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Accueil >> Signaling Pathways >> Ox Stress Reagents >> Lipid Peroxidation

Lipid Peroxidation

Products for  Lipid Peroxidation

  1. Cat.No. Nom du produit Informations
  2. GC45601 α-Linolenic Acid ethyl ester-d5

    ALAEE-d5, Ethyl α-Linolenate-d5, Ethyl Linolenate-d5, LAEE-d5, Linolenic Acid ethyl ester-d5

       α-Linolenic Acid ethyl ester-d5 Chemical Structure
  3. GC41502 β-Myrcene

    NSC 406264

     β-Myrcène (β-β-Myrcène), un composé volatil aromatique, supprime l'activité NF-κB induite par le TNFα. β-Myrcene Chemical Structure
  4. GC41262 (±)-α-CMBHC Vitamin E is a well known antioxidant that exists in eight natural forms: four tocopherols (α, β, δ, and γ) and four tocotrienols (α, β, δ, and γ). (±)-α-CMBHC Chemical Structure
  5. GC41617 (±)-α-Tocopherol

    all-rac-α-Tocopherol, DL-α-Tocopherol

     (±)-α-Le tocophérol est une vitamine E synthétique, À effet antioxydant. (±)-α-Tocopherol Chemical Structure
  6. GC41213 (±)10-HDHA

    10hydroxy Docosahexaenoic Acid, (±)10HDoHE

    (±)10-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro.

     (±)10-HDHA Chemical Structure
  7. GC41214 (±)11-HDHA

    11hydroxy Docosahexaenoic Acid, (±)11-HDoHE

     (±)11-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)11-HDHA Chemical Structure
  8. 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
  9. 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
  10. GC40359 (±)12-HEPE

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

     (±)12-HEPE Chemical Structure
  11. 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
  12. GC48738 (±)12-HETE-d8

    (±)12-Hydroxyeicosatetraenoic Acid-d8

     (±)12-HETE-d8 Chemical Structure
  13. GC41192 (±)13-HDHA

    13hydroxy Docosahexaenoic Acid, (±)13-HDoHE

     (±)13-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)13-HDHA Chemical Structure
  14. GC41649 (±)13-HODE cholesteryl ester (±)13-HODE cholesteryl ester was originally extracted from atherosclerotic lesions and shown to be produced by Cu2+-catalyzed oxidation of LDL. (±)13-HODE cholesteryl ester Chemical Structure
  15. GC40355 (±)13-HpODE

    13-Hydroperoxylinoleic acid; Linoleic acid 13-hydroperoxide

     (±)13-HpODE (acide 13-hydroperoxylinoléique) est un mélange racémique d'hydroperoxydes, qui est produit par l'oxydation de l'acide linoléique par la lipoxygénase. (±)13-HpODE Chemical Structure
  16. GC41193 (±)14-HDHA

    14hydroxy Docosahexaenoic Acid, (±)14-HDoHE

     (±)14-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)14-HDHA Chemical Structure
  17. GC40420 (±)15-HEDE (±)15-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)15-HEDE Chemical Structure
  18. GC40361 (±)15-HEPE

    (±)15-hydroxy Eicosapentaenoic Acid

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

     (±)15-HEPE Chemical Structure
  19. 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
  20. GC48739 (±)15-HETE-d8

    (±)15-Hydroxyeicosatetraenoic Acid-d8

     (±)15-HETE-d8 Chemical Structure
  21. GC41196 (±)16-HDHA

    16hydroxy Docosahexaenoic Acid, (±)16-HDoHE

     (±)16-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)16-HDHA Chemical Structure
  22. GC41197 (±)17-HDHA

    17-hydroxy Docosahexaenoic Acid, 17-hydroxy DHA, (±)17-HDoHE

     (±)17-HDHA is an autoxidation product of docosahexaenoic acid in vitro. (±)17-HDHA Chemical Structure
  23. GC41198 (±)17-HDHA MaxSpec® Standard

    17-hydroxy Docosahexaenoic Acid, 17-hydroxy DHA, (±)17-HDoHE

     (±)17-HDHA is an autoxidation product of docosahexaenoic acid in vitro. (±)17-HDHA MaxSpec® Standard Chemical Structure
  24. GC40362 (±)18-HEPE (±)18-HEPE is produced by non-enzymatic oxidation of EPA. (±)18-HEPE Chemical Structure
  25. GC41202 (±)4-HDHA

    4hydroxy Docosahexaenoic Acid, (±)4HDoHE

     (±)4-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)4-HDHA Chemical Structure
  26. GC40364 (±)5-HEPE (±)5-HEPE is produced by non-enzymatic oxidation of EPA. (±)5-HEPE Chemical Structure
  27. 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
  28. GC40828 (±)5-HETE lactone

    (±)5-Hydroxyeicosatetraenoic Acid lactone

     (±)5-HETE lactone is a cyclic ester formed by acid-catalyzed nucleophilic addition of the C-5 hydroxyl to the C-1 carboxyl of (±)5-HETE. (±)5-HETE lactone Chemical Structure
  29. 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
  30. GC40576 (±)5-iPF2α-VI

    iPF2αI, Isoprostane F2α-I, 5-iso PGF2α-VI, 5-iso Prostaglandin F2α-VI

     Isoprostanes are prostaglandin (PG)-like products of free-radical induced lipid peroxidation. (±)5-iPF2α-VI Chemical Structure
  31. GC46263 (±)5-iPF2α-VI-d11 An internal standard for the quantification of (±)5iPF2αVI (±)5-iPF2α-VI-d11 Chemical Structure
  32. GC41204 (±)7-HDHA

    7hydroxy Docosahexaenoic Acid, (±)7HDoHE

    (±)7-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro.

     (±)7-HDHA Chemical Structure
  33. GC41205 (±)8-HDHA

    8hydroxy Docosahexaenoic Acid, (±)8HDoHE

     (±)8-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)8-HDHA Chemical Structure
  34. GC40366 (±)8-HEPE

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

     (±)8-HEPE Chemical Structure
  35. GC40367 (±)9-HEPE (±)9-HEPE is produced by non-enzymatic oxidation of EPA. (±)9-HEPE Chemical Structure
  36. 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
  37. GC40541 (±)9-HODE

    (±)9-HODE is one of the two racemic monohydroxy fatty acids resulting from the non-enzymatic oxidation of linoleic acid.

     (±)9-HODE Chemical Structure
  38. GC40356 (±)9-HpODE (±)9-HpODE est un hydroperoxyde lipidique à longue chaîne, est un produit de la peroxydation de l'acide linoléique. (±)9-HpODE Chemical Structure
  39. GC40218 (-)-Epigallocatechin Gallate-d3/d4

    EGCG-d3/d4

     (-)-Epigallocatechin gallate-d3/d4 is intended for use as an internal standard for the quantification of (-)-epigallocatechin gallate by GC- or LC-MS. (-)-Epigallocatechin Gallate-d3/d4 Chemical Structure
  40. GC45248 (-)-FINO2 (-)-FINO2 est un peroxyde organique qui peut induire sélectivement la ferroptose et qui est utilisé pour étudier les mécanismes de la ferroptose et les traitements anticancéreux. (-)-FINO2 Chemical Structure
  41. GC49690 (3R,5R)-Rosuvastatin (calcium salt) A potential impurity found in bulk preparations of rosuvastatin (3R,5R)-Rosuvastatin (calcium salt) Chemical Structure
  42. GC26181 (±)-Catechin

    rel-Cianidanol; rel-Catechuic acid

    (±) - Catechin (rel Xianidanol) is the racemate of Catechin.

     (±)-Catechin Chemical Structure
  43. GC19824 (±)-Pinocembrin

    (+)-Pinocembrin, Dihydrochrysin, NSC 279005

     La (±)-pinocembrine ((±)-5,7-dihydroxyflavanone) est un ligand du GPR120 capable de favoriser la cicatrisation des plaies dans la lignée cellulaire HaCaT. (±)-Pinocembrin Chemical Structure
  44. GC19461 (±)13-HODE (±)13-HODE (13-acide hydroxyoctadécadiénoïque) est un mélange racémique de 13(S)-HODE et 13(R)-HODE, ce qui est formé par l'oxydation de l'acide linoléique par des lipoxygénases ou des cyclooxygénases. (±)13-HODE Chemical Structure
  45. GC49034 1(R)-(Trifluoromethyl)oleyl alcohol An oleic acid analog 1(R)-(Trifluoromethyl)oleyl alcohol Chemical Structure
  46. GC41837 1,3,7-Trimethyluric Acid

    8-oxo Caffeine, NSC 11259

     L'acide 1,3,7-triméthylurique est le métabolite de la caféine. Le rapport métabolique de l'acide 1,3,7-triméthylurique À la caféine peut être évalué en tant que biomarqueur pour décrire la variabilité de l'activité du CYP3A dans une cohorte. 1,3,7-Trimethyluric Acid Chemical Structure
  47. GC46387 1,3,7-Trimethyluric Acid-d9

    TMU-d9, 8-oxo Caffeine-d9

     An internal standard for the quantification of 1,3,7-trimethyluric acid 1,3,7-Trimethyluric Acid-d9 Chemical Structure
  48. GC48782 10,13-epoxy-11-methyl-Octadecadienoic Acid

    F2 Furan Fatty Acid, 3-methyl-5-pentyl-2-Furannonanoic Acid, 9M5

     A furan fatty acid 10,13-epoxy-11-methyl-Octadecadienoic Acid Chemical Structure
  49. GC41893 13(R)-HODE cholesteryl ester 13(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. 13(R)-HODE cholesteryl ester Chemical Structure
  50. GC46442 15(S)-HETE-d8

    15(S)-Hydroxyeicosatetraenoic Acid-d8

     An internal standard for the quantification of 15-HETE 15(S)-HETE-d8 Chemical Structure
  51. GC90081 2,3-dinor-8-iso Prostaglandin F1α

    Un métabolite actif de l'acide arachidonique et 8-iso PGF2α.

     2,3-dinor-8-iso Prostaglandin F1α Chemical Structure
  52. GC40416 2,3-dinor-8-iso Prostaglandin F2α

    2,3-dinor-iPF2α-III, 2,3-dinor-8-iso PGF2α

     8-iso Prostaglandin F2α (8-iso PGF2α; 8-isoprostane) is a prostaglandin-like product of non-specific lipid peroxidation. 2,3-dinor-8-iso Prostaglandin F2α Chemical Structure
  53. GC40503 2-HOBA

    2-(Aminomethyl)phenol, 2-Hydroxybenzylamine, NSC 127870

     Le 2-HOBA (2-HOBA), un piégeur sélectif de dicarbonyle, est un antioxydant et un piégeur de radicaux libres et d'isolevuglandines (IsoLG). 2-HOBA Chemical Structure
  54. GC49172 2-hydroxy Estrone

    Catecholestrone, 2-hydroxy E1, 2-OHE1

     La 2-hydroxyestrone (catécholestrone) est un agent anti-œstrogénique médié par des récepteurs spécifiques. 2-hydroxy Estrone Chemical Structure
  55. GC49840 2-Methylbutyrylglycine

    2-MBG, N-sec-Valerylglycine

     A metabolite of isoleucine 2-Methylbutyrylglycine Chemical Structure
  56. GC42195 2-Thiobarbituric Acid

    4,6-dihydroxy-2-mercaptopyrimidine, TBA, Thiobarbituric acid

     2-Thiobarbituric acid is a colorimetric reagent commonly used in the detection of malondialdehyde (MDA), a marker of lipid peroxidation. 2-Thiobarbituric Acid Chemical Structure
  57. GC41210 22-HDHA

    22-hydroxy Docosahexaenoic Acid, 22-OH DHA

     22-HDHA is an oxidation product of docosahexaenoic acid. 22-HDHA Chemical Structure
  58. GC18205 3,5-Diiodothyroacetic Acid

    Diac, NSC 90463, T2A, TA2

     3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. 3,5-Diiodothyroacetic Acid Chemical Structure
  59. GC49364 3-Hydroxycoumarin

    3-Coumarinol, NSC 74691

     La 3-hydroxycoumarine est un inhibiteur puissant et redox de la 15-LOX-1 humaine. 3-Hydroxycoumarin Chemical Structure
  60. GC42400 4-hydroperoxy 2-Nonenal

    4HpNE

     4-hydroxy Nonenal is a lipid peroxidation product derived from oxidized ω-6 polyunsaturated fatty acids, such as linoleic acid and arachidonic acid, that is widely used as a marker of oxidative stress. 4-hydroperoxy 2-Nonenal Chemical Structure
  61. GC40778 4-hydroxy Hexenal

    4-HHE

    4-hydroxy Hexenal is a lipid peroxidation product derived from oxidized ω-3 fatty acids such as DHA.

     4-hydroxy Hexenal Chemical Structure
  62. GC46656 4-hydroxy Hexenal-d3

    4-HHE-d3

     An internal standard for the quantification of 4-hydroxy hexenal 4-hydroxy Hexenal-d3 Chemical Structure
  63. GC42411 4-hydroxy Nonenal Alkyne

    Click Tag 4HNE Alkyne

    4-hydroxy Nonenal (4-HNE) is a major aldehyde produced during the lipid peroxidation of ω-6 polyunsaturated fatty acids, such as arachidonic acid and linoleic acid.

     4-hydroxy Nonenal Alkyne Chemical Structure
  64. GC42412 4-hydroxy Nonenal Glutathione (trifluoroacetate salt)

    4HNEGSH

     4-hydroxy Nonenal Glutathione (HNE-GSH) is a major adduct formed by the reaction of 4-HNE with GSH. 4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Chemical Structure
  65. GC92022 4-hydroxy Nonenal Glutathione-d3

    4-HNE-GSH-d3

     4-hydroxy Nonenal Glutathione-d3 (4 - Hne - GSh - D3) est destiné à être utilisé comme étalon interne pour la quantification du 4 - Hne - glutathion par GC ou LC - MS. 4-hydroxy Nonenal Glutathione-d3 Chemical Structure
  66. GC46659 4-hydroxy Nonenal Glutathione-d3 (trifluoroacetate salt)

    4HNEGSHd3

     A neuropeptide with diverse biological activities 4-hydroxy Nonenal Glutathione-d3 (trifluoroacetate salt) Chemical Structure
  67. GC42413 4-hydroxy Nonenal Mercapturic Acid Peroxidation of common ω-6 polyunsaturated fatty acids (PUFAs) such as linoleic acid, DGLA, and arachidonic acid can give rise to 4-HNE. 4-hydroxy Nonenal Mercapturic Acid Chemical Structure
  68. GC46660 4-hydroxy Nonenal Mercapturic Acid-d3 A neuropeptide with diverse biological activities 4-hydroxy Nonenal Mercapturic Acid-d3 Chemical Structure
  69. GC42464 4-oxo-2-Nonenal

    4-ONE

    4-hydroxy Nonenal is a lipid peroxidation product derived from oxidized ω-6 polyunsaturated fatty acids such as arachidonic acid and linoleic acid.

     4-oxo-2-Nonenal Chemical Structure
  70. GC40498 4-oxo-2-Nonenal Alkyne

    4-ONE Alkyne, Alkynyl 4-oxo-2-Nonenal, Click Tag 4-oxo-2-Nonenal Alkyne

     4-oxo-2-Nonenal is a product of lipid peroxidation that actively modifies histidine and lysine residues on proteins and causes protein cross-linking. 4-oxo-2-Nonenal Alkyne Chemical Structure
  71. GC46674 4-oxo-2-Nonenal-d3

    4ONEd3

     An internal standard for the quantification of 4oxo-2nonenal 4-oxo-2-Nonenal-d3 Chemical Structure
  72. GC40053 5α,6α-epoxy Cholestanol

    NSC 18176

     5α,6α-epoxy Cholestanol est un dérivé du cholestérol qui peut être généré par voie de catalyse par le système d'enzyme cytochrome P450 dans les mitochondries ou peut être induit lors de la peroxydation des lipides. 5α,6α-epoxy Cholestanol peut réguler la biosynthèse des acides biliaires et induire la différenciation et la mort des cellules tumorales. 5α,6α-epoxy Cholestanol Chemical Structure
  73. GC40693 5α-hydroxy-6-keto Cholesterol

    6Oxo3,5diol, Cholestane6oxo3β,5αdiol

     5α-hydroxy-6-céto Le cholestérol est le principal métabolite de β-époxyde (5α,6β-époxycholestérol) lors de l'exposition directe À l'ozone de cellules épithéliales bronchiques humaines intactes cultivées (16-HBE). 5α-hydroxy-6-keto Cholesterol Chemical Structure
  74. GC40418 5β,6β-epoxy Cholestanol

    NSC 148940

    5β,6β-epoxy Cholestanol is an oxidative metabolite of cholesterol that is formed via radical and non-radical oxidation of cholesterol at the 5,6-double bond.

     5β,6β-epoxy Cholestanol Chemical Structure
  75. GC20095 5,7-Dihydroxy-4-methylcoumarin

    NSC 5302

    5,7-Dihydroxy-4-methylcoumarin is a coumarin derivative from Mexican tarragon. 5,7-Dihydroxy-4-methylcoumarin possesses antifungal and antibacterial activities.

     5,7-Dihydroxy-4-methylcoumarin Chemical Structure
  76. GC90889 5-(3'-Hydroxyphenyl)-γ-Valerolactone

    Un métabolite de divers polyphénols.

     5-(3'-Hydroxyphenyl)-γ-Valerolactone Chemical Structure
  77. GC52413 5-Aminosalicylic Acid-d7

    5-ASA-d7, Mesalamine-d7, Mesalazine-d7

     An internal standard for the quantification of 5-aminosalicylic acid 5-Aminosalicylic Acid-d7 Chemical Structure
  78. GC42563 5-methyl-2-HOBA (hydrochloride)

    5-Me-2-HOBA, 5-methyl-2Hydroxybenzylamine

     5-methyl-2-HOBA is an isoketal scavenger. 5-methyl-2-HOBA (hydrochloride) Chemical Structure
  79. GC45772 6(5H)-Phenanthridinone

    NSC 11021, NSC 40943, NSC 61083

     An inhibitor of PARP1 and 2 6(5H)-Phenanthridinone Chemical Structure
  80. GC40572 7-keto Cholesterol

    SC-4722

     7-keto Cholesterol est un oxy-stérol majeur qui est associé aux maladies vasculaires. C'est largement présent dans les plaques athéroscléreuses et possède un effet athérogène plus puissant que le cholestérol. 7-keto Cholesterol Chemical Structure
  81. GC46241 7-keto Cholesterol-d7

    7-oxo Cholesterol-d7

    7-keto Cholesterol is a bioactive sterol and a major oxysterol component of oxidized LDL

     7-keto Cholesterol-d7 Chemical Structure
  82. GC40587 8,12-iso-iPF2α-VI

    8,12-iso-Isoprostane-F2α-VI, 12-iso-5,6E,14Z-PGF2α, 12iso5,6E,14ZProstaglandin F2α

     8,12-iso-iPF2α-VI is an isoprostane produced by non-enzymatic, free radical-induced peroxidative damage to membrane lipids. 8,12-iso-iPF2α-VI Chemical Structure
  83. GC41137 8,12-iso-iPF2α-VI-1,5-lactone F2 isoprostanes (F2-iPs) are thought to arise from the free radical-mediated peroxidation of phospholipid-bound arachidonic acid. 8,12-iso-iPF2α-VI-1,5-lactone Chemical Structure
  84. GC46743 8,12-iso-iPF2α-VI-d11

    8,12-iso-Isoprostane-F2α-VI-d11, 12-iso-5,6E,14Z-PGF2α-d11, 12-iso-5,6E,14Z-Prostaglandin F2α-d11

     A neuropeptide with diverse biological activities 8,12-iso-iPF2α-VI-d11 Chemical Structure
  85. GC41138 8-iso Prostaglandin A1

    8-epi PGA1, 8-iso PGA1

     8-iso Prostaglandin A1 (8-iso PGA1) is an isoprostane and a member in a large family of prostanoids of non-cyclooxygenase origin. 8-iso Prostaglandin A1 Chemical Structure
  86. GC18781 8-iso Prostaglandin A2

    A2 Isoprostane, 15-A2t-IsoP, 15-A2t-Isoprostane, 8-epi PGA2, 8-iso PGA2

     Isoprostanes are prostaglandin (PG)-like compounds produced in vivo by free radical-catalyzed peroxidation of arachidonoyl-containing lipids. 8-iso Prostaglandin A2 Chemical Structure
  87. GC42628 8-iso Prostaglandin A2-biotin

    8iso PGA2biotin

     Isoprostanes are prostaglandin (PG)-like compounds produced in vivo by free radical-catalyzed peroxidation of arachidonoyl-containing lipids. 8-iso Prostaglandin A2-biotin Chemical Structure
  88. GC18737 8-iso Prostaglandin E1

    8epi PGE1, 8iso PGE1, Ovinonic acid

     Isoprostanes are a family of prostanoid molecules of non-cyclooxygenase origin. 8-iso Prostaglandin E1 Chemical Structure
  89. GC41425 8-iso Prostaglandin E2

    8iso PGE2, 8epi PGE2

     La 8-iso prostaglandine E2 (iPE2-III) fait partie de la classe des isoprostanes des prostanoïdes. 8-iso Prostaglandin E2 Chemical Structure
  90. GC42629 8-iso Prostaglandin E2 isopropyl ester

    8iso PGE2 isopropyl ester

     8-iso PGE2 isopropyl ester is a more lipophilic form of the free acid, 8-iso PGE2. 8-iso Prostaglandin E2 isopropyl ester Chemical Structure
  91. GC41437 8-iso Prostaglandin F1α

    8epi PGF1α

     8-iso PGF1α is an isoprostane that was first identified in human semen. 8-iso Prostaglandin F1α Chemical Structure
  92. GC46746 8-iso Prostaglandin F1α-d9

    8epi PGF1αd9

     A neuropeptide with diverse biological activities 8-iso Prostaglandin F1α-d9 Chemical Structure
  93. GC41438 8-iso Prostaglandin F1β

    8epi9βPGF1α, 8iso PGF1β

     8-iso PGF1β is a potential autoxidation product of DGLA. 8-iso Prostaglandin F1β Chemical Structure
  94. GC41405 8-iso Prostaglandin F2α Ethanolamide

    iPF2αIII Ethanolamide, 8Isoprostane Ethanolamide, 8iso PGF2α Ethanolamide, 8epi PGF2α Ethanolamide

     It has been reported that anandamide (AEA) can be used directly by cyclooxygenase-2 and specific prostaglandin H2 (PGH2) isomerases to produce ethanolamide congeners of the classical PGs, including PGF2α. 8-iso Prostaglandin F2α Ethanolamide Chemical Structure
  95. GC46747 8-iso Prostaglandin F2α-d4

    iPF2αIIId4, 8Isoprostaned4, 15F2tIsoprostaned4, 8epi PGF2αd4

     An internal standard for the quantification of 8iso prostaglandin F2α 8-iso Prostaglandin F2α-d4 Chemical Structure
  96. GC90100 8-iso Prostaglandin F2β

    Un isomère de PGF2α produit par la peroxydation radicalaire libre de l'acide arachidonique.

     8-iso Prostaglandin F2β Chemical Structure
  97. GC18829 8-iso Prostaglandin F3α

    8-epi PGF3α

    8-iso PGF3α is an isoprostane produced from the free-radical peroxidation of EPA.

     8-iso Prostaglandin F3α Chemical Structure
  98. GC40588 8-iso-13,14-dihydro-15-keto Prostaglandin F2α

    8iso13,14dihydro15keto PGF2α

     8-iso-13,14-dihydro-15-keto Prostaglandin F2α (8-iso-13,14-dihydro-15-keto PGF2α) is a metabolite of the isoprostane, 8-isoprostane (8-iso PGF2α), in rabbits, monkeys and humans. 8-iso-13,14-dihydro-15-keto Prostaglandin F2α Chemical Structure
  99. GC40589 8-iso-15(R)-Prostaglandin F2α

    8iso15epi PGF2α

    8-iso-15(R) PGF2α is one member of a large family of prostaglandin-like eicosanoids formed by the free radical peroxidation of arachidonic acid in membrane phospholipids.

     8-iso-15(R)-Prostaglandin F2α Chemical Structure
  100. GC41426 8-iso-15-keto Prostaglandin F2α

    8epi15keto PGF2α, 8iso15keto PGF2α

     8-iso-15-keto Prostaglandin F2α (8-iso-15-keto PGF2α) is a metabolite of the isoprostane 8-iso PGF2α in rabbits, monkeys, and humans. 8-iso-15-keto Prostaglandin F2α Chemical Structure
  101. GC41427 8-iso-15-keto Prostaglandin F2β

    8epi15keto PGF2α, 8iso15keto PGF2α

     8-iso Prostaglandin F2β (8-iso PGF2β) is an isomer of PGF2α of non-enzymatic origin. 8-iso-15-keto Prostaglandin F2β Chemical Structure

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