dihydroxybenzoate 2,3-dioxygenase
2,3-dihydroxybenzoate_2,3-dioxygenase
Analytical technique for protein identification
peptide mix. Common matrices are sinapinic acid, Alpha-Cyano-4-hydroxycinnamic acid, and 2,3-Dihydroxybenzoic acid. The matrix molecules are required for
Peptide_mass_fingerprinting
Species of legume
(2,4-dihydroxybenzoic acid), flavonoids (ampelopsin, butein, dihydrorobinetin, and robinetin), terpenoids (echinocystic acid and oleanolic acid), steroids
Adenanthera_pavonina
Protein-coding gene in the species Homo sapiens
lactic acid (and its conjugate base, lactate). More recently, 3,5-dihydroxybenzoic acid has been reported to activate HCA1. Lactate was initially found
Hydroxycarboxylic acid receptor 1
Hydroxycarboxylic_acid_receptor_1
Chemical compound
Cannabidiolic acid (CBDA), is a cannabinoid produced in cannabis plants. It is the precursor to cannabidiol (CBD). It is most abundant in the glandular
Cannabidiolic_acid
Chemical compound found in some lichens
Barbatic acid is an organic compound that is made by some lichens. It is in the structural class known as depsides. It is particularly common in the genera
Barbatic_acid
G-protein coupled receptor which binds free fatty acids
acid. A more recent study reported that it is also activated by the compound 3,5-dihydroxybenzoic acid. GPR109B (also known as hydroxycarboxylic acid
Free_fatty_acid_receptor
Chemical compound
identification and properties of isochorismic acid. An intermediate in the biosynthesis of 2,3-dihydroxybenzoic acid". Biochimica et Biophysica Acta (BBA) -
Isochorismic_acid
Salt, anion or ester of a sulfonic acid
15227/orgsyn.003.0037. Arthur W. Weston, C. M. Suter (1941). "3,5-Dihydroxybenzoic Acid". Organic Syntheses. 21: 27. doi:10.15227/orgsyn.021.0027. Fiege
Sulfonate
Chemical compound
investigation based on eriodictyol and homoeriodictyol, found 2,4-Dihydroxybenzoic acid vanillylamide to elicits bitter-masking activity. At 0.1g/L, this
Homoeriodictyol
Natural plant compounds
4-Hydroxybenzoic acid, 3,4-dihydroxybenzoic acid (protocatechuic acid), 3-methoxy-4-hydroxy-hippuric acid and 3-methoxy-4-hydroxybenzoic acid (vanillic acid) are
Phenolic_content_in_tea
Class of enzymes
and a proton. Its products are protocatechuic acid (3,4-dihydroxybenzoic acid), NAD+, and sulfurous acid. This enzyme is an oxidoreductase, which uses
4-sulfobenzoate 3,4-dioxygenase
4-sulfobenzoate_3,4-dioxygenase
Chemical compound
Orsellinic acid, more specifically o-orsellinic acid, is a phenolic acid. It is of importance in the biochemistry of lichens, from which it can be extracted
Orsellinic_acid
Chemical compound
racemic platensimycin, its structure consists of a 3-amino-2,4-dihydroxybenzoic acid polar part linked through an amide bond to a lipophilic tetracyclic
Platensimycin
Enzyme class
Anthranilic acid + NADP + H+ O2 NH3 2,3-Dihydroxybenzoic acid + NADP+ The four substrates of this enzyme are anthranilic acid, reduced nicotinamide
Anthranilate 3-monooxygenase (deaminating)
Anthranilate_3-monooxygenase_(deaminating)
Chemical compound
testa. It is also present in wine. It is the ethylic ester of protocatechuic acid. The compound is a prolyl 4-hydroxylase inhibitor and can be used to protect
Ethyl_protocatechuate
Class of enzymes
"Structural and functional analysis of AsbF: origin of the stealth 3,4-dihydroxybenzoic acid subunit for petrobactin biosynthesis". Proceedings of the National
3-dehydroshikimate dehydratase
3-dehydroshikimate_dehydratase
Group of chemical compounds
Phenolic acids such as protocatechuic, p-hydroxybenzoic, 2,3-dihydroxybenzoic, chlorogenic, vanillic, caffeic, p-coumaric and salicylic acid, cinnamic acid and
Naturally_occurring_phenols
Chemical compound produced by lichens
Diffractaic acid is a β-orcinol depside with the molecular formula C20H22O7, which is produced by lichens. Diffractaic acid has cytotoxic, cytogenetic
Diffractaic_acid
Study of complete lipid profile in organisms
successfully for lipids. The lipid is mixed with a matrix, such as 2,5-dihydroxybenzoic acid, and applied to a sample holder as a small spot. A laser is fired
Lipidomics
Chemical compound
vibriobactin are three 2,3-dihydroxybenzoic acid (DHB), two threonine (Thr), and one norspermidine (NSPD). DHB is synthesized from chorismic acid by a series of enzymes:
Vibriobactin
Class of chemical compounds
intake. Alkylresorcinol metabolites, 3,5-dihydroxybenzoic acid (DHBA) and 3,5-dihydroxyphenylpropionoic acid (DHPPA) were first identified in urine and
Alkylresorcinol
Chemical compound
needed][better source needed] Separately, 3,4-dihydroxybenzoic acid is produced by AsbF from 3-dehydroshikimic acid, and this benzoic acid is used to produce a thioester
Petrobactin
"Regulation of the enzymes involved in the biosynthesis of 2,3-dihydroxybenzoic acid in Aerobacter aerogenes and Escherichia coli". Biochim. Biophys
Isochorismatase
Chemical compound
acid is a hydrolysable tannin. It is a component of some hydrolysable tannins such as mallojaponin. The difference with its isomer sanguisorbic acid is
Valoneic_acid
Chemical compound
Sanguisorbic acid is a constituent of some ellagitannins. It is constituted by a hexahydroxydiphenic acid unit linked by an O-C bond to a gallic acid. The differences
Sanguisorbic_acid
Protein-coding gene in the species Homo sapiens
to bacterial siderophores, also to the mammalian siderophore 2,5-dihydroxybenzoic acid (2,5-DHBA). This complex ensures that excess free iron does not
Lipocalin-2
99–50–3 2,3-dihydroxybenzoic acid 303–38–8 C7H6O5 gallic acid 149–91–7 C7H7BO4 4-carboxyphenylboronic acid 14047–29–1 C7H7NO2 4-aminobenzoic acid 150–13–0
Glossary_of_chemical_formulae
6-dihydroxybenzoic acid The two substrates of this enzyme are quercetin and oxygen. Its products are 2-(3,4-dihydroxybenzoyloxy)-4,6-dihydroxybenzoic acid
Quercetin_2,3-dioxygenase
Device that creates charged atoms and molecules (ions)
atmospheric pressure inlet. Less volatile matrices such as 2,5-dihydroxybenzoic acid require a hot inlet tube to produce analyte ions by MAI, but more
Ion_source
that can be used include: 2,5-dihydroxybenzoic acid, 2,5-dihydroxyacetophenone, 2-aminobenzyl alcohol, anthranilic acid, and 2-hydroxyacetophenone. Laserspray
Matrix-assisted_ionization
Class of enzymes
degradation via hydroxylation. Ribbons DW (1966). "Bacterial oxidation of 2,3-dihydroxybenzoic acid - a new oxygenase". Biochem. J. 99: 30. Portal: Biology
2,3-dihydroxybenzoate 3,4-dioxygenase
2,3-dihydroxybenzoate_3,4-dioxygenase
Species of alga
Phenolic acids such as protocatechuic, p-hydroxybenzoic, 2,3-dihydroxybenzoic, chlorogenic, vanillic, caffeic, p-coumaric and salicylic acid, cinnamic acid and
Spongiochloris_spongiosa
(1950). "4-Aminosalicylic acid and its derivatives. Part II. The synthesis of 4-amino-2 : 5- and 4-amino-2 : 3-dihydroxybenzoic acid". J. Chem. Soc.: 1139–1140
Sasanka_Chandra_Bhattacharyya
Species of flowering plant
chlorogenic, caffeic, and neochlorogenic acid, smaller amounts of hyperforin and adhyperforin, and dihydroxybenzoic acid. The species' characteristic goat-like
Hypericum_hircinum
Beavis, R. C.; Chaudhary, T.; Chait, B. T. (1992). "α-Cyano-4-hydroxycinnamic acid as a matrix for matrix-assisted laser desorption mass spectrometry". Organic
Matrix_(mass_spectrometry)
Chemical compound
synthetase. Mirubactin assembly uses two nonproteinogenic units, 2,3-dihydroxybenzoic acid (2,3-DHB) and δ-N-formyl-δ-N-hydroxyornithine (fhOrn). MrbC and
Mirubactin
Species of flowering plant
amentoflavone, and catechin. In the leaves, neochlorogenic and dihydroxybenzoic acid can be found. The concentrations of these chemicals is generally
Hypericum_russeggeri
Species of legume
mostly phenolic acids, namely, 3,4-dihydroxybenzoic, 4-hydroxybenzoic, vanillic, caffeic, p-coumaric, ferulic, syringic and sinapic acids. Though both require
Macrotyloma_uniflorum
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