Exact Mass: 116.0109584

Exact Mass Matches: 116.0109584

Found 277 metabolites which its exact mass value is equals to given mass value 116.0109584, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Maleic acid

(2Z)-but-2-enedioic acid

C4H4O4 (116.01095839999999)


Maleic acid is a colorless crystalline solid having a faint odor. It is combustible though it may take some effort to ignite. It is soluble in water. It is used to make other chemicals and for dyeing and finishing naturally occurring fibers. Maleic acid is a butenedioic acid in which the double bond has cis- (Z)-configuration. It has a role as a plant metabolite, an algal metabolite and a mouse metabolite. It is a conjugate acid of a maleate(1-) and a maleate. Maleic acid is a natural product found in Populus tremula, Ardisia crenata, and other organisms with data available. Maleic Acid is an organic salt or ester of maleic acid that could be conjugated to free base compounds/drugs to improve the physiochemical properties including stability, solubility and dissolution rate. (NCI) Maleic acid is an industrial raw material for the production of glyoxylic acid by ozonolysis. Maleic acid is an organic compound which is a dicarboxylic acid (molecule with two carboxyl groups). The molecule consists of an ethylene group flanked by two carboxylic acid groups. Maleic acid is the cis isomer of butenedioic acid, whereas fumaric acid is the trans isomer. The cis isomer is the less stable one of the two; the difference in heat of combustion is 22.7 kJ/mol. The physical properties of maleic acid are very different from that of fumaric acid. Maleic acid is soluble in water whereas fumaric acid is not and the melting point of maleic acid (130 - 131 degree centigrade) is also much lower than that of fumaric acid (287 degree centigrade). Both properties of maleic acid can be explained on account of the intramolecular hydrogen bonding that takes place at the expense of intermolecular interactions. Maleic acid is converted into maleic anhydride by dehydration, to malic acid by hydration, and to succinic acid by hydrogenation. It reacts with thionyl chloride or phosphorus pentachloride to give the maleic acid chloride (it is not possible to isolate the mono acid chloride). Maleic acid is a reactant in many Diels-Alder reactions. See also: Surfomer (monomer of); Ferropolimaler (monomer of). Maleic acid is an industrial raw material for the production of glyoxylic acid by ozonolysis. Maleic acid is an organic compound which is a dicarboxylic acid (molecule with two carboxyl groups). The molecule consists of an ethylene group flanked by two carboxylic acid groups. Maleic acid is the cis isomer of butenedioic acid, whereas fumaric acid is the trans isomer. The cis isomer is the less stable one of the two; the difference in heat of combustion is 22.7 kJ/mol. The physical properties of maleic acid are very different from that of fumaric acid. Maleic acid is soluble in water whereas fumaric acid is not and the melting point of maleic acid (130 - 131 degree centigrade) is also much lower than that of fumaric acid (287 degree centigrade). Both properties of maleic acid can be explained on account of the intramolecular hydrogen bonding that takes place at the expense of intermolecular interactions. Maleic acid is converted into maleic anhydride by dehydration, to malic acid by hydration, and to succinic acid by hydrogenation. It reacts with thionyl chloride or phosphorus pentachloride to give the maleic acid chloride (it is not possible to isolate the mono acid chloride). Maleic acid is a reactant in many Diels-Alder reactions. [HMDB]. Maleic acid is found in many foods, some of which are cocoa bean, lovage, roselle, and corn. Maleic acid is a dicarboxylic acid, a molecule with two carboxyl groups. It consists of an ethylene group flanked by two carboxylic acid groups. Maleic acid is the cis isomer of butenedioic acid, whereas fumaric acid is the trans isomer. The cis isomer is the less stable one of the two; the difference in heat of combustion is 22.7 kJ/mol. The physical properties of maleic acid are very different from that of fumaric acid. Maleic acid is soluble in water whereas fumaric acid is not and the melting point of maleic acid (130 - 131 oC) is also much lower than that of fumaric acid (287 oC). Maleic acid is converted into maleic anhydride by dehydration, to malic acid by hydration, and to succinic acid by hydrogenation. Maleic acid is used in making polyesters for fibre-reinforced laminated moldings and paint vehicles. More specifically it is used in the manufacture of phthalic-type alkyd and polyester resins, surface coatings, copolymers, plasticizers, lubricant additives and agricultural chemicals. It is also found in adhesives and sealants and as a preservative for oils and fats. In the natural world, maleic acid has been identified in ginseng, pineapple, cacao plants, sour cherries and corn. A large number of microbes are able to convert maleic acid to D-malate using the enzyme maleate hydratase (PMID: 1444397). A butenedioic acid in which the double bond has cis- (Z)-configuration. Maleic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=110-16-7 (retrieved 2024-06-29) (CAS RN: 110-16-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Maleic Acid is a Glutamate Decarboxylase (GAD) inhibitor of E. coli and L. monocytogenes. Maleic Acid is a Glutamate Decarboxylase (GAD) inhibitor of E. coli and L. monocytogenes.

   

Fumaric acid

(2E)-but-2-enedioic acid

C4H4O4 (116.0109584)


Fumaric acid appears as a colorless crystalline solid. The primary hazard is the threat to the environment. Immediate steps should be taken to limit spread to the environment. Combustible, though may be difficult to ignite. Used to make paints and plastics, in food processing and preservation, and for other uses. Fumaric acid is a butenedioic acid in which the C=C double bond has E geometry. It is an intermediate metabolite in the citric acid cycle. It has a role as a food acidity regulator, a fundamental metabolite and a geroprotector. It is a conjugate acid of a fumarate(1-). Fumaric acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Fumaric acid is a precursor to L-malate in the Krebs tricarboxylic acid cycle. It is formed by the oxidation of succinate by succinate dehydrogenase. Fumarate is converted by fumarase to malate. A fumarate is a salt or ester of the organic compound fumaric acid, a dicarboxylic acid. Fumarate has recently been recognized as an oncometabolite. (A15199). As a food additive, fumaric acid is used to impart a tart taste to processed foods. It is also used as an antifungal agent in boxed foods such as cake mixes and flours, as well as tortillas. Fumaric acid is also added to bread to increase the porosity of the final baked product. It is used to impart a sour taste to sourdough and rye bread. In cake mixes, it is used to maintain a low pH and prevent clumping of the flours used in the mix. In fruit drinks, fumaric acid is used to maintain a low pH which, in turn, helps to stabilize flavor and color. Fumaric acid also prevents the growth of E. coli in beverages when used in combination with sodium benzoate. When added to wines, fumaric acid helps to prevent further fermentation and yet maintain low pH and eliminate traces of metallic elements. In this fashion, it helps to stabilize the taste of wine. Fumaric acid can also be added to dairy products, sports drinks, jams, jellies and candies. Fumaric acid helps to break down bonds between gluten proteins in wheat and helps to create a more pliable dough. Fumaric acid is used in paper sizing, printer toner, and polyester resin for making molded walls. Fumaric acid is a dicarboxylic acid. It is a precursor to L-malate in the Krebs tricarboxylic acid (TCA) cycle. It is formed by the oxidation of succinic acid by succinate dehydrogenase. Fumarate is converted by the enzyme fumarase to malate. Fumaric acid has recently been identified as an oncometabolite or an endogenous, cancer causing metabolite. High levels of this organic acid can be found in tumors or biofluids surrounding tumors. Its oncogenic action appears to due to its ability to inhibit prolyl hydroxylase-containing enzymes. In many tumours, oxygen availability becomes limited (hypoxia) very quickly due to rapid cell proliferation and limited blood vessel growth. The major regulator of the response to hypoxia is the HIF transcription factor (HIF-alpha). Under normal oxygen levels, protein levels of HIF-alpha are very low due to constant degradation, mediated by a series of post-translational modification events catalyzed by the prolyl hydroxylase domain-containing enzymes PHD1, 2 and 3, (also known as EglN2, 1 and 3) that hydroxylate HIF-alpha and lead to its degradation. All three of the PHD enzymes are inhibited by fumarate. Fumaric acid is found to be associated with fumarase deficiency, which is an inborn error of metabolism. It is also a metabolite of Aspergillus. Produced industrially by fermentation of Rhizopus nigricans, or manufactured by catalytic or thermal isomerisation of maleic anhydride or maleic acid. Used as an antioxidant, acidulant, leavening agent and flavouring agent in foods. Present in raw lean fish. Dietary supplement. Used in powdered products since fumaric acid is less hygroscopic than other acids. A precursor to L-malate in the Krebs tricarboxylic acid cycle. It is formed by the oxidation of succinate by succinate dehydrogenase (wikipedia). Fumaric acid is also found in garden tomato, papaya, wild celery, and star fruit. Fumaric acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=110-17-8 (retrieved 2024-07-01) (CAS RN: 110-17-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Fumaric acid, associated with fumarase deficiency, is identified as an oncometabolite or an endogenous, cancer causing metabolite. Fumaric acid, associated with fumarase deficiency, is identified as an oncometabolite or an endogenous, cancer causing metabolite.

   

N-NITROSOMORPHOLINE

alpha-Acetoxy-N-nitrosomorpholine

C4H8N2O2 (116.0585748)


CONFIDENCE standard compound; EAWAG_UCHEM_ID 3454 CONFIDENCE standard compound; INTERNAL_ID 4127 CONFIDENCE standard compound; INTERNAL_ID 8689 D009676 - Noxae > D002273 - Carcinogens D009676 - Noxae > D009153 - Mutagens

   

alpha-Ketoisovaleric acid

3-Methyl-2-oxobutyric acid sodium salt

C5H8O3 (116.0473418)


alpha-Ketoisovaleric acid is an abnormal metabolite that arises from the incomplete breakdown of branched-chain amino acids. alpha-Ketoisovaleric acid is a neurotoxin, an acidogen, and a metabotoxin. A neurotoxin causes damage to nerve cells and nerve tissues. An acidogen is an acidic compound that induces acidosis, which has multiple adverse effects on many organ systems. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Chronically high levels of alpha-ketoisovaleric acid are associated with maple syrup urine disease. MSUD is a metabolic disorder caused by a deficiency of the branched-chain alpha-keto acid dehydrogenase complex (BCKDC), leading to a buildup of the branched-chain amino acids (leucine, isoleucine, and valine) and their toxic by-products (ketoacids) in the blood and urine. The symptoms of MSUD often show in infancy and lead to severe brain damage if untreated. MSUD may also present later depending on the severity of the disease. If left untreated in older individuals, during times of metabolic crisis, symptoms of the condition include uncharacteristically inappropriate, extreme, or erratic behaviour and moods, hallucinations, anorexia, weight loss, anemia, diarrhea, vomiting, dehydration, lethargy, oscillating hypertonia and hypotonia, ataxia, seizures, hypoglycemia, ketoacidosis, opisthotonus, pancreatitis, rapid neurological decline, and coma. In maple syrup urine disease, the brain concentration of branched-chain ketoacids can increase 10- to 20-fold. This leads to a depletion of glutamate and a consequent reduction in the concentration of brain glutamine, aspartate, alanine, and other amino acids. The result is a compromise of energy metabolism because of a failure of the malate-aspartate shuttle and a diminished rate of protein synthesis (PMID: 15930465). alpha-Ketoisovaleric acid is a keto-acid, which is a subclass of organic acids. Abnormally high levels of organic acids in the blood (organic acidemia), urine (organic aciduria), the brain, and other tissues lead to general metabolic acidosis. Acidosis typically occurs when arterial pH falls below 7.35. In infants with acidosis, the initial symptoms include poor feeding, vomiting, loss of appetite, weak muscle tone (hypotonia), and lack of energy (lethargy). These can progress to heart, liver, and kidney abnormalities, seizures, coma, and possibly death. These are also the characteristic symptoms of untreated MSUD. Many affected children with organic acidemias experience intellectual disability or delayed development. Flavouring ingredient for use in butter-type flavours. Found in banana, bread, cheeses, asparagus, beer and cocoa KEIO_ID M006 3-Methyl-2-oxobutanoic acid is a precursor of pantothenic acid in Escherichia coli.

   

2-Oxovaleric acid

2-Ketopentanoic acid, sodium salt

C5H8O3 (116.0473418)


2-Oxovaleric acid is an alpha-ketoacid is a metabolite usually found in human biofluids. Ketoacids have been known to play an important part in the metabolism of valine, leucine, isoleucine. 2-Oxovaleric acid presence has been determined in human blood serum and urine in numerous scientific documents, although its origin remains unclear. (PMID: 11482739, 9869358, 3235498). Acquisition and generation of the data is financially supported in part by CREST/JST. Isolated from Trigonella caerulea (sweet trefoil) 2-Oxovaleric acid is a keto acid that is found in human blood.

   
   

3-Oxopentanoic acid

3-oxo-pentanoic acid

C5H8O3 (116.0473418)


   

Glutarate semialdehyde

Glutaric acid semialdehyde

C5H8O3 (116.0473418)


In the lysine degradation IV pathway, glutarate semialdehyde reacts with NADP+ and H2O to produce glutarate, NADPH, and H+. In this pathway, glutarate semialdehyde is produced by the reaction between 5-aminopentanoate and 2-ketoglutarate, with L-glutamate as a byproduct. The enzyme responsible for this reaction is 5-aminovalerate aminotransferase. In the lysine degradation III pathway, glutarate semialdehyde reacts with NAD+ and H2O to produce glutarate and NADH. In this pathway, glutarate semialdehyde is produced by the reaction between 5-aminopentanoate and 2-ketoglutarate, with L-glutamate as a byproduct. The enzyme responsible for this reaction is 5-aminovalerate aminotransferase. In the lysine degradation IV pathway, glutarate semialdehyde reacts with NADP+ and H2O to produce glutarate, NADPH, and H+. In this pathway, glutarate semialdehyde is produced by the reaction between 5-aminopentanoate and 2-ketoglutarate, with L-glutamate as a byproduct. The enzyme responsible for this reaction is 5-aminovalerate aminotransferase.

   

N,N'-Diacetylhydrazine

N-Acetylacetohydrazide

C4H8N2O2 (116.0585748)


N,N-Diacetylhydrazine is a metabolite of isoniazid. Isoniazid (Laniazid, Nydrazid), also known as isonicotinylhydrazine (INH), is an organic compound that is the first-line medication in prevention and treatment of tuberculosis. (Wikipedia)

   

3-(Methylnitrosoamino)-propanal

3-(N-Nitrosomethylamino)propionaldehyde

C4H8N2O2 (116.0585748)


   

Levulinic acid

3-Ketobutane-1-carboxylic acid

C5H8O3 (116.0473418)


Found in beet, caramel etcand is also reported in papaya (Carica papaya), wheat bread, rice bran, sake and Chinese quince fruit (Chaenomeles legenaria)and is also production by lychee (Litchi chinensis), Malabar spinach (Basella rubra) and Phyllophora subspecies Flavour ingredient. Levulinic acid is a crystalline keto acid prepared from levulose, inulin, starch, etc., by boiling them with dilute hydrochloric or sulfuric acids. D004791 - Enzyme Inhibitors Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate. Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate.

   

Methylacetoacetic acid

3-oxo-Butanoic acid methyl ester

C5H8O3 (116.0473418)


Methylacetoacetic acid, also known as 3-oxo-butanoate or methyl acetylacetate, belongs to the class of organic compounds known as beta-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C3 carbon atom. Methylacetoacetic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). Methylacetoacetic acid is a citrus, fresh, and fruity tasting compound. Methylacetoacetic acid has been identified in the urine of patients with an inherited deficiency of propionyl-CoA carboxylase (PMID 630060), and after isoleucine loading in the diagnosis of 2-methylacetoacetyl-CoA thiolase deficiency. Methylacetoacetic acid has been identified in the urine of patients with an inherited deficiency of propionyl-CoA carboxylase (PMID 630060), and after isoleucine loading in the diagnosis of 2-methylacetoacetyl-CoA thiolase deficiency. (PMID 1861461) [HMDB] Methyl acetylacetate is an endogenous metabolite. Methyl acetylacetate is an endogenous metabolite.

   

4-hydroxy-2-methylbut-2-enoic acid

4-hydroxy-2-methylbut-2-enoic acid

C5H8O3 (116.0473418)


   

Ethyl pyruvate

Propanoic acid, 2-oxo-, ethyl ester

C5H8O3 (116.0473418)


Ethyl pyruvate, also known as pyruvic acid ethyl ester or 2-oxo-propionate ethyl ester, belongs to the family of alpha-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the adjacent carbon. Ethyl pyruvate is soluble (in water) and an extremely weak acidic compound (based on its pKa). When given as a drug, ethyl pyruvate (known as CTI-01) inhibits the systemic release of cytokines (e.g. TNF-alpha and HMGB1), which promote the bodys inflammatory response. The over-expression of these cytokines has been linked to diseases that occur in critical care settings, such as severe organ damage following cardiopulmonary bypass (CPB) and post-operative ileus following abdominal surgery (DrugBank). Ethyl pyruvate is a flavouring ingredient. Flavouring ingredient Ethyl pyruvate is a simple derivative of the endogenous metabolite, pyruvic acid. Ethyl pyruvate is an anti-inflammatory agent[1].

   

Acetoxyacetone

ACETIC ACID,(2-oxopropyl) ester acetonylacetATE

C5H8O3 (116.0473418)


Acetoxyacetone is found in pineapple. Acetoxyacetone is a maillard produc Maillard product. Acetoxyacetone is found in pineapple.

   

2-(hydroxymethyl)but-2-enoic acid

2-(hydroxymethyl)but-2-enoic acid

C5H8O3 (116.0473418)


   

2-Methylacetoacetic acid

(+/-)-2-methyl-3-oxobutanoic acid

C5H8O3 (116.0473418)


2-Methylacetoacetic acid (CAS: 2382-59-4) is a metabolite that has an increased excretion in patients with acetoacetyl-CoA thiolase (EC 2.3.1.9) deficiency (OMIM: 607809, ACAT1; OMIM: 100678, ACAT2; OMIM: 604770, ACAA2; OMIM: 607809). Thiolases are ubiquitous and important enzymes. Several isoenzymes are known, which can occur in the cytosol (ACAT2), the mitochondria (ACAT1), or the peroxisomes (ACAA2). Thiolases are CoA-dependent enzymes which catalyze the formation of a carbon-carbon bond in a Claisen condensation step and its reverse reaction via a thiolytic degradation mechanism. Mitochondrial acetoacetyl-coenzyme A (CoA) thiolase (T2) is important in the pathways for the synthesis and degradation of ketone bodies as well as for the degradation of 2-methylacetoacetyl-CoA (PMID: 17371050, 14518824, 9744475, 9001814). Moreover, 2-methylacetoacetic acid is found to be associated with beta-ketothiolase deficiency, which is also an inborn error of metabolism. 2-Methylacetoacetic acid is found in urine and can be used as a biomarker for the diagnosis of beta-ketothiolase deficiency. 2-Methylacetoacetic acid is a metabolite that has an increased excretion in patients with acetoacetyl-CoA thiolase (EC 2.3.1.9) deficiency (OMIM 607809, ACAT1; OMIM 100678, ACAT2; OMIM 604770, ACAA2; OMIM 607809). Thiolases are ubiquitous and important enzymes. Several isoenzymes are known, which can occur in the cytosol (ACAT2), the mitochondria (ACAT1) , or the peroxisomes(ACAA2).

   

Diazenedicarboxamide

(E)-N-[(C-hydroxycarbonimidoyl)imino]carbamimidic acid

C2H4N4O2 (116.0334244)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents Bleaching agent for flour Bleaching agent for flou

   

2-Thiophenethiol

2-Thienyl hydrosulfide

C4H4S2 (115.97544239999999)


2-Thiophenethiol is a flavouring ingredien Flavouring ingredient

   

xI-Dihydro-2-methyl-3(2H)-thiophenone

xI-Dihydro-2-methyl-3(2H)-thiophenone

C5H8OS (116.0295838)


xI-Dihydro-2-methyl-3(2H)-thiophenone, also known as 2-methyltetrahydrothiophen-3-one, and 2-methylthiolan-3-one, is a member of the class of tetrahydrothiophenes that is thiolane substituted by a methyl group at position 2 and an oxo group at position 3 respectively. It has a role as a flavouring agent and as a metabolite. It is a member of tetrahydrothiophenes and a cyclic ketone. It derives from a hydride of a tetrahydrothiophene. xI-Dihydro-2-methyl-3(2H)-thiophenone is a berry-like, cabbage-like, and fruity-like tasting compound. It is used as a food additive

   

Dihydro-5-methyl-2(3H)-thiophenone

4-Mercaptopentanoic acid g-lactone

C5H8OS (116.0295838)


Dihydro-5-methyl-2(3H)-thiophenone is a maillard product. Maillard product

   

xi-2-Acetylthietane

1-(thietan-2-yl)ethan-1-one

C5H8OS (116.0295838)


Thiamine thermal degradation product formed in meat aroma model systems. Thiamine thermal degradation product formed in meat aroma model systems

   

Dihydro-2-methyl-3(2H)-furanthione

4,5-dihydro-2-Methyl-3-furanthiol, 9ci

C5H8OS (116.0295838)


Dihydro-2-methyl-3(2H)-furanthione is found in animal foods. Dihydro-2-methyl-3(2H)-furanthione is a component of roasted meat aroma. Dihydro-2-methyl-3(2H)-furanthione is a food flavouring agent. Component of roasted meat aroma. Food flavouring agent. Dihydro-2-methyl-3(2H)-furanthione is found in animal foods.

   

N-Nitroso-3-hydroxypyrrolidine

3-Hydroxy-1-nitrosopyrrolidine

C4H8N2O2 (116.0585748)


N-Nitroso-3-hydroxypyrrolidine is a metabolite of piperazine. Piperazine is an organic compound that consists of a six-membered ring containing two opposing nitrogen atoms. Piperazine exists as small alkaline deliquescent crystals with a saline taste. The piperazines are a broad class of chemical compounds, many with important pharmacological properties, which contain a core piperazine functional group. (Wikipedia)

   
   

2-Thiohydantoin

2-sulfanylideneimidazolidin-4-one

C3H4N2OS (116.0044334)


   

2,3-Dinitrosobutanbildung

2,3-Dinitrosobutanbildung

C4H8N2O2 (116.0585748)


   

3-Amino-1-hydroxypyrrolidin-2-one

2-Pyrrolidinone, 3-amino-1-hydroxy-, hydrochloride (1:1)

C4H8N2O2 (116.0585748)


D018377 - Neurotransmitter Agents > D018683 - Excitatory Amino Acid Agents > D018691 - Excitatory Amino Acid Antagonists D018377 - Neurotransmitter Agents > D018683 - Excitatory Amino Acid Agents > D018690 - Excitatory Amino Acid Agonists

   

3-Amino-5-mercapto-1,2,4-triazole

5-imino-2,5-dihydro-1H-1,2,4-triazole-3-thiol

C2H4N4S (116.0156664)


   

2-Methyl-2H-tetrazole-5-thiol

2-methyl-2,5-dihydro-1H-1,2,3,4-tetrazole-5-thione

C2H4N4S (116.0156664)


   

5-(Methylthio)-1H-tetrazole

5-(methylsulfanyl)-2H-1,2,3,4-tetrazole

C2H4N4S (116.0156664)


   

5-Mercapto-1-methyltetrazole

1-methyl-1H-1,2,3,4-tetrazole-5-thiol

C2H4N4S (116.0156664)


   

Biacetyl dioxime

N-[3-(hydroxyimino)butan-2-ylidene]hydroxylamine

C4H8N2O2 (116.0585748)


   
   

1,2-Diazenedicarboxamide

1,2-Diazenedicarboxamide

C2H4N4O2 (116.0334244)


   

Chlorotrifluoroethylene

1-chloro-1,2,2-trifluoroethene

C2ClF3 (115.9640626)


   

(Diaminomethylideneamino) thiocyanate

(Diaminomethylideneamino) thiocyanate

C2H4N4S (116.0156664)


   

n-methylthiotetrazole

1-(methylsulfanyl)-1H-1,2,3,4-tetrazole

C2H4N4S (116.0156664)


   

pyrazole triol

4,5-dihydroxy-2,3-dihydro-1H-pyrazol-3-one

C3H4N2O3 (116.0221914)


   

3-Amino-4-oxobutanamide

3-Amino-4-oxobutanimidate

C4H8N2O2 (116.0585748)


   

Succinamide

Butanediamide

C4H8N2O2 (116.0585748)


   

N-Carbamimidoyliminomethanethioamide

N-(carbamimidoylimino)methanethioamide

C2H4N4S (116.0156664)


   

3-thienyl mercaptan

3-thienyl mercaptan

C4H4S2 (115.97544239999999)


Flavouring compound [Flavornet]

   

Ketovaline

3-Methyl-2-oxobutanoic acid

C5H8O3 (116.0473418)


3-Methyl-2-oxobutanoic acid is a precursor of pantothenic acid in Escherichia coli.

   

Maleic Acid

Maleic Acid

C4H4O4 (116.01095839999999)


D004791 - Enzyme Inhibitors Maleic Acid is a Glutamate Decarboxylase (GAD) inhibitor of E. coli and L. monocytogenes. Maleic Acid is a Glutamate Decarboxylase (GAD) inhibitor of E. coli and L. monocytogenes.

   
   

4-Methylimidazolidine-2-thione

4-Methylimidazolidine-2-thione

C4H8N2S (116.0408168)


   

3-hydroxy-2-methyl-gamma-butyrolacton

3-hydroxy-2-methyl-gamma-butyrolacton

C5H8O3 (116.0473418)


   

cyclopent-4-ene-1,2,3-triol

cyclopent-4-ene-1,2,3-triol

C5H8O3 (116.0473418)


   

SCHEMBL7679321

SCHEMBL7679321

C5H8O3 (116.0473418)


   

Butanediamide

Succinic acid diamide

C4H8N2O2 (116.0585748)


   

Butanoic acid, 3-hydroxy-2-methylene-

Butanoic acid, 3-hydroxy-2-methylene-

C5H8O3 (116.0473418)


   

(+/-)-2-hydroxy-2-methyldihydrofuran-3(2h)-one

(+/-)-2-hydroxy-2-methyldihydrofuran-3(2h)-one

C5H8O3 (116.0473418)


   
   

N,N-Dimethyloxamide

N,N-Dimethyloxamide

C4H8N2O2 (116.0585748)


   
   

5-(hydroxymethyl)dihydrofuran-2(3H)-one

5-(hydroxymethyl)dihydrofuran-2(3H)-one

C5H8O3 (116.0473418)


   

4-Hydroxy-2-methylenebutanoic acid

4-Hydroxy-2-methylenebutanoic acid

C5H8O3 (116.0473418)


   

3-hydroxypent-4-enoic acid

3-hydroxypent-4-enoic acid

C5H8O3 (116.0473418)


   

S-Allyl ethanethioate

S-Allyl ethanethioate

C5H8OS (116.0295838)


   

Methyl 4-oxobutanoate

Methyl 4-oxobutanoate

C5H8O3 (116.0473418)


   

UNII-TX9B6RN1RM

UNII-TX9B6RN1RM

C5H8O3 (116.0473418)


   

fumarate

Fumaric Acid

C4H4O4 (116.01095839999999)


Fumaric acid, also known as fumarate or trans-butenedioic acid, belongs to dicarboxylic acids and derivatives class of compounds. Those are organic compounds containing exactly two carboxylic acid groups. Fumaric acid is soluble (in water) and a weakly acidic compound (based on its pKa). Fumaric acid can be found in a number of food items such as cardoon, irish moss, sapodilla, and oregon yampah, which makes fumaric acid a potential biomarker for the consumption of these food products. Fumaric acid can be found primarily in most biofluids, including saliva, cerebrospinal fluid (CSF), urine, and sweat, as well as in human prostate tissue. Fumaric acid exists in all living species, ranging from bacteria to humans. In humans, fumaric acid is involved in several metabolic pathways, some of which include azathioprine action pathway, the oncogenic action of succinate, thioguanine action pathway, and arginine and proline metabolism. Fumaric acid is also involved in several metabolic disorders, some of which include gout or kelley-seegmiller syndrome, the oncogenic action of d-2-hydroxyglutarate in hydroxygluaricaciduria, ornithine transcarbamylase deficiency (OTC deficiency), and mitochondrial complex II deficiency. Moreover, fumaric acid is found to be associated with alzheimers disease, fumarase deficiency, and lung Cancer. Fumaric acid is a non-carcinogenic (not listed by IARC) potentially toxic compound. Fumaric acid or trans-butenedioic acid is the chemical compound with the formula HO2CCH=CHCO2H. It is produced in eukaryotic organisms from succinate in complex 2 of the electron transport chain via the enzyme succinate dehydrogenase. It is one of two isomeric unsaturated dicarboxylic acids, the other being maleic acid. In fumaric acid the carboxylic acid groups are trans (E) and in maleic acid they are cis (Z). Fumaric acid has a fruit-like taste . Acute exposure: EYES: irrigate opened eyes for several minutes under running water. INGESTION: do not induce vomiting. Rinse mouth with water (never give anything by mouth to an unconscious person). Seek immediate medical advice. SKIN: should be treated immediately by rinsing the affected parts in cold running water for at least 15 minutes, followed by thorough washing with soap and water. If necessary, the person should shower and change contaminated clothing and shoes, and then must seek medical attention. Fumaric acid, associated with fumarase deficiency, is identified as an oncometabolite or an endogenous, cancer causing metabolite. Fumaric acid, associated with fumarase deficiency, is identified as an oncometabolite or an endogenous, cancer causing metabolite.

   

2-Oxovaleric acid

2-Oxopentanoic acid

C5H8O3 (116.0473418)


An oxopentanoic acid carrying an oxo group at position 2. 2-Oxovaleric acid is a keto acid that is found in human blood.

   

α-Ketoisovaleric acid

3-Methyl-2-oxobutanoic acid

C5H8O3 (116.0473418)


A 2-oxo monocarboxylic acid that is the 2-oxo derivative of isovaleric acid. 3-Methyl-2-oxobutanoic acid is a precursor of pantothenic acid in Escherichia coli.

   

Fumaric Acid

(2Z)-2-Butenedioic acid

C4H4O4 (116.01095839999999)


Fumaric acid, associated with fumarase deficiency, is identified as an oncometabolite or an endogenous, cancer causing metabolite. Fumaric acid, associated with fumarase deficiency, is identified as an oncometabolite or an endogenous, cancer causing metabolite.

   

METHYL ACETOACETATE

3-Oxobutanoic acid methyl ester, Acetoacetic acid methyl ester, MAA

C5H8O3 (116.0473418)


Methyl acetylacetate is an endogenous metabolite. Methyl acetylacetate is an endogenous metabolite.

   

LEVULINIC ACID

4-oxo-pentanoic acid

C5H8O3 (116.0473418)


D004791 - Enzyme Inhibitors Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate. Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate.

   

Ketoisovaleric acid

Ketoisovaleric acid

C5H8O3 (116.0473418)


   

Fumaric acid (not validated)

Fumaric acid (not validated)

C4H4O4 (116.01095839999999)


Annotation level-3

   

Methylacetoacetate

Methylacetoacetate

C5H8O3 (116.0473418)


   

Fumaric acid; LC-tDDA; CE10

Fumaric acid; LC-tDDA; CE10

C4H4O4 (116.01095839999999)


   
   

3-Methyl-2-oxobutanoic acid

3-Methyl-2-oxobutanoic acid

C5H8O3 (116.0473418)


   

2methyl-3-ketovaleric acid

2-methyl-3-oxo-pentanoic acid

C5H8O3 (116.0473418)


   

AZM 2S

Azodicarboxylic acid diamide

C2H4N4O2 (116.0334244)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents

   

Thienylmercaptan

2-Thienyl hydrosulfide

C4H4S2 (115.97544239999999)


   

ammonium sulfite

Sulfurous acid, ammonium salt (1:2)

H8N2O3S (116.02556179999999)


Food additive listed in the EAFUS Food Additive Database (Jan 2001)

   

Acetol acetate

ACETIC ACID,(2-oxopropyl) ester acetonylacetATE

C5H8O3 (116.0473418)


   

2-Methylthiolan-3-one

xI-Dihydro-2-methyl-3(2H)-thiophenone

C5H8OS (116.0295838)


A member of the class of tetrahydrothiophenes that is thiolane substituted by a methyl group at position 2 and an oxo group at position 3 respectively.

   

5-methylthiolan-2-one

4-Mercaptopentanoic acid g-lactone

C5H8OS (116.0295838)


   

xi-2-Acetylthietane

1-(thietan-2-yl)ethan-1-one

C5H8OS (116.0295838)


   

FA 5:1;O

2-methyl-3-oxo-pentanoic acid

C5H8O3 (116.0473418)


   

Levulic acid

4-oxo-pentanoic acid

C5H8O3 (116.0473418)


D004791 - Enzyme Inhibitors Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate. Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate.

   

SFE 5:1;O

methyl 3-hydroxybut-2-enoate

C5H8O3 (116.0473418)


   
   

2-methylpropanediamide

2-methylpropanediamide

C4H8N2O2 (116.0585748)


   
   

1-Methyl-2-imidazolidinethione

1-Methyl-2-imidazolidinethione

C4H8N2S (116.0408168)


   

3-Methyl-3-oxetanecarboxylic acid

3-Methyl-3-oxetanecarboxylic acid

C5H8O3 (116.0473418)


   

(S)-(-)-Tetrahydro-2-furoic acid

(S)-(-)-Tetrahydro-2-furoic acid

C5H8O3 (116.0473418)


   
   

Ethyl 3-oxopropanoate

Ethyl 3-oxopropanoate

C5H8O3 (116.0473418)


   

3-Oxetaneacetic acid

3-Oxetaneacetic acid

C5H8O3 (116.0473418)


   

Tetrahydro-3-furoic acid

Tetrahydro-3-furoic acid

C5H8O3 (116.0473418)


   

2-Methyl-1,3-dioxolane-2-carbaldehyde

2-Methyl-1,3-dioxolane-2-carbaldehyde

C5H8O3 (116.0473418)


   

2-(Prop-2-yn-1-ylsulfanyl)ethanol

2-(Prop-2-yn-1-ylsulfanyl)ethanol

C5H8OS (116.0295838)


   

NN-Dimethyloxamide

NN-Dimethyloxamide

C4H8N2O2 (116.0585748)


   

1,3,4-thiadiazol-2-ylmethanol

1,3,4-thiadiazol-2-ylmethanol

C3H4N2OS (116.0044334)


   
   

3-AMINO-2-BUTENETHIOAMIDE

3-AMINO-2-BUTENETHIOAMIDE

C4H8N2S (116.0408168)


   
   
   
   

Trifluoroacetyl fluoride

Trifluoroacetyl fluoride

C2F4O (115.9885278)


   
   

Ethyl (2R)-2,3-epoxypropanoate

Ethyl (2R)-2,3-epoxypropanoate

C5H8O3 (116.0473418)


   
   

2,2-dimethyl-1,3-dioxolan-4-one

2,2-dimethyl-1,3-dioxolan-4-one

C5H8O3 (116.0473418)


   

Methyl 2-(hydroxymethyl)acrylate

Methyl 2-(hydroxymethyl)acrylate

C5H8O3 (116.0473418)


   

METHYL 3-METHOXYACRYLATE

METHYL 3-METHOXYACRYLATE

C5H8O3 (116.0473418)


   
   

methyl 2-methylglycidate

methyl 2-methylglycidate

C5H8O3 (116.0473418)


   

Methyl 1-hydroxycyclopropanecarboxylate

Methyl 1-hydroxycyclopropanecarboxylate

C5H8O3 (116.0473418)


   

2-methyloxetane-2-carboxylic acid

2-methyloxetane-2-carboxylic acid

C5H8O3 (116.0473418)


   

Chlorotrifluoroethylene

fluorolube grease, gr-362

C2ClF3 (115.9640626)


   

4-METHYLDIHYDROTHIOPHEN-3(2H)-ONE

4-METHYLDIHYDROTHIOPHEN-3(2H)-ONE

C5H8OS (116.0295838)


   

2-fluoro-5-methylthiophene

2-fluoro-5-methylthiophene

C5H5FS (116.0095982)


   

2-methylsulfanyl-4,5-dihydro-1H-imidazole

2-methylsulfanyl-4,5-dihydro-1H-imidazole

C4H8N2S (116.0408168)


   

2(1H)-Pyrimidinethione,tetrahydro-

2(1H)-Pyrimidinethione,tetrahydro-

C4H8N2S (116.0408168)


   

5-(Hydroxymethyl)dihydro-2(3H)-furanone

5-(Hydroxymethyl)dihydro-2(3H)-furanone

C5H8O3 (116.0473418)


   
   

Acetamide,N-[(methylamino)carbonyl]-

Acetamide,N-[(methylamino)carbonyl]-

C4H8N2O2 (116.0585748)


   

Diammonium hydrogen phosphite

Diammonium hydrogen phosphite

H9N2O3P (116.0350774)


   
   

Potassium acetate hydrate, Puratronic®

Potassium acetate hydrate, Puratronic®

C2H5KO3 (115.987576)


   
   

3-Hydroxytetrahydro-2H-pyran-2-one

3-Hydroxytetrahydro-2H-pyran-2-one

C5H8O3 (116.0473418)


   
   

(5R)-5-(Hydroxymethyl)dihydro-2(3H)-furanone

(5R)-5-(Hydroxymethyl)dihydro-2(3H)-furanone

C5H8O3 (116.0473418)


   

3-Hydroxycyclobutanecarboxylic acid

3-Hydroxycyclobutanecarboxylic acid

C5H8O3 (116.0473418)


   
   
   

Urea, (2-oxopropyl)- (9CI)

Urea, (2-oxopropyl)- (9CI)

C4H8N2O2 (116.0585748)


   

4-Thioxo-2-imidazolidinone

4-Thioxo-2-imidazolidinone

C3H4N2OS (116.0044334)


   
   

1,4-DIOXANE-2-CARBOXALDEHYDE

1,4-DIOXANE-2-CARBOXALDEHYDE

C5H8O3 (116.0473418)


   
   

Glycolide

1,4-Dioxane-2,5-dione

C4H4O4 (116.01095839999999)


   
   
   

1-methoxycyclopropane-1-carboxylic acid

1-methoxycyclopropane-1-carboxylic acid

C5H8O3 (116.0473418)


   

3-Ethoxyacrylic acid

3-Ethoxyacrylic acid

C5H8O3 (116.0473418)


   
   

N2-Acetylglycinamide

N2-Acetylglycinamide

C4H8N2O2 (116.0585748)


   

allylthiourea

allylthiourea

C4H8N2S (116.0408168)


A thiourea with a prop-2-enyl group attached to one of the amines.

   

4-Amino-2,4-dihydro-3H-1,2,4-triazole-3-thione

4-Amino-2,4-dihydro-3H-1,2,4-triazole-3-thione

C2H4N4S (116.0156664)


   

Ethyl 2,3-epoxypropanoate

Ethyl 2,3-epoxypropanoate

C5H8O3 (116.0473418)


   

4-Thiazolol, 2-amino-

4-Thiazolol, 2-amino-

C3H4N2OS (116.0044334)


   

2-Amino-4-hydroxythiazole

2-Amino-4-hydroxythiazole

C3H4N2OS (116.0044334)


   
   

METHYL 2-METHOXYACRYLATE

METHYL 2-METHOXYACRYLATE

C5H8O3 (116.0473418)


   

(R)-(+)-2-Tetrahydrofuroic acid

(R)-(+)-2-Tetrahydrofuroic acid

C5H8O3 (116.0473418)


   
   

2,5-dihydro-1-methyl-1H-phosphole 1-oxide

2,5-dihydro-1-methyl-1H-phosphole 1-oxide

C5H9OP (116.03909940000001)


   
   
   

5,6-DIHYDRO-2H-1,4-THIAZIN-3-AMINE

5,6-DIHYDRO-2H-1,4-THIAZIN-3-AMINE

C4H8N2S (116.0408168)


   

1,2,3-Thiadiazol-4-methanol ,97

1,2,3-Thiadiazol-4-methanol ,97

C3H4N2OS (116.0044334)


   

Poly(chlorotrifluoroethylene-co-vinylide ne fluoride) 26 mole\\% vinylidene fluori

Poly(chlorotrifluoroethylene-co-vinylide ne fluoride) 26 mole\\% vinylidene fluori

C2ClF3 (115.9640626)


   
   
   

2-METHOXYCROTONIC ACID

2-METHOXYCROTONIC ACID

C5H8O3 (116.0473418)


   
   

2-(1,3-dioxolan-2-yl)acetaldehyde

2-(1,3-dioxolan-2-yl)acetaldehyde

C5H8O3 (116.0473418)


   
   

ethyl (2S)-oxirane-2-carboxylate

ethyl (2S)-oxirane-2-carboxylate

C5H8O3 (116.0473418)


   

3-Oxopropyl acetate

3-Oxopropyl acetate

C5H8O3 (116.0473418)


   

(1,2,3-Thiadiazol-5-yl)methanol

(1,2,3-Thiadiazol-5-yl)methanol

C3H4N2OS (116.0044334)


   

Methyl 2-oxobutanoate

Methyl 2-oxobutanoate

C5H8O3 (116.0473418)


   
   

1,2,4-Thiadiazole-3,5-diamine

1,2,4-Thiadiazole-3,5-diamine

C2H4N4S (116.0156664)


   

1,3-Bis(Hydroxyimino)Propan-2-One

1,3-Bis(Hydroxyimino)Propan-2-One

C3H4N2O3 (116.0221914)


   

2-Hydroxyethyl acrylate

2-Hydroxyethyl acrylate

C5H8O3 (116.0473418)


   
   
   

1-(Dimethylamino)-2-nitroethene

1-(Dimethylamino)-2-nitroethene

C4H8N2O2 (116.0585748)


   

2,3-epoxypropyl acetate

2,3-epoxypropyl acetate

C5H8O3 (116.0473418)


   

1,5-dioxepan-2-one

1,5-dioxepan-2-one

C5H8O3 (116.0473418)


   
   

2-Tetrahydrofuroic acid

Tetrahydrofuran-2-carboxylic acid

C5H8O3 (116.0473418)


   

methyl 2-hydroxybut-3-enoate

methyl 2-hydroxybut-3-enoate

C5H8O3 (116.0473418)


   

ACETIC PROPIONIC ANHYDRIDE

ACETIC PROPIONIC ANHYDRIDE

C5H8O3 (116.0473418)


   

HYL 2-AMINO-2-IMINOACETATE

HYL 2-AMINO-2-IMINOACETATE

C4H8N2O2 (116.0585748)


   
   

1,2,4-Triazolidine-3,5-dione,4-amino-

1,2,4-Triazolidine-3,5-dione,4-amino-

C2H4N4O2 (116.0334244)


   

1,3,4-thiadiazole-2,5-diamine

1,3,4-thiadiazole-2,5-diamine

C2H4N4S (116.0156664)


   
   
   
   
   

2-Imidazolidinethione,4-methyl-

2-Imidazolidinethione,4-methyl-

C4H8N2S (116.0408168)


   
   

Pseudothiohydantoin

Pseudothiohydantoin

C3H4N2OS (116.0044334)


   

Poly(ethylene glycol) acrylate

Poly(ethylene glycol) acrylate

C5H8O3 (116.0473418)


   

3-Hydroxy-3-methyl-4-butanolide

3-Hydroxy-3-methyl-4-butanolide

C5H8O3 (116.0473418)


   

4-Hydroxy-4-methyl-4-butanolide

4-Hydroxy-4-methyl-4-butanolide

C5H8O3 (116.0473418)


   

2-Hydroxy-4-methyl-4-butanolide

2-Hydroxy-4-methyl-4-butanolide

C5H8O3 (116.0473418)


   

1,2-Butylene Carbonate

1,2-Butylene Carbonate

C5H8O3 (116.0473418)


   

LITHIUM THIOPHENOXIDE

LITHIUM THIOPHENOXIDE

C6H5LiS (116.0272)


   

2-Oxiranemethanol,2-acetate, (2S)

2-Oxiranemethanol,2-acetate, (2S)

C5H8O3 (116.0473418)


   

1-Cyclopropylthiourea

1-Cyclopropylthiourea

C4H8N2S (116.0408168)


   
   

5-mercapto-1-methyltetrazole

5-mercapto-1-methyltetrazole

C2H4N4S (116.0156664)


   

3-AMINO-5-MERCAPTO-1,2,4-TRIAZOLE

3-AMINO-5-MERCAPTO-1,2,4-TRIAZOLE

C2H4N4S (116.0156664)


   
   
   

(R)-(+)-HA-966

(R)-(+)-HA-966

C4H8N2O2 (116.0585748)


(R)-(+)-HA-966 ((+)-HA-966) is a partial agonist/antagonist of glycine site of the N-methyl-D-aspartate (NMDA) receptor complex. (R)-(+)-HA-966 selectively blocks the activation of the mesolimbic dopamine system by amphetamine[1][2]. (R)-(+)-HA-966 can cross the blood-brain barrier and has the potential for neuropathic and acute pain[3].

   
   

Tetrahydro-2H-thiopyran-3-one

Tetrahydro-2H-thiopyran-3-one

C5H8OS (116.0295838)


   

N-(2-formamidoethyl)formamide

N-(2-formamidoethyl)formamide

C4H8N2O2 (116.0585748)


   

Sodium phenoxide

Sodium benzenolate

C6H5NaO (116.02380800000002)


C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent D019999 - Pharmaceutical Solutions > D012597 - Sclerosing Solutions D000890 - Anti-Infective Agents D002317 - Cardiovascular Agents D004202 - Disinfectants

   
   

2-HYDROXY-2-METHYL-BUT-3-ENOIC ACID

2-HYDROXY-2-METHYL-BUT-3-ENOIC ACID

C5H8O3 (116.0473418)


   

Allyl methyl carbonate

Allyl methyl carbonate

C5H8O3 (116.0473418)


   

(5S)-5-(Hydroxymethyl)dihydro-2(3H)-furanone

(5S)-5-(Hydroxymethyl)dihydro-2(3H)-furanone

C5H8O3 (116.0473418)


   

Tetrahydrothiopyran-4-one

Tetrahydrothiopyran-4-one

C5H8OS (116.0295838)


   

Isoxazole,4,5-dihydro-3-nitro-

Isoxazole,4,5-dihydro-3-nitro-

C3H4N2O3 (116.0221914)


   

5-METHYL-[1,3,4]OXADIAZOLE-2-THIOL

5-METHYL-[1,3,4]OXADIAZOLE-2-THIOL

C3H4N2OS (116.0044334)


   

1-hydroxycyclobutanecarboxylic acid

1-hydroxycyclobutanecarboxylic acid

C5H8O3 (116.0473418)


   

2-chloro-2,2-difluoroethanol

2-chloro-2,2-difluoroethanol

C2H3ClF2O (115.9840482)


   

2-Amino-5,6-dihydro-4H-1,3-thiazine

2-Amino-5,6-dihydro-4H-1,3-thiazine

C4H8N2S (116.0408168)


   

alpha-Methylacetoacetic acid

alpha-Methylacetoacetic acid

C5H8O3 (116.0473418)


   

2-Acetylthietane

2-Acetylthietane

C5H8OS (116.0295838)


   

2-Acetoxypropanal

2-Acetoxypropanal

C5H8O3 (116.0473418)


An aldehyde that is propanal substituted by an acetoxy group at position 2.

   

2-Hydroxy-3-methylbut-2-enoic acid

2-Hydroxy-3-methylbut-2-enoic acid

C5H8O3 (116.0473418)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

2-Butenoic acid, 4-hydroxy-3-methyl-

2-Butenoic acid, 4-hydroxy-3-methyl-

C5H8O3 (116.0473418)


   

Carbamimidamidoacetate

Carbamimidamidoacetate

C3H6N3O2- (116.0459996)


   

5-Hydroxyhydantoin

5-Hydroxyhydantoin

C3H4N2O3 (116.0221914)


An imidazolidine-2,4-dione that is hydantoin substituted by a hydroxy group at position 5.

   

3,3-Dimethyloxirane-2-carboxylic acid

3,3-Dimethyloxirane-2-carboxylic acid

C5H8O3 (116.0473418)


   

(Z)-2-(hydroxymethyl)but-2-enoic acid

(Z)-2-(hydroxymethyl)but-2-enoic acid

C5H8O3 (116.0473418)


   

2,3-Dimethyloxirane-2-carboxylic acid

2,3-Dimethyloxirane-2-carboxylic acid

C5H8O3 (116.0473418)


   

Diaziridine, tetrafluoro-

Diaziridine, tetrafluoro-

CF4N2 (115.99976079999999)


   

Bisomer 2HEA

2-Propenoic acid, 2-hydroxyethyl ester, homopolymer

C5H8O3 (116.0473418)


   

Usaf cz-1

InChI=1\C5H8O3\c1-4(6)2-3-5(7)8\h2-3H2,1H3,(H,7,8

C5H8O3 (116.0473418)


D004791 - Enzyme Inhibitors Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate. Levulinic acid is a precursor for the synthesis of biofuels, such as ethyl levulinate.

   

2-Methyl-4,5-dihydro-3-furanthiol

2-Methyl-4,5-dihydro-3-furanthiol

C5H8OS (116.0295838)


Flavouring compound [Flavornet]

   

methyl (E)-3-hydroxybut-2-enoate

methyl (E)-3-hydroxybut-2-enoate

C5H8O3 (116.0473418)


   

Oxomalonate

Oxomalonate

C3O5-2 (115.974575)


   
   

Succinamate

Succinamate

C4H6NO3- (116.0347666)


A monocarboxylic acid anion resulting from the deprotonation of the carboxy group of succinamic acid; major species at pH 7.3.

   
   

N-acetylglycinate

N-acetylglycinate

C4H6NO3- (116.0347666)


An N-acylglycinate arising from deprotonation of the carboxy group of N-acetylglycine; major species at pH 7.3.

   
   
   

3-(Methylamino)pyruvate

3-(Methylamino)pyruvate

C4H6NO3- (116.0347666)


   
   

L-Aspartate 4-semialdehyde

L-Aspartate 4-semialdehyde

C4H6NO3- (116.0347666)


An alpha-amino-acid anion that is the conjugate base of L-aspartic 4-semialdehyde, arising from deprotonation of the carboxy group.

   

(2E,4S)-4,5-dihydroxypent-2-enal

(2E,4S)-4,5-dihydroxypent-2-enal

C5H8O3 (116.0473418)


   

4-Hydroxy-3-methylbut-2-enoic acid

4-Hydroxy-3-methylbut-2-enoic acid

C5H8O3 (116.0473418)


   
   
   

1,1,2,2-tetramethyldisilane

1,1,2,2-tetramethyldisilane

C4H12Si2 (116.0477512)


   
   

Tetramethyldisilane

Tetramethyldisilane

C4H12Si2 (116.0477512)


   

N-NITROSOMORPHOLINE

N-NITROSOMORPHOLINE

C4H8N2O2 (116.0585748)


D009676 - Noxae > D002273 - Carcinogens D009676 - Noxae > D009153 - Mutagens

   

5-oxopentanoic acid

5-oxopentanoic acid

C5H8O3 (116.0473418)


An oxopentanoic acid with the oxo group in the 5-position.

   

3-Ketovaleric acid

3-Oxopentanoic acid

C5H8O3 (116.0473418)


   

3-methylnitrosaminopropionaldehyde

3-(N-Nitrosomethylamino)propionaldehyde

C4H8N2O2 (116.0585748)


   

4-Oxopentanoic acid

4-Oxopentanoic acid

C5H8O3 (116.0473418)


An oxopentanoic acid with the oxo group in the 4-position.

   

Ethylpyruvate

ETHYL PYRUVATE

C5H8O3 (116.0473418)


Ethyl pyruvate is a simple derivative of the endogenous metabolite, pyruvic acid. Ethyl pyruvate is an anti-inflammatory agent[1].

   
   

succinate(2-)

succinate(2-)

C4H4O4 (116.01095839999999)


A dicarboxylic acid dianion resulting from the removal of a proton from both of the carboxy groups of succinic acid.

   

2-methylacetoacetic acid

2-methylacetoacetic acid

C5H8O3 (116.0473418)


   

Azodicarbonamide

Azodicarbonamide

C2H4N4O2 (116.0334244)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents

   

Acetoxyacetone

1-Acetoxyacetone

C5H8O3 (116.0473418)


   

Diacetylhydrazine

N-Acetylacetohydrazide

C4H8N2O2 (116.0585748)


   
   

2-methyl-4,5-dihydrofuran-3-thiol

2-methyl-4,5-dihydrofuran-3-thiol

C5H8OS (116.0295838)


   

N-Nitroso-3-hydroxypyrrolidine

N-Nitroso-3-hydroxypyrrolidine

C4H8N2O2 (116.0585748)


   

Dihydro-5-methyl-2(3H)-thiophenone

Dihydro-5-methyl-2(3H)-thiophenone

C5H8OS (116.0295838)


   

2-hydroxy-3-methyl-2-butenoic acid

2-hydroxy-3-methyl-2-butenoic acid

C5H8O3 (116.0473418)


An alpha,beta-unsaturated monocarboxylic acid that is 3-methylbut-2-enoic acid in which the hydrogen at position 2 has been replaced by a hydroxy group.

   

L-2-Amino-3-oxobutanoate

L-2-Amino-3-oxobutanoate

C4H6NO3 (116.0347666)


   

Guanidinoacetate

Guanidinoacetate

C3H6N3O2 (116.0459996)


A monocarboxylic acid anion that is the conjugate base of guanidinoacetic acid, obtained by deprotonation of the carboxy group.

   

methylmalonate(2-)

methylmalonate(2-)

C4H4O4 (116.01095839999999)


A C4-dicarboxylate resulting from the removal of a proton from both carboxylic acid groups of methylmalonic acid.

   

Ketovaleric acid

Ketovaleric acid

C5H8O3 (116.0473418)


   

(3r,4r)-3-hydroxy-4-methyloxolan-2-one

(3r,4r)-3-hydroxy-4-methyloxolan-2-one

C5H8O3 (116.0473418)