Exact Mass: 146.0552

Exact Mass Matches: 146.0552

Found 500 metabolites which its exact mass value is equals to given mass value 146.0552, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

L-Glutamine

(2S)-2,5-diamino-5-oxopentanoic acid

C5H10N2O3 (146.0691)


Glutamine (Gln), also known as L-glutamine is an alpha-amino acid. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). Amino acids are organic compounds that contain amino (–NH2) and carboxyl (–COOH) functional groups, along with a side chain (R group) specific to each amino acid. Structurally, glutamine is similar to the amino acid glutamic acid. However, instead of having a terminal carboxylic acid, it has an amide. Glutamine is one of 20 proteinogenic amino acids, i.e., the amino acids used in the biosynthesis of proteins. Glutamine is found in all organisms ranging from bacteria to plants to animals. It is classified as an aliphatic, polar amino acid. In humans glutamine is considered a non-essential amino acid. Enzymatically, glutamine is formed by replacing a side-chain hydroxyl of glutamic acid with an amine functional group. More specifically, glutamine is synthesized by the enzyme glutamine synthetase from glutamate and ammonia. The most relevant glutamine-producing tissue are skeletal muscles, accounting for about 90\\\\\\% of all glutamine synthesized. Glutamine is also released, in small amounts, by the lungs and brain. In human blood, glutamine is the most abundant free amino acid. Dietary sources of glutamine include protein-rich foods such as beef, chicken, fish, dairy products, eggs, beans, beets, cabbage, spinach, carrots, parsley, vegetable juices, wheat, papaya, Brussels sprouts, celery and kale. Glutamine is one of the few amino acids that can directly cross the blood–brain barrier. Glutamine is often used as a supplement in weightlifting, bodybuilding, endurance and other sports, as well as by those who suffer from muscular cramps or pain, particularly elderly people. In 2017, the U.S. Food and Drug Administration (FDA) approved L-glutamine oral powder, marketed as Endari, to reduce severe complications of sickle cell disease in people aged five years and older with the disorder. Subjects who were treated with L-glutamine oral powder experienced fewer hospital visits for pain treated with a parenterally administered narcotic or ketorolac. The main use of glutamine within the diet of either group is as a means of replenishing the bodys stores of amino acids that have been used during exercise or everyday activities. Studies which have looked into problems with excessive consumption of glutamine thus far have proved inconclusive. However, normal supplementation is healthy mainly because glutamine is supposed to be supplemented after prolonged periods of exercise (for example, a workout or exercise in which amino acids are required for use) and replenishes amino acid stores. This is one of the main reasons glutamine is recommended during fasting or for people who suffer from physical trauma, immune deficiencies, or cancer. There is a significant body of evidence that links glutamine-enriched diets with positive intestinal effects. These include maintenance of gut barrier function, aiding intestinal cell proliferation and differentiation, as well as generally reducing septic morbidity and the symptoms of Irritable Bowel Syndrome (IBS). The reason for such "cleansing" properties is thought to stem from the fact that the intestinal extraction rate of glutamine is higher than that for other amino acids, and is therefore thought to be the most viable option when attempting to alleviate conditions relating to the gastrointestinal tract. These conditions were discovered after comparing plasma concentration within the gut between glutamine-enriched and non glutamine-enriched diets. However, even though glutamine is thought to have "cleansing" properties and effects, it is unknown to what extent glutamine has clinical benefits, due to the varied concentrations of glutamine in varieties of food. It is also known that glutamine has positive effects in reducing healing time after operations. Hospital waiting times after abdominal s... L-glutamine, also known as L-2-aminoglutaramic acid or levoglutamide, is a member of the class of compounds known as L-alpha-amino acids. L-alpha-amino acids are alpha amino acids which have the L-configuration of the alpha-carbon atom. L-glutamine is soluble (in water) and a moderately acidic compound (based on its pKa). L-glutamine can be found in a number of food items such as acorn, yautia, ohelo berry, and oregon yampah, which makes L-glutamine a potential biomarker for the consumption of these food products. L-glutamine can be found primarily in most biofluids, including blood, sweat, breast milk, and cerebrospinal fluid (CSF), as well as throughout most human tissues. L-glutamine exists in all living species, ranging from bacteria to humans. In humans, L-glutamine is involved in several metabolic pathways, some of which include amino sugar metabolism, the oncogenic action of 2-hydroxyglutarate, mercaptopurine metabolism pathway, and transcription/Translation. L-glutamine is also involved in several metabolic disorders, some of which include the oncogenic action of d-2-hydroxyglutarate in hydroxygluaricaciduria, tay-sachs disease, xanthinuria type I, and adenosine deaminase deficiency. Moreover, L-glutamine is found to be associated with carbamoyl Phosphate Synthetase Deficiency, epilepsy, schizophrenia, and alzheimers disease. L-glutamine is a non-carcinogenic (not listed by IARC) potentially toxic compound. L-glutamine is a drug which is used for nutritional supplementation, also for treating dietary shortage or imbalance. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2].

   

Adipic acid

1,4-Butanedicarboxylic acid

C6H10O4 (146.0579)


Adipic acid is an important inudstrial dicarboxylic acid with about 2.5 billion kilograms produced per year. It is used mainly in the production of nylon. It occurs relatively rarely in nature. It has a tart taste and is also used as an additive and gelling agent in jello or gelatins. It is also used in some calcium carbonate antacids to make them tart. Adipic acid has also been incorporated into controlled-release formulation matrix tablets to obtain pH-independent release for both weakly basic and weakly acidic drugs. Adipic acid in the urine and in the blood is typically exogenous in origin and is a good biomarker of jello consumption. In fact, a condition known as adipic aciduria is actually an artifact of jello consumption (PMID: 1779643). However, certain disorders (such as diabetes and glutaric aciduria type I.) can lead to elevated levels of adipic acid snd other dicarboxcylic acids (such as suberic acid) in urine (PMID: 17520433; PMID: 6778884). Moreover, adipic acid is also found to be associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency, carnitine-acylcarnitine translocase deficiency, malonyl-Coa decarboxylase deficiency, and medium Chain acyl-CoA dehydrogenase deficiency, which are inborn errors of metabolism. Adipic acid is also microbial metabolite found in Escherichia. Constituent of beet juice, pork fat, guava fruit (Psidium guajava), papaya (Carica papaya) and raspberry (Rubus idaeus). Food acidulant Adipic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=124-04-9 (retrieved 2024-07-16) (CAS RN: 124-04-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Adipic acid is found to be associated with HMG-CoA lyase deficiency, carnitine-acylcarnitine translocase deficiency, malonyl-Coa decarboxylase deficiency, and medium Chain acyl-CoA dehydrogenase deficiency, which are inborn errors of metabolism.

   

(S)-2-Aceto-2-hydroxybutanoic acid

2-Aceto-2-hydroxybutyric acid

C6H10O4 (146.0579)


   

Mevaldate

4,6-dihydroxy-4-methyloxan-2-one

C6H10O4 (146.0579)


   

2-dehydropantoate

4-hydroxy-3,3-dimethyl-2-oxobutanoic acid

C6H10O4 (146.0579)


2-dehydropantoic acid, also known as ketopantoate, belongs to short-chain keto acids and derivatives class of compounds. Those are keto acids with an alkyl chain the contains less than 6 carbon atoms. 2-dehydropantoic acid is soluble (in water) and a weakly acidic compound (based on its pKa). 2-dehydropantoic acid can be found in a number of food items such as radish (variety), red algae, cherimoya, and avocado, which makes 2-dehydropantoic acid a potential biomarker for the consumption of these food products. 2-dehydropantoic acid exists in E.coli (prokaryote) and yeast (eukaryote).

   

AC1L978Q

2-hydroxy-3,3-dimethyl-4-oxo-butanoic acid

C6H10O4 (146.0579)


   

3-Hydroxy-3-methyl-2-oxopentanoic acid

3-hydroxy-3-methyl-2-oxo-pentanoic acid

C6H10O4 (146.0579)


A 3-hydroxylated derivative of 3-methyl-2-oxovaleric acid.

   

3-ureido-isobutyrate

3-((Aminocarbonyl)amino)-2-methylpropanoic acid

C5H10N2O3 (146.0691)


Ureidoisobutyric acid, also known as 3-ureidoisobutyrate or beta-uba, is a member of the class of compounds known as ureas. Ureas are compounds containing two amine groups joined by a carbonyl (C=O) functional group. Ureidoisobutyric acid is soluble (in water) and a weakly acidic compound (based on its pKa). Ureidoisobutyric acid can be found in a number of food items such as pili nut, breakfast cereal, bitter gourd, and scarlet bean, which makes ureidoisobutyric acid a potential biomarker for the consumption of these food products. Ureidoisobutyric acid can be found primarily in blood, cerebrospinal fluid (CSF), and urine. Ureidoisobutyric acid exists in all living organisms, ranging from bacteria to humans. In humans, ureidoisobutyric acid is involved in the pyrimidine metabolism. Ureidoisobutyric acid is also involved in few metabolic disorders, which include beta ureidopropionase deficiency, dihydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and UMP synthase deficiency (orotic aciduria). Moreover, ureidoisobutyric acid is found to be associated with beta-ureidopropionase deficiency.

   

4-Hydroxy-2-oxohexanoic acid

2-oxo-4-hydroxy-hexanoic acid

C6H10O4 (146.0579)


A hydroxy- and oxo- fatty acid comprising hexanoic acid substituted at C-2 and C-4 with oxo and hydroxy groups respectively.

   

THTA

2-Tetrahydrothiopheneacetic acid

C6H10O2S (146.0401)


   

Phthalazone

1(2H)-PHTHALAZINONE

C8H6N2O (146.048)


   

3-Hydroxy-5-oxohexanoate

3-Hydroxy-5-oxohexanoic acid

C6H10O4 (146.0579)


   

Isoglutamine

4,5-Diamino-5-oxopentanoic acid

C5H10N2O3 (146.0691)


   

D-Glutamine

(2R)-2-Amino-4-carbamoylbutanoic acid

C5H10N2O3 (146.0691)


D-Glutamine, also known as DGN or D glutamine, belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. Supplementation does not appear to be useful in adults or children with Crohns disease or inflammatory bowel disease, but clinical studies as of 2016 were underpowered. D-Glutamine is a drug. D-Glutamine exists in all living species, ranging from bacteria to humans. D-Glutamine is a potentially toxic compound. Adverse effects of glutamine have been described for people receiving home parenteral nutrition and those with liver-function abnormalities. Glutamine is the most abundant naturally occurring, nonessential amino acid in the human body, and one of the few amino acids that can directly cross the blood-brain barrier. Glutamine can exist in either of two enantiomeric forms, L-glutamine and D-glutamine. A non-essential amino acid present abundantly throughout the body and is involved in many metabolic processes. It is synthesized from glutamic acid and ammonia. It is the principal carrier of nitrogen in the body and is an important energy source for many cells. [HMDB] KEIO_ID G006 D-Glutamine is a cell-permeable D type stereoisomer of Glutamine. D-Glutamine is a cell-permeable D type stereoisomer of Glutamine.

   

(S)-2-Aceto-2-hydroxybutanoic acid

(2S)-2-Ethyl-2-hydroxy-3-oxobutanoic acid

C6H10O4 (146.0579)


(S)-2-Aceto-2-hydroxybutanoic acid is an intermediate in branched chain amino acid metabolism. It is converted from 2-oxobutanoate or 2-hydoxyethyl ThPP via acetolactate synthase. [HMDB] (S)-2-Aceto-2-hydroxybutanoic acid is an intermediate in branched chain amino acid metabolism. It is converted from 2-oxobutanoate or 2-hydoxyethyl ThPP via acetolactate synthase.

   

DL-Glutamine

DL-Glutamine

C5H10N2O3 (146.0691)


DL-Glutamine is used for biochemical research and drug synthesis.

   

(R)-3-Ureidoisobutyrate

(R)-3-Ureidoisobutyrate

C5H10N2O3 (146.0691)


   

FA 6:1;O2

(3R)-3-hydroxy-3-methyl-2-oxopentanoic acid

C6H10O4 (146.0579)


The (R)-enantiomer of 3-hydroxy-3-methyl-2-oxopentanoic acid.

   

Isosorbide

Isosorbide

C6H10O4 (146.0579)


C78274 - Agent Affecting Cardiovascular System > C29707 - Vasodilating Agent D002317 - Cardiovascular Agents > D045283 - Natriuretic Agents D045283 - Natriuretic Agents > D004232 - Diuretics

   

4-quinazolinol

InChI=1/C8H6N2O/c11-8-6-3-1-2-4-7(6)9-5-10-8/h1-5H,(H,9,10,11)

C8H6N2O (146.048)


1H-quinazolin-4-one is a member of quinazolines. 4-Hydroxyquinazoline is a natural product found in Hydrangea febrifuga, Streptomyces, and other organisms with data available. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2]. 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2].

   

2,2-Dimethylsuccinic acid

alpha,alpha-Dimethyl-succinic acid

C6H10O4 (146.0579)


2,2-dimethylsuccinic acid is an alpha,omega-dicarboxylic acid that is succinic acid substituted by two methyl groups at positions 2 and 2 respectively. It derives from a succinic acid. 2,2-Dimethylsuccinic acid, also known as 2,2-dimethylbutanedioate, belongs to the class of organic compounds known as methyl-branched fatty acids. These are fatty acids with an acyl chain that has a methyl branch. Usually, they are saturated and contain only one or more methyl group. However, branches other than methyl may be present. 2,2-Dimethylsuccinic acid is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. 2,2-Dimethylsuccinic acid has been identified in urine samples from children investigated for a possible inherited metabolic disease (PMID 2134344), and in children fed elemental or protein-hydrolysate formulas that use Octanylsuccinic acid-modified cornstarch as an emulsifying agent (PMID 1805153) [HMDB] 2,2-Dimethylsuccinic acid belongs to the class of organic compounds known as methyl-branched fatty acids.

   

2-Methylglutaric acid

alpha-Methylene glutarate, ion(2-)

C6H10O4 (146.0579)


2-Methylglutaric acid, also known as alpha-methylglutarate or 2-methylpentanedioate, belongs to the class of organic compounds known as methyl-branched fatty acids. These are fatty acids with an acyl chain that has a methyl branch. Usually, they are saturated and contain only one or more methyl group. However, branches other than methyl may be present. 2-Methylglutaric acid is also classified as an alpha,omega-dicarboxylic acid. It is glutaric acid substituted at position 2 by a methyl group. 2-Methylglutaric acid arises from the microbial metabolism of the isoprenoid alkaloid pristane (PMID: 4327007; PMID: 20143352). 2-Methylglutaric acid is an organic acid normally found in human urine, in healthy adults and children. 2-Methylglutaric acid is a metabolite of succinic acid, a citric acid cycle intermediate. (PMID: 2925825, 8087979, 16379391, 1688138) [HMDB] 2-Methylpentanedioic acid is a metabolite of succinic acid, a citric acid cycle intermediate.

   

Methylglutaric acid

3-Methylpentanedioic acid

C6H10O4 (146.0579)


Methylglutaric acid is a leucine metabolite. A large amount of methylglutaric acid is identified in urine of patients with deficiency of 3-methylglutaconyl coenzyme A hydratase (PMID 6181239). Methylglutaric acid is also found to be associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency, another inborn error of metabolism. Methylglutaric acid is a leucine metabolite. A large amount of methylglutaric acid is identified in urine of patients with deficiency of 3-methylglutaconyl coenzyme A hydratase (PMID 6181239). [HMDB] 3-Methylglutaric acid, a leucine metabolite, is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies, 3-hydroxy-3-methylglutaryl CoA lyase (HMGCL) and 3-methylglutaconyl CoA hydratase (AUH)[1][2].

   

Dimethyl succinate

Butanedioic acid, 1,4-dimethyl ester

C6H10O4 (146.0579)


Dimethyl succinate, also known as DBE-4 or fema 2396, belongs to the class of organic compounds known as fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR, where R=fatty aliphatic tail or organyl group and R=methyl group. Present in roasted filberts. Flavouring ingredient. Dimethyl succinate is found in nuts.

   

Benzylideneacetone

3-BUTEN,2-one,4-phenyl (trans) benzalacetone

C10H10O (146.0732)


Benzylideneacetone is a flavouring ingredient. Benzylideneacetone is present in hydrolysed soy protei Flavouring ingredient. Present in hydrolysed soy protein Benzylideneacetone is an endogenous metabolite. Benzylideneacetone is an endogenous metabolite. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1]. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1]. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1].

   

Ureidoisobutyric acid

(2S)-3-[(C-Hydroxycarbonimidoyl)amino]-2-methylpropanoate

C5H10N2O3 (146.0691)


Ureidoisobutyric acid, also known as 3-ureidoisobutyrate or beta-UBA, belongs to the class of organic compounds known as ureas. Ureas are compounds containing two amine groups joined by a carbonyl (C=O) functional group. Ureidoisobutyric acid is an extremely weak basic (essentially neutral) compound (based on its pKa). Ureidoisobutyric acid exists in all living organisms, ranging from bacteria to humans. Within humans, ureidoisobutyric acid participates in a number of enzymatic reactions. In particular, ureidoisobutyric acid can be biosynthesized from dihydrothymine through its interaction with the enzyme dihydropyrimidinase. Outside of the human body, ureidoisobutyric acid has been detected, but not quantified in, several different foods, such as bread, squashberries, black elderberries, black crowberries, and climbing beans. This could make ureidoisobutyric acid a potential biomarker for the consumption of these foods. Ureidoisobutyric acid is increased in the urine of patients with beta-ureidopropionase (EC 3.5.1.6) deficiency (PMID: 12271438), a genetic disorder. Ureidoisobutyric acid can be used to predict a patients individual phenotypes of enzyme deficiencies in pyrimidine metabolism when associated with a risk for severe toxicity against the antineoplastic agent 5-fluorouracil (PMID: 12798197).

   

2-Phenyl-2-butenal

2-Phenylacetaldehyde, alpha -ethylidene

C10H10O (146.0732)


(E)-2-Phenyl-2-butenal is found in tea. (E)-2-Phenyl-2-butenal is a flavouring ingredient. (E)-2-Phenyl-2-butenal is a odorous component of black tea Glutamic acid (Glu), also referred to as glutamate (the anion), is one of the 20 proteinogenic amino acids. It is not among the essential amino acids. Glutamate is a key molecule in cellular metabolism. In humans, dietary proteins are broken down by digestion into amino acids, which serves as metabolic fuel or other functional roles in the body. Glutamate is the most abundant fast excitatory neurotransmitter in the mammalian nervous system. At chemical synapses, glutamate is stored in vesicles. Nerve impulses trigger release of glutamate from the pre-synaptic cell. In the opposing post-synaptic cell, glutamate receptors, such as the NMDA receptor, bind glutamate and are activated. Because of its role in synaptic plasticity, it is believed that glutamic acid is involved in cognitive functions like learning and memory in the brain. Glutamate transporters are found in neuronal and glial membranes. They rapidly remove glutamate from the extracellular space. In brain injury or disease, they can work in reverse and excess glutamate can accumulate outside cells. This process causes calcium ions to enter cells via NMDA receptor channels, leading to neuronal damage and eventual cell death, and is called excitotoxicity. The mechanisms of cell death include: * Damage to mitochondria from excessively high intracellular Ca2+. * Glu/Ca2+-mediated promotion of transcription factors for pro-apoptotic genes, or downregulation of transcription factors for anti-apoptotic genes. Excitotoxicity due to glutamate occurs as part of the ischemic cascade and is associated with stroke and diseases like amyotrophic lateral sclerosis, lathyrism, and Alzheimers disease. glutamic acid has been implicated in epileptic seizures. Microinjection of glutamic acid into neurons produces spontaneous depolarization around one second apart, and this firing pattern is similar to what is known as paroxysmal depolarizing shift in epileptic attacks. This change in the resting membrane potential at seizure foci could cause spontaneous opening of voltage activated calcium channels, leading to glutamic acid release and further depolarization. (http://en.wikipedia.org/wiki/Glutamic_acid); In addition to being one of the building blocks in protein synthesis, it is the most widespread neurotransmitter in brain function, as an excitatory neurotransmitter and as a precursor for the synthesis of GABA in GABAergic neurons. It is used as a food additive .

   

4-Phenyl-2-butenal

(2E)-4-phenylbut-2-enal

C10H10O (146.0732)


4-Phenyl-2-butenal is found in mushrooms. 4-Phenyl-2-butenal is a odorous component of Phallus impudicus (common stinkhorn

   

4-(1-Methylethenyl)benzaldehyde

4-(1-Methylethenyl)benzaldehyde

C10H10O (146.0732)


4-(1-Methylethenyl)benzaldehyde is found in herbs and spices. 4-(1-Methylethenyl)benzaldehyde is a constituent of Roman chamomile oil (Anthemis nobilis) Constituent of Roman chamomile oil (Anthemis nobilis). 4-(1-Methylethenyl)benzaldehyde is found in roman camomile and herbs and spices.

   

Monomethyl glutaric acid

4-Carboxybutanoic acid methyl ester

C6H10O4 (146.0579)


Monomethyl glutaric acid, also known as 4-(methoxycarbonyl)butyrate or 2-methyleneglutarate, belongs to the class of organic compounds known as fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR, where R=fatty aliphatic tail or organyl group and R=methyl group. Metabolism of dibasic esters(DBEs) by nasal respiratory and olfactory mucosae in vitro demonstrated that hydrolysis of DBEs yields mainly the monomethyl esters (monomethyl adipate, monomethyl 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite. 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite.

   

4-Ethoxy-4-oxobutanoic acid

Succinic acid monoethyl ester

C6H10O4 (146.0579)


4-Ethoxy-4-oxobutanoic acid belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

   

Alanylglycine

{[(2S)-2-ammoniopropanoyl]amino}acetate

C5H10N2O3 (146.0691)


Alanylglycine is a dipeptide composed of alanine and glycine that is found in human urine. It is a breakdown product from endogenous and exogenous proteins. This peptide is generated by dipeptidyl-dipeptidase (or tetrapeptide dipeptidase) which leads to the release of dipeptides from a tetrapeptide (more specifically: Ala-GlyAla-Gly). The enzyme acts more slowly on Ala-AlaAla-Ala and Gly-GlyGly-Gly.

   

Solerol

dihydro-5-(1-Hydroxyethyl)-2(3H)-furanone

C6H10O4 (146.0579)


Solerol, also known as 4,5-dihydroxyhexanoic acid lactone, is a volatile component originally identified in extracts of grape wines and numerous fruits, with aroma being among the most important factors in determining wine character and quality (PMID: 11052736 ). Solerol (4,5-dihydroxyhexanoic acid lactone) also appears to be a marker for Succinic semialdehyde dehydrogenase (SSADH) deficiency and probably arises from the reaction of succinic semialdehyde with an intermediate in the pyruvate dehydrogenase pathway (PMID: 3126356 ). SSADH is a disorder that arises from a defect in gamma-aminobutyric acid catabolism, resulting in the accumulation of gamma-hydroxybutyric acid (GHB), 2,4-dihydroxybutyric acid, adipic acid as well as elevated levels of 4,5-dihydroxyhexanoic acid, and 4,5-dihydroxyhexanoic acid lactone and causing neurological and cognitive disorders of varying severity (PMID: 3126356 ). Children with SSADH deficiency usually manifest with developmental delay, behavioral symptoms, language dysfunction, seizures, hypotonia, extrapyramidal symptoms, and ataxia (PMID: 32055132). Solerol is a volatile component identified in extracts of grape wines and numerous fruits, with aroma being among the most important factors in determining wine character and quality. (PMID: 11052736). Solerol (4,5-dihydroxyhexanoic acid lactone) also appears to be a marker for Succinic semialdehyde dehydrogenase (SSADH) deficiency and probably arises from the reaction of succinic semialdehyde with an intermediate in the pyruvate dehydrogenase pathway (PMID: 3126356). SSADH is a defect in gamma-aminobutyric acid catabolism, resulting in the accumulation of gamma-hydroxybutyric acid (GHB) and causing neurological and cognitive disorders of varying severity. [HMDB]

   

3-(4-Methylphenyl)-2-propenal

(2E)-3-(4-Methylphenyl)-2-propenal

C10H10O (146.0732)


3-(4-Methylphenyl)-2-propenal is a flavouring ingredien Flavouring ingredient

   

2-Methyl-3-phenyl-2-propenal

(2Z)-2-methyl-3-phenylprop-2-enal

C10H10O (146.0732)


2-Methyl-3-phenyl-2-propenal is found in herbs and spices. 2-Methyl-3-phenyl-2-propenal is present in peppermint oil (Mentha piperita). 2-Methyl-3-phenyl-2-propenal is a flavour ingredien Present in peppermint oil (Mentha piperita). Flavour ingredient. 2-Methyl-3-phenyl-2-propenal is found in peppermint and herbs and spices.

   

2,3-Dimethylbenzofuran

2,3-dimethyl-1-benzofuran

C10H10O (146.0732)


Present in coffee and roasted onion. Flavorant. 2,3-Dimethylbenzofuran is found in onion-family vegetables and coffee and coffee products. 2,3-Dimethylbenzofuran is found in coffee and coffee products. 2,3-Dimethylbenzofuran is present in coffee and roasted onion. Flavorant.

   

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

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

C6H10O2S (146.0401)


Dihydro-2-methoxy-2-methyl-3(2H)-thiophenone is a component of meat aroma model systems. Component of meat aroma model systems

   

Benzofuran, 4,7-dimethyl-

4,7-dimethyl-1-benzofuran

C10H10O (146.0732)


Benzofuran, 4,7-dimethyl- belongs to the family of Benzofurans. These are organic compounds containing a benzene ring fused to a furan

   

2-methyl-1,3-thiazolidine-2-carboxamide

2-methyl-1,3-thiazolidine-2-carboximidic acid

C5H10N2OS (146.0514)


2-methyl-1,3-thiazolidine-2-carboxamide is classified as an alpha amino acid or an Alpha amino acid derivative. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. 2-methyl-1,3-thiazolidine-2-carboxamide is considered to be soluble (in water) and relatively neutral

   

1,2,4-Benzotriazin-3-amine

3-Amino-1,2,4-benzotriazine

C7H6N4 (146.0592)


   

1,8-Naphthyridin-2(1H)-one

1,2-dihydro-1,8-naphthyridin-2-one

C8H6N2O (146.048)


   

Purpald

4-amino-5-hydrazinylidene-4,5-dihydro-1H-1,2,4-triazole-3-thiol

C2H6N6S (146.0375)


   

2-Ethylbutanedioic acid

2-Ethylbutanedioic acid

C6H10O4 (146.0579)


   

2-Hydroxyquinoxaline

1,2-dihydroquinoxalin-2-one

C8H6N2O (146.048)


   

2,3-Dimethylsuccinic acid

DL-2,3-dimethylsuccinic acid

C6H10O4 (146.0579)


   

(5S)-5,6-Dihydroxy-2-oxohexanal

(5S)-5,6-Dihydroxy-2-oxohexanal

C6H10O4 (146.0579)


   

4-Hydroxyquinazoline

4-Hydroxyquinazoline

C8H6N2O (146.048)


   

Ethylidene diacetate

1-(Acetyloxy)ethyl acetic acid

C6H10O4 (146.0579)


D001697 - Biomedical and Dental Materials > D003764 - Dental Materials

   

Acetone lactate

2-oxopropyl 2-hydroxypropanoate

C6H10O4 (146.0579)


   

1-Tetralone

1,2,3,4-tetrahydronaphthalen-1-one

C10H10O (146.0732)


   

Conduritol B

Conduritol b, (1R-(1alpha,2alpha,3beta,4alpha))-isomer

C6H10O4 (146.0579)


D007004 - Hypoglycemic Agents > D065089 - Glycoside Hydrolase Inhibitors D004791 - Enzyme Inhibitors

   

Cyclic Urea

5,6-Dihydroxyhexahydro-2H-1,3-diazepine-2-one

C5H10N2O3 (146.0691)


   

Diallyl sulfone

3-(prop-2-ene-1-sulfonyl)prop-1-ene

C6H10O2S (146.0401)


   

Dianhydrodulcitol

1,2-bis(oxiran-2-yl)ethane-1,2-diol

C6H10O4 (146.0579)


   

Glucal

2-(hydroxymethyl)-3,4-dihydro-2H-pyran-3,4-diol

C6H10O4 (146.0579)


   

Glycyl-D-Alanine

2-[(2-Amino-1-hydroxyethylidene)amino]propanoate

C5H10N2O3 (146.0691)


   

Glycylsarcosine

2-(2-amino-N-methylacetamido)acetic acid

C5H10N2O3 (146.0691)


   

isosorbide

hexahydrofuro[3,2-b]furan-3,6-diol

C6H10O4 (146.0579)


   

3-(Hydroxymethyl)-5-oxopentanoic acid

3-(Hydroxymethyl)-5-oxopentanoic acid

C6H10O4 (146.0579)


   

D-Alanyl glycine

2-{[(2R)-2-amino-1-hydroxypropylidene]amino}acetic acid

C5H10N2O3 (146.0691)


D-alanyl glycine, also known as ag, is a member of the class of compounds known as dipeptides. Dipeptides are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. D-alanyl glycine is slightly soluble (in water) and a weakly acidic compound (based on its pKa). D-alanyl glycine can be found in rice, which makes D-alanyl glycine a potential biomarker for the consumption of this food product.

   

GLUTAMINE

l-glutamine-13c5, 15n2, 99 atom \\% 13c, 9

C5H10N2O3 (146.0691)


A - Alimentary tract and metabolism > A16 - Other alimentary tract and metabolism products > A16A - Other alimentary tract and metabolism products > A16AA - Amino acids and derivatives COVID info from COVID-19 Disease Map, PDB, Protein Data Bank, clinicaltrial, clinicaltrials, clinical trial, clinical trials Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2].

   

Conduritol B

Conduritol B

C6H10O4 (146.0579)


D007004 - Hypoglycemic Agents > D065089 - Glycoside Hydrolase Inhibitors D004791 - Enzyme Inhibitors

   

(E,Z)-Matricarianol

(E,Z)-Matricarianol

C10H10O (146.0732)


   

methyl 5-hydroxy-4-oxopentanoate

methyl 5-hydroxy-4-oxopentanoate

C6H10O4 (146.0579)


   

Succinic acid monoethyl ester

Succinic acid monoethyl ester

C6H10O4 (146.0579)


   

Methyl beta,gamma-dihydroxy-alpha-methylene butylate

Methyl beta,gamma-dihydroxy-alpha-methylene butylate

C6H10O4 (146.0579)


   

4,7-Dimethylbenzofuran

4,7-Dimethylbenzofuran

C10H10O (146.0732)


   

4-Hydroxyquinazoline

4-Hydroxyquinazoline

C8H6N2O (146.048)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2]. 4(3H)-Quinazolinone is a building block in chemical synthesis. Biologically active nitrogen heterocyclic compounds. Possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anti-HIV, anticancerous and analgesic activities[1][2].

   

5-Phenyl-1H-tetrazole

5-Phenyl-1H-tetrazole

C7H6N4 (146.0592)


CONFIDENCE standard compound; INTERNAL_ID 772; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3191; ORIGINAL_PRECURSOR_SCAN_NO 3190 CONFIDENCE standard compound; INTERNAL_ID 772; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3200; ORIGINAL_PRECURSOR_SCAN_NO 3199 CONFIDENCE standard compound; INTERNAL_ID 772; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3211; ORIGINAL_PRECURSOR_SCAN_NO 3210 CONFIDENCE standard compound; INTERNAL_ID 772; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3190; ORIGINAL_PRECURSOR_SCAN_NO 3189 CONFIDENCE standard compound; INTERNAL_ID 772; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3213; ORIGINAL_PRECURSOR_SCAN_NO 3212 CONFIDENCE standard compound; INTERNAL_ID 772; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3230; ORIGINAL_PRECURSOR_SCAN_NO 3229

   

Dimethyl-butanedioic acid

2,3-Dimethylsuccinic acid

C6H10O4 (146.0579)


   

hept-4-enoyl chloride

hept-4-enoyl chloride

C7H11ClO (146.0498)


   

1-TETRALONE

3,4-Dihydronaphthalen-1(2H)-one

C10H10O (146.0732)


   

5-Oxy-2-oxymethyl-4-pyron

5-Oxy-2-oxymethyl-4-pyron

C6H10O4 (146.0579)


   

Cyclohexanecarbonyl chloride

Cyclohexanecarbonyl chloride

C7H11ClO (146.0498)


   

Isomannide

Isomannide

C6H10O4 (146.0579)


   

deca-5,7,9-triynol

deca-5,7,9-triynol

C10H10O (146.0732)


   

3,4-Dihydroxy-2-methylenebutanoic acid methyl ester

3,4-Dihydroxy-2-methylenebutanoic acid methyl ester

C6H10O4 (146.0579)


   

6-Methyl-1-indanone

6-Methyl-1-indanone

C10H10O (146.0732)


   

5-METHYL-1-INDANONE

5-METHYL-1-INDANONE

C10H10O (146.0732)


   

(E)-5-Hydroxy-3-methoxy-2-pentenoec acid

(E)-5-Hydroxy-3-methoxy-2-pentenoec acid

C6H10O4 (146.0579)


   

(3aR,6R,6aR)-hexahydrofuro[3,2-b]furan-2,6-diol|3,6-anhydro-2-deoxy-D-arabino-hexofuranose|3,6-anhydro-2-deoxy-D-arabinohexofuranose|3,6-anhydro-2-deoxy-D-glucose

(3aR,6R,6aR)-hexahydrofuro[3,2-b]furan-2,6-diol|3,6-anhydro-2-deoxy-D-arabino-hexofuranose|3,6-anhydro-2-deoxy-D-arabinohexofuranose|3,6-anhydro-2-deoxy-D-glucose

C6H10O4 (146.0579)


   

b-Tetralone

b-Tetralone

C10H10O (146.0732)


   

3,4-Dimethyl-2-pentenoylchloride

3,4-Dimethyl-2-pentenoylchloride

C7H11ClO (146.0498)


   

5-methylsulfanyl-pentane-2,3-dione

5-methylsulfanyl-pentane-2,3-dione

C6H10O2S (146.0401)


   

2,3-dihydro-1H-indene-4-carbaldehyde

2,3-dihydro-1H-indene-4-carbaldehyde

C10H10O (146.0732)


   

3-Methyl-1-indanone

3-Methyl-1-indanone

C10H10O (146.0732)


   

5-Methoxy-1H-indene

5-Methoxy-1H-indene

C10H10O (146.0732)


   

3,6-Dideoxy-D-erythro-hexos-4-ulose

3,6-Dideoxy-D-erythro-hexos-4-ulose

C6H10O4 (146.0579)


   

2-(furan-2-yl)pyrazine

2-(furan-2-yl)pyrazine

C8H6N2O (146.048)


   
   

5,6-Dimethylbenzofuran

5,6-Dimethylbenzofuran

C10H10O (146.0732)


   

4-Methyl-1-indanone

4-Methyl-1-indanone

C10H10O (146.0732)


   

4,5-dihydroxyhex-2-enoic acid

4,5-dihydroxyhex-2-enoic acid

C6H10O4 (146.0579)


   

4,5-Dimethylbenzofuran

4,5-Dimethylbenzofuran

C10H10O (146.0732)


   

1H-Indazole-3-Carbaldehyde

1H-Indazole-3-Carbaldehyde

C8H6N2O (146.048)


   

4-methoxy-3-methyl-4-oxobutanoic acid

4-methoxy-3-methyl-4-oxobutanoic acid

C6H10O4 (146.0579)


   

5-Hydroxy-4-oxohexanoic acid

5-Hydroxy-4-oxohexanoic acid

C6H10O4 (146.0579)


   

Gloiosiphone B

Gloiosiphone B

C6H10O4 (146.0579)


   

methyl 2-hydroxy-4-oxopentanoate

methyl 2-hydroxy-4-oxopentanoate

C6H10O4 (146.0579)


   

5,7-Dimethylbenzofuran

5,7-Dimethylbenzofuran

C10H10O (146.0732)


   

Indan-5-carbaldehyde

Indan-5-carbaldehyde

C10H10O (146.0732)


   

SCHEMBL17866808

SCHEMBL17866808

C6H10O4 (146.0579)


   

4-Ureido-butyric acid

4-Ureido-butyric acid

C5H10N2O3 (146.0691)


   

(Ra)-deca-4,5-diene-7,9-diyn-1-ol|Deca-4,5-dien-7,9-diin-1-ol

(Ra)-deca-4,5-diene-7,9-diyn-1-ol|Deca-4,5-dien-7,9-diin-1-ol

C10H10O (146.0732)


   

Glycyl-dl-alanine

Glycyl-dl-alanine

C5H10N2O3 (146.0691)


   

2-(acetyloxy)-2-methylpropanoic acid

2-(acetyloxy)-2-methylpropanoic acid

C6H10O4 (146.0579)


   

3-acetoxybutyric acid

3-acetoxybutyric acid

C6H10O4 (146.0579)


   

Allophanic acid propyl ester

Allophanic acid propyl ester

C5H10N2O3 (146.0691)


   

4,6,8-decatriyn-1-ol|Deca-4,6,8-triin-1-ol|deca-4,6,8-triyn-1-ol|deca-4,6,8-triynol|Decatriin-(2.4.6)-ol-(10)

4,6,8-decatriyn-1-ol|Deca-4,6,8-triin-1-ol|deca-4,6,8-triyn-1-ol|deca-4,6,8-triynol|Decatriin-(2.4.6)-ol-(10)

C10H10O (146.0732)


   

threo-6-amino-5-hydroxy-5-methyl-1,3-oxazinan-4-one

threo-6-amino-5-hydroxy-5-methyl-1,3-oxazinan-4-one

C5H10N2O3 (146.0691)


   

(+)-Deca-3,4-dien-6,8-diin-1-ol|(+-)-Deca-3,4-dien-6,8-diin-1-ol|(+/-)-9-methyl-marasin|(-)-Deca-3,4-dien-6,8-diin-1-ol|(Sa)-deca-3,4-diene-6,8-diyn-1-ol|deca-3,4-diene-6,8-diyn-1-ol|R-(-)-9-Methylmarasin

(+)-Deca-3,4-dien-6,8-diin-1-ol|(+-)-Deca-3,4-dien-6,8-diin-1-ol|(+/-)-9-methyl-marasin|(-)-Deca-3,4-dien-6,8-diin-1-ol|(Sa)-deca-3,4-diene-6,8-diyn-1-ol|deca-3,4-diene-6,8-diyn-1-ol|R-(-)-9-Methylmarasin

C10H10O (146.0732)


   

4-Phenyl-3-butyn-1-ol

4-Phenyl-3-butyn-1-ol

C10H10O (146.0732)


   

2-hydroxyethyl prop-2-en-1-yl carbonate

2-hydroxyethyl prop-2-en-1-yl carbonate

C6H10O4 (146.0579)


   

SCHEMBL542282

SCHEMBL542282

C5H10N2O3 (146.0691)


   

2,6,8-Decatrien-4-ynal,9CI,8CI-(2E,6E,8E)-form|all-trans-Decatrien-(2.6.8)-in-(4)-al-(1)|deca-2t,6t,8t-trien-4-ynal|Decatrien-(2,6,8)-in-(4)-al-(1)

2,6,8-Decatrien-4-ynal,9CI,8CI-(2E,6E,8E)-form|all-trans-Decatrien-(2.6.8)-in-(4)-al-(1)|deca-2t,6t,8t-trien-4-ynal|Decatrien-(2,6,8)-in-(4)-al-(1)

C10H10O (146.0732)


   

(E)-dec-2-ene-4,6-diynal|2-Decene-4,6-diynal, 9CI-(E)-form|Dec-2t-en-4,6-diinal|dec-2t-ene-4,6-diynal|trans-8,9-dihydro-matricarianal

(E)-dec-2-ene-4,6-diynal|2-Decene-4,6-diynal, 9CI-(E)-form|Dec-2t-en-4,6-diinal|dec-2t-ene-4,6-diynal|trans-8,9-dihydro-matricarianal

C10H10O (146.0732)


   

L-Glutamine

l-glutamine-13c5, 15n2, 99 atom \\% 13c, 9

C5H10N2O3 (146.0691)


An alpha-amino acid that consists of butyric acid bearing an amino substituent at position 2 and a carbamoyl substituent at position 4. Glutamine (symbol Gln or Q)[4] is an α-amino acid that is used in the biosynthesis of proteins. Its side chain is similar to that of glutamic acid, except the carboxylic acid group is replaced by an amide. It is classified as a charge-neutral, polar amino acid. It is non-essential and conditionally essential in humans, meaning the body can usually synthesize sufficient amounts of it, but in some instances of stress, the body's demand for glutamine increases, and glutamine must be obtained from the diet.[5][6] It is encoded by the codons CAA and CAG. It is named after glutamic acid, which in turn is named after its discovery in cereal proteins, gluten.[7] In human blood, glutamine is the most abundant free amino acid.[8] The dietary sources of glutamine include especially the protein-rich foods like beef, chicken, fish, dairy products, eggs, vegetables like beans, beets, cabbage, spinach, carrots, parsley, vegetable juices and also in wheat, papaya, Brussels sprouts, celery, kale and fermented foods like miso. The one-letter symbol Q for glutamine was assigned in alphabetical sequence to N for asparagine, being larger by merely one methylene –CH2– group. Note that P was used for proline, and O was avoided due to similarity with D. The mnemonic Qlutamine was also proposed.[7] A - Alimentary tract and metabolism > A16 - Other alimentary tract and metabolism products > A16A - Other alimentary tract and metabolism products > A16AA - Amino acids and derivatives COVID info from COVID-19 Disease Map, PDB, Protein Data Bank, clinicaltrial, clinicaltrials, clinical trial, clinical trials Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 13 Acquisition and generation of the data is financially supported by the Max-Planck-Society L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2].

   

2-Methylglutaric acid

(2R)-2-Methylpentanedioic acid

C6H10O4 (146.0579)


An alpha,omega-dicarboxylic acid that is glutaric acid substituted at position 2 by a methyl group. Acquisition and generation of the data is financially supported in part by CREST/JST. 2-Methylpentanedioic acid is a metabolite of succinic acid, a citric acid cycle intermediate.

   

L-Glutamine

L-Glutamine

C5H10N2O3 (146.0691)


An optically active form of glutamine having L-configuration. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2]. L-Glutamine (L-Glutamic acid 5-amide) is a non-essential amino acid present abundantly throughout the body and involved in many metabolic processes. L-Glutamine provides a source of carbons for oxidation in some cells[1][2].

   

Methylglutaric acid

3-METHYLGLUTARIC ACID

C6H10O4 (146.0579)


An alpha,omega-dicarboxylic acid that is glutaric acid substituted at position 3 by a methyl group. 3-Methylglutaric acid, a leucine metabolite, is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies, 3-hydroxy-3-methylglutaryl CoA lyase (HMGCL) and 3-methylglutaconyl CoA hydratase (AUH)[1][2].

   

Methyl Hydrogen Glutarate

Methyl Hydrogen Glutarate

C6H10O4 (146.0579)


5-Methoxy-5-oxopentanoic acid is an endogenous metabolite. 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite.

   

Benzylidenacetone

Benzylidenacetone

C10H10O (146.0732)


CONFIDENCE standard compound; INTERNAL_ID 8174

   

Phenyltetrazole

5-Phenyl-1H-tetrazole

C7H6N4 (146.0592)


CONFIDENCE standard compound; INTERNAL_ID 8368

   

adipic acid

hexanedioic acid

C6H10O4 (146.0579)


An alpha,omega-dicarboxylic acid that is the 1,4-dicarboxy derivative of butane. CONFIDENCE standard compound; INTERNAL_ID 664; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2444; ORIGINAL_PRECURSOR_SCAN_NO 2443 CONFIDENCE standard compound; INTERNAL_ID 664; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2464; ORIGINAL_PRECURSOR_SCAN_NO 2463 CONFIDENCE standard compound; INTERNAL_ID 664; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2427; ORIGINAL_PRECURSOR_SCAN_NO 2425 CONFIDENCE standard compound; INTERNAL_ID 664; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2445; ORIGINAL_PRECURSOR_SCAN_NO 2444 CONFIDENCE standard compound; INTERNAL_ID 664; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2437; ORIGINAL_PRECURSOR_SCAN_NO 2436 Adipic acid is found to be associated with HMG-CoA lyase deficiency, carnitine-acylcarnitine translocase deficiency, malonyl-Coa decarboxylase deficiency, and medium Chain acyl-CoA dehydrogenase deficiency, which are inborn errors of metabolism.

   

Monomethyl glutaric acid

Methyl Hydrogen Glutarate

C6H10O4 (146.0579)


A dicarboxylic acid monoester that the monomethyl ester of glutaric acid. 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite. 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite.

   

2,2-Dimethylsuccinic acid

2,2-Dimethylsuccinic acid

C6H10O4 (146.0579)


2,2-Dimethylsuccinic acid belongs to the class of organic compounds known as methyl-branched fatty acids.

   

D-Glutamine

D-Glutamine

C5H10N2O3 (146.0691)


The D-enantiomer of glutamine. D-Glutamine is a cell-permeable D type stereoisomer of Glutamine. D-Glutamine is a cell-permeable D type stereoisomer of Glutamine.

   

3-Methylglutaric acid

3-METHYLGLUTARIC ACID

C6H10O4 (146.0579)


3-Methylglutaric acid, a leucine metabolite, is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies, 3-hydroxy-3-methylglutaryl CoA lyase (HMGCL) and 3-methylglutaconyl CoA hydratase (AUH)[1][2]. 3-Methylglutaric acid, a leucine metabolite, is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies, 3-hydroxy-3-methylglutaryl CoA lyase (HMGCL) and 3-methylglutaconyl CoA hydratase (AUH)[1][2].

   

delta-Hydroxylysine

delta-Hydroxylysine

C5H10N2O3 (146.0691)


   

Glutamine (L)

Glutamine (L)

C5H10N2O3 (146.0691)


   

Glutamine (D)

Glutamine (D)

C5H10N2O3 (146.0691)


   

1,3-Diaminopropane dihydrochloride

1,3-Diaminopropane dihydrochloride

C3H12Cl2N2 (146.0377)


   

4-PHENYL-3-BUTEN-2-ONE

4-PHENYL-3-BUTEN-2-ONE

C10H10O (146.0732)


CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 6 INTERNAL_ID 6; CONFIDENCE Reference Standard (Level 1)

   

Asparagine methyl ester

Asparagine methyl ester

C5H10N2O3 (146.0691)


   

Benzalacetone

Methyl trans-styryl ketone

C10H10O (146.0732)


CONFIDENCE standard compound; INTERNAL_ID 1224; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10297; ORIGINAL_PRECURSOR_SCAN_NO 10295 CONFIDENCE standard compound; INTERNAL_ID 1224; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10312; ORIGINAL_PRECURSOR_SCAN_NO 10307 CONFIDENCE standard compound; INTERNAL_ID 1224; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10338; ORIGINAL_PRECURSOR_SCAN_NO 10333 CONFIDENCE standard compound; INTERNAL_ID 1224; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10359; ORIGINAL_PRECURSOR_SCAN_NO 10356 CONFIDENCE standard compound; INTERNAL_ID 1224; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10386; ORIGINAL_PRECURSOR_SCAN_NO 10382 CONFIDENCE standard compound; INTERNAL_ID 1224; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 10360; ORIGINAL_PRECURSOR_SCAN_NO 10356 Benzylideneacetone is an endogenous metabolite. Benzylideneacetone is an endogenous metabolite. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1]. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1]. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1].

   

3-METHYGLUTARIC ACID

3-METHYGLUTARIC ACID

C6H10O4 (146.0579)


   

Glutamine; LC-tDDA; CE10

Glutamine; LC-tDDA; CE10

C5H10N2O3 (146.0691)


   

Glutamine; LC-tDDA; CE20

Glutamine; LC-tDDA; CE20

C5H10N2O3 (146.0691)


   

Glutamine; LC-tDDA; CE30

Glutamine; LC-tDDA; CE30

C5H10N2O3 (146.0691)


   

Glutamine; LC-tDDA; CE40

Glutamine; LC-tDDA; CE40

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; LC-tDDA; CE10

3-Ureidoisobutyric acid; LC-tDDA; CE10

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; LC-tDDA; CE20

3-Ureidoisobutyric acid; LC-tDDA; CE20

C5H10N2O3 (146.0691)


   

Glutamine; AIF; CE0; CorrDec

Glutamine; AIF; CE0; CorrDec

C5H10N2O3 (146.0691)


   

Glutamine; AIF; CE10; CorrDec

Glutamine; AIF; CE10; CorrDec

C5H10N2O3 (146.0691)


   

Glutamine; AIF; CE30; CorrDec

Glutamine; AIF; CE30; CorrDec

C5H10N2O3 (146.0691)


   

Glutamine; AIF; CE0; MS2Dec

Glutamine; AIF; CE0; MS2Dec

C5H10N2O3 (146.0691)


   

Glutamine; AIF; CE10; MS2Dec

Glutamine; AIF; CE10; MS2Dec

C5H10N2O3 (146.0691)


   

Glutamine; AIF; CE30; MS2Dec

Glutamine; AIF; CE30; MS2Dec

C5H10N2O3 (146.0691)


   

Glutamine [M+2H-NH4]+; AIF; CE0; MS2Dec

Glutamine [M+2H-NH4]+; AIF; CE0; MS2Dec

C5H10N2O3 (146.0691)


   

Glutamine [M+2H-NH4]+; AIF; CE10; MS2Dec

Glutamine [M+2H-NH4]+; AIF; CE10; MS2Dec

C5H10N2O3 (146.0691)


   

Glutamine [M+2H-NH4]+; AIF; CE30; MS2Dec

Glutamine [M+2H-NH4]+; AIF; CE30; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; AIF; CE0; CorrDec

3-Ureidoisobutyric acid; AIF; CE0; CorrDec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; AIF; CE10; CorrDec

3-Ureidoisobutyric acid; AIF; CE10; CorrDec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; AIF; CE30; CorrDec

3-Ureidoisobutyric acid; AIF; CE30; CorrDec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; AIF; CE0; MS2Dec

3-Ureidoisobutyric acid; AIF; CE0; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; AIF; CE10; MS2Dec

3-Ureidoisobutyric acid; AIF; CE10; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; AIF; CE30; MS2Dec

3-Ureidoisobutyric acid; AIF; CE30; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE0; MS2Dec

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE0; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE10; MS2Dec

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE10; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE30; MS2Dec

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE30; MS2Dec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE0; CorrDec

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE0; CorrDec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE10; CorrDec

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE10; CorrDec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE30; CorrDec

3-Ureidoisobutyric acid [M+H-H2O]+; AIF; CE30; CorrDec

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; LC-tDDA; CE30

3-Ureidoisobutyric acid; LC-tDDA; CE30

C5H10N2O3 (146.0691)


   

3-Ureidoisobutyric acid; LC-tDDA; CE40

3-Ureidoisobutyric acid; LC-tDDA; CE40

C5H10N2O3 (146.0691)


   
   

METHYGLUTARATE

METHYGLUTARATE

C6H10O4 (146.0579)


   

Ala-gly

2-(2-aminopropanoylamino)acetic acid

C5H10N2O3 (146.0691)


A dipeptide formed from L-alanyl and glycine residues.

   

Glutamine (D)_major

Glutamine (D)_major

C5H10N2O3 (146.0691)


   

Glutamine (L)_major

Glutamine (L)_major

C5H10N2O3 (146.0691)


   

Glutamine (D)_57.3\\%

Glutamine (D)_57.3\\%

C5H10N2O3 (146.0691)


   

2-Methylglutarate

(2R)-2-Methylpentanedioic acid

C6H10O4 (146.0579)


   
   
   

Methylglutarate

β-methyl-Glutaric acid

C6H10O4 (146.0579)


3-Methylglutaric acid, a leucine metabolite, is a conspicuous C6 dicarboxylic organic acid classically associated with two distinct leucine pathway enzyme deficiencies, 3-hydroxy-3-methylglutaryl CoA lyase (HMGCL) and 3-methylglutaconyl CoA hydratase (AUH)[1][2].

   

Pentanedioate

4-Carboxybutanoic acid methyl ester

C6H10O4 (146.0579)


5-Methoxy-5-oxopentanoic acid is an endogenous metabolite. 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite.

   

2,2-Dimethylsuccinate

α,α-Dimethyl-succinic acid

C6H10O4 (146.0579)


2,2-Dimethylsuccinic acid belongs to the class of organic compounds known as methyl-branched fatty acids.

   

2-methyl-glutaric acid

2-methyl-pentanedioic acid

C6H10O4 (146.0579)


   

4-Phenylcrotonaldehyde

(2E)-4-phenylbut-2-enal

C10H10O (146.0732)


   

FEMA 3640

(2E)-3-(4-Methylphenyl)-2-propenal

C10H10O (146.0732)


   

FEMA 2697

(2Z)-2-methyl-3-phenylprop-2-enal

C10H10O (146.0732)


   

T-Pbo

3-BUTEN,2-one,4-phenyl (trans) benzalacetone

C10H10O (146.0732)


Benzylideneacetone is an endogenous metabolite. Benzylideneacetone is an endogenous metabolite. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1]. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1]. trans-Benzylideneacetone (trans-Benzalacetone), a metabolite of gram-negative entomopathogenic bacterium Xenorhabdus nematophila, is an enzyme inhibitor against phospholipase A2 (PLA2). trans-Benzylideneacetone is an immunosuppressant[1].

   

&alpha

alpha-Ethylidene-benzeneacetaldehyde

C10H10O (146.0732)


   

FEMA 3535

2,3-dimethyl-1-benzofuran

C10H10O (146.0732)


   

DBE-4

Butanedioic acid, 1,4-dimethyl ester

C6H10O4 (146.0579)


   

4-Isopropenylbenzaldehyde

4-(1-Methylethenyl)benzaldehyde

C10H10O (146.0732)


   

2-methoxy-2-methylthiolan-3-one

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

C6H10O2S (146.0401)


   

AAAHB

Butanoic acid, 2-ethyl-2-hydroxy-3-oxo-

C6H10O4 (146.0579)


   

FOH 10:6

4,5(R)-octadien-7,9-diyn-1-ol

C10H10O (146.0732)


   

1H-pyrrolo[2,3-c]pyridine-3-carbaldehyde

1H-pyrrolo[2,3-c]pyridine-3-carbaldehyde

C8H6N2O (146.048)


   

Benzamide, 2-cyano-

Benzamide, 2-cyano-

C8H6N2O (146.048)


   

D-Galactal

D-Galactal

C6H10O4 (146.0579)


   

2,3-Dihydroxypropyl acrylate

2,3-Dihydroxypropyl acrylate

C6H10O4 (146.0579)


   

2-Imidazolidinone,1,3-bis(hydroxymethyl)-

2-Imidazolidinone,1,3-bis(hydroxymethyl)-

C5H10N2O3 (146.0691)


   

(S)-2-METHOXYCYCLOHEXANONE

(S)-2-METHOXYCYCLOHEXANONE

C6H10O4 (146.0579)


   

beta-Aspartyl methylamide

beta-Aspartyl methylamide

C5H10N2O3 (146.0691)


   

1H-Pyrrolo[2,3-c]pyridine-2-carbaldehyde

1H-Pyrrolo[2,3-c]pyridine-2-carbaldehyde

C8H6N2O (146.048)


   

(S)-(+)-2-INDOLINEMETHANOL

(S)-(+)-2-INDOLINEMETHANOL

C6H10O4 (146.0579)


   

Isopropylmalonic acid

Isopropylmalonic acid

C6H10O4 (146.0579)


   

gly-d-ala

Glycyl-D-Alanine

C5H10N2O3 (146.0691)


   

2-fluoronaphthalene

2-fluoronaphthalene

C10H7F (146.0532)


   

1,6-naphthyridin-5-ol

1,6-naphthyridin-5-ol

C8H6N2O (146.048)


   

2-CYCLOPROPYLBENZALDEHYDE

2-CYCLOPROPYLBENZALDEHYDE

C10H10O (146.0732)


   

5-Methyl-indanone

5-Methyl-indanone

C10H10O (146.0732)


   

piperidine-3-carbonitrile hydrochloride

piperidine-3-carbonitrile hydrochloride

C6H11ClN2 (146.0611)


   

4-(PYRIDIN-3-YL)OXAZOLE

4-(PYRIDIN-3-YL)OXAZOLE

C8H6N2O (146.048)


   

4-(PYRIDIN-4-YL)OXAZOLE

4-(PYRIDIN-4-YL)OXAZOLE

C8H6N2O (146.048)


   

1h-indene-2-methanol

1h-indene-2-methanol

C10H10O (146.0732)


   

2-prop-2-enylbenzaldehyde

2-prop-2-enylbenzaldehyde

C10H10O (146.0732)


   

Pyrimido[6,1-c][1,2,4]triazepine (9CI)

Pyrimido[6,1-c][1,2,4]triazepine (9CI)

C7H6N4 (146.0592)


   

Pyrimidine, 4-(1H-pyrazol-1-yl)- (9CI)

Pyrimidine, 4-(1H-pyrazol-1-yl)- (9CI)

C7H6N4 (146.0592)


   

Imidazo[1,5-a]pyridine-5-carboxaldehyde (9CI)

Imidazo[1,5-a]pyridine-5-carboxaldehyde (9CI)

C8H6N2O (146.048)


   

4-Ethoxyphenylacetylene

4-Ethoxyphenylacetylene

C10H10O (146.0732)


   

3-Pyridazinecarboxylicacid,hexahydro-5-hydroxy-(9CI)

3-Pyridazinecarboxylicacid,hexahydro-5-hydroxy-(9CI)

C5H10N2O3 (146.0691)


   

5-(3-PYRIDYL)-1,3-OXAZOLE

5-(3-PYRIDYL)-1,3-OXAZOLE

C8H6N2O (146.048)


   

pyrazolo[1,5-a]pyridine-7-carbaldehyde

pyrazolo[1,5-a]pyridine-7-carbaldehyde

C8H6N2O (146.048)


   

Cyclopropyl phenyl ketone

Cyclopropyl phenyl ketone

C10H10O (146.0732)


   

PIPERIDINE-4-CARBONITRILE HYDROCHLORIDE

PIPERIDINE-4-CARBONITRILE HYDROCHLORIDE

C6H11ClN2 (146.0611)


   

(S)-2,2-Dimethyl-1,3-dioxolane-4-carboxylic acid

(S)-2,2-Dimethyl-1,3-dioxolane-4-carboxylic acid

C6H10O4 (146.0579)


   

2-chloro-6-methylcyclohexan-1-one

2-chloro-6-methylcyclohexan-1-one

C7H11ClO (146.0498)


   

Pyrido[2,3-d]pyrimidin-4-amine (9CI)

Pyrido[2,3-d]pyrimidin-4-amine (9CI)

C7H6N4 (146.0592)


   

Pyrazolo[1,5-a]pyridine-2-carbaldehyde

Pyrazolo[1,5-a]pyridine-2-carbaldehyde

C8H6N2O (146.048)


   

Pyrido[3,4-b]pyrazine, 8-amino- (6CI)

Pyrido[3,4-b]pyrazine, 8-amino- (6CI)

C7H6N4 (146.0592)


   

Pyrido[3,2-d][1,3]oxazepine (9CI)

Pyrido[3,2-d][1,3]oxazepine (9CI)

C8H6N2O (146.048)


   

Imidazo[1,2-a]pyridine-6-carbaldehyde

Imidazo[1,2-a]pyridine-6-carbaldehyde

C8H6N2O (146.048)


   

3-amino-1H-1,2,4-triazole-5-carboxylic acid,hydrate

3-amino-1H-1,2,4-triazole-5-carboxylic acid,hydrate

C3H6N4O3 (146.044)


   

Cinnolin-4(1H)-one

Cinnolin-4(1H)-one

C8H6N2O (146.048)


   

2-(cyclopropylmethylsulfanyl)acetic acid

2-(cyclopropylmethylsulfanyl)acetic acid

C6H10O2S (146.0401)


   

2,2,4-trimethyl-1,3-oxathiolan-5-one

2,2,4-trimethyl-1,3-oxathiolan-5-one

C6H10O2S (146.0401)


   

2H-cinnolin-3-one

2H-cinnolin-3-one

C8H6N2O (146.048)


   

Propanoic acid,2-(acetyloxy)-2-methyl-

Propanoic acid,2-(acetyloxy)-2-methyl-

C6H10O4 (146.0579)


   

Pyrido[2,3-b]pyrazin-6-amine

Pyrido[2,3-b]pyrazin-6-amine

C7H6N4 (146.0592)


   

1,3-Dimethyl-4,5-dihydroxy-2-imidazolidinone

1,3-Dimethyl-4,5-dihydroxy-2-imidazolidinone

C5H10N2O3 (146.0691)


   

2H-Indol-2-one,1,3-dihydro-3-imino-

2H-Indol-2-one,1,3-dihydro-3-imino-

C8H6N2O (146.048)


   

(R)-(+)-2-CHLOROPROPIONICACID

(R)-(+)-2-CHLOROPROPIONICACID

C6H10O4 (146.0579)


   

1,1,2-Trimethylhydrazine dihydrochloride

1,1,2-Trimethylhydrazine dihydrochloride

C3H12Cl2N2 (146.0377)


   

Benzonitrile, 4-[(hydroxyimino)methyl]- (9CI)

Benzonitrile, 4-[(hydroxyimino)methyl]- (9CI)

C8H6N2O (146.048)


   

Naphth[1,2-b]oxirene,1a,2,3,7b-tetrahydro-

Naphth[1,2-b]oxirene,1a,2,3,7b-tetrahydro-

C10H10O (146.0732)


   

2H-Thiopyran-2-Carboxylicacid,Tetrahydro-

2H-Thiopyran-2-Carboxylicacid,Tetrahydro-

C6H10O2S (146.0401)


   

1H-Indazole-7-carbaldehyde

1H-Indazole-7-carbaldehyde

C8H6N2O (146.048)


   

(R)-4-Methoxy-2-methyl-4-oxobutanoic acid

(R)-4-Methoxy-2-methyl-4-oxobutanoic acid

C6H10O4 (146.0579)


   

3-Thiophenecarboxylicacid,tetrahydro-,methylester(9CI)

3-Thiophenecarboxylicacid,tetrahydro-,methylester(9CI)

C6H10O2S (146.0401)


   

5-Hydroxyquinoxaline

5-Hydroxyquinoxaline

C8H6N2O (146.048)


   

3-Oxo-3-(4-pyridinyl)propanenitrile

3-Oxo-3-(4-pyridinyl)propanenitrile

C8H6N2O (146.048)


   

2-Chlorocycloheptanone

2-Chlorocycloheptanone

C7H11ClO (146.0498)


   

(6R)-6-amino-1,4-thiazepan-5-one

(6R)-6-amino-1,4-thiazepan-5-one

C5H10N2OS (146.0514)


   

Imidazo[1,2-a]pyridine-3-carbaldehyde

Imidazo[1,2-a]pyridine-3-carbaldehyde

C8H6N2O (146.048)


   

Boronic acid, (4-ethynylphenyl)- (9CI)

Boronic acid, (4-ethynylphenyl)- (9CI)

C8H7BO2 (146.0539)


   

PIPERIDINE-2-CARBONITRILE HYDROCHLORIDE

PIPERIDINE-2-CARBONITRILE HYDROCHLORIDE

C6H11ClN2 (146.0611)


   

1-VINYL-1,3-DIHYDRO-ISOBENZOFURAN

1-VINYL-1,3-DIHYDRO-ISOBENZOFURAN

C10H10O (146.0732)


   

1H-Pyrrolo[2,3-b]pyridin-2-carbaldehyd

1H-Pyrrolo[2,3-b]pyridin-2-carbaldehyd

C8H6N2O (146.048)


   

2-Methyl-indanone

2-Methyl-indanone

C10H10O (146.0732)


   

Pyrrolo[1,2-a]pyrazine-4-carboxaldehyde (9CI)

Pyrrolo[1,2-a]pyrazine-4-carboxaldehyde (9CI)

C8H6N2O (146.048)


   

3,4-Dihydro-1(2H)-azulenone

3,4-Dihydro-1(2H)-azulenone

C10H10O (146.0732)


   

1H-Inden-4-ol, 2,3-dihydro-1-methylene- (9CI)

1H-Inden-4-ol, 2,3-dihydro-1-methylene- (9CI)

C10H10O (146.0732)


   

chlorocarbonylcyclohexane

chlorocarbonylcyclohexane

C7H11ClO (146.0498)


   

L-Isoglutamine

L-Isoglutamine

C5H10N2O3 (146.0691)


   

1H-Pyrrolo[3,2-b]pyridine-3-carbaldehyde

1H-Pyrrolo[3,2-b]pyridine-3-carbaldehyde

C8H6N2O (146.048)


   

3-Methoxy-2,2-dimethyl-3-oxopropanoic acid

3-Methoxy-2,2-dimethyl-3-oxopropanoic acid

C6H10O4 (146.0579)


   

5-pyridin-2-yl-1,3-oxazole

5-pyridin-2-yl-1,3-oxazole

C8H6N2O (146.048)


   

PHENYL DIAZOMETHYL KETONE

PHENYL DIAZOMETHYL KETONE

C8H6N2O (146.048)


   

3-Oxo-3-(2-pyridinyl)propanenitrile

3-Oxo-3-(2-pyridinyl)propanenitrile

C8H6N2O (146.048)


   

propylmalonic acid

propylmalonic acid

C6H10O4 (146.0579)


   

Dimethyl methylmalonate

Dimethyl methylmalonate

C6H10O4 (146.0579)


   

7-Azaindole-3-carboxaldehyde

7-Azaindole-3-carboxaldehyde

C8H6N2O (146.048)


   

Oxalyl monoguanylhydrazide

Oxalyl monoguanylhydrazide

C3H6N4O3 (146.044)


   

2-Chloro-2-methylcyclohexanone

2-Chloro-2-methylcyclohexanone

C7H11ClO (146.0498)


   

1,7-Naphthyridin-2(1H)-One

1,7-Naphthyridin-2(1H)-One

C8H6N2O (146.048)


   

2-phenyl-1,3,4-oxadiazole

2-phenyl-1,3,4-oxadiazole

C8H6N2O (146.048)


   

1,5-Naphthyridin-4-ol

1,5-Naphthyridin-4-ol

C8H6N2O (146.048)


   

N1-methylethane-1,2-diamine dihydrochloride

N1-methylethane-1,2-diamine dihydrochloride

C3H12Cl2N2 (146.0377)


   

2(1H)-quinazolinone

2(1H)-quinazolinone

C8H6N2O (146.048)


   

1H-Pyrrolo[3,2-b]pyridine-6-carbaldehyde

1H-Pyrrolo[3,2-b]pyridine-6-carbaldehyde

C8H6N2O (146.048)


   

2-(dimethylcarbamoylamino)acetic acid

2-(dimethylcarbamoylamino)acetic acid

C5H10N2O3 (146.0691)


   

5-(4-PYRIDYL)-1,3-OXAZOLE

5-(4-PYRIDYL)-1,3-OXAZOLE

C8H6N2O (146.048)


   

1H-Benzimidazole-5-carbaldehyde

1H-Benzimidazole-5-carbaldehyde

C8H6N2O (146.048)


   

Dimethyl Fumarate-2,3-d2

Dimethyl Fumarate-2,3-d2

C6H6D2O4 (146.0548)


   

(hydroxyimino)phenylacetonitrile

(Hydroxyimino)(phenyl)acetonitrile

C8H6N2O (146.048)


   

1H-[1,5] NAPHTHYRIDIN-4-ONE

1H-[1,5] NAPHTHYRIDIN-4-ONE

C8H6N2O (146.048)


   

1,4-Dioxa-7-thiaspiro[4.4]nonane

1,4-Dioxa-7-thiaspiro[4.4]nonane

C6H10O2S (146.0401)


   

6-Acetylnicotinonitrile

6-Acetylnicotinonitrile

C8H6N2O (146.048)


   

Pyrrolo[1,2-c]pyrimidine-7-carboxaldehyde(9CI)

Pyrrolo[1,2-c]pyrimidine-7-carboxaldehyde(9CI)

C8H6N2O (146.048)


   

Pyrrolo[1,2-c]pyrimidine-1-carboxaldehyde (9CI)

Pyrrolo[1,2-c]pyrimidine-1-carboxaldehyde (9CI)

C8H6N2O (146.048)


   

8H-1,8-Naphthyridin-2-one

1,8-Naphthyridin-2(1H)-one

C8H6N2O (146.048)


   

pyrazolo[1,5-a]pyridine-3-carbaldehyde

pyrazolo[1,5-a]pyridine-3-carbaldehyde

C8H6N2O (146.048)


   

1,6-naphthyridin-2-ol

1,6-naphthyridin-2-ol

C8H6N2O (146.048)


   

1,6-Naphthyridin-4-ol

1,6-Naphthyridin-4-ol

C8H6N2O (146.048)


   

1H-PYRROLO[3,2-B]PYRIDINE-2-CARBALDEHYDE

1H-PYRROLO[3,2-B]PYRIDINE-2-CARBALDEHYDE

C8H6N2O (146.048)


   

1,5-Naphthyridin-2-ol

1,5-Naphthyridin-2-ol

C8H6N2O (146.048)


   

5-Acetyl-2-cyanopyridine

5-Acetyl-2-cyanopyridine

C8H6N2O (146.048)


   

4-Acetyl-2-pyridinecarbonitrile

4-Acetyl-2-pyridinecarbonitrile

C8H6N2O (146.048)


   

1,2-dihydro-2,7-naphthyridin-1-one

1,2-dihydro-2,7-naphthyridin-1-one

C8H6N2O (146.048)


   

1-Formyl-imidazo[1,5-a]pyridine

1-Formyl-imidazo[1,5-a]pyridine

C8H6N2O (146.048)


   

Quinazolin-8-ol

Quinazolin-8-ol

C8H6N2O (146.048)


   

1,2-Propanediamine dihydrochloride

1,2-Propanediamine dihydrochloride

C3H12Cl2N2 (146.0377)


   

Acetic acid,2-(2-propen-1-ylthio)-, methyl ester

Acetic acid,2-(2-propen-1-ylthio)-, methyl ester

C6H10O2S (146.0401)


   

Cyclobutanecarbonyl chloride, 3,3-dimethyl- (9CI)

Cyclobutanecarbonyl chloride, 3,3-dimethyl- (9CI)

C7H11ClO (146.0498)


   
   

1,3,5-Triazine-2,4,6-triamine hydrofluoride (1:1)

1,3,5-Triazine-2,4,6-triamine hydrofluoride (1:1)

C3H7FN6 (146.0716)


   

1-(2-Hydroxyethyl)imidazolidine-2-thione

1-(2-Hydroxyethyl)imidazolidine-2-thione

C5H10N2OS (146.0514)


   

pyrrolo[1,2-a]pyrazine-8-carbaldehyde

pyrrolo[1,2-a]pyrazine-8-carbaldehyde

C8H6N2O (146.048)


   

1-Ethyl-3-methylimidazolium chloride

1-Ethyl-3-methylimidazolium chloride

C6H11ClN2 (146.0611)


   

methyl 2-hydroxy-2-methyl-3-oxobutanoate

methyl 2-hydroxy-2-methyl-3-oxobutanoate

C6H10O4 (146.0579)


   

Quinoxaline, 1-oxide

Quinoxaline, 1-oxide

C8H6N2O (146.048)


   

Formamide,N-(4-cyanophenyl)-

Formamide,N-(4-cyanophenyl)-

C8H6N2O (146.048)


   

2-(1H-Pyrazol-4-yl)pyrazine

2-(1H-Pyrazol-4-yl)pyrazine

C7H6N4 (146.0592)


   

Pyrimidine, 4-(1H-pyrazol-4-yl)- (9CI)

Pyrimidine, 4-(1H-pyrazol-4-yl)- (9CI)

C7H6N4 (146.0592)


   

Thiomorpholine-3-carboxamide

Thiomorpholine-3-carboxamide

C5H10N2OS (146.0514)


   

beta-Alanylglycine

beta-Alanylglycine

C5H10N2O3 (146.0691)


   

1,3-Propanediamine dihydrochloride

1,3-Propanediamine dihydrochloride

C3H12Cl2N2 (146.0377)


   

Pyrido[2,3-b]pyrazin-3-amine (9CI)

Pyrido[2,3-b]pyrazin-3-amine (9CI)

C7H6N4 (146.0592)


   

1,3-Dioxolane-2-carboxylicacid,ethylester(9CI)

1,3-Dioxolane-2-carboxylicacid,ethylester(9CI)

C6H10O4 (146.0579)


   

3-Ethyl-2,5-dihydrothiophene-1,1-dioxide

3-Ethyl-2,5-dihydrothiophene-1,1-dioxide

C6H10O2S (146.0401)


   

1-Fluoronaphthalene

1-Fluoronaphthalene

C10H7F (146.0532)


   

2-(1H-PYRAZOL-3-YL)PYRAZINE

2-(1H-PYRAZOL-3-YL)PYRAZINE

C7H6N4 (146.0592)


   

1-aminocyclopentane-1-carbonitrile,hydrochloride

1-aminocyclopentane-1-carbonitrile,hydrochloride

C6H11ClN2 (146.0611)


   

1H-Pyrrolo[2,3-b]pyridin-5-carbaldehyd

1H-Pyrrolo[2,3-b]pyridin-5-carbaldehyd

C8H6N2O (146.048)


   

imidazo[1,5-a]pyridine-3-carbaldehyde

imidazo[1,5-a]pyridine-3-carbaldehyde

C8H6N2O (146.048)


   

(2R)-1,2-Propanediamine dihydrochloride

(2R)-1,2-Propanediamine dihydrochloride

C3H12Cl2N2 (146.0377)


   

3-Cyanobenzamide

3-Cyanobenzamide

C8H6N2O (146.048)


   

4-Cyanobenzamide

4-Cyanobenzamide

C8H6N2O (146.048)


   

Quinazoline, 3-oxide

Quinazoline, 3-oxide

C8H6N2O (146.048)


   

VAL-083

Dianhydrogalactitol

C6H10O4 (146.0579)


C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D009676 - Noxae > D000477 - Alkylating Agents D000970 - Antineoplastic Agents

   

(S)-(-)-1,2-Diaminopropane dihydrochloride

(S)-(-)-1,2-Diaminopropane dihydrochloride

C3H12Cl2N2 (146.0377)


   

1H-Pyrrolo[2,3-c]pyridine-7-carbaldehyde

1H-Pyrrolo[2,3-c]pyridine-7-carbaldehyde

C8H6N2O (146.048)


   

H-DL-Ala-Gly-OH

H-DL-Ala-Gly-OH

C5H10N2O3 (146.0691)


   

Butanedioic acid,2,3-dimethyl-, (2R,3S)-rel-

Butanedioic acid,2,3-dimethyl-, (2R,3S)-rel-

C6H10O4 (146.0579)


   

Tetrahydro-2H-thiopyran-4-carboxylic acid

Tetrahydro-2H-thiopyran-4-carboxylic acid

C6H10O2S (146.0401)


   

Glycine,N-(aminocarbonyl)-, ethyl ester

Glycine,N-(aminocarbonyl)-, ethyl ester

C5H10N2O3 (146.0691)


   

Pyrrolo[1,2-a]pyrimidine-6-carboxaldehyde (9CI)

Pyrrolo[1,2-a]pyrimidine-6-carboxaldehyde (9CI)

C8H6N2O (146.048)


   

2-Propylmalonic acid

2-Propylmalonic acid

C6H10O4 (146.0579)


   

4-(1H-1,2,4-triazol-5-yl)pyridine

4-(1H-1,2,4-triazol-5-yl)pyridine

C7H6N4 (146.0592)


   

2-(2-Pyrrolyl)ethylamine Hydrochloride

2-(2-Pyrrolyl)ethylamine Hydrochloride

C6H11ClN2 (146.0611)


   

Pyrazolo[1,5-a]pyridine-5-carboxaldehyde(9CI)

Pyrazolo[1,5-a]pyridine-5-carboxaldehyde(9CI)

C8H6N2O (146.048)


   

propanoyl propaneperoxoate

propanoyl propaneperoxoate

C6H10O4 (146.0579)


   

1H-Pyrrolo[2,3-c]pyridine-5-carbaldehyde

1H-Pyrrolo[2,3-c]pyridine-5-carbaldehyde

C8H6N2O (146.048)


   

6-Quinoxalinol

6-Quinoxalinol

C8H6N2O (146.048)


   

3-(1,3-Dioxolan-2-yl)propanoic acid

3-(1,3-Dioxolan-2-yl)propanoic acid

C6H10O4 (146.0579)


   

3,5-dimethyl-1,3,5-oxadiazinane-4-thione

3,5-dimethyl-1,3,5-oxadiazinane-4-thione

C5H10N2OS (146.0514)


   

1,4-Dihydro-1,6-naphthyridin-4-one

1,4-Dihydro-1,6-naphthyridin-4-one

C8H6N2O (146.048)


   

H-Gly-Ala-OH

Glycyl-L-alanine

C5H10N2O3 (146.0691)


   

2-[1-(Mercaptomethyl)cyclopropyl]acetic acid

2-[1-(Mercaptomethyl)cyclopropyl]acetic acid

C6H10O2S (146.0401)


   

4-Morpholinecarbothioamide

4-Morpholinecarbothioamide

C5H10N2OS (146.0514)


   

(2-OXO-CYCLOHEXYL)-ACETICACIDMETHYLESTER

(2-OXO-CYCLOHEXYL)-ACETICACIDMETHYLESTER

C6H10O4 (146.0579)


   

2-(1,3-Thiazol-4-yl)ethanamine

2-(1,3-Thiazol-4-yl)ethanamine

C8H6N2O (146.048)


   

Methyl D-asparaginate

Methyl D-asparaginate

C5H10N2O3 (146.0691)


   

hexanedioic acid

hexanedioic acid

C6H10O4 (146.0579)


   

7-Aminopyrido[2,3-b]pyrazine

7-Aminopyrido[2,3-b]pyrazine

C7H6N4 (146.0592)


   

methyl 1,3-dioxane-5-carboxylate

methyl 1,3-dioxane-5-carboxylate

C6H10O4 (146.0579)


   

Pyrido[2,3-b]pyrazin-8-amine (9CI)

Pyrido[2,3-b]pyrazin-8-amine (9CI)

C7H6N4 (146.0592)


   

1-phenyltetrazole

1-phenyltetrazole

C7H6N4 (146.0592)


   

3-Oxo-3-(3-pyridinyl)propanenitrile

3-Oxo-3-(3-pyridinyl)propanenitrile

C8H6N2O (146.048)


   

Pyrido[2,3-d]pyrimidin-7-amine

Pyrido[2,3-d]pyrimidin-7-amine

C7H6N4 (146.0592)


   

2-Ethyl-1H-imidazole-4,5-dicarbonitrile

2-Ethyl-1H-imidazole-4,5-dicarbonitrile

C7H6N4 (146.0592)


   

D-Alanylglycine

D-Alanylglycine

C5H10N2O3 (146.0691)


   

Imidazo[1,2-a]pyridine-7-carboxaldehyde (9CI)

Imidazo[1,2-a]pyridine-7-carboxaldehyde (9CI)

C8H6N2O (146.048)


   

L-Glutamine (alpha-15N)

L-Glutamine (alpha-15N)

C5H10N2O3 (146.0691)


   

1,7-Naphthyridin-4(1H)-one

1,7-Naphthyridin-4(1H)-one

C8H6N2O (146.048)


   

Pyrido[2,3-b][1,4]oxazepine (9CI)

Pyrido[2,3-b][1,4]oxazepine (9CI)

C8H6N2O (146.048)


   

Pyrrolo[1,2-c]pyrimidine-3-carboxaldehyde (9CI)

Pyrrolo[1,2-c]pyrimidine-3-carboxaldehyde (9CI)

C8H6N2O (146.048)


   

Thiourea, N-[imino(methylamino)methyl]-N-methyl- (9CI)

Thiourea, N-[imino(methylamino)methyl]-N-methyl- (9CI)

C4H10N4S (146.0626)


   

Pyrido[4,3-b][1,4]oxazepine (9CI)

Pyrido[4,3-b][1,4]oxazepine (9CI)

C8H6N2O (146.048)


   

Diethyloxalate

Diethyl oxalate

C6H10O4 (146.0579)


   

Cyclopentanecarbonyl chloride, 1-methyl- (8CI,9CI)

Cyclopentanecarbonyl chloride, 1-methyl- (8CI,9CI)

C7H11ClO (146.0498)


   

6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine-2-carbonitrile

6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine-2-carbonitrile

C7H6N4 (146.0592)


   

Ethyl malonyl hydrazide

Ethyl malonyl hydrazide

C5H10N2O3 (146.0691)


   

1H-Benzimidazole-2-carboxaldehyde

1H-Benzimidazole-2-carboxaldehyde

C8H6N2O (146.048)


   

Imidazo[1,2-a]pyridine-2-carbaldehyde

Imidazo[1,2-a]pyridine-2-carbaldehyde

C8H6N2O (146.048)


   

1H-Indazole-4-carbaldehyde

1H-Indazole-4-carbaldehyde

C8H6N2O (146.048)


   

1H-Indazole-5-carbaldehyde

1H-Indazole-5-carbaldehyde

C8H6N2O (146.048)


   

Indazole-6-carboxaldehyde

Indazole-6-carboxaldehyde

C8H6N2O (146.048)


   

N-(PHENYL)CYANOFORMAMIDE

N-(PHENYL)CYANOFORMAMIDE

C8H6N2O (146.048)


   

7-Azaindole-4-carboxaldehyde

7-Azaindole-4-carboxaldehyde

C8H6N2O (146.048)


   

1H-Pyrrolo[3,2-c]pyridine-2-carbaldehyde

1H-Pyrrolo[3,2-c]pyridine-2-carbaldehyde

C8H6N2O (146.048)


   

3-Piperidinecarbonitrile hydrochloride (1:1)

3-Piperidinecarbonitrile hydrochloride (1:1)

C6H11ClN2 (146.0611)


   

5,6-Dihydroxy-4-hexanolide

5,6-Dihydroxy-4-hexanolide

C6H10O4 (146.0579)


   

VINYLMETHYLSILOXANE - DIMETHYLSILOXANE COPOLYMERS, TRIMETHYLSILOXY TERMINATED

VINYLMETHYLSILOXANE - DIMETHYLSILOXANE COPOLYMERS, TRIMETHYLSILOXY TERMINATED

C5H14OSi2 (146.0583)


   

2-prop-2-enylsulfanylpropanoic acid

2-prop-2-enylsulfanylpropanoic acid

C6H10O2S (146.0401)


   

1,5-Naphthyridin-3-ol

1,5-Naphthyridin-3-ol

C8H6N2O (146.048)


   

D-Isoglutamine

(R)-4,5-Diamino-5-oxopentanoic acid

C5H10N2O3 (146.0691)


   
   

3-Ethyl-4-methyl-1H-pyrazole hydrochloride

3-Ethyl-4-methyl-1H-pyrazole hydrochloride

C6H11ClN2 (146.0611)


   

Pyrido[3,4-e]-1,2,4-triazine, 5-methyl- (9CI)

Pyrido[3,4-e]-1,2,4-triazine, 5-methyl- (9CI)

C7H6N4 (146.0592)


   

Quinazoline, 1-oxide (7CI,9CI)

Quinazoline, 1-oxide (7CI,9CI)

C8H6N2O (146.048)


   

2-(1H-1,2,4-Triazol-3-yl)pyridine

2-(1H-1,2,4-Triazol-3-yl)pyridine

C7H6N4 (146.0592)


   

2-AMINO-2-(3,3-DIFLUOROCYCLOBUTYL)ACETONITRILE

2-AMINO-2-(3,3-DIFLUOROCYCLOBUTYL)ACETONITRILE

C6H8F2N2 (146.0656)


   
   

1H-1,2,3-Triazol-5-amine,4-hydrazino-1-mercapto-(9CI)

1H-1,2,3-Triazol-5-amine,4-hydrazino-1-mercapto-(9CI)

C2H6N6S (146.0375)


   

2-(1H-Imidazol-2-yl)pyrazine

2-(1H-Imidazol-2-yl)pyrazine

C7H6N4 (146.0592)


   

2-(1H-Imidazol-2-yl)pyrimidine

2-(1H-Imidazol-2-yl)pyrimidine

C7H6N4 (146.0592)


   

2-Chloro-1-cyclopentylethanone

2-Chloro-1-cyclopentylethanone

C7H11ClO (146.0498)


   

1,7-Naphthyridin-8-ol

1,7-Naphthyridin-8-ol

C8H6N2O (146.048)


   

3-aminoisoindol-1-one

3-aminoisoindol-1-one

C8H6N2O (146.048)


   

PYRAZOLO[1,5-A]PYRIDINE-7-CARBOXALDEHYDE

PYRAZOLO[1,5-A]PYRIDINE-7-CARBOXALDEHYDE

C8H6N2O (146.048)


   

Pyrrolo[1,2-a]pyrazine-6-carboxaldehyde(9CI)

Pyrrolo[1,2-a]pyrazine-6-carboxaldehyde(9CI)

C8H6N2O (146.048)


   

4-Cinnolinol

4-Cinnolinol

C8H6N2O (146.048)


   

cyclopentylacetyl chloride

cyclopentylacetyl chloride

C7H11ClO (146.0498)


   

2-Acetyl-4-cyanopyridine

2-Acetyl-4-cyanopyridine

C8H6N2O (146.048)


   

Tetrahydro-2H-thiopyran-3-carboxylic acid

Tetrahydro-2H-thiopyran-3-carboxylic acid

C6H10O2S (146.0401)


   

Methyl 4-methoxyacetoacetate

Methyl 4-methoxyacetoacetate

C6H10O4 (146.0579)


   

glycol diacetate

Ethylene glycol diacetate

C6H10O4 (146.0579)


   

Conduritol a

(1R,2S,3R,4S)-5-Cyclohexene-1,2,3,4-tetrol

C6H10O4 (146.0579)


A conduritol in which the hydroxy groups at positions 2, 3, and 4 are in a trans,trans,cis- relationship to that at position 1. D007004 - Hypoglycemic Agents > D065089 - Glycoside Hydrolase Inhibitors D004791 - Enzyme Inhibitors

   

Pyrido[2,3-d]pyrimidin-2-amine

Pyrido[2,3-d]pyrimidin-2-amine

C7H6N4 (146.0592)


   

Imidazo[1,2-a]pyridine-8-carbaldehyde

Imidazo[1,2-a]pyridine-8-carbaldehyde

C8H6N2O (146.048)


   

2,2-Dimethyl-1,3-Dioxolane-4-Carboxylic Acid

2,2-Dimethyl-1,3-Dioxolane-4-Carboxylic Acid

C6H10O4 (146.0579)


   

Dianhydrodulcitol

Dianhydrodulcitol

C6H10O4 (146.0579)


D009676 - Noxae > D000477 - Alkylating Agents D000970 - Antineoplastic Agents

   
   

N-Nitroso-N-methyl-4-aminobutyric acid

N-Nitroso-N-methyl-4-aminobutyric acid

C5H10N2O3 (146.0691)


A nitrosamine that has methyl and 3-carboxypropyl substituents. It is a tobacco-derived nitrosamino acid that is a known animal and potential human carcinogen. It induces bladder transitional cell carcinomas in rats and has recently been identified as a contaminant in certain blood pressure medications.

   

(+)-Conduritol B

(+)-Conduritol B

C6H10O4 (146.0579)


D007004 - Hypoglycemic Agents > D065089 - Glycoside Hydrolase Inhibitors D004791 - Enzyme Inhibitors

   

(-)-Conduritol B

(-)-Conduritol B

C6H10O4 (146.0579)


D007004 - Hypoglycemic Agents > D065089 - Glycoside Hydrolase Inhibitors D004791 - Enzyme Inhibitors

   

6-Hydroxy-2-oxohexanoic acid

6-Hydroxy-2-oxohexanoic acid

C6H10O4 (146.0579)


   

4-Cyanobenzaldoxime

4-Cyanobenzaldoxime

C8H6N2O (146.048)


   

Aspartic acid methyl ester

Aspartic acid methyl ester

C5H10N2O3 (146.0691)


   

95-92-1

InChI=1\C6H10O4\c1-3-9-5(7)6(8)10-4-2\h3-4H2,1-2H

C6H10O4 (146.0579)


   

LS-406

InChI=1\C6H10O4\c1-9-5(7)3-4-6(8)10-2\h3-4H2,1-2H

C6H10O4 (146.0579)


   

FR-0632

Glutaric acid, monomethyl ester (8CI)

C6H10O4 (146.0579)


5-Methoxy-5-oxopentanoic acid is an endogenous metabolite. 5-Methoxy-5-oxopentanoic acid is an endogenous metabolite.

   

Alanylglycine

Alanylglycine

C5H10N2O3 (146.0691)


Alanylglycine is a dipeptide found in human urine. It is a breakdown product from endogenous and exogenous proteins. This peptide is generated by dipeptidyl-dipeptidase (or tetrapeptide dipeptidase which leads to the release of dipeptides from a tetrapeptide, more specifically: Ala-GlyAla-Gly. The enzyme acts more slowly on Ala-AlaAla-Ala and Gly-GlyGly-Gly. [HMDB]

   

(2R)-5-amino-2-azaniumyl-5-oxopentanoate

(2R)-5-amino-2-azaniumyl-5-oxopentanoate

C5H10N2O3 (146.0691)


   

glutamate

glutamate

C5H8NO4- (146.0453)


D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids

   

L-glutamate(1-)

L-glutamate(1-)

C5H8NO4- (146.0453)


An alpha-amino-acid anion that is the conjugate base of L-glutamic acid, having anionic carboxy groups and a cationic amino group

   

(2S)-5-amino-2-ammonio-5-oxopentanoate

(2S)-5-amino-2-ammonio-5-oxopentanoate

C5H10N2O3 (146.0691)


   

threo-3-methyl-L-aspartate(1-)

threo-3-methyl-L-aspartate(1-)

C5H8NO4- (146.0453)


Conjugate base of threo-3-methyl-L-aspartic acid.

   

(2R)-2-ammoniopentanedioate

(2R)-2-ammoniopentanedioate

C5H8NO4- (146.0453)


   

Glycylsarcosine zwitterion

Glycylsarcosine zwitterion

C5H10N2O3 (146.0691)


   

3-Aminopentanedioate

3-Aminopentanedioate

C5H8NO4- (146.0453)


   

N-(carboxylatomethyl)-D-alanine

N-(carboxylatomethyl)-D-alanine

C5H8NO4- (146.0453)


   

N-hydroxy-N-isopropyloxamate, IpOHA

N-hydroxy-N-isopropyloxamate, IpOHA

C5H8NO4- (146.0453)


   

(4S)-5-amino-4-azaniumyl-5-oxopentanoate

(4S)-5-amino-4-azaniumyl-5-oxopentanoate

C5H10N2O3 (146.0691)


   

Mevaldsaure

Mevaldsaure

C6H10O4 (146.0579)


   

2-Methylaspartate

2-Methylaspartate

C5H8NO4- (146.0453)


   

3-(Carboxymethyl-amino)-propanoate

3-(Carboxymethyl-amino)-propanoate

C5H8NO4- (146.0453)


   

(R)-4-dehydropantoic acid

(R)-4-dehydropantoic acid

C6H10O4 (146.0579)


   

cinerulose B

cinerulose B

C6H10O4 (146.0579)


   

(2R)-2-(methylazaniumyl)butanedioate

(2R)-2-(methylazaniumyl)butanedioate

C5H8NO4- (146.0453)


   

4-deoxy-L-fucono-1,5-lactone

4-deoxy-L-fucono-1,5-lactone

C6H10O4 (146.0579)


   
   

2-[Carbamoyl(methyl)amino]propanoic acid

2-[Carbamoyl(methyl)amino]propanoic acid

C5H10N2O3 (146.0691)


   

(2S)-2-acetamido-3-hydroxypropanoate

(2S)-2-acetamido-3-hydroxypropanoate

C5H8NO4- (146.0453)


   

(2R)-2-acetamido-3-hydroxypropanoate

(2R)-2-acetamido-3-hydroxypropanoate

C5H8NO4- (146.0453)


   

Mevaldic acid

Mevaldic acid

C6H10O4 (146.0579)


   

2-(Carboxyethoxy)propanal

2-(Carboxyethoxy)propanal

C6H10O4 (146.0579)


An oxo carboxylic acid that is propanal substituted by a carboxyethoxy group at position 2.

   

(2S)-2-(2-Acetylhydrazino)propanoic acid

(2S)-2-(2-Acetylhydrazino)propanoic acid

C5H10N2O3 (146.0691)


   

erythro-3-methyl-L-aspartate(1-)

erythro-3-methyl-L-aspartate(1-)

C5H8NO4- (146.0453)


   

(2R)-2-[carbamoyl(methyl)amino]propanoic acid

(2R)-2-[carbamoyl(methyl)amino]propanoic acid

C5H10N2O3 (146.0691)


   

Ethylene glycol dideuteroacetyl ester

Ethylene glycol dideuteroacetyl ester

C6H10O4 (146.0579)


   

beta-Ureidoisobutyric acid

beta-Ureidoisobutyric acid

C5H10N2O3 (146.0691)


   

2-dehydropantoate

2-dehydropantoate

C6H10O4 (146.0579)


   

2-aceto-2-hydroxybutanoate

2-aceto-2-hydroxybutanoate

C6H10O4 (146.0579)


   

(2S)-2-Ethyl-2-hydroxy-3-oxobutanoic acid

(2S)-2-Ethyl-2-hydroxy-3-oxobutanoic acid

C6H10O4 (146.0579)


   

Glycylsarcosine

Glycylsarcosine

C5H10N2O3 (146.0691)


   

{[(2S)-2-ammoniopropanoyl]amino}acetate

{[(2S)-2-ammoniopropanoyl]amino}acetate

C5H10N2O3 (146.0691)


   

D-glutamate(1-)

D-glutamate(1-)

C5H8NO4 (146.0453)


An alpha-amino-acid anion that is the conjugate base of D-glutamic acid, having anionic carboxy groups and a cationic amino group

   

(S)-4-hydroxy-2-oxohexanoic acid

(S)-4-hydroxy-2-oxohexanoic acid

C6H10O4 (146.0579)


An optically active form of 4-hydroxy-2-oxohexanoic acid having 4S-configuration.

   

DIMETHYL SUCCINATE

DIMETHYL SUCCINATE

C6H10O4 (146.0579)


   

quinoxalin-2-ol

quinoxalin-2-ol

C8H6N2O (146.048)


A hydroxyquinoxaline that consists of quinoxaline having a single hydroxy substituent located at position 2.

   

4-Ethoxy-4-oxobutanoic acid

4-Ethoxy-4-oxobutanoic acid

C6H10O4 (146.0579)


   
   

2-Ethylsuccinic acid

2-Ethylbutanedioic acid

C6H10O4 (146.0579)


   

2-methyl-1,3-thiazolidine-2-carboxamide

2-methyl-1,3-thiazolidine-2-carboxamide

C5H10N2OS (146.0514)


A thiazolidinecarboxamide that is 1,3-thiazolidine-2-carboxamide substituted by a methyl group at position 2.

   

N(4)-methyl-L-asparagine

N(4)-methyl-L-asparagine

C5H10N2O3 (146.0691)


An N-methyl-L-asparagine with a single methyl substituent attached to the amide nitrogen.

   

(S)-3-hydroxy-3-methyl-2-oxopentanoic acid

(S)-3-hydroxy-3-methyl-2-oxopentanoic acid

C6H10O4 (146.0579)


The S enantiomer of 3-hydroxy-3-methyl-2-oxopentanoic acid.

   

2-Dehydropantoic acid

2-Dehydropantoic acid

C6H10O4 (146.0579)


An oxo monocarboxylic acid that is 2-oxobutanoic acid in which both of the hydrogens at position 3 are substituted by methyl groups and one of the hydrogens at position 4 is substituted by a hydroxy group.

   

(S)-2-acetyl-2-hydroxybutanoic acid

(S)-2-acetyl-2-hydroxybutanoic acid

C6H10O4 (146.0579)


A 3-oxo monocarboxylic acid that is butanoic acid in which the hydrogens at position 2 are replaced by an acetyl and a hydroxy group (the S enantiomer).

   

D-glutamine zwitterion

D-glutamine zwitterion

C5H10N2O3 (146.0691)


Zwitterionic form of D-glutamine arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3.

   

isoglutamate(1-)

isoglutamate(1-)

C5H8NO4 (146.0453)


A beta-amino-acid anion that is the conjugate base of isoglutamic acid, obtained by deprotonation of the carboxy groups and protonation of the amino group; major species at pH 7.3.

   

D-Ala-Gly

D-Ala-Gly

C5H10N2O3 (146.0691)


A dipeptide formed from D-alanine and glycine residues.

   

Gly-ala

Gly-ala

C5H10N2O3 (146.0691)


A dipeptide formed from glycine and L-alanine residues.

   

Ala-Gly zwitterion

Ala-Gly zwitterion

C5H10N2O3 (146.0691)


A peptide zwitterion obtained by transfer of a proton from the carboxy to the amino terminus of Ala-Gly.

   

glutamate(1-)

glutamate(1-)

C5H8NO4 (146.0453)


An alpha-amino-acid anion that is the conjugate base of glutamic acid, having anionic carboxy groups and a cationic amino group

   

3-Ureidoisobutyric acid

3-Ureidoisobutyric acid

C5H10N2O3 (146.0691)


A ureidocarboxylic acid that is 2-methylpropanoic acid substituted by a carbamoylamino group at position 3.

   

L-glutamine zwitterion

L-glutamine zwitterion

C5H10N2O3 (146.0691)


An amino acid zwitterion arising from transfer of a proton from the carboxy to the amino group of L-glutamine; major species at pH 7.3.

   

Dimethylsuccinic acid

Dimethylsuccinic acid

C6H10O4 (146.0579)


   

2-Oxo-4-hydroxyhexanoic acid

2-Oxo-4-hydroxyhexanoic acid

C6H10O4 (146.0579)


   

Oxohydroxyhexanoic acid

Oxohydroxyhexanoic acid

C6H10O4 (146.0579)


   

Dehydropantoic acid

Dehydropantoic acid

C6H10O4 (146.0579)


   

Tetrahydrothiopheneacetic acid

Tetrahydrothiopheneacetic acid

C6H10O2S (146.0401)


   

3-TYP

3-TYP

C7H6N4 (146.0592)


3-TYP is an inhibitor of SIRT3 (IC50: ~377 μM) and an inhibitor of Methionine Adenosyltransferase (MAT) 2 and Indoleamine 2,3-Dioxygenase (IDO). There may be many off-target sites for 3-TYP that need to be examined, such as NAD-dependent enzymes, including dehydrogenases[1][2][3].

   

4-(c-hydroxycarbonimidoylamino)butanoic acid

4-(c-hydroxycarbonimidoylamino)butanoic acid

C5H10N2O3 (146.0691)


   

4-(hydroxymethyl)cyclopent-4-ene-1,2,3-triol

4-(hydroxymethyl)cyclopent-4-ene-1,2,3-triol

C6H10O4 (146.0579)


   

(1s,2r,3s,4s)-cyclohex-5-ene-1,2,3,4-tetrol

(1s,2r,3s,4s)-cyclohex-5-ene-1,2,3,4-tetrol

C6H10O4 (146.0579)


   

(1s,2s,3r)-4-(hydroxymethyl)cyclopent-4-ene-1,2,3-triol

(1s,2s,3r)-4-(hydroxymethyl)cyclopent-4-ene-1,2,3-triol

C6H10O4 (146.0579)


   

6-amino-5-methyl-2,6-dihydro-1,3-oxazine-4,5-diol

6-amino-5-methyl-2,6-dihydro-1,3-oxazine-4,5-diol

C5H10N2O3 (146.0691)


   

(2e)-5-hydroxy-3-methoxypent-2-enoic acid

(2e)-5-hydroxy-3-methoxypent-2-enoic acid

C6H10O4 (146.0579)


   

2-hydroxy-2-(methoxymethyl)oxolan-3-one

2-hydroxy-2-(methoxymethyl)oxolan-3-one

C6H10O4 (146.0579)


   

(2s,5s)-5-hydroxy-2-(hydroxymethyl)oxan-4-one

(2s,5s)-5-hydroxy-2-(hydroxymethyl)oxan-4-one

C6H10O4 (146.0579)


   

(5s,6s)-6-amino-5-methyl-2,6-dihydro-1,3-oxazine-4,5-diol

(5s,6s)-6-amino-5-methyl-2,6-dihydro-1,3-oxazine-4,5-diol

C5H10N2O3 (146.0691)


   

3-nitro-2h-1,2,3-triazole-1,5-diamine

3-nitro-2h-1,2,3-triazole-1,5-diamine

C2H6N6O2 (146.0552)


   

(1r,2s,3s,4s)-cyclohex-5-ene-1,2,3,4-tetrol

(1r,2s,3s,4s)-cyclohex-5-ene-1,2,3,4-tetrol

C6H10O4 (146.0579)


   

2-{[(prop-2-en-1-yloxy)carbonyl]oxy}ethanol

2-{[(prop-2-en-1-yloxy)carbonyl]oxy}ethanol

C6H10O4 (146.0579)


   

2-[(2-amino-1-hydroxyethylidene)amino]propanoic acid

2-[(2-amino-1-hydroxyethylidene)amino]propanoic acid

C5H10N2O3 (146.0691)


   

(2s)-2-amino-3-[(1-hydroxyethylidene)amino]propanoic acid

(2s)-2-amino-3-[(1-hydroxyethylidene)amino]propanoic acid

C5H10N2O3 (146.0691)


   

(2r)-2-[(2-amino-1-hydroxyethylidene)amino]propanoic acid

(2r)-2-[(2-amino-1-hydroxyethylidene)amino]propanoic acid

C5H10N2O3 (146.0691)


   

3-(acetyloxy)-2-methylpropanoic acid

3-(acetyloxy)-2-methylpropanoic acid

C6H10O4 (146.0579)


   

(1r,2s,3r,4s)-cyclohex-5-ene-1,2,3,4-tetrol

(1r,2s,3r,4s)-cyclohex-5-ene-1,2,3,4-tetrol

C6H10O4 (146.0579)


   

(2r)-2-amino-4-(c-hydroxycarbonimidoyl)butanoic acid

(2r)-2-amino-4-(c-hydroxycarbonimidoyl)butanoic acid

C5H10N2O3 (146.0691)


   

2-(hydroxymethyl)-2-methyl-3-oxobutanoic acid

2-(hydroxymethyl)-2-methyl-3-oxobutanoic acid

C6H10O4 (146.0579)


   

5-hydroxy-2-(hydroxymethyl)oxan-4-one

5-hydroxy-2-(hydroxymethyl)oxan-4-one

C6H10O4 (146.0579)


   

2-amino-3-[(1-hydroxyethylidene)amino]propanoic acid

2-amino-3-[(1-hydroxyethylidene)amino]propanoic acid

C5H10N2O3 (146.0691)


   

(1r,2r,3r,4s)-cyclohex-5-ene-1,2,3,4-tetrol

(1r,2r,3r,4s)-cyclohex-5-ene-1,2,3,4-tetrol

C6H10O4 (146.0579)


   

[(1r,2r)-2-carboxylatocyclopropyl]dimethylsulfanium

[(1r,2r)-2-carboxylatocyclopropyl]dimethylsulfanium

C6H10O2S (146.0401)