Exact Mass: 228.994

Exact Mass Matches: 228.994

Found 39 metabolites which its exact mass value is equals to given mass value 228.994, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Dimethoate

Phosphorodithioic acid, O,O-dimethyl S-(2-(methylamino)-2-oxoethyl) ester

C5H12NO3PS2 (228.9996)


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

Phosphorothioic acid, O-(4-cyanophenyl) O-methyl ester

C8H8NO3PS (228.9963)


   

Picric acid

2-Hydroxy-1,3,5-trinitrobenzene

C6H3N3O7 (228.9971)


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).

   

MLS002207196-01!Dimethoate60-51-5

MLS002207196-01!Dimethoate60-51-5

C5H12NO3PS2 (228.9996)


   

dimethoate

Pesticide1_Dimethoate_C5H12NO3PS2_Phosphorodithioic acid, O,O-dimethyl S-[2-(methylamino)-2-oxoethyl] ester

C5H12NO3PS2 (228.9996)


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

   

Sulfamide, 2-benzothiazolyl- (9CI)

Sulfamide, 2-benzothiazolyl- (9CI)

C7H7N3O2S2 (228.998)


   

2-(Chloromethyl)thiazole-2yl Guanidine Hydrochloride

2-(Chloromethyl)thiazole-2yl Guanidine Hydrochloride

C5H9Cl2N3OS (228.9843)


   

POTASSIUM (6-CARBOXYPYRIDIN-3-YL)TRIFLUOROBORATE

POTASSIUM (6-CARBOXYPYRIDIN-3-YL)TRIFLUOROBORATE

C6H4BF3KNO2 (228.9924)


   

3-(pentafluoro-λ6-sulfanyl)benzonitrile

3-(pentafluoro-λ6-sulfanyl)benzonitrile

C7H4F5NS (228.9985)


   

2,3,6-trinitrophenol

2,3,6-trinitrophenol

C6H3N3O7 (228.9971)


   

3-amino-4-mercaptobenzotrifluoride hydrochloride

3-amino-4-mercaptobenzotrifluoride hydrochloride

C7H7ClF3NS (228.994)


   

1-methylindole-7-sulfonyl chloride

1-methylindole-7-sulfonyl chloride

C9H8ClNO2S (228.9964)


   

2-[(4-CHLOROBENZYL)SULFONYL]ACETONITRILE

2-[(4-CHLOROBENZYL)SULFONYL]ACETONITRILE

C9H8ClNO2S (228.9964)


   

Lamprecide

Phenol, 4-nitro-3-(trifluoromethyl)-, sodium salt (1:1)

C7H3F3NNaO3 (228.9963)


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).

   

N-(5-Amino-3-bromo-2-pyridinyl)acetamide

N-(5-Amino-3-bromo-2-pyridinyl)acetamide

C7H8BrN3O (228.9851)


   

6-bromo-2,4-dimethylpyridine-3-boronic acid

6-bromo-2,4-dimethylpyridine-3-boronic acid

C7H9BBrNO2 (228.991)


   

2-Chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acid ethyl ester

2-Chloro-6H-thieno[2,3-b]pyrrole-5-carboxylic acid ethyl ester

C9H8ClNO2S (228.9964)


   

2-AMINOBENZO[D]THIAZOLE-6-SULFONAMIDE

2-AMINOBENZO[D]THIAZOLE-6-SULFONAMIDE

C7H7N3O2S2 (228.998)


   

1-Methyl-1H-indole-4-sulfonyl chloride

1-Methyl-1H-indole-4-sulfonyl chloride

C9H8ClNO2S (228.9964)


   

4-(pentafluoro-λ6-sulfanyl)benzonitrile

4-(pentafluoro-λ6-sulfanyl)benzonitrile

C7H4F5NS (228.9985)


   

2-AMINO-5-BROMO-4-METHYL NICOTINAMIDE

2-AMINO-5-BROMO-4-METHYL NICOTINAMIDE

C7H8BrN3O (228.9851)


   

Pyridinium trifluoromethanesulfonate

Pyridinium trifluoromethanesulfonate

C6H6F3NO3S (229.002)


   

potassium (4-nitrophenyl)trifluoroborate

potassium (4-nitrophenyl)trifluoroborate

C6H4BF3KNO2 (228.9924)


   

2-CHLORO-5,6-DIMETHOXY-BENZOTHIAZOLE

2-CHLORO-5,6-DIMETHOXY-BENZOTHIAZOLE

C9H8ClNO2S (228.9964)


   

6-chloro-1-methylsulfonylindole

6-chloro-1-methylsulfonylindole

C9H8ClNO2S (228.9964)


   

O,O-Dimethyl S-[2-(methylamino)-2-oxoethyl] phosphorodithioate

O,O-Dimethyl S-[2-(methylamino)-2-oxoethyl] phosphorodithioate

C5H12NO3PS2 (228.9996)


   

2-AMINO-5-BROMO-6-METHYL NICOTINAMIDE

2-AMINO-5-BROMO-6-METHYL NICOTINAMIDE

C7H8BrN3O (228.9851)


   

5-Chloro-2,4-dimethoxyphenyl isothiocyanate

5-Chloro-2,4-dimethoxyphenyl isothiocyanate

C9H8ClNO2S (228.9964)


   

1-METHYL-1H-INDOLE-5-SULFONYLCHLORIDE

1-METHYL-1H-INDOLE-5-SULFONYLCHLORIDE

C9H8ClNO2S (228.9964)


   

5-Bromo-2-(trimethylsilyl)pyridine

5-Bromo-2-(trimethylsilyl)pyridine

C8H12BrNSi (228.9922)


   

N-(5-Bromopyridin-2-yl)acetohydrazide

N-(5-Bromopyridin-2-yl)acetohydrazide

C7H8BrN3O (228.9851)


   

4-CHLORO-2,5-DIMETHOXYPHENYL ISOTHIOCYANATE

4-CHLORO-2,5-DIMETHOXYPHENYL ISOTHIOCYANATE

C9H8ClNO2S (228.9964)


   

Potassium trifluoro(3-nitrophenyl)borate(1-)

Potassium trifluoro(3-nitrophenyl)borate(1-)

C6H4BF3KNO2 (228.9924)


   

Potassium (2-nitrophenyl)trifluoroborate

Potassium (2-nitrophenyl)trifluoroborate

C6H4BF3KNO2 (228.9924)


   

Phosphorothioic acid, O-(4-cyanophenyl) O-methyl ester

Phosphorothioic acid, O-(4-cyanophenyl) O-methyl ester

C8H8NO3PS (228.9963)


   

3-[(4-Chlorophenyl)sulfonyl]propanenitrile

3-[(4-Chlorophenyl)sulfonyl]propanenitrile

C9H8ClNO2S (228.9964)


   

N(omega)-phosphohypotaurocyamine(2-)

N(omega)-phosphohypotaurocyamine(2-)

C3H8N3O5PS-2 (228.9922)


   

2-{[Iminio(phosphonatoamino)methyl]amino}ethanesulfinate

2-{[Iminio(phosphonatoamino)methyl]amino}ethanesulfinate

C3H8N3O5PS-2 (228.9922)


   

Picric acid

Trinitrophenol

C6H3N3O7 (228.9971)


C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents D004791 - Enzyme Inhibitors > D014475 - Uncoupling Agents