Exact Mass: 212.0385892
Exact Mass Matches: 212.0385892
Found 147 metabolites which its exact mass value is equals to given mass value 212.0385892,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Urolithin B
Urolithin B is a secondary metabolite of ellagic acid which may be glucuronidated by liver enzymes during phase II metabolism. A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2]. Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2].
2-Hydroxyxanthone
2-Hydroxyxanthone belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. 2-Hydroxyxanthone exists as a solid and is considered to be practically insoluble (in water) and relatively neutral. Within the cell, 2-hydroxyxanthone is primarily located in the membrane (predicted from logP). Outside of the human body, 2-hydroxyxanthone can be found in fruits, herbs and spices, and mammee apple. This makes 2-hydroxyxanthone a potential biomarker for the consumption of these food products. Constituent of Hypericum subspecies, Mammea americana (mamey). 2-Hydroxyxanthone is found in herbs and spices, fruits, and mammee apple.
4-Hydroxyxanthone
4-Hydroxyxanthone is found in fruits. 4-Hydroxyxanthone is from seeds of Mammea americana (mamey). From seeds of Mammea americana (mamey). 4-Hydroxyxanthone is found in fruits.
1-(Methylsulfinyl)propyl propyl disulfide
1-(Methylsulfinyl)propyl propyl disulfide is found in onion-family vegetables. 1-(Methylsulfinyl)propyl propyl disulfide is a constituent of Allium cepa (onion) juice and Allium tricoccum (wood leek). Constituent of Allium cepa (onion) juice and Allium tricoccum (wood leek). 1-(Methylsulfinyl)propyl propyl disulfide is found in garden onion and onion-family vegetables.
Methyl 1-(propylsulfinyl)propyl disulfide
Methyl 1-(propylsulfinyl)propyl disulfide is found in onion-family vegetables. Methyl 1-(propylsulfinyl)propyl disulfide is a constituent of Allium sp Constituent of Allium species Methyl 1-(propylsulfinyl)propyl disulfide is found in onion-family vegetables.
N-phosphocreatinate(2-)
N-phosphocreatinate(2-) is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). N-phosphocreatinate(2-) is considered to be soluble (in water) and acidic
2-(3,4-Epoxy-1-butynyl)-5-(1,3-pentadiynyl)thiophene|2-<3,4-Epoxy-but-1-inyl>-5-but-1,3-diinyl-thiophen|2--5-<3.4-epoxy-butin-(1)-yl>-thiophen|2-[(5-penta-1,3-diynyl-thiophen-2-yl)-ethynyl]-oxirane|2-[5-(penta-1,3-diynyl)-thiophen-2-ylethynyl]-oxirane
2-(hydroxyprop-1-ynyl)-5-(5-hexen-3-yn-1-ynyl)-thiophene|3-(5-hex-5-ene-1,3-diynyl-thiophen-2-yl)-prop-2-yn-1-ol
2-formyl-3,5-dihydroxy-4-hydroxymethylbenzoic acid
2--5-<5-formyl-buten-(3)-in-(1)-yl>-thiophen|5-(5-but-3-en-1-ynyl-thiophen-2-yl)-pent-2-en-4-ynal
2-(1-propynyl)-5-(5,6-epoxyhex-3-yn-1-ynyl)-thiophene
urolithin B
Coumarins Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2]. Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2].
2,2,2-TRIFLUORO-1-PYRIDIN-3-YL-ETHYLAMINE
C7H8ClF3N2 (212.03280739999997)
4-(2-Chloro-acetylamino)-benzamide
C9H9ClN2O2 (212.03525240000002)
2,2,2-TRIFLUORO-1-PYRIDIN-3-YL-ETHYL-AMMONIUM, CHLORIDE
C7H8ClF3N2 (212.03280739999997)
2-Chloro-N-(phenylcarbamoyl)acetamide
C9H9ClN2O2 (212.03525240000002)
2-(2-CHLORO-ACETYLAMINO)-BENZAMIDE
C9H9ClN2O2 (212.03525240000002)
2-(4-HYDROXYPHENYL)-2-METHYL-1,3-DITHIOLAN
C10H12OS2 (212.03295419999998)
(4-(Trifluoromethyl)phenyl)hydrazine hydrochloride
C7H8ClF3N2 (212.03280739999997)
3-Pyridinemethanamine, 4-(trifluoromethyl)-, hydrochloride (1:1)
C7H8ClF3N2 (212.03280739999997)
N1-(4-CHLORO-2-METHYLPHENYL)-2-HYDROXYIMINOACETAMIDE
C9H9ClN2O2 (212.03525240000002)
Methyl imidazo[1,2-a]pyridine-6-carboxylate hydrochloride
C9H9ClN2O2 (212.03525240000002)
Cyclopropanamine, 1-(4-chloro-3-nitrophenyl)
C9H9ClN2O2 (212.03525240000002)
1H-INDAZOLE-7-CARBOXYLIC ACID,METHYL ESTER,HYDROCHLORIDE
C9H9ClN2O2 (212.03525240000002)
methyl 2-chloro-2-n-(phenyl)hydrazino acetate
C9H9ClN2O2 (212.03525240000002)
methyl 7-fluoro-2,3-dihydro-1,4-benzodioxine-5-carboxylate
2-Chloro-1-cyclopropyl-2-(2-fluorophenyl)ethanone
C11H10ClFO (212.04041719999998)
(2-(TRIFLUOROMETHYL)PYRIDIN-4-YL)METHANAMINE HYDROCHLORIDE
C7H8ClF3N2 (212.03280739999997)
2,4,5,6-Pyrimidinetetramine dihydrochloride
C4H10Cl2N6 (212.03439600000002)
N-(2-Acetamido)iminodiacetic acid monosodium salt
C6H9N2NaO5 (212.04091440000002)
[2-(Trifluormethyl)phenyl]hydrazinhydrochlorid
C7H8ClF3N2 (212.03280739999997)
2-(6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile
(3-(Trifluoromethyl)phenyl)hydrazine hydrochloride
C7H8ClF3N2 (212.03280739999997)
4-(3-Chloro-2-fluorophenyl)-2-methylbut-3-yn-2-ol
C11H10ClFO (212.04041719999998)
1H-Benzimidazole-5-carboxylicacid,6-methyl-(9CI)
C9H9ClN2O2 (212.03525240000002)
Depsidone
The simplest member of the class of depsidones comprising of a heterotricyclic system that is 11H-dibenzo[b,e][1,4]dioxepine substituted by an oxo group at position 11.
[(2R)-3-[acetyl(hydroxy)amino]-2-hydroxypropyl]phosphonic acid
2,2,3,3-tetrafluoro-N-(1H-1,2,4-triazol-5-yl)propanamide
C5H4F4N4O (212.03212219999998)