Chemical Formula: C38H69NO4

Chemical Formula C38H69NO4

Found 85 metabolite its formula value is C38H69NO4

Cer(d18:0/20:3(5Z,8Z,11Z)-O(14R,15S))

(5Z,8Z,11Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-13-(3-pentyloxiran-2-yl)trideca-5,8,11-trienimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:3(5Z,8Z,11Z)-O(14R,15S)) 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(d18:0/20:3(5Z,8Z,14Z)-O(11S,12R))

(5Z,8Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-10-{3-[(2Z)-oct-2-en-1-yl]oxiran-2-yl}deca-5,8-dienimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:3(5Z,8Z,14Z)-O(11S,12R)) 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(d18:0/20:3(5Z,11Z,14Z)-O(8,9))

(5Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-7-{3-[(2Z,5Z)-undeca-2,5-dien-1-yl]oxiran-2-yl}hept-5-enimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:3(5Z,11Z,14Z)-O(8,9)) 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(d18:0/20:3(8Z,11Z,14Z)-O(5,6))

N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-4-{3-[(2Z,5Z,8Z)-tetradeca-2,5,8-trien-1-yl]oxiran-2-yl}butanimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:3(8Z,11Z,14Z)-O(5,6)) 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(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(20))

(5Z,8Z,11Z,14Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-20-hydroxyicosa-5,8,11,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(20)) 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(d18:0/20:4(6E,8Z,11Z,14Z)-OH(5S))

(5R,6E,8Z,11Z,14Z)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]-5-hydroxyicosa-6,8,11,14-tetraenamide

C38H69NO4 (603.5226)


Cer(d18:0/20:4(6E,8Z,11Z,14Z)-OH(5S)) 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(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(19S))

(5Z,8Z,11Z,14Z,19S)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-19-hydroxyicosa-5,8,11,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(19S)) 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(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(18R))

(5Z,8Z,11Z,14Z,18R)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-18-hydroxyicosa-5,8,11,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-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(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(17))

(5Z,8Z,11Z,14Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-17-hydroxyicosa-5,8,11,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-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(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(16R))

(5Z,8Z,11Z,14Z,16R)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-16-hydroxyicosa-5,8,11,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(16R)) 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(d18:0/20:4(5Z,8Z,11Z,13E)-OH(15S))

(5Z,8Z,11Z,13E,15S)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-15-hydroxyicosa-5,8,11,13-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,11Z,13E)-OH(15S)) 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(d18:0/20:4(5Z,8Z,10E,14Z)-OH(12S))

(5Z,8Z,10E,12S,14Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-12-hydroxyicosa-5,8,10,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,8Z,10E,14Z)-OH(12S)) 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(d18:0/20:4(5E,8Z,12Z,14Z)-OH(11R))

(5E,8Z,11R,12Z,14Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-11-hydroxyicosa-5,8,12,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5E,8Z,12Z,14Z)-OH(11R)) 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(d18:0/20:4(5Z,7E,11Z,14Z)-OH(9))

(5E,7Z,11Z,14Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-9-hydroxyicosa-5,7,11,14-tetraenimidate

C38H69NO4 (603.5226)


Cer(d18:0/20:4(5Z,7E,11Z,14Z)-OH(9)) 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(d18:1/20:3(6,8,11)-OH(5))

(6E,8E,11E)-N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]-5-hydroxyicosa-6,8,11-trienamide

C38H69NO4 (603.5226)


Cer(d18:1/20:3(6,8,11)-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).

   

Cer(d20:1/18:2(10E,12Z)+=O(9))

(10E,12Z)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-9-oxooctadeca-10,12-dienamide

C38H69NO4 (603.5226)


Cer(d20:1/18:2(10E,12Z)+=O(9)) 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(d20:1/18:2(9Z,11E)+=O(13))

(9Z,11E)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-13-oxooctadeca-9,11-dienamide

C38H69NO4 (603.5226)


Cer(d20:1/18:2(9Z,11E)+=O(13)) 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(d20:1/18:3(10,12,15)-OH(9))

(10E,12E,15E)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-9-hydroxyoctadeca-10,12,15-trienamide

C38H69NO4 (603.5226)


Cer(d20:1/18:3(10,12,15)-OH(9)) 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(d20:1/18:3(9,11,15)-OH(13))

(9E,11E,15E)-N-[(2S,3R,4E)-1,3-dihydroxyicos-4-en-2-yl]-13-hydroxyoctadeca-9,11,15-trienamide

C38H69NO4 (603.5226)


Cer(d20:1/18:3(9,11,15)-OH(13)) 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(d18:1/20:3(6,8,11)-OH(5))

Cer(d18:1/20:3(6,8,11)-OH(5))

C38H69NO4 (603.5226)


   

Cer(d20:1/18:2(10E,12Z)+=O(9))

Cer(d20:1/18:2(10E,12Z)+=O(9))

C38H69NO4 (603.5226)


   

Cer(d20:1/18:2(9Z,11E)+=O(13))

Cer(d20:1/18:2(9Z,11E)+=O(13))

C38H69NO4 (603.5226)


   

Cer(d20:1/18:3(10,12,15)-OH(9))

Cer(d20:1/18:3(10,12,15)-OH(9))

C38H69NO4 (603.5226)


   

Cer(d20:1/18:3(9,11,15)-OH(13))

Cer(d20:1/18:3(9,11,15)-OH(13))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:3(5Z,8Z,11Z)-O(14R,15S))

Cer(d18:0/20:3(5Z,8Z,11Z)-O(14R,15S))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:3(5Z,8Z,14Z)-O(11S,12R))

Cer(d18:0/20:3(5Z,8Z,14Z)-O(11S,12R))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:3(5Z,11Z,14Z)-O(8,9))

Cer(d18:0/20:3(5Z,11Z,14Z)-O(8,9))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:3(8Z,11Z,14Z)-O(5,6))

Cer(d18:0/20:3(8Z,11Z,14Z)-O(5,6))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(20))

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(20))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(6E,8Z,11Z,14Z)-OH(5S))

Cer(d18:0/20:4(6E,8Z,11Z,14Z)-OH(5S))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(19S))

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(19S))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(18R))

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(18R))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(17))

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(17))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(16R))

Cer(d18:0/20:4(5Z,8Z,11Z,14Z)-OH(16R))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,11Z,13E)-OH(15S))

Cer(d18:0/20:4(5Z,8Z,11Z,13E)-OH(15S))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,8Z,10E,14Z)-OH(12S))

Cer(d18:0/20:4(5Z,8Z,10E,14Z)-OH(12S))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5E,8Z,12Z,14Z)-OH(11R))

Cer(d18:0/20:4(5E,8Z,12Z,14Z)-OH(11R))

C38H69NO4 (603.5226)


   

Cer(d18:0/20:4(5Z,7E,11Z,14Z)-OH(9))

Cer(d18:0/20:4(5Z,7E,11Z,14Z)-OH(9))

C38H69NO4 (603.5226)


   

N-arachidonoylphytosphingosine

N-arachidonoylphytosphingosine

C38H69NO4 (603.5226)


A phytoceramide in which the N-acyl group is specified as arachidonoyl.

   

1-O-linoleoyl-N-acetylsphingosine

1-O-linoleoyl-N-acetylsphingosine

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 25:3;2O/13:1;(2OH)

Cer 25:3;2O/13:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 14:3;2O/24:1;(3OH)

Cer 14:3;2O/24:1;(3OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 16:3;2O/22:1;(3OH)

Cer 16:3;2O/22:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 19:3;2O/19:1;(3OH)

Cer 19:3;2O/19:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 22:3;2O/16:1;(3OH)

Cer 22:3;2O/16:1;(3OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 18:3;2O/20:1;(3OH)

Cer 18:3;2O/20:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 20:3;2O/18:1;(3OH)

Cer 20:3;2O/18:1;(3OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 17:3;2O/21:1;(2OH)

Cer 17:3;2O/21:1;(2OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 18:3;2O/20:1;(2OH)

Cer 18:3;2O/20:1;(2OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 24:3;2O/14:1;(2OH)

Cer 24:3;2O/14:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 19:3;2O/19:1;(2OH)

Cer 19:3;2O/19:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 26:3;2O/12:1;(2OH)

Cer 26:3;2O/12:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 20:3;2O/18:1;(2OH)

Cer 20:3;2O/18:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 23:3;2O/15:1;(3OH)

Cer 23:3;2O/15:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 15:3;2O/23:1;(2OH)

Cer 15:3;2O/23:1;(2OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 26:3;2O/12:1;(3OH)

Cer 26:3;2O/12:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 23:3;2O/15:1;(2OH)

Cer 23:3;2O/15:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 16:3;2O/22:1;(2OH)

Cer 16:3;2O/22:1;(2OH)

C38H69NO4 (603.5226)


   

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

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

C38H69NO4 (603.5226)


   

Cer 14:3;2O/24:1;(2OH)

Cer 14:3;2O/24:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 17:3;2O/21:1;(3OH)

Cer 17:3;2O/21:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 15:3;2O/23:1;(3OH)

Cer 15:3;2O/23:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 22:3;2O/16:1;(2OH)

Cer 22:3;2O/16:1;(2OH)

C38H69NO4 (603.5226)


   

Cer 25:3;2O/13:1;(3OH)

Cer 25:3;2O/13:1;(3OH)

C38H69NO4 (603.5226)


   

Cer 24:3;2O/14:1;(3OH)

Cer 24:3;2O/14:1;(3OH)

C38H69NO4 (603.5226)


   

Cer(38:4)

Cer(t20:1_18:3)

C38H69NO4 (603.5226)


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Cer 14:0;O3/24:4

Cer 14:0;O3/24:4

C38H69NO4 (603.5226)


   

Cer 16:0;O3/22:4

Cer 16:0;O3/22:4

C38H69NO4 (603.5226)


   

Cer 18:0;O3/20:4

Cer 18:0;O3/20:4

C38H69NO4 (603.5226)


   

Cer 20:0;O3/18:4

Cer 20:0;O3/18:4

C38H69NO4 (603.5226)