Exact Mass: 228.998
Exact Mass Matches: 228.998
Found 48 metabolites which its exact mass value is equals to given mass value 228.998,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Chloranocryl
CONFIDENCE standard compound; INTERNAL_ID 512; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4881; ORIGINAL_PRECURSOR_SCAN_NO 4879 CONFIDENCE standard compound; INTERNAL_ID 512; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4870; ORIGINAL_PRECURSOR_SCAN_NO 4866 CONFIDENCE standard compound; INTERNAL_ID 512; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4842; ORIGINAL_PRECURSOR_SCAN_NO 4840 CONFIDENCE standard compound; INTERNAL_ID 512; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4863; ORIGINAL_PRECURSOR_SCAN_NO 4858 CONFIDENCE standard compound; INTERNAL_ID 512; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4866; ORIGINAL_PRECURSOR_SCAN_NO 4863 CONFIDENCE standard compound; INTERNAL_ID 512; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4881; ORIGINAL_PRECURSOR_SCAN_NO 4876
Dimethoate
D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor CONFIDENCE standard compound; EAWAG_UCHEM_ID 2761 EAWAG_UCHEM_ID 2761; CONFIDENCE standard compound CONFIDENCE standard compound; INTERNAL_ID 8379 CONFIDENCE standard compound; INTERNAL_ID 4003 CONFIDENCE standard compound; INTERNAL_ID 3009 D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals
Phosphorothioic acid, O-(4-cyanophenyl) O-methyl ester
Picric acid
Picric acid, also known as acide picrique or c.i. 10305, belongs to the class of organic compounds known as nitrophenols. Nitrophenols are compounds containing a nitrophenol moiety, which consists of a benzene ring bearing both a hydroxyl group and a nitro group on two different ring carbon atoms. Based on a literature review a significant number of articles have been published on Picric acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Picric acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Picric acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources. Picric acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=88-89-1 (retrieved 2024-07-10) (CAS RN: 88-89-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
dimethoate
D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals CONFIDENCE standard compound; INTERNAL_ID 3009
Lamprecide
A lampricide is any chemical designed to target the larvae of lampreys in river systems before they develop into parasitic adults. One lampricide is used in the headwaters of Lake Champlain and the Great Lakes to control the sea lamprey (Petromyzon marinus), an invasive species to these lakes.[1] TFM (3-trifluoromethyl-4-nitrophenol) is the main chemical used for this purpose. As it is hydrophobic, it passes through biological membranes.[2] TFM is a metabolic uncoupler—that is, TFM separates the electron transport chain from ATP synthesis, resulting in the failure of the aerobic respiration process. It accomplishes this by disrupting the electrochemical gradient that powers ATP synthase—as an acid, it donates H+ ions to the mitochondrial matrix. The electron transport chain is not affected and continues using oxygen, without producing ATP. While the general opinion is that TFM typically does not harm other fish (due to the relationship between true fish and lampreys), lampricide can be problematic for many amphibians, such as mudpuppies (genus Necturus) which often share the same habitats. Also, some more "primitive" species of fish, such as the sturgeon in the Great Lakes are sensitive to chemicals such as TFM. Lamprecide is a metabolic compound that has been identified in various biological contexts, although it is not as widely recognized as some other metabolites. The term "lamprecide" is less commonly used in scientific literature, and therefore, detailed information about this specific metabolite may be limited. However, the name suggests that it could be associated with the metabolism of lampreys, which are a type of jawless fish, or it might be a compound with a similar structure to other known metabolites or alkaloids. As a metabolite, lamprecide is likely to be a small molecule that is produced as part of the normal metabolic processes within an organism. It may have various biological roles, such as serving as a signaling molecule, a precursor to other compounds, or having a specific physiological function within the organism that produces it. In the context of its chemical structure, lamprecide might be characterized by a unique arrangement of atoms that gives it specific properties. These properties could include a particular reactivity, solubility, or interaction with biological macromolecules like proteins or nucleic acids. Without specific details on the exact structure and function of lamprecide, a more precise description is not possible. If lamprecide is a novel or less-studied metabolite, further research would be needed to determine its: - Chemical structure: The exact arrangement of atoms and functional groups that define the molecule. - Biosynthesis: The metabolic pathways and enzymes involved in the production of lamprecide. - Bioactivity: Any potential pharmacological or toxicological effects it may have on biological systems. - Role in metabolism: Its function within the organism, such as enzyme inhibition, hormone activity, or as a structural component. For a more accurate and detailed description, one would need to refer to the scientific literature or research studies that specifically investigate this compound. Phenol, 4-nitro-3-(trifluoromethyl)-, sodium salt (1:1). CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=654-66-0 (retrieved 2024-07-10) (CAS RN: 654-66-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
2-Chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acid ethyl ester
O,O-Dimethyl S-[2-(methylamino)-2-oxoethyl] phosphorodithioate
Phosphorothioic acid, O-(4-cyanophenyl) O-methyl ester
2-{[Iminio(phosphonatoamino)methyl]amino}ethanesulfinate
Picric acid
C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents D004791 - Enzyme Inhibitors > D014475 - Uncoupling Agents
