Exact Mass: 173.9632
Exact Mass Matches: 173.9632
Found 280 metabolites which its exact mass value is equals to given mass value 173.9632,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
4-Sulfophenol
4-Hydroxybenzenesulfonic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=98-67-9 (retrieved 2024-08-06) (CAS RN: 98-67-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Phenyl dihydrogen phosphate
CONFIDENCE standard compound; INTERNAL_ID 2498 KEIO_ID P033
Phenol sulfate
Phenol sulphate, also known as phenylsulfate or aryl sulphate, belongs to the class of organic compounds known as phenylsulfates. Phenylsulfates are compounds containing a sulfate group conjugated to a phenyl group. In normal humans, phenol sulphate is primarily a gut-derived metabolite that arises from the activity of the bacterial enzyme tyrosine phenol-lyase, which is responsible for the synthesis of phenol from dietary tyrosine (PMID: 31015435). Phenol sulphate can also arise from the consumption of phenol or from phenol poisoning (PMID: 473790). Phenol sulphate is produced from the conjugation of phenol with sulphate in the liver. In particular, phenol sulphate can be biosynthesized from phenol and phosphoadenosine phosphosulfate through the action of the enzyme sulfotransferase 1A1 in the liver. Phenol sulphate can be found in most mammals (mice, rats, sheep, dogs, humans) and likely most animals. Phenol sulphate is a uremic toxin (PMID: 30068866). It is a protein-bound uremic solute that induces reactive oxygen species (ROS) production and decreases glutathione levels, rendering cells vulnerable to oxidative stress (PMID: 29474405). In experimental models of diabetes, phenol sulphate administration has been shown to induce albuminuria and podocyte damage. In a diabetic patient cohort, phenol sulphate levels were found to significantly correlate with basal and predicted 2-year progression of albuminuria in patients with microalbuminuria (PMID: 31015435).
cis-2-Chloro-4-carboxymethylenebut-2-en-1,4-olide
This compound belongs to the family of Butenolides. These are dihydrofurans with a carbonyk group at the C2 carbon atom.
Magnesium hydrogen phosphate trihydrate
It is used as a food additive
phosphoric acid-(2-chloro-ethyl ester)-methyl ester|Phosphorsaeure-(2-chlor-aethylester)-methylester
3-chloro-2-hydroxypropanesulphonic acid
CONFIDENCE standard compound; INTERNAL_ID 309; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 685; ORIGINAL_PRECURSOR_SCAN_NO 683 CONFIDENCE standard compound; INTERNAL_ID 309; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 687; ORIGINAL_PRECURSOR_SCAN_NO 683 CONFIDENCE standard compound; INTERNAL_ID 309; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 696; ORIGINAL_PRECURSOR_SCAN_NO 693 CONFIDENCE standard compound; INTERNAL_ID 309; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 681; ORIGINAL_PRECURSOR_SCAN_NO 679 CONFIDENCE standard compound; INTERNAL_ID 309; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 693; ORIGINAL_PRECURSOR_SCAN_NO 691 CONFIDENCE standard compound; INTERNAL_ID 309; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 678; ORIGINAL_PRECURSOR_SCAN_NO 677
1H-Imidazole-4-carboxylic acid, 5-(chlorocarbonyl)- (9CI)
4-(Aminomethyl)thiophene-2-carbonitrile hydrochloride
1-Cyclopentene-1-carboxylic acid, 2-(chlorocarbonyl)- (9CI)
5-(Aminomethyl)thiophene-2-carbonitrile hydrochloride
tert-Butyl chromate solution in carbon tetrachloride
5-CHLORO-6-OXO-1,6-DIHYDROPYRIMIDINE-4-CARBOXYLIC ACID
Tetracyclo[3.3.0.02,8.03,6]octane, 4,4-dichloro- (9CI)
(2-AMINO-3-PYRIDINYL)-[1,1-BIPHENYL]-4-YL-METHANONE
Ytterbium
Ytterbium, also known as 70yb or yterbio, is a member of the class of compounds known as homogeneous lanthanide compounds. Homogeneous lanthanide compounds are inorganic compounds containing only metal atoms, with the largest atom being a lanthanide atom. Ytterbium can be found in a number of food items such as corn, almond, white cabbage, and pistachio, which makes ytterbium a potential biomarker for the consumption of these food products. In 1878, the Swiss chemist Jean Charles Galissard de Marignac separated from the rare earth "erbia" another independent component, which he called "ytterbia", for Ytterby, the village in Sweden near where he found the new component of erbium. He suspected that ytterbia was a compound of a new element that he called "ytterbium" (in total, four elements were named after the village, the others being yttrium, terbium and erbium). In 1907, the new earth "lutecia" was separated from ytterbia, from which the element "lutecium" (now lutetium) was extracted by Georges Urbain, Carl Auer von Welsbach, and Charles James. After some discussion, Marignacs name "ytterbium" was retained. A relatively pure sample of the metal was not obtained until 1953. At present, ytterbium is mainly used as a dopant of stainless steel or active laser media, and less often as a gamma ray source .
Bicyclo[3.1.0]hexane, 3-(bromomethyl)-, cis- (8CI)
(5E)-3-imino-4-sulfanyl-5-(sulfanylmethylidene)pyrrolidin-2-one
Hydroxy-[[hydroxy(oxido)phosphoryl]methyl]phosphinate
Phenyl phosphate
An aryl phosphate resulting from the mono-esterification of phosphoric acid with phenol.
Phenylsulfate
An aryl sulfate that is phenol bearing an O-sulfo substituent.
trans-2-Chloro-4-carboxymethylenebut-2-en-1,4-olide
3-hydroxybenzenesulfonic acid
An arenesulfonic acid that is phenol substituted by a sulfo group at C-3.
2-hydroxybenzenesulfonic acid
An arenesulfonic acid that is phenol substituted by a sulfo group at C-2.
