Chemical Formula: C19H37O6P

Chemical Formula C19H37O6P

Found 11 metabolite its formula value is C19H37O6P

CPA(16:0/0:0)

(2-Hydroxy-2-oxo-1,3,2λ⁵-dioxaphospholan-4-yl)methyl hexadecanoic acid

C19H37O6P (392.2327632)


cPA(16:0/0:0) is a cyclic phosphatidic acid or cyclic lysophosphatidic acid. It is a glycerophospholipid in which a cyclic phosphate moiety occupies two glycerol substitution sites. Lysophosphatidic acids can have different combinations of fatty acids of varying lengths and saturation attached at the C-1 (sn-1). Fatty acids containing 16 and 18 carbons are the most common. Cyclic phosphatidic acids have been detected in a wide range of organisms including humans, especially in the brain but also in serum (at a concentration of 10-7M). cPAs have a cyclic phosphate at the sn-2 and sn-3 positions of the glycerol carbons, and this structure is absolutely necessary for their activities. In particular, it is found in tissues subject to injury, and while it may have some similar signalling functions to lysophosphatidic acid per se, it also has some quite distinct biological activities. For example, cyclic phosphatidic acid is known to be a specific inhibitor of DNA polymerase alpha. It has an appreciable effect on the inhibition of cancer cell invasion and metastasis. [HMDB] cPA(16:0/0:0) is a cyclic phosphatidic acid or cyclic lysophosphatidic acid. It is a glycerophospholipid in which a cyclic phosphate moiety occupies two glycerol substitution sites. Lysophosphatidic acids can have different combinations of fatty acids of varying lengths and saturation attached at the C-1 (sn-1). Fatty acids containing 16 and 18 carbons are the most common. Cyclic phosphatidic acids have been detected in a wide range of organisms including humans, especially in the brain but also in serum (at a concentration of 10-7M). cPAs have a cyclic phosphate at the sn-2 and sn-3 positions of the glycerol carbons, and this structure is absolutely necessary for their activities. In particular, it is found in tissues subject to injury, and while it may have some similar signalling functions to lysophosphatidic acid per se, it also has some quite distinct biological activities. For example, cyclic phosphatidic acid is known to be a specific inhibitor of DNA polymerase alpha. It has an appreciable effect on the inhibition of cancer cell invasion and metastasis.

   

16:0 cyclic LPA

1-hexadecanoyl-sn-glycero-2,3-cyclic-phosphate

C19H37O6P (392.2327632)


   

CPA(16:0)

1-hexadecanoyl-sn-glycero-2,3-cyclic-phosphate

C19H37O6P (392.2327632)


   

1-palmitoleyl glycerone-3-phosphate

1-(9Z-hexadecenyl)-glycerone 3-phosphate

C19H37O6P (392.2327632)


   

CPA 16:0

1-hexadecanoyl-sn-glycero-2,3-cyclic-phosphate

C19H37O6P (392.2327632)


   

1-Hexadecanoyl-cyclophosphatidic acid

1-Hexadecanoyl-cyclophosphatidic acid

C19H37O6P (392.2327632)


   

1-Palmitylglycerone 3-phosphate(2-)

1-Palmitylglycerone 3-phosphate(2-)

C19H37O6P (392.2327632)


A 1-alkylglycerone 3-phosphate(2-) obtained by deprotonation of the phosphate OH groups of 1-palmitylglycerone 3-phosphate; major species at pH 7.3.

   

1-hexadecanoyl-sn-glycero-2,3-cyclic-phosphate

1-hexadecanoyl-sn-glycero-2,3-cyclic-phosphate

C19H37O6P (392.2327632)


   
   
   

LPA P-16:1 or LPA O-16:2

LPA P-16:1 or LPA O-16:2

C19H37O6P (392.2327632)