Exact Mass: 244.0403
Exact Mass Matches: 244.0403
Found 174 metabolites which its exact mass value is equals to given mass value 244.0403,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Fucose 1-phosphate
Fucose 1-phosphate (CAS: 16562-58-6) belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphate group linked to the carbohydrate unit. Fucose 1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, EC 2.7.7.30). The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose (PMID: 16185085, 14686921). Fucose-1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose, in a reaction catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, E.C. 2.7.7.30) . The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose. (PMID: 16185085, 14686921) [HMDB]
Gentisein
Gentisein is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. It has a role as a plant metabolite. It is a member of xanthones and a polyphenol. Gentisein is a natural product found in Hypericum scabrum, Cratoxylum formosum, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. Gentisein is found in alcoholic beverages. Gentisein is isolated from Gentiana lutea (yellow gentian Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].
Mesuaxanthone B
A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 5 and 6.
1,3,5-Trihydroxyxanthone
A member of the class of xanthones that is xanthone substituted by hydroxy groups at positions 1, 3 and 5. It has been isolated from Anaxagorea luzonensis.
L-Rhamnulose 1-phosphate
A deoxyketohexose phosphate consisting of L-rhamnulose having a monophosphate group at the 1-position.
Urolithin C
Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].
Urolithin C
A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin C is a biomarker of nut consumption in urine. Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].
4-phenylbutanic acid-O-sulphate
4-phenylbutanic acid-O-sulphate is a conjugate of 4-phenylbutanic acid and sulphate. 4-phenylbutyric acid is a monocarboxylic acid the structure of which is that of butyric acid substituted with a phenyl group at C-4. It is a histone deacetylase inhibitor that displays anticancer activity. It inhibits cell proliferation, invasion and migration and induces apoptosis in glioma cells. It also inhibits protein isoprenylation, depletes plasma glutamine, increases production of foetal haemoglobin through transcriptional activation of the γ-globin gene and affects hPPARγ activation. (CHEBI:41500)
2-Deoxy-D-arabino-hexose 6-(dihydrogen phosphate)
1,2,5-Trihydroxyxanthone
A member of the class of xanthones that is 9H-xanthen-9-one substituted bybhydroxy groups at positions 1, 2 and 5. It is isolated from Garcinia subelliptica.
8-Chloro-5,10-dihydro-11H-dibenzo[b,e][1,4]-diazepin-11-one
7,8-Dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione
1,2,3,4-Tetrahydro-6-hydroxy-2-methyl-1,3,4-trioxo-pyrazino<1,2-a>indol|6-Hydroxy-1,3,4-trioxo-2-methyl-1,2,3,4-tetrahydro-pyrazino<1,2-a>indol|6-hydroxy-2-methyl-pyrazino[1,2-a]indole-1,3,4-trione
5-hydroxy-6-methoxynaphtho<2,3-b>furan-4,9-quinone
alpha-L-(-)-Fucose 1-phosphate bis(cyclohexylammonium) salt
8-Chloro-11-oxo-10,11-dihydro-5H-dibenzo-1,4-diazepine
CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1093
methyl 5-(trifluoromethyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
1,2-BIS(PHENYLTHIO)ETHYLENE (CIS- AND TRANS- MIXTURE)
Mesulfen
P - Antiparasitic products, insecticides and repellents > P03 - Ectoparasiticides, incl. scabicides, insecticides and repellents > P03A - Ectoparasiticides, incl. scabicides > P03AA - Sulfur containing products D - Dermatologicals > D10 - Anti-acne preparations > D10A - Anti-acne preparations for topical use > D10AB - Preparations containing sulfur C308 - Immunotherapeutic Agent > C574 - Immunosuppressant
2-thiophen-3-yl-3H-benzimidazole-5-carboxylic acid
2-THIOPHEN-2-YL-3H-BENZOIMIDAZOLE-4-CARBOXYLIC ACID
2-THIOPHEN-2-YL-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID
ETHYL 2-CHLORO-2-[2-(2-FLUOROPHENYL)HYDRAZONO]-ACETATE
methyl 6-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
5-(1H-BENZOIMIDAZOL-2-YLSULFANYL)-FURAN-2-CARBALDEHYDE
N-(5-bromo-2-pyrimidinyl)-N,N-dimethylethane-1,2-diamine
Benzenemethanol, alpha,alpha-bis(trifluoromethyl)-
methyl 2-(trifluoromethyl)-1H-benzo[d]imidazole-7-carboxylate
(2-trifluoromethyl-benzoimidazol-1-yl)-acetic acid
4-chloro-6-(1,3-dihydrobenzimidazol-2-ylidene)cyclohexa-2,4-dien-1-one
6-TRIFLUOROMETHYL-1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER
Imidazo[1,2-a]pyridine-7-carboxylic acid, 2-(2-thienyl)
1-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)-3,5-DIMETHYL-1H-PYRAZOLE HYDROBROMIDE
(2-Chloro-4-methoxy-5-(methoxycarbonyl)phenyl)boronic acid
methyl 4-(trifluoromethyl)-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
Methyl 7-(trifluoromethyl)-1-benzofuran-2-carboxylate
n-(2-formyl-5,8-dioxo-5,8-dihydroquinolin-7-yl)acetamide
[(3S,4R,5S)-3,4,5-trihydroxy-2-keto-hexyl] dihydrogen phosphate
Gentisein
Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].
1-methyl-3-[(Z)-(4-oxo-3-prop-2-enyl-1,3-thiazolidin-2-ylidene)amino]thiourea
5-Chloro-2-hydroxy-3,7-bis(methoxymethyl)cyclohepta-2,4,6-trien-1-one
2-Deoxy-D-glucose 6-phosphate
A deoxyaldohexose phosphate comprising 2-deoxy-D-glucose having the phosphate group at the 6-position.
N-(3-carboxylatopropanoyl)-L-glutamate(3-)
Trianion of N(2)-succinyl-L-glutamic acid arising from global deprotonation of the carboxy groups.
