Exact Mass: 573.5120671999999

Exact Mass Matches: 573.5120671999999

Found 110 metabolites which its exact mass value is equals to given mass value 573.5120671999999, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Cer(d16:1/20:3(5Z,8Z,11Z)-O(14R,15S))

(5Z,8Z,11Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-13-(3-pentyloxiran-2-yl)trideca-5,8,11-trienamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:3(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(d16:1/20:3(5Z,8Z,14Z)-O(11S,12R))

(5Z,8Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-10-{3-[(2Z)-oct-2-en-1-yl]oxiran-2-yl}deca-5,8-dienamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:3(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(d16:1/20:3(5Z,11Z,14Z)-O(8,9))

(5Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-7-{3-[(2Z,5Z)-undeca-2,5-dien-1-yl]oxiran-2-yl}hept-5-enamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:3(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(d16:1/20:3(8Z,11Z,14Z)-O(5,6))

N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-4-{3-[(2Z,5Z,8Z)-tetradeca-2,5,8-trien-1-yl]oxiran-2-yl}butanamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:3(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(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(20))

(5Z,8Z,11Z,14Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-20-hydroxyicosa-5,8,11,14-tetraenamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(6E,8Z,11Z,14Z)-OH(5S))

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

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(19S))

(5Z,8Z,11Z,14Z,19S)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-19-hydroxyicosa-5,8,11,14-tetraenamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(18R))

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

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(17))

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

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(16R))

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

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,8Z,11Z,13E)-OH(15S))

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

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,8Z,10E,14Z)-OH(12S))

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

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5E,8Z,12Z,14Z)-OH(11R))

(5E,8Z,11R,12Z,14Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-11-hydroxyicosa-5,8,12,14-tetraenamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d16:1/20:4(5Z,7E,11Z,14Z)-OH(9))

(5E,7Z,11Z,14Z)-N-[(2S,3R,4E)-1,3-dihydroxyhexadec-4-en-2-yl]-9-hydroxyicosa-5,7,11,14-tetraenamide

C36H63NO4 (573.4756838000001)


Cer(d16:1/20:4(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(d18:2(4E,14Z)/18:2(10E,12Z)+=O(9))

(10E,12Z)-N-[(2S,3R,4E,14Z)-1,3-dihydroxyoctadeca-4,14-dien-2-yl]-9-oxooctadeca-10,12-dienamide

C36H63NO4 (573.4756838000001)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/18:2(9Z,11E)+=O(13))

(9Z,11E)-N-[(2S,3R,4E,14Z)-1,3-dihydroxyoctadeca-4,14-dien-2-yl]-13-oxooctadeca-9,11-dienamide

C36H63NO4 (573.4756838000001)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/18:3(10,12,15)-OH(9))

(10E,12E,15E)-N-[(2S,3R,4E,14Z)-1,3-dihydroxyoctadeca-4,14-dien-2-yl]-9-hydroxyoctadeca-10,12,15-trienamide

C36H63NO4 (573.4756838000001)


Cer(d18:2(4E,14Z)/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(d18:2(4E,14Z)/18:3(9,11,15)-OH(13))

(9E,11E,15E)-N-[(2S,3R,4E,14Z)-1,3-dihydroxyoctadeca-4,14-dien-2-yl]-13-hydroxyoctadeca-9,11,15-trienamide

C36H63NO4 (573.4756838000001)


Cer(d18:2(4E,14Z)/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).

   
   

(2S,3R,4E,8E,9Z,12Z)-N-(9,12)-octadecadienoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol|(2S,3R,4E,8E,9Z,12Z)-N-9,12-Octadecadienoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol

(2S,3R,4E,8E,9Z,12Z)-N-(9,12)-octadecadienoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol|(2S,3R,4E,8E,9Z,12Z)-N-9,12-Octadecadienoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol

C37H67NO3 (573.5120671999999)


   

DG(16:0/0:0/16:0) (d5)

1,3-dihexadecanoyl-2-hydroxy-sn-glycerol-d5

C35H63D5O5 (573.53803369)


   

ALPHA,ALPHA,ALPHA,ALPHA,4,5-HEXABROMO-O-XYLENE

ALPHA,ALPHA,ALPHA,ALPHA,4,5-HEXABROMO-O-XYLENE

C8H4Br6 (573.5413143999999)


   

3,6-bis(bromomethyl)-1,2,4,5-tetrabromobenzene

3,6-bis(bromomethyl)-1,2,4,5-tetrabromobenzene

C8H4Br6 (573.5413143999999)


   

Dimethyldipalmitylammonium Bromide

Dimethyldipalmitylammonium Bromide

C34H72BrN (573.4847811999999)


   

Cer(d16:1/20:3(5Z,8Z,11Z)-O(14R,15S))

Cer(d16:1/20:3(5Z,8Z,11Z)-O(14R,15S))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:3(5Z,8Z,14Z)-O(11S,12R))

Cer(d16:1/20:3(5Z,8Z,14Z)-O(11S,12R))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:3(5Z,11Z,14Z)-O(8,9))

Cer(d16:1/20:3(5Z,11Z,14Z)-O(8,9))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:3(8Z,11Z,14Z)-O(5,6))

Cer(d16:1/20:3(8Z,11Z,14Z)-O(5,6))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(20))

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(20))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(6E,8Z,11Z,14Z)-OH(5S))

Cer(d16:1/20:4(6E,8Z,11Z,14Z)-OH(5S))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(19S))

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(19S))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(18R))

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(18R))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(17))

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(17))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(16R))

Cer(d16:1/20:4(5Z,8Z,11Z,14Z)-OH(16R))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,11Z,13E)-OH(15S))

Cer(d16:1/20:4(5Z,8Z,11Z,13E)-OH(15S))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,8Z,10E,14Z)-OH(12S))

Cer(d16:1/20:4(5Z,8Z,10E,14Z)-OH(12S))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5E,8Z,12Z,14Z)-OH(11R))

Cer(d16:1/20:4(5E,8Z,12Z,14Z)-OH(11R))

C36H63NO4 (573.4756838000001)


   

Cer(d16:1/20:4(5Z,7E,11Z,14Z)-OH(9))

Cer(d16:1/20:4(5Z,7E,11Z,14Z)-OH(9))

C36H63NO4 (573.4756838000001)


   

Cer(d18:2(4E,14Z)/18:2(10E,12Z)+=O(9))

Cer(d18:2(4E,14Z)/18:2(10E,12Z)+=O(9))

C36H63NO4 (573.4756838000001)


   

Cer(d18:2(4E,14Z)/18:2(9Z,11E)+=O(13))

Cer(d18:2(4E,14Z)/18:2(9Z,11E)+=O(13))

C36H63NO4 (573.4756838000001)


   

Cer(d18:2(4E,14Z)/18:3(10,12,15)-OH(9))

Cer(d18:2(4E,14Z)/18:3(10,12,15)-OH(9))

C36H63NO4 (573.4756838000001)


   

Cer(d18:2(4E,14Z)/18:3(9,11,15)-OH(13))

Cer(d18:2(4E,14Z)/18:3(9,11,15)-OH(13))

C36H63NO4 (573.4756838000001)


   

(14Z,17Z,20Z)-N-[(E)-1,3-dihydroxynon-4-en-2-yl]octacosa-14,17,20-trienamide

(14Z,17Z,20Z)-N-[(E)-1,3-dihydroxynon-4-en-2-yl]octacosa-14,17,20-trienamide

C37H67NO3 (573.5120671999999)


   

(16Z,19Z,22Z,25Z)-N-(1,3-dihydroxynonan-2-yl)octacosa-16,19,22,25-tetraenamide

(16Z,19Z,22Z,25Z)-N-(1,3-dihydroxynonan-2-yl)octacosa-16,19,22,25-tetraenamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(10Z,13Z,16Z)-N-[(E)-1,3-dihydroxypentadec-4-en-2-yl]docosa-10,13,16-trienamide

(10Z,13Z,16Z)-N-[(E)-1,3-dihydroxypentadec-4-en-2-yl]docosa-10,13,16-trienamide

C37H67NO3 (573.5120671999999)


   

(13Z,16Z)-N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]docosa-13,16-dienamide

(13Z,16Z)-N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]docosa-13,16-dienamide

C37H67NO3 (573.5120671999999)


   

(13Z,16Z)-N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]tetracosa-13,16-dienamide

(13Z,16Z)-N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]tetracosa-13,16-dienamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]octadec-9-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]octadec-9-enamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(11Z,14Z)-N-[(4E,8E)-1,3-dihydroxyhexadeca-4,8-dien-2-yl]henicosa-11,14-dienamide

(11Z,14Z)-N-[(4E,8E)-1,3-dihydroxyhexadeca-4,8-dien-2-yl]henicosa-11,14-dienamide

C37H67NO3 (573.5120671999999)


   

(8Z,11Z,14Z,17Z)-N-(1,3-dihydroxyheptadecan-2-yl)icosa-8,11,14,17-tetraenamide

(8Z,11Z,14Z,17Z)-N-(1,3-dihydroxyheptadecan-2-yl)icosa-8,11,14,17-tetraenamide

C37H67NO3 (573.5120671999999)


   

(11Z,14Z,17Z)-N-[(E)-1,3-dihydroxyheptadec-4-en-2-yl]icosa-11,14,17-trienamide

(11Z,14Z,17Z)-N-[(E)-1,3-dihydroxyheptadec-4-en-2-yl]icosa-11,14,17-trienamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyicosa-4,8,12-trien-2-yl]heptadec-9-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyicosa-4,8,12-trien-2-yl]heptadec-9-enamide

C37H67NO3 (573.5120671999999)


   

(12Z,15Z,18Z)-N-[(E)-1,3-dihydroxyundec-4-en-2-yl]hexacosa-12,15,18-trienamide

(12Z,15Z,18Z)-N-[(E)-1,3-dihydroxyundec-4-en-2-yl]hexacosa-12,15,18-trienamide

C37H67NO3 (573.5120671999999)


   

(9Z,12Z,15Z)-N-[(E)-1,3-dihydroxynonadec-4-en-2-yl]octadeca-9,12,15-trienamide

(9Z,12Z,15Z)-N-[(E)-1,3-dihydroxynonadec-4-en-2-yl]octadeca-9,12,15-trienamide

C37H67NO3 (573.5120671999999)


   

(14Z,17Z,20Z,23Z)-N-(1,3-dihydroxyundecan-2-yl)hexacosa-14,17,20,23-tetraenamide

(14Z,17Z,20Z,23Z)-N-(1,3-dihydroxyundecan-2-yl)hexacosa-14,17,20,23-tetraenamide

C37H67NO3 (573.5120671999999)


   

(12Z,15Z,18Z,21Z)-N-(1,3-dihydroxytridecan-2-yl)tetracosa-12,15,18,21-tetraenamide

(12Z,15Z,18Z,21Z)-N-(1,3-dihydroxytridecan-2-yl)tetracosa-12,15,18,21-tetraenamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]docos-13-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]docos-13-enamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhexadeca-4,8,12-trien-2-yl]henicos-11-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhexadeca-4,8,12-trien-2-yl]henicos-11-enamide

C37H67NO3 (573.5120671999999)


   

(10Z,13Z,16Z,19Z)-N-(1,3-dihydroxypentadecan-2-yl)docosa-10,13,16,19-tetraenamide

(10Z,13Z,16Z,19Z)-N-(1,3-dihydroxypentadecan-2-yl)docosa-10,13,16,19-tetraenamide

C37H67NO3 (573.5120671999999)


   

(4Z,7Z,10Z,13Z)-N-(1,3-dihydroxyhenicosan-2-yl)hexadeca-4,7,10,13-tetraenamide

(4Z,7Z,10Z,13Z)-N-(1,3-dihydroxyhenicosan-2-yl)hexadeca-4,7,10,13-tetraenamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhenicosa-4,8,12-trien-2-yl]hexadec-9-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhenicosa-4,8,12-trien-2-yl]hexadec-9-enamide

C37H67NO3 (573.5120671999999)


   

(6Z,9Z,12Z,15Z)-N-(1,3-dihydroxynonadecan-2-yl)octadeca-6,9,12,15-tetraenamide

(6Z,9Z,12Z,15Z)-N-(1,3-dihydroxynonadecan-2-yl)octadeca-6,9,12,15-tetraenamide

C37H67NO3 (573.5120671999999)


   

(10Z,13Z,16Z)-N-[(E)-1,3-dihydroxytridec-4-en-2-yl]tetracosa-10,13,16-trienamide

(10Z,13Z,16Z)-N-[(E)-1,3-dihydroxytridec-4-en-2-yl]tetracosa-10,13,16-trienamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]icos-11-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyheptadeca-4,8,12-trien-2-yl]icos-11-enamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyoctadeca-4,8,12-trien-2-yl]nonadec-9-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyoctadeca-4,8,12-trien-2-yl]nonadec-9-enamide

C37H67NO3 (573.5120671999999)


   
   
   
   
   
   
   
   
   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxytetradeca-4,8,12-trien-2-yl]tricos-11-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxytetradeca-4,8,12-trien-2-yl]tricos-11-enamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhexadeca-4,8,12-trien-2-yl]henicos-9-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhexadeca-4,8,12-trien-2-yl]henicos-9-enamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxytetracosa-4,8,12-trien-2-yl]tridec-8-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxytetracosa-4,8,12-trien-2-yl]tridec-8-enamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]octadec-11-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxynonadeca-4,8,12-trien-2-yl]octadec-11-enamide

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

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

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

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhenicosa-4,8,12-trien-2-yl]hexadec-7-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxyhenicosa-4,8,12-trien-2-yl]hexadec-7-enamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxypentacosa-4,8,12-trien-2-yl]dodec-5-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxypentacosa-4,8,12-trien-2-yl]dodec-5-enamide

C37H67NO3 (573.5120671999999)


   

(Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]docos-11-enamide

(Z)-N-[(4E,8E,12E)-1,3-dihydroxypentadeca-4,8,12-trien-2-yl]docos-11-enamide

C37H67NO3 (573.5120671999999)


   

(9E,12E)-N-[(2S,3R,4E,8E)-1,3-dihydroxynonadeca-4,8-dien-2-yl]octadeca-9,12-dienamide

(9E,12E)-N-[(2S,3R,4E,8E)-1,3-dihydroxynonadeca-4,8-dien-2-yl]octadeca-9,12-dienamide

C37H67NO3 (573.5120671999999)


   
   
   
   
   
   
   
   
   
   
   
   
   
   

(2s,3r,4 e,8 e,9'z,12'z)-n-9',12'-octadecadieno-yl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol

NA

C37H67NO3 (573.5120671999999)


{"Ingredient_id": "HBIN006632","Ingredient_name": "(2s,3r,4 e,8 e,9'z,12'z)-n-9',12'-octadecadieno-yl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol","Alias": "NA","Ingredient_formula": "C37H67NO3","Ingredient_Smile": "CCCCCCCCCC(=CCCC=CC(C(CO)NC(=O)CCCCCCCC=CCC=CCCCCC)O)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "15933","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

n-(1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl)octadeca-9,12-dienimidic acid

n-(1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl)octadeca-9,12-dienimidic acid

C37H67NO3 (573.5120671999999)


   

(9z,12z)-n-[(2s,3r,4e,8e)-1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl]octadeca-9,12-dienimidic acid

(9z,12z)-n-[(2s,3r,4e,8e)-1,3-dihydroxy-9-methyloctadeca-4,8-dien-2-yl]octadeca-9,12-dienimidic acid

C37H67NO3 (573.5120671999999)


   

3-{8-[(3s,3as,6ar)-1-[(6z)-14-(pyridin-3-yl)tetradec-6-en-1-yl]-hexahydrocyclopenta[c][1,2]oxazol-3-yl]octyl}pyridine

3-{8-[(3s,3as,6ar)-1-[(6z)-14-(pyridin-3-yl)tetradec-6-en-1-yl]-hexahydrocyclopenta[c][1,2]oxazol-3-yl]octyl}pyridine

C38H59N3O (573.4657884000001)