Chemical Formula: C17H34O4

Chemical Formula C17H34O4

Found 39 metabolite its formula value is C17H34O4

MG(0:0/14:0/0:0)

1,3-dihydroxypropan-2-yl tetradecanoate

C17H34O4 (302.2456964)


MG(0:0/14:0/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed alpha-monoacylglycerols, while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well. MG(0:0/14:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/14:0/0:0) is made up of one tetradecanoyl(R2).

   

MG(14:0/0:0/0:0)

(2S)-2,3-dihydroxypropyl tetradecanoate

C17H34O4 (302.2456964)


MG(14:0/0:0/0:0) is a monoacylglyceride. A monoglyceride, more correctly known as a monoacylglycerol, is a glyceride consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage. Monoacylglycerol can be broadly divided into two groups; 1-monoacylglycerols (or 3-monoacylglycerols) and 2-monoacylglycerols, depending on the position of the ester bond on the glycerol moiety. Normally the 1-/3-isomers are not distinguished from each other and are termed alpha-monoacylglycerols, while the 2-isomers are beta-monoacylglycerols. Monoacylglycerols are formed biochemically via release of a fatty acid from diacylglycerol by diacylglycerol lipase or hormone sensitive lipase. Monoacylglycerols are broken down by monoacylglycerol lipase. They tend to be minor components only of most plant and animal tissues, and indeed would not be expected to accumulate because their strong detergent properties would have a disruptive effect on membranes. 2-Monoacylglycerols are a major end product of the intestinal digestion of dietary fats in animals via the enzyme pancreatic lipase. They are taken up directly by the intestinal cells and converted to triacylglycerols via the monoacylglycerol pathway before being transported in lymph to the liver. Mono- and Diglycerides are commonly added to commercial food products in small quantities. They act as emulsifiers, helping to mix ingredients such as oil and water that would not otherwise blend well. MG(14:0/0:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(14:0/0:0/0:0) is made up of one tetradecanoyl(R1).

   

MG(0:0/i-14:0/0:0)

1,3-dihydroxypropan-2-yl 12-methyltridecanoate

C17H34O4 (302.2456964)


MG(0:0/i-14:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/i-14:0/0:0) is made up of one 12-methyltridecanoyl(R2).

   

MG(i-14:0/0:0/0:0)

[(2R)-2,3-dihydroxypropyl] 12-methyltridecanoate

C17H34O4 (302.2456964)


MG(i-14:0/0:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(i-14:0/0:0/0:0) is made up of one 12-methyltridecanoyl(R1).

   

Glycerol 1-myristate

2,3-Dihydroxypropyl tetradecanoate

C17H34O4 (302.2456964)


1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3]. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3]. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3].

   

methyl 10,16-dihydroxyhexadecanoate

methyl 10,16-dihydroxyhexadecanoate

C17H34O4 (302.2456964)


   

METHYL 9,16-DIHYDROXYHEXADECANOATE

METHYL 9,16-DIHYDROXYHEXADECANOATE

C17H34O4 (302.2456964)


   

methyl 3,11-dihydroxyhexadecanoate

methyl 3,11-dihydroxyhexadecanoate

C17H34O4 (302.2456964)


   

methyl 8,16-dihydroxyhexadecanoate

methyl 8,16-dihydroxyhexadecanoate

C17H34O4 (302.2456964)


   

Me ester-4, 12-Dihydroxyhexadecanoic acid

Me ester-4, 12-Dihydroxyhexadecanoic acid

C17H34O4 (302.2456964)


   
   

OC(CCCCCCCCC(=O)O)CCCCCCCO

OC(CCCCCCCCC(=O)O)CCCCCCCO

C17H34O4 (302.2456964)


   

(+)-(3S,12S)-3,12-dihydroxypalmitic acid methyl ester|Methyl-3,12-Dihydroxyhexadecanoic acid

(+)-(3S,12S)-3,12-dihydroxypalmitic acid methyl ester|Methyl-3,12-Dihydroxyhexadecanoic acid

C17H34O4 (302.2456964)


   

MG 14:0

Tetradecanoic acid, monoester with 1,2,3-propanetriol

C17H34O4 (302.2456964)


1-monomyristoylglycerol is a 1-monoglyceride with tetradecanoyl (myristoyl) as the acyl group. It has a role as a Caenorhabditis elegans metabolite. It is a 1-monoglyceride and a tetradecanoate ester. 2,3-Dihydroxypropyl tetradecanoate is a natural product found in Caenorhabditis elegans and Aeromonas veronii with data available. A 1-monoglyceride with tetradecanoyl (myristoyl) as the acyl group. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3]. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3]. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3].

   

2,3-dihydroxypropyl 12-methyltridecanoate

NCGC00381197-01!2,3-dihydroxypropyl 12-methyltridecanoate

C17H34O4 (302.2456964)


   

2-Myristoylglycerol

2-Myristoylglycerol

C17H34O4 (302.2456964)


   
   

rac-Glycerol 1-myristate

rac-Glycerol 1-myristate

C17H34O4 (302.2456964)


   

GLYCEROL-MYRISTATE

rac-Glycerol 1-myristate

C17H34O4 (302.2456964)


1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3]. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3]. 1-Monomyristin, extracted from Serenoa repens, inhibits the hydrolysis of 2-oleoylglycerol (IC50=32 μM) and fatty acid amide hydrolase (FAAH) activity (IC50=18 μM). 1-Monomyristin shows antibacterial activity against Staphylococcus aureus and Aggregatibacter actinomycetemcomitans and also antifungal activity against Candida albicans[1][2][3].

   

MG(14:0)

1-Tetradecanoyl-rac-glycerol

C17H34O4 (302.2456964)


   

2,3-Dihydroxypropyl 12-methyltridecanoate

2,3-Dihydroxypropyl 12-methyltridecanoate

C17H34O4 (302.2456964)


   

FA 17:0;O2

3,4-dihydroxy-4-methylhexadecanoic acid

C17H34O4 (302.2456964)


   

MG O-14:1;O

1-O-(2R-hydroxy-4Z-tetradecenyl)-sn-glycerol

C17H34O4 (302.2456964)


   

1,1-Bis(t-butylperoxy)-3,3,5-trimethylcyclohexane

1,1-Bis(t-butylperoxy)-3,3,5-trimethylcyclohexane

C17H34O4 (302.2456964)


   

1-Myristoyl-sn-glycerol

1-Myristoyl-sn-glycerol

C17H34O4 (302.2456964)


A 1-acyl-sn-glycerol that is the S-enantiomer of 1-myristoyl glycerol.

   

3-Myristoyl-sn-glycerol

3-Myristoyl-sn-glycerol

C17H34O4 (302.2456964)


A 3-acyl-sn-glycerol that is the R-enantiomer of 1-myristoyl glycerol.

   

(3R)-3,17-dihydroxymargaric acid

(3R)-3,17-dihydroxymargaric acid

C17H34O4 (302.2456964)


A dihydroxy monocarboxylic acid that is 17-hydroxymargaric acid (17-hydroxyheptadecanoic acid) in which the pro-R hydrogen beta to the carboxy group is replaced by a hydroxy group.

   

(3R,16R)-3,16-dihydroxymargaric acid

(3R,16R)-3,16-dihydroxymargaric acid

C17H34O4 (302.2456964)


An (omega-1)-hydroxy fatty acid that is (16R)-16-hydroxymargaric acid ((16R)-16-hydroxyheptadecanoic acid) in which the 3-pro-R hydrogen is replaced by a hydroxy group.

   

(1-Hydroxy-3-nonoxypropan-2-yl) pentanoate

(1-Hydroxy-3-nonoxypropan-2-yl) pentanoate

C17H34O4 (302.2456964)


   

(1-Hydroxy-3-octoxypropan-2-yl) hexanoate

(1-Hydroxy-3-octoxypropan-2-yl) hexanoate

C17H34O4 (302.2456964)


   

(1-Decoxy-3-hydroxypropan-2-yl) butanoate

(1-Decoxy-3-hydroxypropan-2-yl) butanoate

C17H34O4 (302.2456964)


   

(1-Dodecoxy-3-hydroxypropan-2-yl) acetate

(1-Dodecoxy-3-hydroxypropan-2-yl) acetate

C17H34O4 (302.2456964)


   

(1-Hydroxy-3-undecoxypropan-2-yl) propanoate

(1-Hydroxy-3-undecoxypropan-2-yl) propanoate

C17H34O4 (302.2456964)


   

2-tetradecanoylglycerol

2-tetradecanoylglycerol

C17H34O4 (302.2456964)


A 2-monoglyceride where the acyl group is tetradecanoyl (myristoyl).

   

3,4-dihydroxy-4-methylhexadecanoic acid

3,4-dihydroxy-4-methylhexadecanoic acid

C17H34O4 (302.2456964)


A dihydroxy monocarboxylic acid that consists of palmitic acid bearing two hydroxy substituents at positions 3 and 4 and a methyl substituent at position 4.

   

1-O-(2R-hydroxy-4Z-tetradecenyl)-sn-glycerol

1-O-(2R-hydroxy-4Z-tetradecenyl)-sn-glycerol

C17H34O4 (302.2456964)


   

monoacylglycerol 14:0

monoacylglycerol 14:0

C17H34O4 (302.2456964)


A monoglyceride in which the acyl contains a total of 14 carbon atoms and 0 double bonds.

   

DG(14:0)

DG(8:0(1)_6:0)

C17H34O4 (302.2456964)


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