Exact Mass: 597.525073

Exact Mass Matches: 597.525073

Found 183 metabolites which its exact mass value is equals to given mass value 597.525073, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Cer(d16:1/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4))

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

C38H63NO4 (597.4756838)


Cer(d16:1/22:6(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(d16:1/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7))

(4Z,8Z,10Z,13Z,16Z,19Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-7-hydroxydocosa-4,8,10,13,16,19-hexaenamide

C38H63NO4 (597.4756838)


Cer(d16:1/22:6(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(d16:1/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

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

C38H63NO4 (597.4756838)


Cer(d16:1/22:6(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(d16:1/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17))

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

C38H63NO4 (597.4756838)


Cer(d16:1/22:6(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(d16:1/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17))

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

C38H63NO4 (597.4756838)


Cer(d16:1/22:5(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(d18:0/18:1(12Z)-2OH(9,10))

(9S,10S,12Z)-N-[(2S,3R)-1,3-Dihydroxyoctadecan-2-yl]-9,10-dihydroxyoctadec-12-enimidate

C36H71NO5 (597.5331956)


Cer(d18:0/18:1(12Z)-2OH(9,10)) 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(d18:2(4E,14Z)/20:4(6E,8Z,11Z,14Z)+=O(5))

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

C38H63NO4 (597.4756838)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/20:4(5Z,8Z,11Z,13E)+=O(15))

(5Z,8Z,11Z,13E)-N-[(2S,3R,4E,14Z)-1,3-dihydroxyoctadeca-4,14-dien-2-yl]-15-oxoicosa-5,8,11,13-tetraenamide

C38H63NO4 (597.4756838)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R))

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

C38H63NO4 (597.4756838)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/20:5(5Z,8Z,11Z,14Z,16E)-OH(18))

(5Z,8Z,11Z,13E,17Z)-N-[(2S,3R,4E,14Z)-1,3-dihydroxyoctadeca-4,14-dien-2-yl]-16-hydroxyicosa-5,8,11,13,17-pentaenamide

C38H63NO4 (597.4756838)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/20:5(5Z,8Z,10E,14Z,17Z)-OH(12))

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

C38H63NO4 (597.4756838)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/20:5(6E,8Z,11Z,14Z,17Z)-OH(5))

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

C38H63NO4 (597.4756838)


Cer(d18:2(4E,14Z)/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-nonadecanoylamino-octadecane-1,3,4-triol|Trufflesphingolipid B

(2S,3S,4R)-2-nonadecanoylamino-octadecane-1,3,4-triol|Trufflesphingolipid B

C37H75NO4 (597.569579)


   
   

(2R)-2-hydroxy-N-((E,2S,3S,4R)-1,3,4-trihydroxyhexacos-8-en-2-yl) decanamide

(2R)-2-hydroxy-N-((E,2S,3S,4R)-1,3,4-trihydroxyhexacos-8-en-2-yl) decanamide

C36H71NO5 (597.5331956)


   
   

Cer 36:1;O4

(2R)-2-hydroxy-N-((E,2S,3S,4R)-1,3,4-trihydroxyhexacos-8-en-2-yl) decanamide

C36H71NO5 (597.5331956)


   

Cer[NP]

N-(nonadecanoyl)-4R-hydroxysphinganine

C37H75NO4 (597.569579)


   

zirconium iodide

zirconium iodide

I4Zr (597.522616)


   

diiron trimolybdenum dodecaoxide

diiron trimolybdenum dodecaoxide

Fe2Mo3O12 (597.525073)


   

N-(1,3,4-trihydroxyoctadecan-2-yl)nonadecanamide

N-(1,3,4-trihydroxyoctadecan-2-yl)nonadecanamide

C37H75NO4 (597.569579)


   

Cer(d18:0/18:1(12Z)-2OH(9,10))

Cer(d18:0/18:1(12Z)-2OH(9,10))

C36H71NO5 (597.5331956)


   

Cer(d16:1/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4))

Cer(d16:1/22:6(5Z,7Z,10Z,13Z,16Z,19Z)-OH(4))

C38H63NO4 (597.4756838)


   

Cer(d16:1/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7))

Cer(d16:1/22:6(4Z,8Z,10Z,13Z,16Z,19Z)-OH(7))

C38H63NO4 (597.4756838)


   

Cer(d16:1/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

Cer(d16:1/22:6(4Z,7Z,10Z,12E,16Z,19Z)-OH(14))

C38H63NO4 (597.4756838)


   

Cer(d16:1/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17))

Cer(d16:1/22:6(4Z,7Z,10Z,13E,15E,19Z)-OH(17))

C38H63NO4 (597.4756838)


   

Cer(d16:1/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17))

Cer(d16:1/22:5(4Z,7Z,10Z,13Z,19Z)-O(16,17))

C38H63NO4 (597.4756838)


   

Cer(d18:2(4E,14Z)/20:4(6E,8Z,11Z,14Z)+=O(5))

Cer(d18:2(4E,14Z)/20:4(6E,8Z,11Z,14Z)+=O(5))

C38H63NO4 (597.4756838)


   

Cer(d18:2(4E,14Z)/20:4(5Z,8Z,11Z,13E)+=O(15))

Cer(d18:2(4E,14Z)/20:4(5Z,8Z,11Z,13E)+=O(15))

C38H63NO4 (597.4756838)


   

Cer(d18:2(4E,14Z)/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R))

Cer(d18:2(4E,14Z)/20:5(5Z,8Z,11Z,14Z,16E)-OH(18R))

C38H63NO4 (597.4756838)


   

Cer(d18:2(4E,14Z)/20:5(5Z,8Z,11Z,14Z,16E)-OH(18))

Cer(d18:2(4E,14Z)/20:5(5Z,8Z,11Z,14Z,16E)-OH(18))

C38H63NO4 (597.4756838)


   

Cer(d18:2(4E,14Z)/20:5(5Z,8Z,10E,14Z,17Z)-OH(12))

Cer(d18:2(4E,14Z)/20:5(5Z,8Z,10E,14Z,17Z)-OH(12))

C38H63NO4 (597.4756838)


   

Cer(d18:2(4E,14Z)/20:5(6E,8Z,11Z,14Z,17Z)-OH(5))

Cer(d18:2(4E,14Z)/20:5(6E,8Z,11Z,14Z,17Z)-OH(5))

C38H63NO4 (597.4756838)


   
   

N-icosanoyl-4-hydroxy-15-methylhexadecasphinganine

N-icosanoyl-4-hydroxy-15-methylhexadecasphinganine

C37H75NO4 (597.569579)


   

rubidium tetrabromoaurate(III)

rubidium tetrabromoaurate(III)

AuBr4Rb (597.551704)


   

Cer 18:0;2O/19:0;(3OH)

Cer 18:0;2O/19:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 18:0;2O/19:0;(2OH)

Cer 18:0;2O/19:0;(2OH)

C37H75NO4 (597.569579)


   

(12Z,15Z,18Z,21Z,24Z,27Z)-N-(1,3-dihydroxynonan-2-yl)triaconta-12,15,18,21,24,27-hexaenamide

(12Z,15Z,18Z,21Z,24Z,27Z)-N-(1,3-dihydroxynonan-2-yl)triaconta-12,15,18,21,24,27-hexaenamide

C39H67NO3 (597.5120671999999)


   

(15Z,18Z,21Z,24Z,27Z)-N-[(E)-1,3-dihydroxynon-4-en-2-yl]triaconta-15,18,21,24,27-pentaenamide

(15Z,18Z,21Z,24Z,27Z)-N-[(E)-1,3-dihydroxynon-4-en-2-yl]triaconta-15,18,21,24,27-pentaenamide

C39H67NO3 (597.5120671999999)


   

(8Z,11Z,14Z,17Z,20Z,23Z)-N-(1,3-dihydroxytridecan-2-yl)hexacosa-8,11,14,17,20,23-hexaenamide

(8Z,11Z,14Z,17Z,20Z,23Z)-N-(1,3-dihydroxytridecan-2-yl)hexacosa-8,11,14,17,20,23-hexaenamide

C39H67NO3 (597.5120671999999)


   

(13Z,16Z,19Z,22Z,25Z)-N-[(E)-1,3-dihydroxyundec-4-en-2-yl]octacosa-13,16,19,22,25-pentaenamide

(13Z,16Z,19Z,22Z,25Z)-N-[(E)-1,3-dihydroxyundec-4-en-2-yl]octacosa-13,16,19,22,25-pentaenamide

C39H67NO3 (597.5120671999999)


   

(14Z,17Z,20Z,23Z)-N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]hexacosa-14,17,20,23-tetraenamide

(14Z,17Z,20Z,23Z)-N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]hexacosa-14,17,20,23-tetraenamide

C39H67NO3 (597.5120671999999)


   

(5Z,8Z,11Z,14Z,17Z)-N-[(E)-1,3-dihydroxynonadec-4-en-2-yl]icosa-5,8,11,14,17-pentaenamide

(5Z,8Z,11Z,14Z,17Z)-N-[(E)-1,3-dihydroxynonadec-4-en-2-yl]icosa-5,8,11,14,17-pentaenamide

C39H67NO3 (597.5120671999999)


   

(10Z,13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]tetracosa-10,13,16-trienamide

(10Z,13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]tetracosa-10,13,16-trienamide

C39H67NO3 (597.5120671999999)


   

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

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

C39H67NO3 (597.5120671999999)


   

(4Z,7Z,10Z,13Z,16Z,19Z)-N-(1,3-dihydroxyheptadecan-2-yl)docosa-4,7,10,13,16,19-hexaenamide

(4Z,7Z,10Z,13Z,16Z,19Z)-N-(1,3-dihydroxyheptadecan-2-yl)docosa-4,7,10,13,16,19-hexaenamide

C39H67NO3 (597.5120671999999)


   

(11Z,14Z,17Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]icosa-11,14,17-trienamide

(11Z,14Z,17Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]icosa-11,14,17-trienamide

C39H67NO3 (597.5120671999999)


   

(10Z,13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]docosa-10,13,16-trienamide

(10Z,13Z,16Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]docosa-10,13,16-trienamide

C39H67NO3 (597.5120671999999)


   

(6Z,9Z,12Z,15Z,18Z,21Z)-N-(1,3-dihydroxypentadecan-2-yl)tetracosa-6,9,12,15,18,21-hexaenamide

(6Z,9Z,12Z,15Z,18Z,21Z)-N-(1,3-dihydroxypentadecan-2-yl)tetracosa-6,9,12,15,18,21-hexaenamide

C39H67NO3 (597.5120671999999)


   

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

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

C39H67NO3 (597.5120671999999)


   

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

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

C39H67NO3 (597.5120671999999)


   

(11Z,14Z,17Z,20Z,23Z)-N-[(E)-1,3-dihydroxytridec-4-en-2-yl]hexacosa-11,14,17,20,23-pentaenamide

(11Z,14Z,17Z,20Z,23Z)-N-[(E)-1,3-dihydroxytridec-4-en-2-yl]hexacosa-11,14,17,20,23-pentaenamide

C39H67NO3 (597.5120671999999)


   

(12Z,15Z,18Z,21Z)-N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]tetracosa-12,15,18,21-tetraenamide

(12Z,15Z,18Z,21Z)-N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]tetracosa-12,15,18,21-tetraenamide

C39H67NO3 (597.5120671999999)


   

(7Z,10Z,13Z,16Z,19Z)-N-[(E)-1,3-dihydroxyheptadec-4-en-2-yl]docosa-7,10,13,16,19-pentaenamide

(7Z,10Z,13Z,16Z,19Z)-N-[(E)-1,3-dihydroxyheptadec-4-en-2-yl]docosa-7,10,13,16,19-pentaenamide

C39H67NO3 (597.5120671999999)


   

(9Z,12Z,15Z,18Z,21Z)-N-[(E)-1,3-dihydroxypentadec-4-en-2-yl]tetracosa-9,12,15,18,21-pentaenamide

(9Z,12Z,15Z,18Z,21Z)-N-[(E)-1,3-dihydroxypentadec-4-en-2-yl]tetracosa-9,12,15,18,21-pentaenamide

C39H67NO3 (597.5120671999999)


   

(6Z,9Z,12Z,15Z)-N-[(4E,8E)-1,3-dihydroxyhenicosa-4,8-dien-2-yl]octadeca-6,9,12,15-tetraenamide

(6Z,9Z,12Z,15Z)-N-[(4E,8E)-1,3-dihydroxyhenicosa-4,8-dien-2-yl]octadeca-6,9,12,15-tetraenamide

C39H67NO3 (597.5120671999999)


   

(10Z,13Z,16Z,19Z)-N-[(4E,8E)-1,3-dihydroxyheptadeca-4,8-dien-2-yl]docosa-10,13,16,19-tetraenamide

(10Z,13Z,16Z,19Z)-N-[(4E,8E)-1,3-dihydroxyheptadeca-4,8-dien-2-yl]docosa-10,13,16,19-tetraenamide

C39H67NO3 (597.5120671999999)


   

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

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

C39H67NO3 (597.5120671999999)


   

(7Z,10Z,13Z)-N-[(4E,8E,12E)-1,3-dihydroxytricosa-4,8,12-trien-2-yl]hexadeca-7,10,13-trienamide

(7Z,10Z,13Z)-N-[(4E,8E,12E)-1,3-dihydroxytricosa-4,8,12-trien-2-yl]hexadeca-7,10,13-trienamide

C39H67NO3 (597.5120671999999)


   

(10Z,13Z,16Z,19Z,22Z,25Z)-N-(1,3-dihydroxyundecan-2-yl)octacosa-10,13,16,19,22,25-hexaenamide

(10Z,13Z,16Z,19Z,22Z,25Z)-N-(1,3-dihydroxyundecan-2-yl)octacosa-10,13,16,19,22,25-hexaenamide

C39H67NO3 (597.5120671999999)


   

Cer 8:0;3O/28:1;(2OH)

Cer 8:0;3O/28:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 9:0;3O/27:1;(2OH)

Cer 9:0;3O/27:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 13:1;3O/23:0;(2OH)

Cer 13:1;3O/23:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 12:1;3O/24:0;(2OH)

Cer 12:1;3O/24:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 11:0;3O/25:1;(2OH)

Cer 11:0;3O/25:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 10:0;3O/26:1;(2OH)

Cer 10:0;3O/26:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 13:0;3O/23:1;(2OH)

Cer 13:0;3O/23:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 12:0;3O/24:1;(2OH)

Cer 12:0;3O/24:1;(2OH)

C36H71NO5 (597.5331956)


   

N-(1,3,4-trihydroxytetracosan-2-yl)tridecanamide

N-(1,3,4-trihydroxytetracosan-2-yl)tridecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxypentadecan-2-yl)docosanamide

N-(1,3,4-trihydroxypentadecan-2-yl)docosanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxyhenicosan-2-yl)hexadecanamide

N-(1,3,4-trihydroxyhenicosan-2-yl)hexadecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxytricosan-2-yl)tetradecanamide

N-(1,3,4-trihydroxytricosan-2-yl)tetradecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxypentacosan-2-yl)dodecanamide

N-(1,3,4-trihydroxypentacosan-2-yl)dodecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxydocosan-2-yl)pentadecanamide

N-(1,3,4-trihydroxydocosan-2-yl)pentadecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxynonadecan-2-yl)octadecanamide

N-(1,3,4-trihydroxynonadecan-2-yl)octadecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxyheptadecan-2-yl)icosanamide

N-(1,3,4-trihydroxyheptadecan-2-yl)icosanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxyhexadecan-2-yl)henicosanamide

N-(1,3,4-trihydroxyhexadecan-2-yl)henicosanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxyicosan-2-yl)heptadecanamide

N-(1,3,4-trihydroxyicosan-2-yl)heptadecanamide

C37H75NO4 (597.569579)


   

N-(1,3,4-trihydroxytetradecan-2-yl)tricosanamide

N-(1,3,4-trihydroxytetradecan-2-yl)tricosanamide

C37H75NO4 (597.569579)


   

Cer 18:0;3O/18:1;(2OH)

Cer 18:0;3O/18:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 22:0;2O/15:0;(2OH)

Cer 22:0;2O/15:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 21:0;3O/15:1;(2OH)

Cer 21:0;3O/15:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 20:1;3O/16:0;(2OH)

Cer 20:1;3O/16:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 16:1;3O/20:0;(2OH)

Cer 16:1;3O/20:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 22:0;2O/15:0;(3OH)

Cer 22:0;2O/15:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 22:1;3O/14:0;(2OH)

Cer 22:1;3O/14:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 14:0;2O/23:0;(2OH)

Cer 14:0;2O/23:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 23:1;3O/13:0;(2OH)

Cer 23:1;3O/13:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 23:0;2O/14:0;(3OH)

Cer 23:0;2O/14:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 18:1;3O/18:0;(2OH)

Cer 18:1;3O/18:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 24:0;3O/12:1;(2OH)

Cer 24:0;3O/12:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 21:0;2O/16:0;(3OH)

Cer 21:0;2O/16:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 16:0;2O/21:0;(3OH)

Cer 16:0;2O/21:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 14:0;2O/23:0;(3OH)

Cer 14:0;2O/23:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 17:0;2O/20:0;(3OH)

Cer 17:0;2O/20:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 20:0;2O/17:0;(3OH)

Cer 20:0;2O/17:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 23:0;2O/14:0;(2OH)

Cer 23:0;2O/14:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 16:0;2O/21:0;(2OH)

Cer 16:0;2O/21:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 17:1;3O/19:0;(2OH)

Cer 17:1;3O/19:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 16:0;3O/20:1;(2OH)

Cer 16:0;3O/20:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 21:0;2O/16:0;(2OH)

Cer 21:0;2O/16:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 23:0;3O/13:1;(2OH)

Cer 23:0;3O/13:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 24:1;3O/12:0;(2OH)

Cer 24:1;3O/12:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 20:0;3O/16:1;(2OH)

Cer 20:0;3O/16:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 17:0;3O/19:1;(2OH)

Cer 17:0;3O/19:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 24:0;2O/13:0;(2OH)

Cer 24:0;2O/13:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 25:0;2O/12:0;(2OH)

Cer 25:0;2O/12:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 15:0;3O/21:1;(2OH)

Cer 15:0;3O/21:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 14:0;3O/22:1;(2OH)

Cer 14:0;3O/22:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 19:0;2O/18:0;(2OH)

Cer 19:0;2O/18:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 25:0;2O/12:0;(3OH)

Cer 25:0;2O/12:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 19:0;2O/18:0;(3OH)

Cer 19:0;2O/18:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 20:0;2O/17:0;(2OH)

Cer 20:0;2O/17:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 19:1;3O/17:0;(2OH)

Cer 19:1;3O/17:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 15:0;2O/22:0;(3OH)

Cer 15:0;2O/22:0;(3OH)

C37H75NO4 (597.569579)


   

Cer 15:1;3O/21:0;(2OH)

Cer 15:1;3O/21:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 22:0;3O/14:1;(2OH)

Cer 22:0;3O/14:1;(2OH)

C36H71NO5 (597.5331956)


   

Cer 14:1;3O/22:0;(2OH)

Cer 14:1;3O/22:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 21:1;3O/15:0;(2OH)

Cer 21:1;3O/15:0;(2OH)

C36H71NO5 (597.5331956)


   

Cer 15:0;2O/22:0;(2OH)

Cer 15:0;2O/22:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 17:0;2O/20:0;(2OH)

Cer 17:0;2O/20:0;(2OH)

C37H75NO4 (597.569579)


   

Cer 24:0;2O/13:0;(3OH)

Cer 24:0;2O/13:0;(3OH)

C37H75NO4 (597.569579)


   
   

(5E,8E,11E,14E)-N-[(2S,3R,4E,6E)-1,3-dihydroxypentadeca-4,6-dien-2-yl]tetracosa-5,8,11,14-tetraenamide

(5E,8E,11E,14E)-N-[(2S,3R,4E,6E)-1,3-dihydroxypentadeca-4,6-dien-2-yl]tetracosa-5,8,11,14-tetraenamide

C39H67NO3 (597.5120671999999)


   

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

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

C39H67NO3 (597.5120671999999)


   
   
   
   
   
   
   
   
   

Cer 14:0;O2/23:0;2OH

Cer 14:0;O2/23:0;2OH

C37H75NO4 (597.569579)


   

Cer 14:0;O2/23:0;3OH

Cer 14:0;O2/23:0;3OH

C37H75NO4 (597.569579)


   

Cer 14:0;O2/23:0;O

Cer 14:0;O2/23:0;O

C37H75NO4 (597.569579)


   

Cer 15:0;O2/22:0;2OH

Cer 15:0;O2/22:0;2OH

C37H75NO4 (597.569579)


   

Cer 15:0;O2/22:0;3OH

Cer 15:0;O2/22:0;3OH

C37H75NO4 (597.569579)


   

Cer 15:0;O2/22:0;O

Cer 15:0;O2/22:0;O

C37H75NO4 (597.569579)


   

Cer 16:0;O2/21:0;2OH

Cer 16:0;O2/21:0;2OH

C37H75NO4 (597.569579)


   

Cer 16:0;O2/21:0;3OH

Cer 16:0;O2/21:0;3OH

C37H75NO4 (597.569579)


   

Cer 16:0;O2/21:0;O

Cer 16:0;O2/21:0;O

C37H75NO4 (597.569579)


   

Cer 17:0;O2/20:0;2OH

Cer 17:0;O2/20:0;2OH

C37H75NO4 (597.569579)


   

Cer 17:0;O2/20:0;3OH

Cer 17:0;O2/20:0;3OH

C37H75NO4 (597.569579)


   

Cer 17:0;O2/20:0;O

Cer 17:0;O2/20:0;O

C37H75NO4 (597.569579)


   
   

Cer 18:0;O2/19:0;2OH

Cer 18:0;O2/19:0;2OH

C37H75NO4 (597.569579)


   

Cer 18:0;O2/19:0;3OH

Cer 18:0;O2/19:0;3OH

C37H75NO4 (597.569579)


   

Cer 18:0;O2/19:0;O

Cer 18:0;O2/19:0;O

C37H75NO4 (597.569579)


   

Cer 19:0;O2/18:0;2OH

Cer 19:0;O2/18:0;2OH

C37H75NO4 (597.569579)


   

Cer 19:0;O2/18:0;3OH

Cer 19:0;O2/18:0;3OH

C37H75NO4 (597.569579)


   

Cer 19:0;O2/18:0;O

Cer 19:0;O2/18:0;O

C37H75NO4 (597.569579)


   

Cer 20:0;O2/17:0;2OH

Cer 20:0;O2/17:0;2OH

C37H75NO4 (597.569579)


   

Cer 20:0;O2/17:0;3OH

Cer 20:0;O2/17:0;3OH

C37H75NO4 (597.569579)


   

Cer 20:0;O2/17:0;O

Cer 20:0;O2/17:0;O

C37H75NO4 (597.569579)


   

Cer 21:0;O2/16:0;2OH

Cer 21:0;O2/16:0;2OH

C37H75NO4 (597.569579)


   

Cer 21:0;O2/16:0;3OH

Cer 21:0;O2/16:0;3OH

C37H75NO4 (597.569579)


   

Cer 21:0;O2/16:0;O

Cer 21:0;O2/16:0;O

C37H75NO4 (597.569579)


   

Cer 22:0;O2/15:0;2OH

Cer 22:0;O2/15:0;2OH

C37H75NO4 (597.569579)


   

Cer 22:0;O2/15:0;3OH

Cer 22:0;O2/15:0;3OH

C37H75NO4 (597.569579)


   

Cer 22:0;O2/15:0;O

Cer 22:0;O2/15:0;O

C37H75NO4 (597.569579)


   
   
   

Cer 14:0;O3/22:1;2OH

Cer 14:0;O3/22:1;2OH

C36H71NO5 (597.5331956)


   

Cer 14:0;O3/22:1;3OH

Cer 14:0;O3/22:1;3OH

C36H71NO5 (597.5331956)


   
   
   
   

Cer 16:0;O3/20:1;2OH

Cer 16:0;O3/20:1;2OH

C36H71NO5 (597.5331956)


   

Cer 16:0;O3/20:1;3OH

Cer 16:0;O3/20:1;3OH

C36H71NO5 (597.5331956)


   
   
   
   

Cer 18:0;O3/18:1;2OH

Cer 18:0;O3/18:1;2OH

C36H71NO5 (597.5331956)


   

Cer 18:0;O3/18:1;3OH

Cer 18:0;O3/18:1;3OH

C36H71NO5 (597.5331956)


   
   
   
   
   
   
   

n'-(4-aminobutyl)-n,n'-bis(3-aminopropyl)-n-{4-[(3-aminopropyl)amino]butyl}hexadecanediamide

n'-(4-aminobutyl)-n,n'-bis(3-aminopropyl)-n-{4-[(3-aminopropyl)amino]butyl}hexadecanediamide

C33H71N7O2 (597.5668946)