Exact Mass: 627.5631116

Exact Mass Matches: 627.5631116

Found 140 metabolites which its exact mass value is equals to given mass value 627.5631116, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Cer(d18:0/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4))

(5Z,7Z,10Z,13Z,16Z,19Z)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]-4-hydroxydocosa-5,7,10,13,16,19-hexaenamide

C40H69NO4 (627.5226313999999)


Cer(d18:0/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d18:0/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7))

(4Z,8Z,10Z,13Z,16Z,19Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-7-hydroxydocosa-4,8,10,13,16,19-hexaenimidate

C40H69NO4 (627.5226313999999)


Cer(d18:0/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d18:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

(4Z,7Z,10Z,12E,16Z,19Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-14-hydroxydocosa-4,7,10,12,16,19-hexaenimidate

C40H69NO4 (627.5226313999999)


Cer(d18:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d18:0/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17))

(4Z,7Z,10Z,13E,15E,19Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-17-hydroxydocosa-4,7,10,13,15,19-hexaenimidate

C40H69NO4 (627.5226313999999)


Cer(d18:0/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d18:0/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17))

(4Z,7Z,10Z,13Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-15-{3-[(2Z)-pent-2-en-1-yl]oxiran-2-yl}pentadeca-4,7,10,13-tetraenimidate

C40H69NO4 (627.5226313999999)


Cer(d18:0/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d20:1/20:4(6E,8Z,11Z,14Z)+=O(5))

(6E,8Z,11Z,14Z)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-5-oxoicosa-6,8,11,14-tetraenamide

C40H69NO4 (627.5226313999999)


Cer(d20:1/20:4(6E,8Z,11Z,14Z)+=O(5)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d20:1/20:4(5Z,8Z,11Z,13E)+=O(15))

(5Z,8Z,11Z,13E)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-15-oxoicosa-5,8,11,13-tetraenamide

C40H69NO4 (627.5226313999999)


Cer(d20:1/20:4(5Z,8Z,11Z,13E)+=O(15)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R))

(5Z,8Z,11Z,14Z,16E,18R)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-18-hydroxyicosa-5,8,11,14,16-pentaenamide

C40H69NO4 (627.5226313999999)


Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18))

(5Z,8Z,11Z,13E,17Z)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-16-hydroxyicosa-5,8,11,13,17-pentaenamide

C40H69NO4 (627.5226313999999)


Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d20:1/20:5(5Z,8Z,10E,14Z,17Z)-OH(12))

(5Z,8Z,10E,14Z,17Z)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-12-hydroxyicosa-5,8,10,14,17-pentaenamide

C40H69NO4 (627.5226313999999)


Cer(d20:1/20:5(5Z,8Z,10E,14Z,17Z)-OH(12)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   

Cer(d20:1/20:5(6E,8Z,11Z,14Z,17Z)-OH(5))

(6E,8Z,11Z,14Z,17Z)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-5-hydroxyicosa-6,8,11,14,17-pentaenamide

C40H69NO4 (627.5226313999999)


Cer(d20:1/20:5(6E,8Z,11Z,14Z,17Z)-OH(5)) is an oxidized ceramide (Cer). As all ceramides, oxidized ceramides are members of the class of compounds known as sphingolipids (SPs), or glycosylceramides. SPs are lipids containing a backbone of sphingoid bases (e.g. sphingosine or sphinganine) that are often covalently bound to a fatty acid derivative through N-acylation. SPs are found in cell membranes, particularly in peripheral nerve cells and the cells found in the central nervous system (including the brain and spinal cord). Sphingolipids are extremely versatile molecules that have functions controlling fundamental cellular processes such as cell division, differentiation, and cell death. Impairments associated with sphingolipid metabolism are associated with many common human diseases such as diabetes, various cancers, microbial infections, diseases of the cardiovascular and respiratory systems, Alzheimer’s disease and other neurological syndromes. The biosynthesis and catabolism of sphingolipids involves a large number of intermediate metabolites where many different enzymes are involved. Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways, while complex sphingolipids may be formed by the addition of head groups to the ceramide template (Wikipedia). In humans, ceramides are phosphorylated to ceramide phosphates (CerPs) through the action of a specific ceramide kinase (CerK). Ceramide phosphates are important metabolites of ceramides as they act as a mediators of the inflammatory response. Ceramides are also one of the hydrolysis byproducts of sphingomyelins (SMs) through the action of the enzyme sphingomyelin phosphodiesterase, which has been identified in the subcellular fractions of human epidermis (PMID: 25935) and many other tissues. Ceramides can also be synthesized from serine and palmitate in a de novo pathway and are regarded as important cellular signals for inducing apoptosis (PMID: 14998372). Ceramides are key in the biosynthesis of glycosphingolipids and gangliosides. In terms of its appearance and structure, Cer(d18:1/22:1(13Z)) is a colorless solid that consists of an unsaturated 18-carbon sphingoid base with an attached unsaturated 13Z-docosenoyl fatty acid side chain. In most mammalian SPs, the 18-carbon sphingoid bases are predominant (PMID: 9759481).

   
   
   

(2S,3S,4R)-2-[(2R)-2-hydroxynonadecanoylamino]nonadecane-1,3,4-triol

(2S,3S,4R)-2-[(2R)-2-hydroxynonadecanoylamino]nonadecane-1,3,4-triol

C38H77NO5 (627.5801432)


   

(2S,2R,3S,4R)-2-(2-hydroxy-21-methyldocosanoylamino)-1,3,4-pentadecanetriol|(2S,2R,3S,4S)-2-(2-hydroxy-21-methyl-docosanoylamino)-1,3,4-pentadecanetriol|(2S,3S,4R)-2-[(R)-2-hydroxy-21-methyldocosanoylamino]-1,3,4-pentadecanetriol

(2S,2R,3S,4R)-2-(2-hydroxy-21-methyldocosanoylamino)-1,3,4-pentadecanetriol|(2S,2R,3S,4S)-2-(2-hydroxy-21-methyl-docosanoylamino)-1,3,4-pentadecanetriol|(2S,3S,4R)-2-[(R)-2-hydroxy-21-methyldocosanoylamino]-1,3,4-pentadecanetriol

C38H77NO5 (627.5801432)


   

(R)-2-hydroxy-N-((2S,3S,4R)-1,3,4-trihydroxy-19-methylicosan-2-yl)heptadecanamide|echinoclathriamide

(R)-2-hydroxy-N-((2S,3S,4R)-1,3,4-trihydroxy-19-methylicosan-2-yl)heptadecanamide|echinoclathriamide

C38H77NO5 (627.5801432)


   

Cer[AP] t38:0

Cer[AP] t38:0

C38H77NO5 (627.5801432)


Found in mouse small intestine; TwoDicalId=1381; MgfFile=160907_Small_Intestine_DHA_Neg_11_never; MgfId=1571

   

Cer(t18:0/20:0(2OH))

N-(2-hydroxyeicosanoyl)-4R-hydroxysphinganine

C38H77NO5 (627.5801432)


   

Cer(t20:0/18:0(2OH))

N-(2-hydroxyoctadecanoyl)-4R-hydroxyeicosasphinganine

C38H77NO5 (627.5801432)


   

CAY10614

N-cyclopentyl-N,N-dimethyl-3,4-bis(tetradecyloxy)-benzenemethanaminium, iodide

C42H77NO2 (627.5953982)


   

Cer[AP]

N-(2-hydroxyoctadecanoyl)-4R-hydroxyeicosasphinganine

C38H77NO5 (627.5801432)


   

Cer 38:0;O4

N-(2R-hydroxyheneicosanoyl)-4R-hydroxy-15-methyl-hexadecasphinganine

C38H77NO5 (627.5801432)


   

tin(iv) iodide

tin(iv) iodide

I4Sn (627.520107)


   

2,2-Bi-1H-pyrrole, 3,3,4,4,5,5-hexabromo-1,1-dimethyl-

2,2-Bi-1H-pyrrole, 3,3,4,4,5,5-hexabromo-1,1-dimethyl-

C10H6Br6N2 (627.5631116)


   

N-[1-(Hydroxymethyl)-2,3-dihydroxyheptadecyl]-2-hydroxyicosanamide

N-[1-(Hydroxymethyl)-2,3-dihydroxyheptadecyl]-2-hydroxyicosanamide

C38H77NO5 (627.5801432)


   

Cer 19:0;3O/19:0;(2OH)

Cer 19:0;3O/19:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 16:0;3O/22:0;(2OH)

Cer 16:0;3O/22:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer(d20:1/20:4(6E,8Z,11Z,14Z)+=O(5))

Cer(d20:1/20:4(6E,8Z,11Z,14Z)+=O(5))

C40H69NO4 (627.5226313999999)


   

Cer(d20:1/20:4(5Z,8Z,11Z,13E)+=O(15))

Cer(d20:1/20:4(5Z,8Z,11Z,13E)+=O(15))

C40H69NO4 (627.5226313999999)


   

Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R))

Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R))

C40H69NO4 (627.5226313999999)


   

Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18))

Cer(d20:1/20:5(5Z,8Z,11Z,14Z,16E)-OH(18))

C40H69NO4 (627.5226313999999)


   

Cer(d20:1/20:5(5Z,8Z,10E,14Z,17Z)-OH(12))

Cer(d20:1/20:5(5Z,8Z,10E,14Z,17Z)-OH(12))

C40H69NO4 (627.5226313999999)


   

Cer(d20:1/20:5(6E,8Z,11Z,14Z,17Z)-OH(5))

Cer(d20:1/20:5(6E,8Z,11Z,14Z,17Z)-OH(5))

C40H69NO4 (627.5226313999999)


   

Cer(d18:0/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4))

Cer(d18:0/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4))

C40H69NO4 (627.5226313999999)


   

Cer(d18:0/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7))

Cer(d18:0/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7))

C40H69NO4 (627.5226313999999)


   

Cer(d18:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

Cer(d18:0/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

C40H69NO4 (627.5226313999999)


   

Cer(d18:0/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17))

Cer(d18:0/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17))

C40H69NO4 (627.5226313999999)


   

Cer(d18:0/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17))

Cer(d18:0/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17))

C40H69NO4 (627.5226313999999)


   

1-O-arachidonoyl-N-acetylsphingosine

1-O-arachidonoyl-N-acetylsphingosine

C40H69NO4 (627.5226313999999)


   

N-(2-hydroxyhenicosanoyl)-4-hydroxy-15-methylhexadecasphinganine

N-(2-hydroxyhenicosanoyl)-4-hydroxy-15-methylhexadecasphinganine

C38H77NO5 (627.5801432)


   

(20Z,23Z,26Z,29Z)-N-[(E)-1,3-dihydroxynon-4-en-2-yl]dotriaconta-20,23,26,29-tetraenamide

(20Z,23Z,26Z,29Z)-N-[(E)-1,3-dihydroxynon-4-en-2-yl]dotriaconta-20,23,26,29-tetraenamide

C41H73NO3 (627.5590147999999)


   

(17Z,20Z,23Z,26Z,29Z)-N-(1,3-dihydroxynonan-2-yl)dotriaconta-17,20,23,26,29-pentaenamide

(17Z,20Z,23Z,26Z,29Z)-N-(1,3-dihydroxynonan-2-yl)dotriaconta-17,20,23,26,29-pentaenamide

C41H73NO3 (627.5590147999999)


   

(6Z,9Z,12Z,15Z)-N-[(E)-1,3-dihydroxytricos-4-en-2-yl]octadeca-6,9,12,15-tetraenamide

(6Z,9Z,12Z,15Z)-N-[(E)-1,3-dihydroxytricos-4-en-2-yl]octadeca-6,9,12,15-tetraenamide

C41H73NO3 (627.5590147999999)


   

(11Z,14Z,17Z)-N-[(4E,8E)-1,3-dihydroxyhenicosa-4,8-dien-2-yl]icosa-11,14,17-trienamide

(11Z,14Z,17Z)-N-[(4E,8E)-1,3-dihydroxyhenicosa-4,8-dien-2-yl]icosa-11,14,17-trienamide

C41H73NO3 (627.5590147999999)


   

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxytricosa-4,8,12-trien-2-yl]octadeca-9,12-dienamide

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxytricosa-4,8,12-trien-2-yl]octadeca-9,12-dienamide

C41H73NO3 (627.5590147999999)


   

(3Z,6Z,9Z,12Z,15Z)-N-(1,3-dihydroxytricosan-2-yl)octadeca-3,6,9,12,15-pentaenamide

(3Z,6Z,9Z,12Z,15Z)-N-(1,3-dihydroxytricosan-2-yl)octadeca-3,6,9,12,15-pentaenamide

C41H73NO3 (627.5590147999999)


   

(12Z,15Z,18Z)-N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]hexacosa-12,15,18-trienamide

(12Z,15Z,18Z)-N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]hexacosa-12,15,18-trienamide

C41H73NO3 (627.5590147999999)


   

(14Z,17Z,20Z)-N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]octacosa-14,17,20-trienamide

(14Z,17Z,20Z)-N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]octacosa-14,17,20-trienamide

C41H73NO3 (627.5590147999999)


   

(13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]docosa-13,16-dienamide

(13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]docosa-13,16-dienamide

C41H73NO3 (627.5590147999999)


   

(10Z,13Z,16Z,19Z)-N-[(E)-1,3-dihydroxynonadec-4-en-2-yl]docosa-10,13,16,19-tetraenamide

(10Z,13Z,16Z,19Z)-N-[(E)-1,3-dihydroxynonadec-4-en-2-yl]docosa-10,13,16,19-tetraenamide

C41H73NO3 (627.5590147999999)


   

(11Z,14Z,17Z,20Z,23Z)-N-(1,3-dihydroxypentadecan-2-yl)hexacosa-11,14,17,20,23-pentaenamide

(11Z,14Z,17Z,20Z,23Z)-N-(1,3-dihydroxypentadecan-2-yl)hexacosa-11,14,17,20,23-pentaenamide

C41H73NO3 (627.5590147999999)


   

(15Z,18Z,21Z,24Z,27Z)-N-(1,3-dihydroxyundecan-2-yl)triaconta-15,18,21,24,27-pentaenamide

(15Z,18Z,21Z,24Z,27Z)-N-(1,3-dihydroxyundecan-2-yl)triaconta-15,18,21,24,27-pentaenamide

C41H73NO3 (627.5590147999999)


   

(7Z,10Z,13Z,16Z,19Z)-N-(1,3-dihydroxynonadecan-2-yl)docosa-7,10,13,16,19-pentaenamide

(7Z,10Z,13Z,16Z,19Z)-N-(1,3-dihydroxynonadecan-2-yl)docosa-7,10,13,16,19-pentaenamide

C41H73NO3 (627.5590147999999)


   

(10Z,13Z,16Z)-N-[(4E,8E)-1,3-dihydroxynonadeca-4,8-dien-2-yl]docosa-10,13,16-trienamide

(10Z,13Z,16Z)-N-[(4E,8E)-1,3-dihydroxynonadeca-4,8-dien-2-yl]docosa-10,13,16-trienamide

C41H73NO3 (627.5590147999999)


   

(10Z,13Z,16Z)-N-[(4E,8E)-1,3-dihydroxyheptadeca-4,8-dien-2-yl]tetracosa-10,13,16-trienamide

(10Z,13Z,16Z)-N-[(4E,8E)-1,3-dihydroxyheptadeca-4,8-dien-2-yl]tetracosa-10,13,16-trienamide

C41H73NO3 (627.5590147999999)


   

(5Z,8Z,11Z,14Z,17Z)-N-(1,3-dihydroxyhenicosan-2-yl)icosa-5,8,11,14,17-pentaenamide

(5Z,8Z,11Z,14Z,17Z)-N-(1,3-dihydroxyhenicosan-2-yl)icosa-5,8,11,14,17-pentaenamide

C41H73NO3 (627.5590147999999)


   

(12Z,15Z,18Z,21Z)-N-[(E)-1,3-dihydroxyheptadec-4-en-2-yl]tetracosa-12,15,18,21-tetraenamide

(12Z,15Z,18Z,21Z)-N-[(E)-1,3-dihydroxyheptadec-4-en-2-yl]tetracosa-12,15,18,21-tetraenamide

C41H73NO3 (627.5590147999999)


   

(11Z,14Z)-N-[(4E,8E,12E)-1,3-dihydroxyicosa-4,8,12-trien-2-yl]henicosa-11,14-dienamide

(11Z,14Z)-N-[(4E,8E,12E)-1,3-dihydroxyicosa-4,8,12-trien-2-yl]henicosa-11,14-dienamide

C41H73NO3 (627.5590147999999)


   

(16Z,19Z,22Z,25Z)-N-[(E)-1,3-dihydroxytridec-4-en-2-yl]octacosa-16,19,22,25-tetraenamide

(16Z,19Z,22Z,25Z)-N-[(E)-1,3-dihydroxytridec-4-en-2-yl]octacosa-16,19,22,25-tetraenamide

C41H73NO3 (627.5590147999999)


   

(13Z,16Z,19Z,22Z,25Z)-N-(1,3-dihydroxytridecan-2-yl)octacosa-13,16,19,22,25-pentaenamide

(13Z,16Z,19Z,22Z,25Z)-N-(1,3-dihydroxytridecan-2-yl)octacosa-13,16,19,22,25-pentaenamide

C41H73NO3 (627.5590147999999)


   

(18Z,21Z,24Z,27Z)-N-[(E)-1,3-dihydroxyundec-4-en-2-yl]triaconta-18,21,24,27-tetraenamide

(18Z,21Z,24Z,27Z)-N-[(E)-1,3-dihydroxyundec-4-en-2-yl]triaconta-18,21,24,27-tetraenamide

C41H73NO3 (627.5590147999999)


   

(9Z,12Z,15Z,18Z,21Z)-N-(1,3-dihydroxyheptadecan-2-yl)tetracosa-9,12,15,18,21-pentaenamide

(9Z,12Z,15Z,18Z,21Z)-N-(1,3-dihydroxyheptadecan-2-yl)tetracosa-9,12,15,18,21-pentaenamide

C41H73NO3 (627.5590147999999)


   

(9Z,12Z,15Z)-N-[(4E,8E)-1,3-dihydroxytricosa-4,8-dien-2-yl]octadeca-9,12,15-trienamide

(9Z,12Z,15Z)-N-[(4E,8E)-1,3-dihydroxytricosa-4,8-dien-2-yl]octadeca-9,12,15-trienamide

C41H73NO3 (627.5590147999999)


   

(7Z,10Z,13Z)-N-[(4E,8E)-1,3-dihydroxypentacosa-4,8-dien-2-yl]hexadeca-7,10,13-trienamide

(7Z,10Z,13Z)-N-[(4E,8E)-1,3-dihydroxypentacosa-4,8-dien-2-yl]hexadeca-7,10,13-trienamide

C41H73NO3 (627.5590147999999)


   

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxydocosa-4,8,12-trien-2-yl]nonadeca-9,12-dienamide

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxydocosa-4,8,12-trien-2-yl]nonadeca-9,12-dienamide

C41H73NO3 (627.5590147999999)


   

(4Z,7Z,10Z,13Z)-N-[(E)-1,3-dihydroxypentacos-4-en-2-yl]hexadeca-4,7,10,13-tetraenamide

(4Z,7Z,10Z,13Z)-N-[(E)-1,3-dihydroxypentacos-4-en-2-yl]hexadeca-4,7,10,13-tetraenamide

C41H73NO3 (627.5590147999999)


   

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxytetracosa-4,8,12-trien-2-yl]heptadeca-9,12-dienamide

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxytetracosa-4,8,12-trien-2-yl]heptadeca-9,12-dienamide

C41H73NO3 (627.5590147999999)


   

(13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]tetracosa-13,16-dienamide

(13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]tetracosa-13,16-dienamide

C41H73NO3 (627.5590147999999)


   

(8Z,11Z,14Z,17Z)-N-[(E)-1,3-dihydroxyhenicos-4-en-2-yl]icosa-8,11,14,17-tetraenamide

(8Z,11Z,14Z,17Z)-N-[(E)-1,3-dihydroxyhenicos-4-en-2-yl]icosa-8,11,14,17-tetraenamide

C41H73NO3 (627.5590147999999)


   

(14Z,17Z,20Z,23Z)-N-[(E)-1,3-dihydroxypentadec-4-en-2-yl]hexacosa-14,17,20,23-tetraenamide

(14Z,17Z,20Z,23Z)-N-[(E)-1,3-dihydroxypentadec-4-en-2-yl]hexacosa-14,17,20,23-tetraenamide

C41H73NO3 (627.5590147999999)


   

(15Z,18Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]hexacosa-15,18-dienamide

(15Z,18Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]hexacosa-15,18-dienamide

C41H73NO3 (627.5590147999999)


   

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxypentacosa-4,8,12-trien-2-yl]hexadeca-9,12-dienamide

(9Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxypentacosa-4,8,12-trien-2-yl]hexadeca-9,12-dienamide

C41H73NO3 (627.5590147999999)


   

Cer 9:0;3O/29:0;(2OH)

Cer 9:0;3O/29:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 8:0;3O/30:0;(2OH)

Cer 8:0;3O/30:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 11:0;3O/27:0;(2OH)

Cer 11:0;3O/27:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 10:0;3O/28:0;(2OH)

Cer 10:0;3O/28:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 12:0;3O/26:0;(2OH)

Cer 12:0;3O/26:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 13:0;3O/25:0;(2OH)

Cer 13:0;3O/25:0;(2OH)

C38H77NO5 (627.5801432)


   

(11Z,14Z)-N-[(4E,8E,12E)-1,3-dihydroxyhenicosa-4,8,12-trien-2-yl]icosa-11,14-dienamide

(11Z,14Z)-N-[(4E,8E,12E)-1,3-dihydroxyhenicosa-4,8,12-trien-2-yl]icosa-11,14-dienamide

C41H73NO3 (627.5590147999999)


   

Cer 20:0;3O/18:0;(2OH)

Cer 20:0;3O/18:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 21:0;3O/17:0;(2OH)

Cer 21:0;3O/17:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 23:0;3O/15:0;(2OH)

Cer 23:0;3O/15:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 22:0;3O/16:0;(2OH)

Cer 22:0;3O/16:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 26:0;3O/12:0;(2OH)

Cer 26:0;3O/12:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 24:0;3O/14:0;(2OH)

Cer 24:0;3O/14:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 17:0;3O/21:0;(2OH)

Cer 17:0;3O/21:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 14:0;3O/24:0;(2OH)

Cer 14:0;3O/24:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 15:0;3O/23:0;(2OH)

Cer 15:0;3O/23:0;(2OH)

C38H77NO5 (627.5801432)


   

Cer 25:0;3O/13:0;(2OH)

Cer 25:0;3O/13:0;(2OH)

C38H77NO5 (627.5801432)


   

(14Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]docosa-14,16-dienamide

(14Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]docosa-14,16-dienamide

C41H73NO3 (627.5590147999999)


   

(10Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxytricosa-4,8,12-trien-2-yl]octadeca-10,12-dienamide

(10Z,12Z)-N-[(4E,8E,12E)-1,3-dihydroxytricosa-4,8,12-trien-2-yl]octadeca-10,12-dienamide

C41H73NO3 (627.5590147999999)


   

(18Z,21Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]tetracosa-18,21-dienamide

(18Z,21Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]tetracosa-18,21-dienamide

C41H73NO3 (627.5590147999999)


   

(4Z,7Z)-N-[(4E,8E,12E)-1,3-dihydroxypentacosa-4,8,12-trien-2-yl]hexadeca-4,7-dienamide

(4Z,7Z)-N-[(4E,8E,12E)-1,3-dihydroxypentacosa-4,8,12-trien-2-yl]hexadeca-4,7-dienamide

C41H73NO3 (627.5590147999999)


   

(11Z,14Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]hexacosa-11,14-dienamide

(11Z,14Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]hexacosa-11,14-dienamide

C41H73NO3 (627.5590147999999)


   

(5E,8E,11E,14E)-N-[(E,2S,3R)-1,3-dihydroxyheptadec-8-en-2-yl]tetracosa-5,8,11,14-tetraenamide

(5E,8E,11E,14E)-N-[(E,2S,3R)-1,3-dihydroxyheptadec-8-en-2-yl]tetracosa-5,8,11,14-tetraenamide

C41H73NO3 (627.5590147999999)


   

(5E,8E,11E,14E)-N-[(E,2S,3R)-1,3-dihydroxyheptadec-4-en-2-yl]tetracosa-5,8,11,14-tetraenamide

(5E,8E,11E,14E)-N-[(E,2S,3R)-1,3-dihydroxyheptadec-4-en-2-yl]tetracosa-5,8,11,14-tetraenamide

C41H73NO3 (627.5590147999999)


   

N-(2-hydroxyeicosanoyl)-hydroxysphinganine

N-(2-hydroxyeicosanoyl)-hydroxysphinganine

C38H77NO5 (627.5801432)


   

N-(2-hydroxyoctadecanoyl)-hydroxyeicosasphinganine

N-(2-hydroxyoctadecanoyl)-hydroxyeicosasphinganine

C38H77NO5 (627.5801432)


   

N-(2-hydroxyeicosanoyl)-4-hydroxysphinganine

N-(2-hydroxyeicosanoyl)-4-hydroxysphinganine

C38H77NO5 (627.5801432)


A phytoceramide in which the ceramide N-acyl group is specified as 2-hydroxyeicosanoyl.

   

Cer(42:4)

Cer(m18:1_24:3)

C42H77NO2 (627.5953982)


Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved

   
   
   
   
   
   
   
   
   

Cer 14:0;O3/24:0;2OH

Cer 14:0;O3/24:0;2OH

C38H77NO5 (627.5801432)


   

Cer 14:0;O3/24:0;3OH

Cer 14:0;O3/24:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 15:0;O3/23:0;2OH

Cer 15:0;O3/23:0;2OH

C38H77NO5 (627.5801432)


   

Cer 15:0;O3/23:0;3OH

Cer 15:0;O3/23:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 16:0;O3/22:0;2OH

Cer 16:0;O3/22:0;2OH

C38H77NO5 (627.5801432)


   

Cer 16:0;O3/22:0;3OH

Cer 16:0;O3/22:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 17:0;O3/21:0;2OH

Cer 17:0;O3/21:0;2OH

C38H77NO5 (627.5801432)


   

Cer 17:0;O3/21:0;3OH

Cer 17:0;O3/21:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 18:0;O3/20:0;2OH

Cer 18:0;O3/20:0;2OH

C38H77NO5 (627.5801432)


   

Cer 18:0;O3/20:0;3OH

Cer 18:0;O3/20:0;3OH

C38H77NO5 (627.5801432)


   
   
   

Cer 19:0;O3/19:0;2OH

Cer 19:0;O3/19:0;2OH

C38H77NO5 (627.5801432)


   

Cer 19:0;O3/19:0;3OH

Cer 19:0;O3/19:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 20:0;O3/18:0;2OH

Cer 20:0;O3/18:0;2OH

C38H77NO5 (627.5801432)


   

Cer 20:0;O3/18:0;3OH

Cer 20:0;O3/18:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 21:0;O3/17:0;2OH

Cer 21:0;O3/17:0;2OH

C38H77NO5 (627.5801432)


   

Cer 21:0;O3/17:0;3OH

Cer 21:0;O3/17:0;3OH

C38H77NO5 (627.5801432)


   
   

Cer 22:0;O3/16:0;2OH

Cer 22:0;O3/16:0;2OH

C38H77NO5 (627.5801432)


   

Cer 22:0;O3/16:0;3OH

Cer 22:0;O3/16:0;3OH

C38H77NO5 (627.5801432)


   
   
   

2-hydroxy-n-(1,3,4-trihydroxyhexadecan-2-yl)docosanimidic acid

2-hydroxy-n-(1,3,4-trihydroxyhexadecan-2-yl)docosanimidic acid

C38H77NO5 (627.5801432)