NCBI Taxonomy: 654496

Thelephora aurantiotincta (ncbi_taxid: 654496)

found 31 associated metabolites at species taxonomy rank level.

Ancestor: Thelephora

Child Taxonomies: none taxonomy data.

4-Hydroxybenzoic acid

4-hydroxybenzoic acid

C7H6O3 (138.0317)


4-Hydroxybenzoic acid, also known as p-hydroxybenzoate or 4-carboxyphenol, belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. 4-Hydroxybenzoic acid is a white crystalline solid that is slightly soluble in water and chloroform but more soluble in polar organic solvents such as alcohols and acetone. It is a nutty and phenolic tasting compound. 4-Hydroxybenzoic acid exists in all living species, ranging from bacteria to plants to humans. 4-Hydroxybenzoic acid can be found naturally in coconut. It is one of the main catechins metabolites found in humans after consumption of green tea infusions. It is also found in wine, in vanilla, in A√ßa√≠ oil, obtained from the fruit of the a√ßa√≠ palm (Euterpe oleracea), at relatively high concetrations (892¬±52 mg/kg). It is also found in cloudy olive oil and in the edible mushroom Russula virescens. It has been detected in red huckleberries, rabbiteye blueberries, and corianders and in a lower concentration in olives, red raspberries, and almonds. In humans, 4-hydroxybenzoic acid is involved in ubiquinone biosynthesis. In particular, the enzyme 4-hydroxybenzoate polyprenyltransferase uses a polyprenyl diphosphate and 4-hydroxybenzoate to produce diphosphate and 4-hydroxy-3-polyprenylbenzoate. This enzyme participates in ubiquinone biosynthesis. 4-Hydroxybenzoic acid can be biosynthesized by the enzyme Chorismate lyase. Chorismate lyase is an enzyme that transforms chorismate into 4-hydroxybenzoate and pyruvate. This enzyme catalyses the first step in ubiquinone biosynthesis in Escherichia coli and other Gram-negative bacteria. 4-Hydroxybenzoate is an intermediate in many enzyme-mediated reactions in microbes. For instance, the enzyme 4-hydroxybenzaldehyde dehydrogenase uses 4-hydroxybenzaldehyde, NAD+ and H2O to produce 4-hydroxybenzoate, NADH and H+. This enzyme participates in toluene and xylene degradation in bacteria such as Pseudomonas mendocina. 4-hydroxybenzaldehyde dehydrogenase is also found in carrots. The enzyme 4-hydroxybenzoate 1-hydroxylase transforms 4-hydroxybenzoate, NAD(P)H, 2 H+ and O2 into hydroquinone, NAD(P)+, H2O and CO2. This enzyme participates in 2,4-dichlorobenzoate degradation and is found in Candida parapsilosis. The enzyme 4-hydroxybenzoate 3-monooxygenase transforms 4-hydroxybenzoate, NADPH, H+ and O2 into protocatechuate, NADP+ and H2O. This enzyme participates in benzoate degradation via hydroxylation and 2,4-dichlorobenzoate degradation and is found in Pseudomonas putida and Pseudomonas fluorescens. 4-Hydroxybenzoic acid is a popular antioxidant in part because of its low toxicity. 4-Hydroxybenzoic acid has estrogenic activity both in vitro and in vivo (PMID 9417843). Isolated from many plants, free and combined. Alkyl esters of 4-hydroxybenzoic acid (see below) are used as food and cosmetic preservatives, mainly in their Na salt form, which makes them more water soluble. They are active at low concentrations and more pH-independent than the commonly used Benzoic acid DVN38-Z and 2,4-Hexadienoic acid GMZ10-P. The taste is more detectable than for those preservatives. Effectiveness increases with chain length of the alcohol, but for some microorganisms this reduces cell permeability and thus counteracts the increased efficiency. 4-Hydroxybenzoic acid is found in many foods, some of which are chicory, corn, rye, and black huckleberry. 4-hydroxybenzoic acid is a monohydroxybenzoic acid that is benzoic acid carrying a hydroxy substituent at C-4 of the benzene ring. It has a role as a plant metabolite and an algal metabolite. It is a conjugate acid of a 4-hydroxybenzoate. 4-Hydroxybenzoic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). See also: Vaccinium myrtillus Leaf (part of); Galium aparine whole (part of); Menyanthes trifoliata leaf (part of) ... View More ... A monohydroxybenzoic acid that is benzoic acid carrying a hydroxy substituent at C-4 of the benzene ring. 4-Hydroxybenzoic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=99-96-7 (retrieved 2024-07-01) (CAS RN: 99-96-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). 4-Hydroxybenzoic acid, a phenolic derivative of benzoic acid, could inhibit most gram-positive and some gram-negative bacteria, with an IC50 of 160 μg/mL. 4-Hydroxybenzoic acid, a phenolic derivative of benzoic acid, could inhibit most gram-positive and some gram-negative bacteria, with an IC50 of 160 μg/mL.

   

3-O-Methylatromentin

3-O-Methylatromentin

C19H14O6 (338.079)


   

Vialinin A

4,4",5,6-tetrahydroxy[1,1:4,1"-terphenyl]-2,3-diyl ester benzeneacetic acid

C34H26O8 (562.1628)


   

Thelephantin G

Thelephantin G

C32H22O10 (566.1213)


   

Ganbajunin C

Ganbajunin C

C34H26O8 (562.1628)


   

Ganbajunin E

Ganbajunin E

C34H26O8 (562.1628)


   

Thelephorin A

Thelephorin A

C33H24O9 (564.142)


   

Thelephantin D

Thelephantin D

C30H26O8 (514.1628)


   

Thelephantin F

Thelephantin F

C33H32O8 (556.2097)


   

Thelephantin H

Thelephantin H

C33H22O10 (578.1213)


   

Atromentin

Atromentin

C18H12O6 (324.0634)


A member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxycyclohexa-2,5-diene-1,4-dione which is substituted by a 4-hydroxyphenyl group at positions 3 and 6. It is a mushroom pigment isolated from several fungi species and acts as a smooth muscle stimulant, and exhibits anticoagulant, antibacterial and antineoplastic properties.

   

4-hydroxybenzoate

4-Hydroxybenzoic acid

C7H6O3 (138.0317)


4-Hydroxybenzoic acid, a phenolic derivative of benzoic acid, could inhibit most gram-positive and some gram-negative bacteria, with an IC50 of 160 μg/mL. 4-Hydroxybenzoic acid, a phenolic derivative of benzoic acid, could inhibit most gram-positive and some gram-negative bacteria, with an IC50 of 160 μg/mL.

   

p-Hydroxybenzoic acid

p-Hydroxybenzoic acid

C7H6O3 (138.0317)


4-Hydroxybenzoic acid, a phenolic derivative of benzoic acid, could inhibit most gram-positive and some gram-negative bacteria, with an IC50 of 160 μg/mL. 4-Hydroxybenzoic acid, a phenolic derivative of benzoic acid, could inhibit most gram-positive and some gram-negative bacteria, with an IC50 of 160 μg/mL.

   

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl butanoate

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl butanoate

C30H26O8 (514.1628)


   

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

C33H24O9 (564.142)


   

4-{2,3,5,6-tetrahydroxy-4'-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-4-yl}phenyl 2-phenylacetate

4-{2,3,5,6-tetrahydroxy-4'-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-4-yl}phenyl 2-phenylacetate

C34H26O8 (562.1628)


   

6-(hexanoyloxy)-2,4',5-trihydroxy-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

6-(hexanoyloxy)-2,4',5-trihydroxy-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

C31H28O9 (544.1733)


   

6-[(3,4-dimethylpentanoyl)oxy]-2,4',5-trihydroxy-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

6-[(3,4-dimethylpentanoyl)oxy]-2,4',5-trihydroxy-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

C32H30O9 (558.189)


   

thelephantins

thelephantins

C29H24O9 (516.142)


   

6-{[(3r)-3,4-dimethylpentanoyl]oxy}-2,4',5-trihydroxy-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

6-{[(3r)-3,4-dimethylpentanoyl]oxy}-2,4',5-trihydroxy-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

C32H30O9 (558.189)


   

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 2-phenylacetate

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 2-phenylacetate

C34H26O8 (562.1628)


   

4,11,12-trihydroxy-5-(4-hydroxyphenyl)-3-[(2-phenylacetyl)oxy]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl 4-hydroxybenzoate

4,11,12-trihydroxy-5-(4-hydroxyphenyl)-3-[(2-phenylacetyl)oxy]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-6-yl 4-hydroxybenzoate

C33H22O10 (578.1213)


   

4',5,6-trihydroxy-4-(4-hydroxyphenyl)-2-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl benzoate

4',5,6-trihydroxy-4-(4-hydroxyphenyl)-2-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl benzoate

C33H24O8 (548.1471)


   

2,4',5-trihydroxy-6-(4-hydroxybenzoyloxy)-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

2,4',5-trihydroxy-6-(4-hydroxybenzoyloxy)-4-(4-hydroxyphenyl)-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

C32H22O10 (566.1213)


   

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-{[(3s)-3-methylhexanoyl]oxy}-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-{[(3s)-3-methylhexanoyl]oxy}-[1,1'-biphenyl]-3-yl 4-hydroxybenzoate

C32H30O9 (558.189)


   

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl (3r)-3,4-dimethylpentanoate

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl (3r)-3,4-dimethylpentanoate

C33H32O8 (556.2097)


   

4-{2,3,5-trihydroxy-6-methyl-4'-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-4-yl}phenyl 2-phenylacetate

4-{2,3,5-trihydroxy-6-methyl-4'-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-4-yl}phenyl 2-phenylacetate

C35H28O7 (560.1835)


   

4',5-dihydroxy-4-(4-hydroxyphenyl)-2-methyl-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl 2-phenylacetate

4',5-dihydroxy-4-(4-hydroxyphenyl)-2-methyl-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl 2-phenylacetate

C35H28O7 (560.1835)


   

2-hydroxy-3,6-bis(4-hydroxyphenyl)-5-methoxycyclohexa-2,5-diene-1,4-dione

2-hydroxy-3,6-bis(4-hydroxyphenyl)-5-methoxycyclohexa-2,5-diene-1,4-dione

C19H14O6 (338.079)


   

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 3,4-dimethylpentanoate

3,4',6-trihydroxy-4-(4-hydroxyphenyl)-5-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-2-yl 3,4-dimethylpentanoate

C33H32O8 (556.2097)


   

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl benzoate

2,4',5-trihydroxy-4-(4-hydroxyphenyl)-6-[(2-phenylacetyl)oxy]-[1,1'-biphenyl]-3-yl benzoate

C33H24O8 (548.1471)