Chemical Formula: C12H24N2O3
Chemical Formula C12H24N2O3
Found 57 metabolite its formula value is C12H24N2O3
Leucyl-leucine
Leucylleucine is a dipeptide composed of two leucine residues. It is an incomplete breakdown product of protein digestion or protein catabolism. 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. Leu-Leu-OH, a Leu derivative, is a dipeptide.
6-(6-aminohexanamido)hexanoic acid
C12H24N2O3 (244.17868339999998)
Isoleucyl-Isoleucine
C12H24N2O3 (244.17868339999998)
Isoleucyl-Isoleucine is a dipeptied compoosed of two isoleucine residues. 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. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.
Leucyl-Isoleucine
C12H24N2O3 (244.17868339999998)
Leucyl-Isoleucine is a dipeptide composed of leucine and isoleucine. 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. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.
Isoleucyl-Leucine
C12H24N2O3 (244.17868339999998)
Isoleucyl-Leucine is a dipeptide composed of isoleucine and leucine. 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. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.
(2S)-6-Amino-2-(hexanoylamino)hexanoic Acid
C12H24N2O3 (244.17868339999998)
Leucyl-leucine
C12H24N2O3 (244.17868339999998)
N-Leucyl-leucine; AIF; CE0; CorrDec
C12H24N2O3 (244.17868339999998)
N-Leucyl-leucine; AIF; CE10; CorrDec
C12H24N2O3 (244.17868339999998)
N-Leucyl-leucine; AIF; CE30; CorrDec
C12H24N2O3 (244.17868339999998)
N-Leucyl-leucine; AIF; CE0; MS2Dec
C12H24N2O3 (244.17868339999998)
N-Leucyl-leucine; AIF; CE10; MS2Dec
C12H24N2O3 (244.17868339999998)
N-Leucyl-leucine; AIF; CE30; MS2Dec
C12H24N2O3 (244.17868339999998)
Ile-ile
C12H24N2O3 (244.17868339999998)
A dipeptide formed from two L-isoleucine residues.
Ile-leu
C12H24N2O3 (244.17868339999998)
A dipeptide formed from L-isoleucine and L-leucine residues.
Leu-ile
C12H24N2O3 (244.17868339999998)
A dipeptide formed from L-leucine and L-isoleucine residues.
(S)-2-(3-(TERT-BUTYL)-3-METHYLUREIDO)-3,3-DIMETHYLBUTANOIC ACID
C12H24N2O3 (244.17868339999998)
tert-Butyl 4-(2-aminoethyl)-4-hydroxypiperidine-1-carboxylate
C12H24N2O3 (244.17868339999998)
1-BOC-3-(2-METHOXYETHYLAMINO)PYRROLIDINE
C12H24N2O3 (244.17868339999998)
1-BOC-4-AMINOMETHYL-4-METHOXYPIPERIDINE
C12H24N2O3 (244.17868339999998)
1-(1H-PYRAZOL-5-YL)ETHAN-1-ONEHYDROCHLORIDE
C12H24N2O3 (244.17868339999998)
1-Piperazinecarboxylicacid, 4-(3-hydroxypropyl)-, 1,1-dimethylethyl ester
C12H24N2O3 (244.17868339999998)
1-BOC-3-(3-METHOXY-PROPYLAMINO)-AZETIDINE
C12H24N2O3 (244.17868339999998)
tert-butyl 4-(2-amino-1-hydroxyethyl)piperidine-1-carboxylate
C12H24N2O3 (244.17868339999998)
4-(2-hydroxy-propyl)-piperazine-1-carboxylic acid tert-butyl ester
C12H24N2O3 (244.17868339999998)
Leu-leu
C12H24N2O3 (244.17868339999998)
A dipeptide formed from two L-leucine residues. Leu-Leu-OH, a Leu derivative, is a dipeptide.
N-(6-Aminohexanoyl)-6-aminohexanoate
C12H24N2O3 (244.17868339999998)
Leu-Leu zwitterion
C12H24N2O3 (244.17868339999998)
An L-aminoacyl-L-amino acid zwitterion resulting from transfer of a proton from the carboxy to the amino group of L-leucyl-L-leucine; major species at pH 7.3.
N-(6-aminohexanoyl)-6-aminohexanoic acid zwitterion
C12H24N2O3 (244.17868339999998)
Zwitterionic form N-(6-aminohexanoyl)-6-aminohexanoic acid.
Ile-Leu zwitterion
C12H24N2O3 (244.17868339999998)
A dipeptide zwitterion obtained by transfer of a proton from the carboxy to the amino terminus of Ile-Leu.