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Accueil >> Lipids >> Hydroxy/Hydroperoxy/Epoxy/Oxo Eicosanoids

Hydroxy/Hydroperoxy/Epoxy/Oxo Eicosanoids

Products for  Hydroxy/Hydroperoxy/Epoxy/Oxo Eicosanoids

  1. Cat.No. Nom du produit Informations
  2. GC40279 (±)11(12)-DiHET

    (±)11,12DiHETrE

     Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity. (±)11(12)-DiHET Chemical Structure
  3. GC49439 (±)11(12)-DiHET MaxSpec® Standard

    (±)11,12-DiHETrE

     A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications (±)11(12)-DiHET MaxSpec® Standard Chemical Structure
  4. GC46252 (±)11(12)-DiHET-d11

    (±)11(12)-DHET-d11, (±)11,12-DiHETrE-d11

     A neuropeptide with diverse biological activities (±)11(12)-DiHET-d11 Chemical Structure
  5. GC45271 (±)11(12)-EET Ethanolamide

    (±)11,12-EpETrE Ethanolamide

     Arachidonoyl ethanolamide (AEA; anandamide) is an endogenous lipid neurotransmitter with cannibingeric activity, binding to both the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. (±)11(12)-EET Ethanolamide Chemical Structure
  6. GC40841 (±)11(12)-EET methyl ester

    (±)11,12EpETrE methyl ester

     (±)11(12)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450. (±)11(12)-EET methyl ester Chemical Structure
  7. GC45922 (±)11(12)-EET-d11 methyl ester

    (±)11,12-EpETrE-d11 methyl ester

     A neuropeptide with diverse biological activities (±)11(12)-EET-d11 methyl ester Chemical Structure
  8. GC40386 (±)11(12)-EpETE

    (±)11,12-EEQ, (±)11,12-Epoxyeicosatetraenoic Acid

     Eicosapentaenoic acid is converted to epoxyeicosatetraenoic acids (EpETE) by several cytochrome P450 isoforms. (±)11(12)-EpETE Chemical Structure
  9. GC41143 (±)11,12-DiHETE (±)11,12-DiHETE is a dihydroxy metabolite of EPA produced by cytochrome P450-mediated epoxide formation and subsequent hydrolysis by epoxide hydrolase. (±)11,12-DiHETE Chemical Structure
  10. GC40428 (±)11-HEDE

    11-hydroxy-12,14-Eicosadienoic Acid

     (±)11-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)11-HEDE Chemical Structure
  11. GC40387 (±)11-HEPE (±)11-HEPE is produced by non-enzymatic oxidation of eicosapentaenoic acid. (±)11-HEPE Chemical Structure
  12. GC40467 (±)11-HETE

    (±)11-Hydroxyeicosatetraenoic Acid

     (±)11-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)11-HETE Chemical Structure
  13. GC40359 (±)12-HEPE

    (±)12-HEPE is produced by non-enzymatic oxidation of EPA.

     (±)12-HEPE Chemical Structure
  14. GC40429 (±)12-HETE

    (±)-Hydroxyeicosatetraenoic Acid

     (±)12-HETE, un produit métabolique majeur de l'acide arachidonique utilisant la catalyse 12-LOX, inhibe l'apoptose cellulaire de manière dose-dépendante. (±)12-HETE Chemical Structure
  15. GC48738 (±)12-HETE-d8

    (±)12-Hydroxyeicosatetraenoic Acid-d8

     (±)12-HETE-d8 Chemical Structure
  16. GC41115 (±)12-HpETE (±)12-HpETE is one of the six monohydroperoxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid and consists of an equal mixture of the R and S isomers. (±)12-HpETE Chemical Structure
  17. GC40268 (±)14(15)-DiHET

    (±)14,15DiHETrE

     Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity. (±)14(15)-DiHET Chemical Structure
  18. GC46258 (±)14(15)-DiHET-d11

    (±)14,15-DiHETrE-d11

     A neuropeptide with diverse biological activities (±)14(15)-DiHET-d11 Chemical Structure
  19. GC41116 (±)14(15)-DiHETE

    (±)14,15dihydroxyeicosa5,8,11,17Tetraenoic Acid

     Eicosapentaenoic acid is an ω-3 fatty acid abundantly available in marine organisms. (±)14(15)-DiHETE Chemical Structure
  20. GC40430 (±)14(15)-EET

    (±)14,15-EET, (±)14,15-EpETrE

    (±)14(15)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450.

     (±)14(15)-EET Chemical Structure
  21. GC41650 (±)14(15)-EET Ethanolamide

    (±)14,15EpETrE Ethanolamide, (±)14(15)Epoxy Eicosatrienoyl Ethanolamide

     Arachidonyl ethanolamide (AEA) is an endogenous lipid neurotransmitter with cannabinergic activity, binding to both the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. (±)14(15)-EET Ethanolamide Chemical Structure
  22. GC40835 (±)14(15)-EET methyl ester

    (±)14,15EpETrE methyl ester

     (±)14(15)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450. (±)14(15)-EET methyl ester Chemical Structure
  23. GC45920 (±)14(15)-EET-d11 methyl ester

    (±)14,15-EpETrE-d11 methyl ester

     A neuropeptide with diverse biological activities (±)14(15)-EET-d11 methyl ester Chemical Structure
  24. GC41651 (±)14(15)-EET-SI

    14,15-EpETrE-SI, 14(15)-EET-SI, 14(15)EETsulfonimide

     Arachidonic acid is metabolized in the vascular endothelium to epoxytrienoic acids (EETs or EpETrEs) by cytochrome P450 enzymes. (±)14(15)-EET-SI Chemical Structure
  25. GC41652 (±)14(15)-EpEDE

    (±)14,15Epoxyeicosadienoic Acid

     8,11,14-Eicosatrienoic acid, also known as dihomo-γ-linolenic acid, is a polyunsaturated fatty acid (PUFA) produced from γ-linolenic acid by the action of fatty acid elongases. (±)14(15)-EpEDE Chemical Structure
  26. GC40888 (±)14(15)-EpEDE methyl ester

    (±)14,15Epoxyeicosadienoic Acid methyl ester

     (±)14(15)-EpEDE is an EpEDE formed from 8,11,14-eicosatrienoic acid, also known as dihomo-γ-linolenic acid. (±)14(15)-EpEDE methyl ester Chemical Structure
  27. GC40360 (±)14(15)-EpETE

    (±)14,15 EEQ, (±)14,15epoxy Eicosatetraenoic Acid

     EDHF (endothelium-derived hyperpolarizing factor) is an unidentified mediator released from vascular endothelial cells in response to acetylcholine and bradykinin which is distinct from the NOS- (nitric oxide) and COX-derived (prostacyclin) vasodilators. (±)14(15)-EpETE Chemical Structure
  28. GC40420 (±)15-HEDE (±)15-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)15-HEDE Chemical Structure
  29. GC40361 (±)15-HEPE

    (±)15-hydroxy Eicosapentaenoic Acid

    (±)15-HEPE is produced by non-enzymatic oxidation of EPA.

     (±)15-HEPE Chemical Structure
  30. GC40433 (±)15-HETE MaxSpec® Standard (±)15-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)15-HETE MaxSpec® Standard Chemical Structure
  31. GC48739 (±)15-HETE-d8

    (±)15-Hydroxyeicosatetraenoic Acid-d8

     (±)15-HETE-d8 Chemical Structure
  32. GC41117 (±)17(18)-DiHETE

    (±)17,18-dihydroxy-eicosa-5,8,11,14-Tetraenoic Acid

     Eicosapentaenoic acid is an ω-3 fatty acid abundantly available in marine organisms. (±)17(18)-DiHETE Chemical Structure
  33. GC46260 (±)17(18)-EpETE

    (±)17,18-EEQ, (±)17,18-epoxy Eicosatetraenoic Acid

     A neuropeptide with diverse biological activities (±)17(18)-EpETE Chemical Structure
  34. GC41318 (±)17(18)-EpETE methyl ester

    (±)17,18-EEQ methyl ester, (±)17,18-epoxy Eicosatetraenoic Acid methyl ester

     (±)17(18)-EpETE methyl ester is an analog of the eicosapentaenoic acid (EPA) metabolite (±)17(18)-EpETE that is more lipid soluble. (±)17(18)-EpETE methyl ester Chemical Structure
  35. GC41288 (±)17(18)-EpETE-Ethanolamide

    17,18-EEQ-EA, (±)17,18-EEQ-Ethanolamide, (±)17(18)-EpETE-EA, 17,18-epoxy-Eicosatetraenoic Acid Ethanolamide

     (±)17(18)-EpETE-Ethanolamide is an ω-3 endocannabinoid epoxide. (±)17(18)-EpETE-Ethanolamide Chemical Structure
  36. GC40362 (±)18-HEPE (±)18-HEPE is produced by non-enzymatic oxidation of EPA. (±)18-HEPE Chemical Structure
  37. GC40436 (±)18-HETE

    (±)18-Hydroxyeicosatetraenoic Acid

     (±)18-HETE is the racemic version of a cytochrome P450 (CYP450) metabolite of arachidonic acid. (±)18-HETE Chemical Structure
  38. GC40437 (±)5(6)-DiHET lactone

    (±)5,6DiHETrE lactone

     5,6-DiHET lactone is a lactonized form of 5,6-EET and 5,6-DiHET. (±)5(6)-DiHET lactone Chemical Structure
  39. GC40271 (±)5(6)-DiHET MaxSpec® Standard 5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases. (±)5(6)-DiHET MaxSpec® Standard Chemical Structure
  40. GC41119 (±)5(6)-DiHETE Eicosapentaenoic acid is an ω-3 polyunsaturated fatty acid that is abundant in marine organisms and fish oils. (±)5(6)-DiHETE Chemical Structure
  41. GC40363 (±)5(6)-DiHETE lactone Eicosapentaenoic acid is metabolized, in part, through cytochrome P450-catalyzed epoxidation followed by conversion to the vicinal diols by epoxide hydrolases. (±)5(6)-DiHETE lactone Chemical Structure
  42. GC41662 (±)5(6)-EET Ethanolamide

    (±)5,6EpETrE Ethanolamide

     Arachidonyl ethanolamide is an endogenous lipid neurotransmitter with cannabinergic activity, binding to both the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. (±)5(6)-EET Ethanolamide Chemical Structure
  43. GC40836 (±)5(6)-EET methyl ester

    (±)5,6EpETrE methyl ester

     (±)5(6)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450. (±)5(6)-EET methyl ester Chemical Structure
  44. GC46262 (±)5(6)-EET-d11

    (±)5,6-EET-d11

     A neuropeptide with diverse biological activities (±)5(6)-EET-d11 Chemical Structure
  45. GC45919 (±)5(6)-EET-d11 methyl ester

    (±)5,6-EpETrE-d11 methyl ester

     A neuropeptide with diverse biological activities (±)5(6)-EET-d11 methyl ester Chemical Structure
  46. GC41319 (±)5(6)-EpETE methyl ester

    (±)5,6EEQ methyl ester, (±)5,6epoxy Eicosatetraenoic Acid methyl ester

     (±)5(6)-EpETE methyl ester is a derivative of 5(6)-EpETE which is stable enough to ship and handle routinely. (±)5(6)-EpETE methyl ester Chemical Structure
  47. GC40364 (±)5-HEPE (±)5-HEPE is produced by non-enzymatic oxidation of EPA. (±)5-HEPE Chemical Structure
  48. GC40439 (±)5-HETE

    (±)5-Hydroxyeicosatetraenoic Acid

    (±)5-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid.

     (±)5-HETE Chemical Structure
  49. GC40837 (±)5-HETE methyl ester

    (±)-Hydroxyeicosatetraenoic Acid methyl ester

     (±)5-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)5-HETE methyl ester Chemical Structure
  50. GC40272 (±)8(9)-DiHET

    (±)8,9DiHETrE

     Epoxide hydrolases convert the EETs into vicinal diols, with the concurrent loss of much of their biological activity. (±)8(9)-DiHET Chemical Structure
  51. GC40421 (±)8(9)-EE-14(Z)-E

    (±)8,9-Epoxyeicosa-14(Z)-enoic Acid

     (±)14(15)-EE-8(Z)-E is a potent vasodilator in bovine coronary arteries. (±)8(9)-EE-14(Z)-E Chemical Structure
  52. GC40440 (±)8(9)-EET

    (±)8,9EpETrE

     (±)8(9)-EET is a fully racemic version of the R/S enantiomeric forms biosynthesized from arachidonic acid. (±)8(9)-EET Chemical Structure
  53. GC41665 (±)8(9)-EET Ethanolamide

    (±)8,9-EET Ethanolamide

     Arachidonoyl ethanolamide (AEA; anandamide) is an endogenous lipid neurotransmitter with cannabinergic activity, binding to both the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors. (±)8(9)-EET Ethanolamide Chemical Structure
  54. GC40838 (±)8(9)-EET methyl ester

    (±)8,9EpETrE methyl ester

     (±)8(9)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450. (±)8(9)-EET methyl ester Chemical Structure
  55. GC46264 (±)8(9)-EET-d11

    (±)8,9-EET-d11, (±)8,9-EpETrE-d11

     A neuropeptide with diverse biological activities (±)8(9)-EET-d11 Chemical Structure
  56. GC45921 (±)8(9)-EET-d11 methyl ester

    (±)8,9-EpETrE-d11 methyl ester

     A neuropeptide with diverse biological activities (±)8(9)-EET-d11 methyl ester Chemical Structure
  57. GC40365 (±)8(9)-EpETE

    (±)8,9-EEQ, (±)8,9-epoxy Eicosatetraenoic Acid

     Eicosapentaenoic acid is converted to epoxyeicosatetraenoic acids (EpETEs) by several cytochrome P450 isoforms. (±)8(9)-EpETE Chemical Structure
  58. GC46265 (±)8,9-DiHET-d11

    (±)8,9DiHETrEd11

     A neuropeptide with diverse biological activities (±)8,9-DiHET-d11 Chemical Structure
  59. GC41120 (±)8,9-DiHETE

    (±)8,9-DiHETE is a major metabolite of the 20:5 ω-3 fatty acid eicosapentaenoic acid.

     (±)8,9-DiHETE Chemical Structure
  60. GC40366 (±)8-HEPE

    (±)8-HEPE is produced by non-enzymatic oxidation of EPA.

     (±)8-HEPE Chemical Structure
  61. GC40367 (±)9-HEPE (±)9-HEPE is produced by non-enzymatic oxidation of EPA. (±)9-HEPE Chemical Structure
  62. GC40443 (±)9-HETE

    (±)9-Hydroxyeicosatetraenoic Acid

     (±)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)9-HETE Chemical Structure
  63. GC46268 (±)9-HETE-d8

    (±)9-Hydroxyeicosatetraenoic Acid-d8

     A neuropeptide with diverse biological activities (±)9-HETE-d8 Chemical Structure
  64. GC40444 (5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic Acid

    HETE Analog 1, Hydroxyeicosatetraenoic Acid Analog 1

     (5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic acid is a stable isomer of 15(S)-HETE, a major arachidonic acid metabolite from the 15-lipoxygenase pathway. (5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic Acid Chemical Structure
  65. GC20027 (±)5(6)-DiHET MaxSpec® Standard

    (±)5,6-DiHETrE

    5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases.

     (±)5(6)-DiHET MaxSpec® Standard Chemical Structure
  66. GC40422 11(R)-HEDE 11(R)-HEDE is produced from 11Z,14Z-eicosadienoic acid by COX in a lipoxygenase-type reaction. 11(R)-HEDE Chemical Structure
  67. GC40368 11(R)-HEPE 11(R)-HEPE is produced by the oxidation of EPA by 11(R)-LO. 11(R)-HEPE Chemical Structure
  68. GC40445 11(R)-HETE

    11(R)-Hydroxyeicosatetraenoic Acid

     11(R)-HETE is biosynthesized by 11(R)-LOs of the sea urchin, S. 11(R)-HETE Chemical Structure
  69. GC40423 11(S)-HEDE 11(S)-HEDE is isolated by the chromatographic resolution of (±)11-HEDE. 11(S)-HEDE Chemical Structure
  70. GC40369 11(S)-HEPE 11(S)-HEPE is a monohydroxy fatty acid derived from EPA, theoretically by the action of COX. 11(S)-HEPE Chemical Structure
  71. GC40446 11(S)-HETE

    11(S)-Hydroxyeicosatetraenoic Acid

     11(S)-HETE is an oxylipin and the (S) enantiomer of 11(R)-HETE. It is formed non-enzymatically from arachidonic acid. 11(S)-HETE Chemical Structure
  72. GC91503 11R(12S)-EET

    11R(12S)-EpETrE,11R(12S)-Epoxy-all-cis-5,8,14-Eicosatrienoic Acid,11R(12S)-Epoxyeicosatrienoic Acid,11R(12S)-Epoxy-5(Z),8(Z),14(Z)-ETrE,FA 20:4;O

     11R(12S)-EET is an oxylipin and a metabolite of arachidonic acid . 11R(12S)-EET Chemical Structure
  73. GC40370 12(R)-HEPE

    12(R)-HEPE is a monohydroxy fatty acid synthesized from EPA by the eggs of the sea urchin, S.

     12(R)-HEPE Chemical Structure
  74. GC40447 12(R)-HETE

    12(R)-Hydroxyeicosatetraenoic Acid

     Biosynthesis of 12(R)-HETE in invertebrates is via lipoxygenation of arachidonic acid. 12(R)-HETE Chemical Structure
  75. GC40371 12(S)-HEPE 12(S)-HEPE is a monohydroxy fatty acid synthesized from EPA by the action of 12-LO. 12(S)-HEPE Chemical Structure
  76. GC40448 12(S)-HETE

    12(S)-Hydroxyeicosatetraenoic Acid

    12(S)-HETE is the predominant lipoxygenase product of mammalian platelets.

     12(S)-HETE Chemical Structure
  77. GC40449 12(S)-HETE MaxSpec® Standard 12(S)-HETE is the predominant lipoxygenase product of mammalian platelets. 12(S)-HETE MaxSpec® Standard Chemical Structure
  78. GC40349 12(S)-HETE-19,20-alkyne

    Click Tag 12(S)-HETE-19,20-alkyne, Click Tag 12(S)-Hydroxyeicosatetraenoic Acid-19,20-alkyne

     12(S)-HETE is the predominant lipoxygenase product of mammalian platelets. 12(S)-HETE-19,20-alkyne Chemical Structure
  79. GC41882 12(S)-HETrE 12(S)-HETrE is produced by 12-lipoxygenase oxidation of dihomo-γ-linolenic acid (DGLA). 12(S)-HETrE Chemical Structure
  80. GC41095 12(S)-HpEPE

    12(S)-HpEPE is a monohydroperoxy polyunsaturated fatty acid produced by the action of 12-lipoxygenase on eicosapentaenoic acid.

     12(S)-HpEPE Chemical Structure
  81. GC40372 12-OxoETE

    12KETE

     12-OxoETE is synthesized by human platelets and Aplysia nervous tissue after incubation with arachidonic acid. 12-OxoETE Chemical Structure
  82. GC40424 14,15-EE-5(Z)-E

    14,15Epoxyeicosa5(Z)enoic Acid

     Epoxyeicosatrienoic acids (EETs), such as 11(12)-EET and 14(15)-EET, are cytochrome P450 metabolites of arachidonic acid that have been identified as endothelium-derived hyperpolarizing factors with vasodilator activity. 14,15-EE-5(Z)-E Chemical Structure
  83. GC40425 14,15-EE-8(Z)-E

    14,15Epoxyeicosa8(Z)enoic Acid

     Epoxyeicosatrienoic acids (EETs), such as 11(12)-EET and 14(15)-EET, are cytochrome P450 metabolites of arachidonic acid that have been identified as endothelium-derived hyperpolarizing factors with vasodilator activity. 14,15-EE-8(Z)-E Chemical Structure
  84. GC91697 14R(15S)-EET

    14R(15S)-EpETrE,14R(15S)-epoxy-5(Z),8(Z),11(Z)-ETrE,14R(15S)-epoxy-all-cis-5,8,11-Eicosatrienoic Acid,14R(15S)-Epoxyeicosatrienoic Acid,FA 20:4;O

     14R(15S)-EET is an oxylipin and a metabolite of arachidonic acid . 14R(15S)-EET Chemical Structure
  85. GC46438 14S(15R)-EET

    14S,15R-EpETrE

     A cytochrome P450 metabolite of arachidonic acid 14S(15R)-EET Chemical Structure
  86. GC90350 14S(15R)-EET methyl ester

    Un métabolite de la cytochrome P450 de l'acide arachidonique.

     14S(15R)-EET methyl ester Chemical Structure
  87. GC40426 15(R)-HEDE

    15(R)-Hydroxyeicosatetraenoic Acid

     15(R)-HEDE is isolated by the chromatographic resolution of (±)15-HEDE. 15(R)-HEDE Chemical Structure
  88. GC40450 15(R)-HETE 15(R)-HETE is produced when aspirin-inhibited COX-2 is incubated with arachidonic acid. 15(R)-HETE Chemical Structure
  89. GC40373 15(S)-HEPE

    15S-hydroxy-Eicosapentaenoic Acid

     15(S)-HEPE is a monohydroxy fatty acid synthesized from EPA by the action of 15-LO. 15(S)-HEPE Chemical Structure
  90. GC40374 15(S)-HEPE MaxSpec® Standard 15(S)-HEPE is a monohydroxy fatty acid synthesized from EPA by the action of 15-LO. 15(S)-HEPE MaxSpec® Standard Chemical Structure
  91. GC46441 15(S)-HEPE-d5

    15S-Hydroxyeicosapentaenoic Acid-d5

     A neuropeptide with diverse biological activities 15(S)-HEPE-d5 Chemical Structure
  92. GC40451 15(S)-HETE

    15(S)-Hydroxyeicosatetraenoic Acid

     15(S)-HETE is a major arachidonic acid metabolite from the 15-lipoxygenase pathway. 15(S)-HETE Chemical Structure
  93. GC40452 15(S)-HETE MaxSpec® Standard 15(S)-HETE is a major arachidonic acid metabolite from the 15-lipoxygenase pathway. 15(S)-HETE MaxSpec® Standard Chemical Structure
  94. GC40839 15(S)-HETE methyl ester

    15(S)-Hydroxyeicosatetraenoic Acid methyl ester

     15(S)-HETE methyl ester is a synthetic derivative of 15(S)-HETE, a major arachidonic acid metabolite from the 15-lipoxygenase pathway. 15(S)-HETE methyl ester Chemical Structure
  95. GC41403 15(S)-HpEDE

    15(S)-HpEDE is a monohydroperoxy polyunsaturated fatty acid produced by the action of 15-lipoxygenase on eicosadienoic acid.

     15(S)-HpEDE Chemical Structure
  96. GC41101 15(S)-HpEPE

    15(S)-HpEPE is a monohydroperoxy polyunsaturated fatty acid produced by the action of 15-lipoxygenase on eicosapentaenoic acid.

     15(S)-HpEPE Chemical Structure
  97. GC41124 15(S)-HpETE

    15(S)-HpETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of 15-lipoxygenase (15-LO) on arachidonic acid.

     15(S)-HpETE Chemical Structure
  98. GC41940 15-OxoEDE

    15KEDE

     15-OxoEDE is produced by the oxidation of 15-HEDE. 15-OxoEDE Chemical Structure
  99. GC40376 15-OxoETE

    15KETE

     15-OxoETE is produced by oxidation of the 15-hydroxyl of 15-HETE. 15-OxoETE Chemical Structure
  100. GC49356 17(S)-HDoTE

    17(S)-HDTA, 17(S)-hydroxy Docosatetraenoic Acid

     A metabolite of adrenic acid 17(S)-HDoTE Chemical Structure
  101. GC40457 19(R)-HETE

    19(R)-Hydroxyeicosatetraenoic Acid

     19-HETE is one of the major cytochrome P450 (CYP450) metabolites of arachidonic acid that is released from the kidney in response to angiotensin II. 19(R)-HETE Chemical Structure

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