NCBI Taxonomy: 82087

Ferula tenuisecta (ncbi_taxid: 82087)

found 40 associated metabolites at species taxonomy rank level.

Ancestor: Ferula

Child Taxonomies: none taxonomy data.

PA(16:0/16:0)

2-(Hexadecanoyloxy)-1-[(phosphonooxy)methyl]ethyl hexadecanoate

C35H69O8P (648.4729804)


PA(16:0/16:0) is a phosphatidic acid. It is a glycerophospholipid in which a phosphate moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidic acids can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PA(16:0/16:0), in particular, consists of one chain of palmitic acid at the C-1 position and one chain of palmitic acid at the C-2 position. The palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats, while the palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats. Phosphatidic acids are quite rare but are extremely important as intermediates in the biosynthesis of triacylglycerols and phospholipids. Indeed, the concentration of phosphatidic acids is often over-estimated in tissues and biofluids as it can arise by inadvertent enzymatic hydrolysis during inappropriate storage or extraction conditions during analysis. The main biosynthetic route of phosphatidic acid in animal tissues involves sequential acylation of alpha-glycerophosphate by acyl-coA derivatives of fatty acids. PAs are biologically active lipids that can stimulate a large range of responses in many different cell types, such as platelet aggregation, smooth muscle contraction, in vivo vasoactive effects, chemotaxis, expression of adhesion molecules, increased tight junction permeability of endothelial cells, induction of stress fibres, modulation of cardiac contractility, and many others. Diacylglycerols (DAGs) can be converted to PAs by DAG kinases and indirect evidence supports the notion that PAs alter the excitability of neurons. Phospholipase Ds (PLDs), which catalyze the conversion of glycerolphospholipids, particularly phosphatidylcholine, to PAs and the conversion of N-arachidonoyl-phosphatidylethanolamine (NAPE) to anandamide and PAs are activated by several inflammatory mediators including bradykinin, ATP and glutamate. PAs activate downstream signaling pathways such as PKCs and mitogen-activated protein kinases (MAPKs), which are linked to an increase in sensitivity of sensory neurons either during inflammation or in chronic pain models. Circumstantial evidence that PAs are converted to DAGs. (PMID: 12618218, 16185776). [HMDB] PA(16:0/16:0) is a phosphatidic acid. It is a glycerophospholipid in which a phosphate moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidic acids can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PA(16:0/16:0), in particular, consists of one chain of palmitic acid at the C-1 position and one chain of palmitic acid at the C-2 position. The palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats, while the palmitic acid moiety is derived from fish oils, milk fats, vegetable oils and animal fats. Phosphatidic acids are quite rare but are extremely important as intermediates in the biosynthesis of triacylglycerols and phospholipids. Indeed, the concentration of phosphatidic acids is often over-estimated in tissues and biofluids as it can arise by inadvertent enzymatic hydrolysis during inappropriate storage or extraction conditions during analysis. The main biosynthetic route of phosphatidic acid in animal tissues involves sequential acylation of alpha-glycerophosphate by acyl-CoA derivatives of fatty acids. PAs are biologically active lipids that can stimulate a large range of responses in many different cell types, such as platelet aggregation, smooth muscle contraction, in vivo vasoactive effects, chemotaxis, expression of adhesion molecules, increased tight junction permeability of endothelial cells, induction of stress fibres, modulation of cardiac contractility, and many others. Diacylglycerols (DAGs) can be converted to PAs by DAG kinases and indirect evidence supports the notion that PAs alter the excitability of neurons. Phospholipase Ds (PLDs), which catalyze the conversion of glycerolphospholipids, particularly phosphatidylcholine, to PAs and the conversion of N-arachidonoyl-phosphatidylethanolamine (NAPE) to anandamide and PAs are activated by several inflammatory mediators including bradykinin, ATP and glutamate. PAs activate downstream signaling pathways such as PKCs and mitogen-activated protein kinases (MAPKs), which are linked to an increase in sensitivity of sensory neurons either during inflammation or in chronic pain models. Circumstantial evidence that PAs are converted to DAGs. (PMID: 12618218, 16185776).

   

Lysophosphatidylcholine

(2-{[3-(acetyloxy)-2-hydroxypropyl phosphono]oxy}ethyl)trimethylazanium

C10H22NO7P (299.1133832)


   

1,2-Dipalmitoy

2-(Hexadecanoyloxy)-1-[(phosphonooxy)methyl]ethyl hexadecanoate

C35H69O8P (648.4729804)


   

Dipalmitoyl

Hexadecanoic acid, 1-[(phosphonooxy)methyl]-1,2-ethanediyl ester, (R)-

C35H69O8P (648.4729804)


   

Lysophosphatidylcholine

Lysophosphatidylcholines (egg)

C10H22NO7P (299.1133832)


   

(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate

C22H30O4 (358.214398)


   
   

6-hydroxy-3-isopropyl-1a,6-dimethyl-octahydroazuleno[1,2-b]oxiren-4-yl 4-hydroxybenzoate

6-hydroxy-3-isopropyl-1a,6-dimethyl-octahydroazuleno[1,2-b]oxiren-4-yl 4-hydroxybenzoate

C22H30O5 (374.209313)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

C23H32O4 (372.2300472)


   

(3s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

(3s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

C23H32O5 (388.2249622)


   

6-hydroxy-3-isopropyl-1a,6-dimethyl-octahydroazuleno[1,2-b]oxiren-4-yl 4-hydroxy-3-methoxybenzoate

6-hydroxy-3-isopropyl-1a,6-dimethyl-octahydroazuleno[1,2-b]oxiren-4-yl 4-hydroxy-3-methoxybenzoate

C23H32O6 (404.2198772)


   

2,3-dihydroxypropoxy(3-(hexadecanoyloxy)-2-[(9e,12e)-octadeca-9,12-dienoyloxy]propoxy)phosphinic acid

2,3-dihydroxypropoxy(3-(hexadecanoyloxy)-2-[(9e,12e)-octadeca-9,12-dienoyloxy]propoxy)phosphinic acid

C40H75O10P (746.509758)


   

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

(3r,3as,4s,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxy-3-methoxybenzoate

C23H32O5 (388.2249622)


   

(3s,3ar,4r,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

(3s,3ar,4r,8ar)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl benzoate

C22H30O3 (342.21948299999997)


   

6-hydroxy-3-isopropyl-1a,6-dimethyl-octahydroazuleno[1,2-b]oxiren-4-yl 3-hydroxy-4-methoxybenzoate

6-hydroxy-3-isopropyl-1a,6-dimethyl-octahydroazuleno[1,2-b]oxiren-4-yl 3-hydroxy-4-methoxybenzoate

C23H32O6 (404.2198772)


   

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3-hydroxy-4-methoxybenzoate

3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 3-hydroxy-4-methoxybenzoate

C23H32O5 (388.2249622)


   

(2r)-2-(pentadecanoyloxy)-3-(tridecanoyloxy)propoxyphosphonic acid

(2r)-2-(pentadecanoyloxy)-3-(tridecanoyloxy)propoxyphosphonic acid

C31H61O8P (592.4103835999999)