Chemical Formula: C6H11NO3

Chemical Formula C6H11NO3

Found 200 metabolite its formula value is C6H11NO3

4-Acetamidobutanoate

N-Acetyl-gamma-amino-N-butyric acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid, also known as 4-acetamidobutanoate or N-acetyl-4-aminobutyric acid, is a member of the class of compounds known as gamma amino acids and derivatives. These compounds are amino acids having an -NH2 group attached to the gamma carbon atom. 4-Acetamidobutanoic acid is soluble in water. 4-Acetamidobutanoic acid can be found in a number of food items such as Rubus species (blackberry, raspberry), cassava, pepper (Capsicum frutescens), and napa cabbage, which makes 4-acetamidobutanoic acid a potential biomarker for the consumption of these food products. 4-Acetamidobutanoic acid can be found in blood, feces, and urine, as well as in human prostate tissue. 4-Acetamidobutanoic acid exists in all eukaryotes, ranging from yeast to humans. 4-Acetamidobutanoic acid is a GABA derivative, a product of the urea cycle and the metabolism of amino groups, and the product of NAD-linked aldehyde dehydrogenase (EC 1.2.1.3) (KEGG). 4-Acetamidobutanoic acid is a GABA derivative, product of the Urea cycle and metabolism of amino groups, the product of NAD-linked aldehyde dehydrogenase (EC 1.2.1.3) (KEGG) [HMDB]. 4-Acetamidobutanoic acid is found in many foods, some of which are custard apple, japanese walnut, shiitake, and oxheart cabbage. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

Allysine

alpha-Aminoadipic acid delta-semialdehyde

C6H11NO3 (145.0738896)


Allysine (CAS: 1962-83-0), also known as 2-amino-6-oxohexanoic acid or 6-oxonorleucine, belongs to the class of organic compounds known as alpha-amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). Outside of the human body, allysine has been detected, but not quantified in, several different foods, such as winged beans, wasabi, common verbena, arrowhead, and oats. This could make allysine a potential biomarker for the consumption of these foods. Allysine is a derivative of lysine used in the production of elastin and collagen. It is produced by the actions of the enzyme lysyl oxidase in the extracellular matrix and is essential in the crosslink formation that stabilizes collagen and elastin.

   

2-Keto-6-aminocaproate

alpha-keto-epsilon-Aminohexanoic acid

C6H11NO3 (145.0738896)


2-Keto-6-aminocaproate is an intermediate in lysine degradation and can be formed from L-lysine. L-Lysine is an essential amino-acid that is a necessary building block for all protein in the body. L-Lysine plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. L-Lysine can be converted to 2-keto-6-aminocaproate via the enzyme L-lysine alpha-oxidase. 2-Keto-6-aminocaproate can spontaneously decarboxylate to 5-aminovalerate in the presence of the reaction product, hydrogen peroxide. It can also be spontaneously converted in solution to its cyclic form delta-piperideine-2-carboxylate. This has been demonstrated in vitro in the presence of catalase, which splits hydrogen peroxide. [HMDB] 2-Keto-6-aminocaproate is an intermediate in lysine degradation and can be formed from L-lysine. L-Lysine is an essential amino-acid that is a necessary building block for all protein in the body. L-Lysine plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. L-Lysine can be converted to 2-keto-6-aminocaproate via the enzyme L-lysine alpha-oxidase. 2-Keto-6-aminocaproate can spontaneously decarboxylate to 5-aminovalerate in the presence of the reaction product, hydrogen peroxide. It can also be spontaneously converted in solution to its cyclic form delta-piperideine-2-carboxylate. This has been demonstrated in vitro in the presence of catalase, which splits hydrogen peroxide.

   

(S)-5-Amino-3-oxohexanoate

(5S)-5-Amino-3-oxohexanoic acid

C6H11NO3 (145.0738896)


S)-5-Amino-3-oxohexanoate is an intermediate in lysine degradation. L-Lysine is an essential amino acid that is a necessary building block for all protein in the body and It plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. In lysine degradation pathway, (S)-5-Amino-3-oxohexanoate is a substrate for the enzyme L-erythro-3,5-diaminohexanoate dehydrogenase (EC 1.4.1.11) and can be generated from L-erythro-3,5-Diaminohexanoate. [HMDB] (S)-5-Amino-3-oxohexanoate is an intermediate in lysine degradation. L-Lysine is an essential amino acid that is a necessary building block for all protein in the body and It plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. In lysine degradation pathway, (S)-5-Amino-3-oxohexanoate is a substrate for the enzyme L-erythro-3,5-diaminohexanoate dehydrogenase (EC 1.4.1.11) and can be generated from L-erythro-3,5-Diaminohexanoate.

   

2-Amino-5-oxohexanoate

2-amino-5-oxohexanoic acid

C6H11NO3 (145.0738896)


   

Isobutyrylglycine

2-(2-methylpropanamido)acetic acid

C6H11NO3 (145.0738896)


Isobutyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction: acyl-CoA + glycine < -- > CoA + N-acylglycine. Isobutyrylglycine is identified in large amount in urine of patients with isobutyryl-CoA dehydrogenase deficiency. Isobutyryl-CoA dehydrogenase deficiency is a disorder caused by the deficiency of isobutyryl-CoA dehydrogenase that is involved in the catabolism of the branched-chain amino acid valine (PMID 15505379). Moreover, Isobutyrylglycine is found to be associated with ethylmalonic encephalopathy and propionic acidemia, which are also inborn errors of metabolism. Isobutyrylglycine is a biomarker for the consumption of cheese. Isobutyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction:

   

Butyrylglycine

2-Butyramidoacetic acid

C6H11NO3 (145.0738896)


N-Butyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism, such as ethylmalonic encephalopathy. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13), which is an enzyme that catalyzes the chemical reaction: acyl-CoA + glycine < -- > CoA + N-acylglycine amino acids composed of glycine substituted at the nitrogen rather than the usual carbon position, resulting in the loss of hydrogen bonding donors. Polymers of these compounds are called Peptoids. N-Butyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction:

   

L-cis-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid

(2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid

C6H11NO3 (145.0738896)


(2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid is found in fruits. (2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid is a constituent of the seeds of Eriobotrya japonica (loquat). Constituent of the seeds of Eriobotrya japonica (loquat). (2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid is found in fruits.

   

L-trans-5-Hydroxy-2-piperidinecarboxylic acid

(2S,5R)-trans-5-Hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


L-cis-5-Hydroxy-2-piperidinecarboxylic acid is found in fruits. L-cis-5-Hydroxy-2-piperidinecarboxylic acid is present in the leaves of Morus alba (white mulberry

   

Methyl aminolevulinate

delta-Aminolevulinic acid methyl ester

C6H11NO3 (145.0738896)


Methyl aminolevulinate is only found in individuals that have used or taken this drug. It is a prodrug that is metabolised to Protoporphyrin IX (a photosensitizer) used in photodynamic therapy.Photosensitization following application of methyl aminolevulinate cream occurs through the metabolic conversion of methyl aminolevulinate (prodrug) to photoactive porphyrins (PAP), which accumulates in the skin lesions to which the cream has been applied. When exposed to light of appropriate wavelength and energy, the accumulated photoactive porphyrins produce a photodynamic reaction, resulting in a cytotoxic process dependent upon the simultaneous presence of oxygen. The absorption of light results in an excited state of porphyrin molecules, and subsequent spin transfer from photoactive porphyrins to molecular oxygen generates singlet oxygen, which can further react to form superoxide and hydroxyl radicals. L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01X - Other antineoplastic agents > L01XD - Sensitizers used in photodynamic/radiation therapy D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents C1420 - Photosensitizing Agent D003879 - Dermatologic Agents

   

N-(2-Carboxymethyl)-morpholine

N-(2-Carboxymethyl)-morpholine

C6H11NO3 (145.0738896)


N-(2-Carboxymethyl)-morpholine is a metabolite of mycophenolate mofetil. Mycophenolate mofetil (MMF) (brand names CellCept, Myfortic) is an immunosuppressant and prodrug of mycophenolic acid, used extensively in transplant medicine. It is a reversible inhibitor of inosine monophosphate dehydrogenase (IMPDH) in purine biosynthesis which is necessary for the growth of T cells and B cells. Other cells are able to recover purines via a separate, scavenger, pathway and are, thus, able to escape the effect. MMF is a less toxic alternative to azathioprine. (Wikipedia)

   

N-Propionylalanine

(2S)-2-[(1-hydroxypropylidene)amino]propanoic acid

C6H11NO3 (145.0738896)


N-propionylalanine is classified as a member of the n-acyl-l-alpha-amino acids. N-acyl-L-alpha-amino acids are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. N-propionylalanine is considered to be a slightly soluble (in water) and a weak acidic compound. N-propionylalanine can be found in humans.

   

methyl 2-amino-4-oxopentanoate

Methyl 2-amino-4-oxopentanoic acid

C6H11NO3 (145.0738896)


   

But-2-en-2-yl 2-aminoethaneperoxoate

But-2-en-2-yl 2-aminoethaneperoxoic acid

C6H11NO3 (145.0738896)


   

Amino 6-oxohexanoate

Amino 6-oxohexanoic acid

C6H11NO3 (145.0738896)


   

L-2-Amino-6-oxohexanoic acid

alpha-Aminoadipic acid delta-semialdehyde

C6H11NO3 (145.0738896)


Found in collagen, elastin and heart muscle

   

trans-4-Hydroxy-N-methyl-L-proline

(-)-trans-4-Hydroxy-N-methyl-L-proline

C6H11NO3 (145.0738896)


4-Hydroxyhygric acid is a compound isolated from leaves of five species of the leguminous tropical tree Copuiferq. 4-Hydroxyhygric acid is the inhibitor of larval development of the seed-feeding bruchid beetle Callosobruchus maculatus and to have significant feeding deterrence of the leaf-feeding lepidopteran Spodoprera littoralis[1].

   

cis-5-Hydroxypipecolic acid

cis-5-Hydroxypipecolic acid

C6H11NO3 (145.0738896)


   

epsilon-Amino-alpha-ketocarproic acid

epsilon-Amino-alpha-ketocarproic acid

C6H11NO3 (145.0738896)


   

4-Hydroxypipecolic acid

4-HYDROXYPIPERIDINE-2-CARBOXYLIC ACID

C6H11NO3 (145.0738896)


   

N-acetyl-GABA

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

2-amino-4-oxohexanoic acid

2-amino-4-oxohexanoic acid

C6H11NO3 (145.0738896)


   

2-(2-amino-1-hydroxycyclobutyl)acetic acid

2-(2-amino-1-hydroxycyclobutyl)acetic acid

C6H11NO3 (145.0738896)


   
   

1-amino-3-(hydroxymethyl)cyclobutane-1-carboxylic acid

1-amino-3-(hydroxymethyl)cyclobutane-1-carboxylic acid

C6H11NO3 (145.0738896)


   

ethyl 4-amino-4-oxobutanoate

ethyl 4-amino-4-oxobutanoate

C6H11NO3 (145.0738896)


   
   

3-hydroxypiperidine-2-carboxylic acid

3-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   
   

2-amino-3-(hydroxymethyl)pent-3-enoic acid

2-amino-3-(hydroxymethyl)pent-3-enoic acid

C6H11NO3 (145.0738896)


   

2-hydroxyiminohexanoic acid

2-hydroxyiminohexanoic acid

C6H11NO3 (145.0738896)


   

2-amino-3-methyl-4-oxopentanoic acid

2-amino-3-methyl-4-oxopentanoic acid

C6H11NO3 (145.0738896)


   

3-Hydroxy-4-methylproline #

3-Hydroxy-4-methylproline #

C6H11NO3 (145.0738896)


   
   

hydroxypipecolic acid

2-Piperidinecarboxylicacid,1-hydroxy-(9CI)

C6H11NO3 (145.0738896)


N-hydroxypipecolic acid is an N-hydroxy-alpha-amino-acid resulting from the formal N-hydroxylation of the amino group of piperidine-carboxylic acid (pipecolic acid). It is a N-hydroxy-alpha-amino-acid and a piperidinemonocarboxylic acid. It is functionally related to a pipecolic acid. N-Hydroxypipecolic acid (1-Hydroxy-2-piperidinecarboxylic acid), a plant metabolite and a systemic acquired resistance (SAR) regulator, orchestrates SAR establishment in concert with the immune signal salicylic acid. N-Hydroxypipecolic acid accumulates systemically in the plant foliage in response to pathogen attack. N-Hydroxypipecolic acid induces SAR to bacterial and oomycete infection[1][2][3].

   

NMH-Pro

(2S, 4R)-4-hydroxy-1-methyl-2-pyrrolidinecarboxylic acid

C6H11NO3 (145.0738896)


(R)-4-hydroxy-1-methyl-L-proline is an L-proline derivative that is trans-4-hydroxy-L-proline in which the amino hydrogen has been replaced by a methyl group. It has a role as a plant metabolite and an anti-HIV-1 agent. It is a L-proline derivative and a pyrrolidine alkaloid. It is functionally related to a trans-4-hydroxy-L-proline. An L-proline derivative that is trans-4-hydroxy-L-proline in which the amino hydrogen has been replaced by a methyl group. 4-Hydroxyhygric acid is a compound isolated from leaves of five species of the leguminous tropical tree Copuiferq. 4-Hydroxyhygric acid is the inhibitor of larval development of the seed-feeding bruchid beetle Callosobruchus maculatus and to have significant feeding deterrence of the leaf-feeding lepidopteran Spodoprera littoralis[1].

   

4-Acetamidobutanoate

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

Isobutyrylglycine

Isobutyrylglycine

C6H11NO3 (145.0738896)


   
   

4-Acetamidobutyric acid

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

N-Isobutyrylglycine

N-Isobutyrylglycine

C6H11NO3 (145.0738896)


An N-acylglycine in which the acyl group is specified as isobutryl.

   

Butyrylglycine

Butyrylglycine

C6H11NO3 (145.0738896)


A N-acylglycine obtained by formal condensation of the carboxy group of butyric acid with the amino group of glycine.

   

Allysine (not validated)

Allysine (not validated)

C6H11NO3 (145.0738896)


Annotation level-3

   

4-Acetamidobutanoic acid; LC-tDDA; CE10

4-Acetamidobutanoic acid; LC-tDDA; CE10

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid; LC-tDDA; CE20

4-Acetamidobutanoic acid; LC-tDDA; CE20

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid; LC-tDDA; CE30

4-Acetamidobutanoic acid; LC-tDDA; CE30

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid; LC-tDDA; CE40

4-Acetamidobutanoic acid; LC-tDDA; CE40

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE10

N-Butyrylglycine; LC-tDDA; CE10

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE20

N-Butyrylglycine; LC-tDDA; CE20

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE30

N-Butyrylglycine; LC-tDDA; CE30

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE40

N-Butyrylglycine; LC-tDDA; CE40

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; AIF; CE0; CorrDec

N-Butyrylglycine; AIF; CE0; CorrDec

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; AIF; CE10; CorrDec

N-Butyrylglycine; AIF; CE10; CorrDec

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; AIF; CE30; CorrDec

N-Butyrylglycine; AIF; CE30; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE0; CorrDec

4-Acetamidobutyric acid; AIF; CE0; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE10; CorrDec

4-Acetamidobutyric acid; AIF; CE10; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE30; CorrDec

4-Acetamidobutyric acid; AIF; CE30; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE0; MS2Dec

4-Acetamidobutyric acid; AIF; CE0; MS2Dec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE10; MS2Dec

4-Acetamidobutyric acid; AIF; CE10; MS2Dec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE30; MS2Dec

4-Acetamidobutyric acid; AIF; CE30; MS2Dec

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


An N-acyl-gamma-aminobutyric acid resulting from the monoacetylation of the nitrogen of GABA.

   

Propionylglycine methyl ester

Propionylglycine methyl ester

C6H11NO3 (145.0738896)


   

allysine

allysine

C6H11NO3 (145.0738896)


An alpha-amino acid consisting of lysine having an oxo group in place of the side-chain amino group.

   

Methyl aminolevulinate

5-Aminolevulinic acid methyl ester;Aminolevulinic acid methyl ester

C6H11NO3 (145.0738896)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01X - Other antineoplastic agents > L01XD - Sensitizers used in photodynamic/radiation therapy D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents C1420 - Photosensitizing Agent D003879 - Dermatologic Agents

   

4-(hydroxymethyl)pyrrolidine-2-carboxylic acid

L-cis-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid

C6H11NO3 (145.0738896)


   

5-hydroxypipecolic acid

(2S,5R)-trans-5-Hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


A piperidinemonocarboxylic acid that is pipecolic acid with a hydroxy substituent at position 5.

   

3-oxo-5S-amino-hexanoic acid

(5S)-5-Amino-3-oxohexanoic acid

C6H11NO3 (145.0738896)


   

trans-5-Hydroxypipecolic acid

trans-5-Hydroxypipecolic acid

C6H11NO3 (145.0738896)


   

3-Aminotetrahydro-2H-pyran-3-carboxylic acid

3-Aminotetrahydro-2H-pyran-3-carboxylic acid

C6H11NO3 (145.0738896)


   

N-ACETYL-N-METHYL-BETAALANIN

N-ACETYL-N-METHYL-BETAALANIN

C6H11NO3 (145.0738896)


   

Adipamic acid

6-Amino-6-oxohexanoic acid

C6H11NO3 (145.0738896)


   
   

Morpholin-3-yl-acetic acid

Morpholin-3-yl-acetic acid

C6H11NO3 (145.0738896)


   

Alanine,N-acetyl-2-methyl-

Alanine,N-acetyl-2-methyl-

C6H11NO3 (145.0738896)


   

3-hydroxypipecolic acid

3-hydroxypipecolic acid

C6H11NO3 (145.0738896)


   

2-MORPHOLINEACETIC ACID

2-MORPHOLINEACETIC ACID

C6H11NO3 (145.0738896)


   

1H,3H,5H-Oxazolo[3,4-c]oxazole-7a(7H)-methanol

1H,3H,5H-Oxazolo[3,4-c]oxazole-7a(7H)-methanol

C6H11NO3 (145.0738896)


   

ethyl 2-ethoxy-2-iminoacetate

ethyl 2-ethoxy-2-iminoacetate

C6H11NO3 (145.0738896)


   

2-Piperidinecarboxylicacid,5-hydroxy-,(2R,5S)-(9CI)

2-Piperidinecarboxylicacid,5-hydroxy-,(2R,5S)-(9CI)

C6H11NO3 (145.0738896)


   

(sec-butylamino)(oxo)acetic acid

(sec-butylamino)(oxo)acetic acid

C6H11NO3 (145.0738896)


   

4-Hydroxy-4-piperidinecarboxylic acid

4-Hydroxy-4-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

cis-3-hydroxy-L-proline methyl ester

cis-3-hydroxy-L-proline methyl ester

C6H11NO3 (145.0738896)


   

2-(2-methylpropylamino)-2-oxoacetic acid

2-(2-methylpropylamino)-2-oxoacetic acid

C6H11NO3 (145.0738896)


   

(tert-butylamino)(oxo)acetic acid

(tert-butylamino)(oxo)acetic acid

C6H11NO3 (145.0738896)


   
   

3,3,3-Trimethoxypropionitrile

3,3,3-Trimethoxypropionitrile

C6H11NO3 (145.0738896)


   

2-(propanoylamino)propanoic acid

2-(propanoylamino)propanoic acid

C6H11NO3 (145.0738896)


   

cis-4-hydroxy-d-proline methyl ester

cis-4-hydroxy-d-proline methyl ester

C6H11NO3 (145.0738896)


   
   

1-(Nitromethyl)cyclopentanol

1-(Nitromethyl)cyclopentanol

C6H11NO3 (145.0738896)


   

ethyl N-ethoxycarbonylmethanimidate

ethyl N-ethoxycarbonylmethanimidate

C6H11NO3 (145.0738896)


   

(R)-2-(MORPHOLIN-3-YL)ACETIC ACID

(R)-2-(MORPHOLIN-3-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

(R)-2-(MORPHOLIN-2-YL)ACETIC ACID

(R)-2-(MORPHOLIN-2-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

(S)-2-MORPHOLINEACETIC ACID

(S)-2-MORPHOLINEACETIC ACID

C6H11NO3 (145.0738896)


   

(S)-2-(MORPHOLIN-3-YL)ACETIC ACID

(S)-2-(MORPHOLIN-3-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

N-(2-hydroxyethyl)acetoacetamide

N-(2-hydroxyethyl)acetoacetamide

C6H11NO3 (145.0738896)


   

N-ACETYL-DL-2-AMINO-N-BUTYRIC ACID

N-ACETYL-DL-2-AMINO-N-BUTYRIC ACID

C6H11NO3 (145.0738896)


   

2-MORPHOLIN-4-YL-2-OXOETHANOL

2-MORPHOLIN-4-YL-2-OXOETHANOL

C6H11NO3 (145.0738896)


   

4-hydroxynipecotic acid

4-hydroxynipecotic acid

C6H11NO3 (145.0738896)


   

4-Piperidinecarboxylic acid, 3-hydroxy-, trans- (9CI)

4-Piperidinecarboxylic acid, 3-hydroxy-, trans- (9CI)

C6H11NO3 (145.0738896)


   

2-AMINO-2-(TETRAHYDROFURAN-3-YL)ACETIC ACID

2-AMINO-2-(TETRAHYDROFURAN-3-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

3-Methoxymorpholine-4-carbaldehyde

3-Methoxymorpholine-4-carbaldehyde

C6H11NO3 (145.0738896)


   

2-ACETAMIDOPROPIONIC ACID METHYL ESTER

2-ACETAMIDOPROPIONIC ACID METHYL ESTER

C6H11NO3 (145.0738896)


   

2-Methyl-1,3-dioxolane-2-acetamide

2-Methyl-1,3-dioxolane-2-acetamide

C6H11NO3 (145.0738896)


   

4-methylmorpholine-3-carboxylic acid

4-methylmorpholine-3-carboxylic acid

C6H11NO3 (145.0738896)


   

4-Aminotetrahydro-2H-pyran-4-carboxylic acid

4-Aminotetrahydro-2H-pyran-4-carboxylic acid

C6H11NO3 (145.0738896)


   

oxamic acid n-butyl ester

oxamic acid n-butyl ester

C6H11NO3 (145.0738896)


   

1-ETHYL-4-(PIPERIDIN-4-YLMETHYL)PIPERAZINE

1-ETHYL-4-(PIPERIDIN-4-YLMETHYL)PIPERAZINE

C6H11NO3 (145.0738896)


   

(2S,4R)-METHYL 4-HYDROXYPYRROLIDINE-2-CARBOXYLATE

(2S,4R)-METHYL 4-HYDROXYPYRROLIDINE-2-CARBOXYLATE

C6H11NO3 (145.0738896)


   

(3-Hydroxy-1-pyrrolidinyl)acetic acid

(3-Hydroxy-1-pyrrolidinyl)acetic acid

C6H11NO3 (145.0738896)


   

5-Hydroxy-3-piperidinecarboxylic acid

5-Hydroxy-3-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

(2S,5S)-5-Hydroxy-2-piperidinecarboxylic acid

(2S,5S)-5-Hydroxy-2-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

4-(2-hydroxyethyl)morpholin-3-one

4-(2-hydroxyethyl)morpholin-3-one

C6H11NO3 (145.0738896)


   

4-Morpholineacetic Acid

Morpholin-4-yl-acetic acid

C6H11NO3 (145.0738896)


   

methyl morpholine-4-carboxylate

methyl morpholine-4-carboxylate

C6H11NO3 (145.0738896)


   

Ethyl-N-methyl malonamide

Ethyl-N-methyl malonamide

C6H11NO3 (145.0738896)


   

Methyl (3S)-3-hydroxy-D-prolinate

Methyl (3S)-3-hydroxy-D-prolinate

C6H11NO3 (145.0738896)


   

D-Proline, 4-hydroxy-, methyl ester, (4S)

D-Proline, 4-hydroxy-, methyl ester, (4S)

C6H11NO3 (145.0738896)


   

2-Isoxazolidinecarboxylicacid,ethylester(9CI)

2-Isoxazolidinecarboxylicacid,ethylester(9CI)

C6H11NO3 (145.0738896)


   

Methyl 2-morpholinecarboxylate

Methyl 2-morpholinecarboxylate

C6H11NO3 (145.0738896)


   

5-Hydroxypiperidine-3-carboxylic Acid

5-Hydroxypiperidine-3-carboxylic Acid

C6H11NO3 (145.0738896)


   

Methyl 3-morpholinecarboxylate

Methyl 3-morpholinecarboxylate

C6H11NO3 (145.0738896)


   

ethyl n,n-dimethyloxamate

ethyl n,n-dimethyloxamate

C6H11NO3 (145.0738896)


   

ALLYL N-(2-HYDROXYETHYL)CARBAMATE

ALLYL N-(2-HYDROXYETHYL)CARBAMATE

C6H11NO3 (145.0738896)


   

SUCCINAMICACIDETHYLESTER

SUCCINAMICACIDETHYLESTER

C6H11NO3 (145.0738896)


   

4-Methyl-4-nitrovaleraldehyde

4-Methyl-4-nitrovaleraldehyde

C6H11NO3 (145.0738896)


   
   

Acetyl-D-2-aminobutyric acid

Acetyl-D-2-aminobutyric acid

C6H11NO3 (145.0738896)


   

L-Proline, 4-hydroxy-, methyl ester, (4S)- (9CI)

L-Proline, 4-hydroxy-, methyl ester, (4S)- (9CI)

C6H11NO3 (145.0738896)


   

(R)-Methyl morpholine-3-carboxylate

(R)-Methyl morpholine-3-carboxylate

C6H11NO3 (145.0738896)


   

n,n-dimethylsuccinamic acid

n,n-dimethylsuccinamic acid

C6H11NO3 (145.0738896)


   

4-methoxypyrrolidine-3-carboxylic acid

4-methoxypyrrolidine-3-carboxylic acid

C6H11NO3 (145.0738896)


   

(3-amino-oxetan-3-yl)-acetic acid methyl ester

(3-amino-oxetan-3-yl)-acetic acid methyl ester

C6H11NO3 (145.0738896)


   

BUTANOIC ACID, 2-AMINO-3-OXO-, ETHYL ESTER

BUTANOIC ACID, 2-AMINO-3-OXO-, ETHYL ESTER

C6H11NO3 (145.0738896)


   

N-Acetyl-D-alanine methylester

(R)-Methyl 2-acetamidopropanoate

C6H11NO3 (145.0738896)


   

4-Morpholinylacetic acid

4-Morpholinylacetic acid

C6H11NO3 (145.0738896)


   

(S)-(+)-N-Acetyl-L-Alanine Methyl Ester

(S)-(+)-N-Acetyl-L-Alanine Methyl Ester

C6H11NO3 (145.0738896)


   

(-)-3-oxetanylglycine methyl ester

(-)-3-oxetanylglycine methyl ester

C6H11NO3 (145.0738896)


   

2-(Methoxycarbonylamino)-2-(oxetan-3-yl)acetic acid

2-(Methoxycarbonylamino)-2-(oxetan-3-yl)acetic acid

C6H11NO3 (145.0738896)


   

(2R,5R)-5-Hydroxy-2-piperidinecarboxylic acid

(2R,5R)-5-Hydroxy-2-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

(R)-(3-HYDROXYPYRROLIDIN-1-YL)-ACETIC ACID

(R)-(3-HYDROXYPYRROLIDIN-1-YL)-ACETIC ACID

C6H11NO3 (145.0738896)


   
   

((S)-3-Hydroxy-pyrrolidin-1-yl)-acetic acid

((S)-3-Hydroxy-pyrrolidin-1-yl)-acetic acid

C6H11NO3 (145.0738896)


   

CIS-3-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID

CIS-3-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID

C6H11NO3 (145.0738896)


   

(2S,4R)-1-BOC-4-AMINO-PYRROLIDINE-2-CARBOXYLICACID

(2S,4R)-1-BOC-4-AMINO-PYRROLIDINE-2-CARBOXYLICACID

C6H11NO3 (145.0738896)


   

2-[(Isopropylideneamino)oxy]propanoic acid

2-[(Isopropylideneamino)oxy]propanoic acid

C6H11NO3 (145.0738896)


   

2-Piperidinecarboxylicacid, 4-hydroxy-, (2R,4R)-rel-

2-Piperidinecarboxylicacid, 4-hydroxy-, (2R,4R)-rel-

C6H11NO3 (145.0738896)


   

3-carbamoyl-2,2-dimethyl-propanoic acid

3-carbamoyl-2,2-dimethyl-propanoic acid

C6H11NO3 (145.0738896)


   

5-Oxo-L-norleucine

5-Oxo-L-norleucine

C6H11NO3 (145.0738896)


   

(5S)-5-ammonio-3-oxohexanoate

(5S)-5-ammonio-3-oxohexanoate

C6H11NO3 (145.0738896)


   

(2s,3r)-2-Amino-3-methyl-4-oxopentanoic acid

(2s,3r)-2-Amino-3-methyl-4-oxopentanoic acid

C6H11NO3 (145.0738896)


   

(R)-2-Amino-6-oxohexanoic acid

(R)-2-Amino-6-oxohexanoic acid

C6H11NO3 (145.0738896)


   

2-amino-6-oxohexanoic acid

L-2-Amino-6-oxohexanoic acid

C6H11NO3 (145.0738896)


Found in collagen, elastin and heart muscle

   

(S)-2-Amino-6-oxohexanoate

(S)-2-Amino-6-oxohexanoate

C6H11NO3 (145.0738896)


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

   

6-Amino-2-oxohexanoate

6-Amino-2-oxohexanoate

C6H11NO3 (145.0738896)


   

5-Hydroxypipecolate

5-Hydroxypipecolate

C6H11NO3 (145.0738896)


   

N-hydroxy-L-pipecolic acid

N-hydroxy-L-pipecolic acid

C6H11NO3 (145.0738896)


   

2-Azaniumyl-5-oxohexanoate

2-Azaniumyl-5-oxohexanoate

C6H11NO3 (145.0738896)


   

l-Proline, 3-hydroxy-4-methyl-, (3S,4S)-

l-Proline, 3-hydroxy-4-methyl-, (3S,4S)-

C6H11NO3 (145.0738896)


   

3-hydroxy-4-methyl-L-proline

3-hydroxy-4-methyl-L-proline

C6H11NO3 (145.0738896)


   

(2S,3R)-2-amino-3-methyl-4-ketopentanoate

(2S,3R)-2-amino-3-methyl-4-ketopentanoate

C6H11NO3 (145.0738896)


   
   

But-2-en-2-yl 2-aminoethaneperoxoate

But-2-en-2-yl 2-aminoethaneperoxoate

C6H11NO3 (145.0738896)


   

(2E)-2-(hydroxyimino)isocaproic acid

(2E)-2-(hydroxyimino)isocaproic acid

C6H11NO3 (145.0738896)


   

(E)-2-(methoxyimino)-3-methylbutanoic acid

(E)-2-(methoxyimino)-3-methylbutanoic acid

C6H11NO3 (145.0738896)


   

(4R)-5-oxo-L-leucine

(4R)-5-oxo-L-leucine

C6H11NO3 (145.0738896)


A L-leucine derivative that is L-leucine substituted by an oxo group at position 5.

   

2-Azaniumyl-6-oxohexanoate

2-Azaniumyl-6-oxohexanoate

C6H11NO3 (145.0738896)


   

N-Ethylidenethreonine

N-Ethylidenethreonine

C6H11NO3 (145.0738896)


   

6-amino-2-oxohexanoic acid

6-amino-2-oxohexanoic acid

C6H11NO3 (145.0738896)


   

(S)-5-Amino-3-oxohexanoate

(S)-5-Amino-3-oxohexanoate

C6H11NO3 (145.0738896)


   

2-amino-5-oxohexanoic acid

2-amino-5-oxohexanoic acid

C6H11NO3 (145.0738896)


   

N-Propionylalanine

N-Propionylalanine

C6H11NO3 (145.0738896)


   

allysine zwitterion

allysine zwitterion

C6H11NO3 (145.0738896)


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

   

6-amino-2-oxohexanoic acid zwitterion

6-amino-2-oxohexanoic acid zwitterion

C6H11NO3 (145.0738896)


Zwitterionic form of 6-amino-2-oxohexanoic acid arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3.

   

L-allysine

L-allysine

C6H11NO3 (145.0738896)


An optically active form of allysine having L-configuration.

   

L-allysine zwitterion

L-allysine zwitterion

C6H11NO3 (145.0738896)


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

   
   

Acetamidobutanoic acid

Acetamidobutanoic acid

C6H11NO3 (145.0738896)


   

N-Methyl-4-hydroxyproline

N-Methyl-4-hydroxyproline

C6H11NO3 (145.0738896)


   

Ketoaminocaproate

Ketoaminocaproate

C6H11NO3 (145.0738896)


   

(2r,4s)-4-hydroxypiperidine-2-carboxylic acid

(2r,4s)-4-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s,4r)-4-(hydroxymethyl)pyrrolidine-2-carboxylic acid

(2s,4r)-4-(hydroxymethyl)pyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

(2s)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2r,3s)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid

(2r,3s)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid

C6H11NO3 (145.0738896)


   

(3r,6r)-3,6-dihydroxy-1-methylpiperidin-2-one

(3r,6r)-3,6-dihydroxy-1-methylpiperidin-2-one

C6H11NO3 (145.0738896)


   

(2r,5s)-5-hydroxypiperidine-2-carboxylic acid

(2r,5s)-5-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2R,4S)-4-hydroxypipecolinic acid

(2R,4S)-4-hydroxy-2-piperidinecarboxylic acid; (2R,4S)-4-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


{"Ingredient_id": "HBIN006514","Ingredient_name": "(2R,4S)-4-hydroxypipecolinic acid","Alias": "(2R,4S)-4-hydroxy-2-piperidinecarboxylic acid; (2R,4S)-4-hydroxypiperidine-2-carboxylic acid","Ingredient_formula": "C6H11NO3","Ingredient_Smile": "C1CNC(CC1O)C(=O)O","Ingredient_weight": "145.16 g/mol","OB_score": "70.19561769","CAS_id": "NA","SymMap_id": "SMIT10915","TCMID_id": "NA","TCMSP_id": "MOL009832","TCM_ID_id": "NA","PubChem_id": "11389456","DrugBank_id": "NA"}

   

(2S, 4R)-4-hydroxy-2-piperidine-carboxylic acid

NA

C6H11NO3 (145.0738896)


{"Ingredient_id": "HBIN006745","Ingredient_name": "(2S, 4R)-4-hydroxy-2-piperidine-carboxylic acid","Alias": "NA","Ingredient_formula": "C6H11NO3","Ingredient_Smile": "C1CNC(CC1O)C(=O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "42159","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

(2s,5r)-5-hydroxypiperidine-2-carboxylic acid

(2s,5r)-5-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s,4s)-4-hydroxypiperidine-2-carboxylic acid

(2s,4s)-4-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2r)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

(2r)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

3,6-dihydroxy-1-methylpiperidin-2-one

3,6-dihydroxy-1-methylpiperidin-2-one

C6H11NO3 (145.0738896)


   

4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s,4r)-4-hydroxypiperidine-2-carboxylic acid

(2s,4r)-4-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2r,4r)-4-hydroxypiperidine-2-carboxylic acid

(2r,4r)-4-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s,5s)-5-hydroxypiperidine-2-carboxylic acid

(2s,5s)-5-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s,3z)-2-amino-3-(hydroxymethyl)pent-3-enoic acid

(2s,3z)-2-amino-3-(hydroxymethyl)pent-3-enoic acid

C6H11NO3 (145.0738896)


   

(2r,5r)-5-hydroxypiperidine-2-carboxylic acid

(2r,5r)-5-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

4-[(1-hydroxyethylidene)amino]butanoic acid

4-[(1-hydroxyethylidene)amino]butanoic acid

C6H11NO3 (145.0738896)


   

(2s,4s)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

(2s,4s)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)