NCBI Taxonomy: 252963

Plakortis simplex (ncbi_taxid: 252963)

found 60 associated metabolites at species taxonomy rank level.

Ancestor: Plakortis

Child Taxonomies: none taxonomy data.

cis,cis-Muconic acid

(2Z,4Z)-HEXA-2,4-dienedioIC ACID

C6H6O4 (142.0266076)


cis-cis-Muconic acid is a presumptive metabolite of benzene. Muconic acid was first isolated from the urine of rabbits and dogs in 1909 (M. Jaffe, Z Physiol Chem 62:58-67). It was originally thought that if muconic acid was formed by the opening of the benzene ring in vivo then the cis-cis isomer should be the initial (and primary) product. However subsequent studies conducted in the 1950s proved that trans-trans-muconic acid is a true metabolite of benzene in mammals (Parke DV, Williams RT. Biochem J 51:339-348 (1952)). Furthermore, dosing rabbits with phenol or catechol also resulted in the urinary excretion of trans-trans-muconic acid. The oxidative ring opening of benzene first gives rise to cis-cis-muconaldehyde, which then isomerizes to cis-trans- and trans-trans-muconaldehyde; the latter is oxidized in vivo to trans-trans-muconic acid. Isomerization of the trans-trans form may take place in vivo to yield small amounts if the cis-cis and cis-trans form of muconic acid. cis-cis-Muconic acid may also be generated from microbial fermentation of benzoic acid. Certain strains of arthobacter are particularly efficient at this process. cis-cis-Muconic acid can also be found in Pseudomonas and Escherichia coli (https://link.springer.com/article/10.1007/BF00250491) (PMID:26360870). Cis-cis-muconic acid is a presumptive metabolite of benzene. Muconic acid was first isolated from the urine of rabbits and dogs in 1909 ( M. Jaffe, Z Physiol Chem 62:58-67). It was originally thought that if muconic acid were formed by opening of the benzene ring in vivo then the cis-cis isomer should be the initial (and primary) product. However subsequent studies conducted in the 1950s proved that trans-trans-muconic acid is a true metabolite of benzene in mammals (Parke DV, Williams RT. Biochem J 51:339-348 (1952)). Furthermore, dosing rabbits with phenol or catechol also resulted in the urinary excretion of trans-trans-muconic acid. The oxidative ring opening of benzene first gives rise to cis-cis-muconaldehyde, which then isomerizes to cis-trans- and trans-trans-muconaldehyde; the latter is oxidized in vivo to trans-trans-muconic acid. Isomerization of the trans-trans form may take place in vivo to yield small amounts if the cis-cis and cis-trans form of muconic acid. Cis-cis muconic acid may also be generated from microbial fermentation of benzoic acid. Certain strains of arthobacter are particularly efficient at this process. [HMDB] KEIO_ID M105 cis,cis-Muconic acid, a metabolic intermediate of Klebsiella pneumonia, can be converted to adipic acid and terephthalic acid, which are important monomers of synthetic polymers. cis,cis-Muconic acid is also a biochemical material that can be used for the production of various plastics and polymers and is particularly gaining attention as an adipic acid precursor for the synthesis of nylon-6,6[1][2].

   

3-Oxoadipic acid

3-Oxoadipic acid, disodium salt

C6H8O5 (160.0371718)


3-Oxoadipic acid is a regularly occurring Adipic dicarboxylic acid human metabolite found occasionally in biofluids of healthy individuals. (PMIDs 8340451, 1769109, 2338430) Increased amounts of 3-Oxoadipic acid are excreted after ingestion of Sebacic acid, supporting the hypothesis that dicarboxylic acids are degraded by ordinary beta-oxidation. (PMID 3220884) [HMDB] 3-Oxoadipic acid is a regularly occurring Adipic dicarboxylic acid human metabolite found occasionally in biofluids of healthy individuals. (PMIDs 8340451, 1769109, 2338430) Increased amounts of 3-Oxoadipic acid are excreted after ingestion of Sebacic acid, supporting the hypothesis that dicarboxylic acids are degraded by ordinary beta-oxidation. (PMID 3220884).

   

Bacteriohopanetetrol

Bacteriohopanetetrol; Tetrahydroxybacteriohopane; Bacteriohopane-32,33,34,35-tetrol

C35H62O4 (546.4647851999999)


A hopanoid that is bacteriohopane carrying four hydroxy substituents at positions 32, 33, 34 and 35.

   

trans-trans-Muconic acid

trans,trans-Buta-1,3-diene-1,4-dicarboxylic acid

C6H6O4 (142.0266076)


trans,trans-Muconic acid is a urinary metabolite of benzene and has been used as a biomarker of exposure to benzene in humans exposed to levels as low as 1 ppm. However, muconic acid may also be derived from sorbic acid and its salts. Dietary supplementation with 500 mg sorbic acid significantly increases the urinary trans,trans-muconic acid excretion. Under study conditions, 0.12\\\\% of the sorbic acid dose is excreted in urine as trans,trans-muconic acid thereby indicating that a typical dietary intake of 6-30 mg/day of sorbic acid accounts for 10-50\\\\% of the background of trans,trans-muconic acid excretion in nonsmokers, and for 5-25\\\\% in smokers (PMID: 8021961, 1487326, 9137998, Int Arch Occup Environ Health. 1997;69(4):247-51.). trans,trans-Muconic acid has been found to be a metabolite in Escherichia coli and Pseudomonas putida (PMID: 26360870). cis,cis-Muconic acid, a metabolic intermediate of Klebsiella pneumonia, can be converted to adipic acid and terephthalic acid, which are important monomers of synthetic polymers. cis,cis-Muconic acid is also a biochemical material that can be used for the production of various plastics and polymers and is particularly gaining attention as an adipic acid precursor for the synthesis of nylon-6,6[1][2]. trans-trans-Muconic acid is a urinary metabolite of benzene and has been used as a biomarker of exposure to benzene in human.

   

2-Furanacetic acid, 5-hexadecyl-, methyl ester

2-Furanacetic acid, 5-hexadecyl-, methyl ester

C23H40O3 (364.297729)


   

3-ketoadipate

3-Oxoadipic acid

C6H8O5 (160.0371718)


An oxo dicarboxylic acid consisting of adipic acid having a single oxo group at the 3-position.

   

cis,cis-Muconic acid

cis,cis-Muconic acid

C6H6O4 (142.0266076)


The cis,cis-isomer of muconic acid. It is produced during the degradation of chlorobenzene by bacteria like Bacillus. cis,cis-Muconic acid, a metabolic intermediate of Klebsiella pneumonia, can be converted to adipic acid and terephthalic acid, which are important monomers of synthetic polymers. cis,cis-Muconic acid is also a biochemical material that can be used for the production of various plastics and polymers and is particularly gaining attention as an adipic acid precursor for the synthesis of nylon-6,6[1][2].

   

FA 6:3;O2

(2E,4Z)-4-hydroxy-6-oxohexa-2,4-dienoic acid

C6H6O4 (142.0266076)


cis,cis-Muconic acid, a metabolic intermediate of Klebsiella pneumonia, can be converted to adipic acid and terephthalic acid, which are important monomers of synthetic polymers. cis,cis-Muconic acid is also a biochemical material that can be used for the production of various plastics and polymers and is particularly gaining attention as an adipic acid precursor for the synthesis of nylon-6,6[1][2].

   

FA 22:3;O

13-(5-propyl-3,4-dimethylfuran-2-yl)-tridecanoic acid

C22H38O3 (350.2820798)


   

2-(5-hexadecylfuran-2-yl)-acetic acid

2-(5-hexadecylfuran-2-yl)-acetic acid

C22H38O3 (350.2820798)


   

(2s)-3-(5,6-diiodo-1h-indol-3-yl)-2-(trimethylammonio)propanoate

(2s)-3-(5,6-diiodo-1h-indol-3-yl)-2-(trimethylammonio)propanoate

C14H16I2N2O2 (497.93012559999994)


   

[4,6-diethyl-6-(4-ethyl-2-methyloct-1-en-1-yl)-1,2-dioxan-3-yl]acetic acid

[4,6-diethyl-6-(4-ethyl-2-methyloct-1-en-1-yl)-1,2-dioxan-3-yl]acetic acid

C21H38O4 (354.2769948)


   

methyl 2-[5-(8-butyl-11-oxoundecyl)furan-2-yl]acetate

methyl 2-[5-(8-butyl-11-oxoundecyl)furan-2-yl]acetate

C22H36O4 (364.2613456)


   

10-(2-decylcyclopropyl)-n-[10-(2-decylcyclopropyl)-1-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3-methylbut-2-en-1-yl)oxy]oxan-2-yl]oxy}-3-hydroxydecan-2-yl]-2-hydroxydec-5-enimidic acid

10-(2-decylcyclopropyl)-n-[10-(2-decylcyclopropyl)-1-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3-methylbut-2-en-1-yl)oxy]oxan-2-yl]oxy}-3-hydroxydecan-2-yl]-2-hydroxydec-5-enimidic acid

C57H105NO9 (947.778892)


   

(2r,3s,4s,5s,6s)-2-{[(2s,3r,4r,5s,6r)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2-methyltetratriacontan-17-yl)oxy]oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3s,4s,5s,6s)-2-{[(2s,3r,4r,5s,6r)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2-methyltetratriacontan-17-yl)oxy]oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C47H92O11 (832.6639282)


   

6-methoxy-6-oxohexa-2,4-dienoic acid

6-methoxy-6-oxohexa-2,4-dienoic acid

C7H8O4 (156.0422568)


   

methyl 2-[(3s,6r)-4,6-diethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-3h-1,2-dioxin-3-yl]acetate

methyl 2-[(3s,6r)-4,6-diethyl-6-[(2r,3e)-2-ethylhex-3-en-1-yl]-3h-1,2-dioxin-3-yl]acetate

C19H32O4 (324.2300472)


   

methyl 2-[(2z,3r,5s)-3-ethyl-5-[(2r,3e)-2-ethylhex-3-en-1-yl]-5-methyloxolan-2-ylidene]acetate

methyl 2-[(2z,3r,5s)-3-ethyl-5-[(2r,3e)-2-ethylhex-3-en-1-yl]-5-methyloxolan-2-ylidene]acetate

C18H30O3 (294.21948299999997)


   

(3ar,5r,6ar)-5,6a-diethyl-5-[(4r,5e)-4-ethyloct-5-en-1-yl]-dihydro-3h-furo[3,2-b]furan-2-one

(3ar,5r,6ar)-5,6a-diethyl-5-[(4r,5e)-4-ethyloct-5-en-1-yl]-dihydro-3h-furo[3,2-b]furan-2-one

C20H34O3 (322.25078140000005)


   

(2r,5z)-10-[(1s,2s)-2-decylcyclopropyl]-n-[(2s,3r)-10-[(1s,2s)-2-decylcyclopropyl]-1-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(3-methylbut-2-en-1-yl)oxy]oxan-2-yl]oxy}-3-hydroxydecan-2-yl]-2-hydroxydec-5-enimidic acid

(2r,5z)-10-[(1s,2s)-2-decylcyclopropyl]-n-[(2s,3r)-10-[(1s,2s)-2-decylcyclopropyl]-1-{[(2r,3r,4s,5r,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(3-methylbut-2-en-1-yl)oxy]oxan-2-yl]oxy}-3-hydroxydecan-2-yl]-2-hydroxydec-5-enimidic acid

C57H105NO9 (947.778892)


   

(2s)-3-(5,7-diiodo-1h-indol-3-yl)-2-(trimethylammonio)propanoate

(2s)-3-(5,7-diiodo-1h-indol-3-yl)-2-(trimethylammonio)propanoate

C14H16I2N2O2 (497.93012559999994)


   

(2r,3s,4s)-2-[(3r)-3-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]butyl]oxolane-3,4-diol

(2r,3s,4s)-2-[(3r)-3-[(3r,3as,5ar,5br,7as,11as,11br,13ar,13bs)-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]butyl]oxolane-3,4-diol

C35H60O3 (528.454221)


   

7-ethyl-5-methylundeca-4,8-dien-3-one

7-ethyl-5-methylundeca-4,8-dien-3-one

C14H24O (208.18270539999997)


   

(7e,11e)-4,6,10-triethyl-3,6-dihydroxy-8-methyltetradeca-7,11-dienoic acid

(7e,11e)-4,6,10-triethyl-3,6-dihydroxy-8-methyltetradeca-7,11-dienoic acid

C21H38O4 (354.2769948)


   

(3ar,5r,6ar)-5,6a-diethyl-5-[(2s,4s)-4-ethyl-2-methyloctyl]-dihydro-3h-furo[3,2-b]furan-2-one

(3ar,5r,6ar)-5,6a-diethyl-5-[(2s,4s)-4-ethyl-2-methyloctyl]-dihydro-3h-furo[3,2-b]furan-2-one

C21H38O3 (338.2820798)


   

(2s,3r)-3-[(1e)-3-oxononadec-1-en-1-yl]oxirane-2-carboxylic acid

(2s,3r)-3-[(1e)-3-oxononadec-1-en-1-yl]oxirane-2-carboxylic acid

C22H38O4 (366.2769948)


   

methyl 2-[4-ethyl-6-(2-ethylhex-3-en-1-yl)-6-methyl-1,2-dioxan-3-yl]acetate

methyl 2-[4-ethyl-6-(2-ethylhex-3-en-1-yl)-6-methyl-1,2-dioxan-3-yl]acetate

C18H32O4 (312.2300472)


   

methyl 4-{[4-ethyl-2-methyl-5-(prop-1-en-1-yl)oxolan-2-yl]methyl}-3-hydroxyhexanoate

methyl 4-{[4-ethyl-2-methyl-5-(prop-1-en-1-yl)oxolan-2-yl]methyl}-3-hydroxyhexanoate

C18H32O4 (312.2300472)


   

(2s)-3-(5,6,7-triiodo-1h-indol-3-yl)-2-(trimethylammonio)propanoate

(2s)-3-(5,6,7-triiodo-1h-indol-3-yl)-2-(trimethylammonio)propanoate

C14H15I3N2O2 (623.826778)


   

methyl 2-(5-hexadecylfuran-2-yl)acetate

methyl 2-(5-hexadecylfuran-2-yl)acetate

C23H40O3 (364.297729)


   

[4,6-diethyl-6-(4-ethyl-2-methylocta-1,5-dien-1-yl)-1,2-dioxan-3-yl]acetic acid

[4,6-diethyl-6-(4-ethyl-2-methylocta-1,5-dien-1-yl)-1,2-dioxan-3-yl]acetic acid

C21H36O4 (352.2613456)