Chemical Formula: C8H16N2O4

Chemical Formula C8H16N2O4

Found 68 metabolite its formula value is C8H16N2O4

ACMC-20lajd

N(6)-acetyl-N(6)-hydroxy-L-lysine

C8H16N2O4 (204.1110016)


   

ACMC-20m7bf

N(5)-(L-1-carboxyethyl)-L-ornithine

C8H16N2O4 (204.1110016)


   

N6-Acetyl-5S-hydroxy-L-lysine

2-Amino-5-hydroxy-6-[(1-hydroxyethylidene)amino]hexanoate

C8H16N2O4 (204.1110016)


N6-Acetyl-5S-hydroxy-L-lysine is found in root vegetables. N6-Acetyl-5S-hydroxy-L-lysine is produced by Beta vulgaris (sugar beet). Production by Beta vulgaris (sugar beet). N6-Acetyl-5S-hydroxy-L-lysine is found in root vegetables.

   

3,4-Dihydroxy-2-hydroxymethyl-1-pyrrolidinepropanamide

3-[3,4-Dihydroxy-2-(hydroxymethyl)pyrrolidin-1-yl]propanimidate

C8H16N2O4 (204.1110016)


3,4-Dihydroxy-2-hydroxymethyl-1-pyrrolidinepropanamide is found in fruits. 3,4-Dihydroxy-2-hydroxymethyl-1-pyrrolidinepropanamide is an alkaloid from Morus alba (white mulberry). Alkaloid from Morus alba (white mulberry). 3,4-Dihydroxy-2-hydroxymethyl-1-pyrrolidinepropanamide is found in fruits.

   

Serylvaline

(2S)-2-[(2S)-2-amino-3-hydroxypropanamido]-3-methylbutanoic acid

C8H16N2O4 (204.1110016)


Serylvaline is a dipeptide composed of serine and valine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis.

   

Valylserine

(2S)-2-[(2S)-2-amino-3-methylbutanamido]-3-hydroxypropanoic acid

C8H16N2O4 (204.1110016)


Valylserine is a dipeptide composed of valine and serine. It is an incomplete breakdown product of protein digestion or protein catabolism. Dipeptides are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Some dipeptides are known to have physiological or cell-signalling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis.

   

N6-Carboxymethyllysine

(2S)-2-amino-6-[(carboxymethyl)amino]hexanoic acid

C8H16N2O4 (204.1110016)


N6-Carboxymethyllysine (CML), also known as epsilon-(carboxymethyl)lysine, belongs to the class of organic compounds known as L-alpha-amino acids. These are alpha-amino acids which have the L-configuration of the alpha-carbon atom. CML is a Maillard reaction product, or dietary advanced glycation end-products (d-AGE), formed as a result of the thermal treatment of foods. Due to its chemical stability and its ubiquity in foods and in vivo, CML is used as a biomarker for the ingestion of thermally treated foods. CML is metabolized by intestinal bacteria under anaerobic conditions (PMID: 31091091).

   

N-(3-Amino-2-hydroxy-3-oxopropyl)-L-valine

2-{[2-hydroxy-2-(C-hydroxycarbonimidoyl)ethyl]amino}-3-methylbutanoate

C8H16N2O4 (204.1110016)


   

Carboxy methyl lysine

6-amino-2-[carboxy(methyl)amino]hexanoic acid

C8H16N2O4 (204.1110016)


   

epsilon-(Carboxymethyl)lysine

epsilon-(Carboxymethyl)lysine

C8H16N2O4 (204.1110016)


   

n-carboxymethyllysine

6-amino-2-[(carboxymethyl)amino]hexanoic acid

C8H16N2O4 (204.1110016)


   

2-[(2S)-2,6-Diaminohexanoyl]oxyacetic acid

2-[(2S)-2,6-Diaminohexanoyl]oxyacetic acid

C8H16N2O4 (204.1110016)


   

[(2S)-6-Amino-1-methoxy-1-oxohexan-2-yl]carbamic acid

[(2S)-6-Amino-1-methoxy-1-oxohexan-2-yl]carbamic acid

C8H16N2O4 (204.1110016)


   

5-amino-2-(1-carboxyethylamino)pentanoic Acid

5-amino-2-(1-carboxyethylamino)pentanoic Acid

C8H16N2O4 (204.1110016)


   
   

Me ester;B,HCl 鈥樎橪-D-N-Alanylthreonine

Me ester;B,HCl 鈥樎橪-D-N-Alanylthreonine

C8H16N2O4 (204.1110016)


   

N|A-Carboxymethyl-L-lysine

N|A-Carboxymethyl-L-lysine

C8H16N2O4 (204.1110016)


   

alpha-D-gluco-4-acetylamino-2-amino-2,4,6-trideoxy-hexopyranose; hydrochloride|alpha-D-gluco-4-Acetylamino-2-amino-2,4,6-tridesoxy-hexopyranose; Hydrochlorid

alpha-D-gluco-4-acetylamino-2-amino-2,4,6-trideoxy-hexopyranose; hydrochloride|alpha-D-gluco-4-Acetylamino-2-amino-2,4,6-tridesoxy-hexopyranose; Hydrochlorid

C8H16N2O4 (204.1110016)


   
   
   
   

Suberohydroxamic Acid

N1,N8-dihydroxy-octanediamide

C8H16N2O4 (204.1110016)


   

Ser-val

2-(2-amino-3-methylbutanamido)-3-hydroxypropanoic acid

C8H16N2O4 (204.1110016)


A dipeptide formed from L-serine and L-valine residues.

   

Val-ser

2-(2-amino-3-hydroxypropanamido)-3-methylbutanoic acid

C8H16N2O4 (204.1110016)


A dipeptide formed from L-valine and L-serine residues.

   

N6-Acetyl-5S-hydroxy-L-lysine

2-amino-6-acetamido-5-hydroxyhexanoic acid

C8H16N2O4 (204.1110016)


   

3,4-Dihydroxy-2-hydroxymethyl-1-pyrrolidinepropanamide

3-[3,4-dihydroxy-2-(hydroxymethyl)pyrrolidin-1-yl]propanamide

C8H16N2O4 (204.1110016)


   

HSP;N-hydroxy-N-succinylputrescine

4-[(4-aminobutyl)(hydroxy)amino]-4-oxobutanoic acid

C8H16N2O4 (204.1110016)


   

2-Acetamido-1,2-dideoxynojirimycin

2-Acetamido-1,2-dideoxynojirimycin

C8H16N2O4 (204.1110016)


   

2-(HYDROXYAMINO)CYCLOHEXAN-1-ONE OXIME ACETATE

2-(HYDROXYAMINO)CYCLOHEXAN-1-ONE OXIME ACETATE

C8H16N2O4 (204.1110016)


   

diisopropyl bicarbamate

diisopropyl bicarbamate

C8H16N2O4 (204.1110016)


   
   

(S)-TERT-BUTYL1-(HYDROXYAMINO)-3-(4-BROMOPHENYL)-1-OXOPROPAN-2-YLCARBAMATE

(S)-TERT-BUTYL1-(HYDROXYAMINO)-3-(4-BROMOPHENYL)-1-OXOPROPAN-2-YLCARBAMATE

C8H16N2O4 (204.1110016)


   

Pentabamate

Pentabamate

C8H16N2O4 (204.1110016)


C78272 - Agent Affecting Nervous System > C264 - Anticonvulsant Agent

   

N(Alpha)-Boc-L-2,3-Diaminopropionic Acid

N(Alpha)-Boc-L-2,3-Diaminopropionic Acid

C8H16N2O4 (204.1110016)


   

3-amino-N-(tert-butoxycarbonyl)-L-alanine

3-amino-N-(tert-butoxycarbonyl)-L-alanine

C8H16N2O4 (204.1110016)


   

n-butyloxycarbonyl-dap-oh

n-butyloxycarbonyl-dap-oh

C8H16N2O4 (204.1110016)


   
   

ethylidene diurethan

ethylidene diurethan

C8H16N2O4 (204.1110016)


   

N,N,N,N-Tetramethyl-L-tartramide

N,N,N,N-Tetramethyl-L-tartramide

C8H16N2O4 (204.1110016)


   

(2r,3r,4s,5r)-2-Acetamido-3,4-Dihydroxy-5-Hydroxymethyl-Piperidine

(2r,3r,4s,5r)-2-Acetamido-3,4-Dihydroxy-5-Hydroxymethyl-Piperidine

C8H16N2O4 (204.1110016)


   

N,N-Dihydroxyoctanediamide

N,N-Dihydroxyoctanediamide

C8H16N2O4 (204.1110016)


   

gamma-glutamyl-L-alaninol

gamma-glutamyl-L-alaninol

C8H16N2O4 (204.1110016)


   

N-hydroxy-N-succinyl-putrescine

N-hydroxy-N-succinyl-putrescine

C8H16N2O4 (204.1110016)


   

(2S)-6-[acetyl(hydroxy)amino]-2-azaniumylhexanoate

(2S)-6-[acetyl(hydroxy)amino]-2-azaniumylhexanoate

C8H16N2O4 (204.1110016)


   

2-Acetamido-4-amino-2,4,6-trideoxy-d-galactose

2-Acetamido-4-amino-2,4,6-trideoxy-d-galactose

C8H16N2O4 (204.1110016)


   

N-(gamma-L-glutamyl)-L-alaninol

N-(gamma-L-glutamyl)-L-alaninol

C8H16N2O4 (204.1110016)


A N(5)-alkylglutamine obtained by formal condensation of the side-chain carboxy group of L-glutamic acid with the amino group of L-alaninol.

   

N-Acetylbacillosamine

N-Acetylbacillosamine

C8H16N2O4 (204.1110016)


   

n5-(Carboxy ethyl)ornithine

n5-(Carboxy ethyl)ornithine

C8H16N2O4 (204.1110016)


   

(2S)-2-azaniumyl-5-(2-carboxylatoethylazaniumyl)pentanoate

(2S)-2-azaniumyl-5-(2-carboxylatoethylazaniumyl)pentanoate

C8H16N2O4 (204.1110016)


   

N-[(2S,3S,4S,5S,6S)-2,4,5-trihydroxy-6-methyloxan-3-yl]ethanimidamide

N-[(2S,3S,4S,5S,6S)-2,4,5-trihydroxy-6-methyloxan-3-yl]ethanimidamide

C8H16N2O4 (204.1110016)


   

[(2S)-6-Amino-1-methoxy-1-oxohexan-2-yl]carbamic acid

[(2S)-6-Amino-1-methoxy-1-oxohexan-2-yl]carbamic acid

C8H16N2O4 (204.1110016)


   

(2S)-2-azaniumyl-5-{[(1S)-1-carboxylatoethyl]azaniumyl}pentanoate

(2S)-2-azaniumyl-5-{[(1S)-1-carboxylatoethyl]azaniumyl}pentanoate

C8H16N2O4 (204.1110016)


   

n-carboxymethyllysine

n-carboxymethyllysine

C8H16N2O4 (204.1110016)


   

GALA-N6 glycoloyl lysine

GALA-N6 glycoloyl lysine

C8H16N2O4 (204.1110016)


   

N(6)-acetyl-N(6)-hydroxy-L-lysine

N(6)-acetyl-N(6)-hydroxy-L-lysine

C8H16N2O4 (204.1110016)


   

N(5)-(L-1-carboxyethyl)-L-ornithine

N(5)-(L-1-carboxyethyl)-L-ornithine

C8H16N2O4 (204.1110016)


   

N-(3-carboxypropanoyl)-N-hydroxyputrescine

N-(3-carboxypropanoyl)-N-hydroxyputrescine

C8H16N2O4 (204.1110016)


   

N(6)-carboxymethyl-L-lysine

N(6)-carboxymethyl-L-lysine

C8H16N2O4 (204.1110016)


An L-lysine derivative with a carboxymethyl substituent at the N(6)-position.

   

L-Serine, L-valyl-

2-[(2-Amino-3-methylbutanoyl)amino]-3-hydroxypropanoic acid

C8H16N2O4 (204.1110016)


   

N(5)-(L-1-carboxyethyl)-L-ornithine dizwitterion

N(5)-(L-1-carboxyethyl)-L-ornithine dizwitterion

C8H16N2O4 (204.1110016)


Dizwitterionic form of N(5)-(L-1-carboxyethyl)-L-ornithine having anionic carboxy groups and cationic amino groups; major species at pH 7.3.

   

N(6)-acetyl-N(6)-hydroxy-L-lysine zwitterion

N(6)-acetyl-N(6)-hydroxy-L-lysine zwitterion

C8H16N2O4 (204.1110016)


Zwitterionic form of N(6)-acetyl-N(6)-hydroxy-L-lysine arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3

   

N-(gamma-L-glutamyl)-L-alaninol zwitterion

N-(gamma-L-glutamyl)-L-alaninol zwitterion

C8H16N2O4 (204.1110016)


An amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of N-(gamma-L-glutamyl)-L-alaninol; major species at pH 7.3.

   

N1-Hydroxy-N1-succinylputrescine

N1-Hydroxy-N1-succinylputrescine

C8H16N2O4 (204.1110016)


   

N(6)-Acetyl-N(6)-hydroxy-lysine

N(6)-Acetyl-N(6)-hydroxy-lysine

C8H16N2O4 (204.1110016)


   

N(6)-Carboxymethyl-lysine

N(6)-Carboxymethyl-lysine

C8H16N2O4 (204.1110016)


   

N-Lactoyl ornithine

N-Lactoyl ornithine

C8H16N2O4 (204.1110016)


   

(2s)-2-{[(2s)-2-amino-1-hydroxy-3-methylbutylidene]amino}-3-hydroxypropanoic acid

(2s)-2-{[(2s)-2-amino-1-hydroxy-3-methylbutylidene]amino}-3-hydroxypropanoic acid

C8H16N2O4 (204.1110016)


   

n-[(2r,3s,4r,5r,6s)-5-amino-4,6-dihydroxy-2-methyloxan-3-yl]ethanimidic acid

n-[(2r,3s,4r,5r,6s)-5-amino-4,6-dihydroxy-2-methyloxan-3-yl]ethanimidic acid

C8H16N2O4 (204.1110016)