Exact Mass: 328.279742

Exact Mass Matches: 328.279742

Found 39 metabolites which its exact mass value is equals to given mass value 328.279742, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

N-Lauroyl Lysine

6-amino-2-dodecanamidohexanoic acid

C18H36N2O3 (328.2725786)


N-lauroyl lysine belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Lauric acid amide of Lysine. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Lauroyl Lysine is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Lauroyl Lysine is therefore classified as a long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.

   
   

Trimethylsilyl palmitoate

Hexadecanic acid, trimethylsilyl ester

C19H40O2Si (328.279742)


   

Norcon-5-enine, 3.beta.-(methylamino)-

Norcon-5-enine, 3.beta.-(methylamino)-

C22H36N2 (328.2878336)


   

3alpha-Amino-conanen-(5)

3alpha-Amino-conanen-(5)

C22H36N2 (328.2878336)


   
   
   

3-heptadecadienylphenol

3-heptadecadienylphenol

C23H36O (328.2766006)


   

15S-HETE-d8

15S-hydroxy-5Z,8Z,11Z,13E-eicosatetraenoic acid-d8

C20H24D8O3 (328.285349624)


   

12S-HETE-d8

12S-hydroxy-5Z,8Z,10E,14Z-eicosatetraenoic acid-d8

C20H24D8O3 (328.285349624)


   

(±)11,12-EpETrE-d8

11,12-epoxy-5Z,8Z,14Z-eicosatrienoic acid-d8

C20H24D8O3 (328.285349624)


   

5S-HETE-d8

5S-hydroxy-6E,8Z,11Z,14Z-eicosatetraenoic acid (5,6,8,9,11,12,14,15-d8)

C20H24D8O3 (328.285349624)


   

20:1(9Z)(20F)

20-fluoro-9Z-eicosenoic acid

C20H37FO2 (328.27774339999996)


   

20:1(11Z)(20F)

20-fluoro-11Z-eicosenoic acid

C20H37FO2 (328.27774339999996)


   

(+/-)14,15-EpETrE-(d8)

14,15-epoxy-5Z,8Z,11Z-eicosatrienoic acid-(d8)

C20H24D8O3 (328.285349624)


   

(+/-)8,9-EpETrE-(d8)

8,9-epoxy-5Z,11Z,14Z-eicosatrienoic acid-(d8)

C20H24D8O3 (328.285349624)


   

(+/-)11,12-EpETrE-d8

11,12-epoxy-5Z,8Z,14Z-eicosatrienoic acid-d8

C20H24D8O3 (328.285349624)


   

N-lauroyl lysine

(S)-6-Amino-2-dodecanamidohexanoic acid

C18H36N2O3 (328.2725786)


   

N6-lauroyl lysine

(2S)-2-amino-6-(dodecanoylamino) hexanoic acid

C18H36N2O3 (328.2725786)


   

N2-Dodecanoyl-L-lysine

N2-Dodecanoyl-L-lysine

C18H36N2O3 (328.2725786)


   

N2-(1-Oxododecyl)-L-lysine

N2-(1-Oxododecyl)-L-lysine

C18H36N2O3 (328.2725786)


   

N-[(5S)-5-(hexanoylamino)-6-hydroxyhexyl]hexanamide

N-[(5S)-5-(hexanoylamino)-6-hydroxyhexyl]hexanamide

C18H36N2O3 (328.2725786)


   

Hexadecanoic acid, trimethylsilyl ester

Hexadecanoic acid, trimethylsilyl ester

C19H40O2Si (328.279742)


   

2-Methylpentadecanoic acid trimethylsilyl ester

2-Methylpentadecanoic acid trimethylsilyl ester

C19H40O2Si (328.279742)


   

Isopalmitic acid trimethylsilyl

Isopalmitic acid trimethylsilyl

C19H40O2Si (328.279742)


   
   
   
   
   

3-epicaonamine

NA

C22H36N2 (328.2878336)


{"Ingredient_id": "HBIN008471","Ingredient_name": "3-epicaonamine","Alias": "NA","Ingredient_formula": "C22H36N2","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "25801","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

3-epiconamine

NA

C22H36N2 (328.2878336)


{"Ingredient_id": "HBIN008472","Ingredient_name": "3-epiconamine","Alias": "NA","Ingredient_formula": "C22H36N2","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "6872","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

(2s)-6-amino-2-[(1-hydroxydodecylidene)amino]hexanoic acid

(2s)-6-amino-2-[(1-hydroxydodecylidene)amino]hexanoic acid

C18H36N2O3 (328.2725786)


   

6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-16-amine

6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-16-amine

C22H36N2 (328.2878336)


   

1-{4-decyltetracyclo[5.4.0.0²,⁵.0³,⁹]undec-10-en-8-yl}ethanone

1-{4-decyltetracyclo[5.4.0.0²,⁵.0³,⁹]undec-10-en-8-yl}ethanone

C23H36O (328.2766006)


   

3-(heptadeca-1,3-dien-1-yl)phenol

3-(heptadeca-1,3-dien-1-yl)phenol

C23H36O (328.2766006)


   

1-[(1s,2s,3s,4r,5s,7s,8r)-4-decyltetracyclo[5.4.0.0²,⁵.0³,⁹]undec-10-en-8-yl]ethanone

1-[(1s,2s,3s,4r,5s,7s,8r)-4-decyltetracyclo[5.4.0.0²,⁵.0³,⁹]undec-10-en-8-yl]ethanone

C23H36O (328.2766006)


   

1-[(1s,2s,3s,4r,5s,7s,8r,9r)-4-decyltetracyclo[5.4.0.0²,⁵.0³,⁹]undec-10-en-8-yl]ethanone

1-[(1s,2s,3s,4r,5s,7s,8r,9r)-4-decyltetracyclo[5.4.0.0²,⁵.0³,⁹]undec-10-en-8-yl]ethanone

C23H36O (328.2766006)


   

(2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

(2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

C18H36N2O3 (328.2725786)


   

(1s,2r,5s,6r,9r,12s,13s,16r)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-16-amine

(1s,2r,5s,6r,9r,12s,13s,16r)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-18-en-16-amine

C22H36N2 (328.2878336)