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

Lipid Peroxidation

Products for  Lipid Peroxidation

  1. Cat.No. Product Name Information
  2. GC45601 α-Linolenic Acid ethyl ester-d5   α-Linolenic Acid ethyl ester-d5 Chemical Structure
  3. GC41502 β-Myrcene β-Myrcene is a terpene that has been found in Cannabis and has antioxidative properties. β-Myrcene Chemical Structure
  4. GC41213 (±)10-HDHA

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

     (±)10-HDHA Chemical Structure
  5. GC41214 (±)11-HDHA (±)11-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)11-HDHA Chemical Structure
  6. GC40428 (±)11-HEDE (±)11-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)11-HEDE Chemical Structure
  7. GC40467 (±)11-HETE (±)11-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)11-HETE Chemical Structure
  8. GC40359 (±)12-HEPE

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

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

    (±)12-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid.

     (±)12-HETE Chemical Structure
  10. GC41192 (±)13-HDHA (±)13-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)13-HDHA Chemical Structure
  11. 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
  12. GC40355 (±)13-HpODE

    (±)13-HpODE is a racemic mixture of hydroperoxides derived non-enzymatically from linoleic acid through the action of reactive oxygen species.

     (±)13-HpODE Chemical Structure
  13. GC41193 (±)14-HDHA (±)14-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)14-HDHA Chemical Structure
  14. GC40420 (±)15-HEDE (±)15-HEDE is produced by non-enzymatic oxidation of 11,14-eicosadienoic acid. (±)15-HEDE Chemical Structure
  15. GC40361 (±)15-HEPE

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

     (±)15-HEPE Chemical Structure
  16. GC41196 (±)16-HDHA (±)16-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)16-HDHA Chemical Structure
  17. GC41197 (±)17-HDHA (±)17-HDHA is an autoxidation product of docosahexaenoic acid in vitro. (±)17-HDHA Chemical Structure
  18. GC40362 (±)18-HEPE (±)18-HEPE is produced by non-enzymatic oxidation of EPA. (±)18-HEPE Chemical Structure
  19. GC41202 (±)4-HDHA (±)4-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)4-HDHA Chemical Structure
  20. GC40364 (±)5-HEPE (±)5-HEPE is produced by non-enzymatic oxidation of EPA. (±)5-HEPE Chemical Structure
  21. GC40439 (±)5-HETE

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

     (±)5-HETE Chemical Structure
  22. GC40828 (±)5-HETE 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
  23. GC40837 (±)5-HETE 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
  24. GC40576 (±)5-iPF2α-VI Isoprostanes are prostaglandin (PG)-like products of free-radical induced lipid peroxidation. (±)5-iPF2α-VI Chemical Structure
  25. GC46263 (±)5-iPF2α-VI-d11 An internal standard for the quantification of (±)5iPF2αVI (±)5-iPF2α-VI-d11 Chemical Structure
  26. GC41204 (±)7-HDHA

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

     (±)7-HDHA Chemical Structure
  27. GC41205 (±)8-HDHA (±)8-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)8-HDHA Chemical Structure
  28. GC40366 (±)8-HEPE

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

     (±)8-HEPE Chemical Structure
  29. GC40367 (±)9-HEPE (±)9-HEPE is produced by non-enzymatic oxidation of EPA. (±)9-HEPE Chemical Structure
  30. GC40443 (±)9-HETE (±)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. (±)9-HETE Chemical Structure
  31. 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
  32. GC40356 (±)9-HpODE (±)9-HpODE is a racemic mixture of the fatty acid hydroperoxide product (9(S)-HpODE) formed from lipoxygenase action on linoleic acid. (±)9-HpODE Chemical Structure
  33. GC45248 (-)-FINO2 (-)-FINO2 is a ferroptosis-inducing peroxide compound that indirectly inhibits glutathione peroxidase 4 (GPX4) and oxidizes iron. (-)-FINO2 Chemical Structure
  34. GC49690 (3R,5R)-Rosuvastatin (calcium salt) A potential impurity found in bulk preparations of rosuvastatin (3R,5R)-Rosuvastatin (calcium salt) Chemical Structure
  35. GC19461 (±)13-HODE

    (±)13-HODE is one of the two racemic monohydroxy fatty acids resulting from the non-enzymatic oxidation of linoleic acid.

     (±)13-HODE Chemical Structure
  36. GC49034 1(R)-(Trifluoromethyl)oleyl alcohol An oleic acid analog 1(R)-(Trifluoromethyl)oleyl alcohol Chemical Structure
  37. GC41837 1,3,7-Trimethyluric Acid

    1,3,7-Trimethyluric acid is a methyl derivative of uric acid and a product of C-8 oxidation of caffeine by cytochrome P450 enzymes.

     1,3,7-Trimethyluric Acid Chemical Structure
  38. GC46387 1,3,7-Trimethyluric Acid-d9 An internal standard for the quantification of 1,3,7-trimethyluric acid 1,3,7-Trimethyluric Acid-d9 Chemical Structure
  39. GC48782 10,13-epoxy-11-methyl-Octadecadienoic Acid A furan fatty acid 10,13-epoxy-11-methyl-Octadecadienoic Acid Chemical Structure
  40. GC41893 13(R)-HODE cholesteryl ester 13(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. 13(R)-HODE cholesteryl ester Chemical Structure
  41. GC46442 15(S)-HETE-d8 An internal standard for the quantification of 15-HETE 15(S)-HETE-d8 Chemical Structure
  42. GC40416 2,3-dinor-8-iso Prostaglandin F2α 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
  43. GC40503 2-HOBA 2-HOBA (2-HOBA) a selective dicarbonyl scavenger, is an antioxidant and scavanger of free radicals and isolevuglandins (IsoLGs). 2-HOBA Chemical Structure
  44. GC49172 2-hydroxy Estrone An active metabolite of estrone 2-hydroxy Estrone Chemical Structure
  45. GC49840 2-Methylbutyrylglycine A metabolite of isoleucine 2-Methylbutyrylglycine Chemical Structure
  46. GC42195 2-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
  47. GC41210 22-HDHA 22-HDHA is an oxidation product of docosahexaenoic acid. 22-HDHA Chemical Structure
  48. GC18205 3,5-Diiodothyroacetic Acid 3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. 3,5-Diiodothyroacetic Acid Chemical Structure
  49. GC49364 3-Hydroxycoumarin A coumarin with diverse biological activities 3-Hydroxycoumarin Chemical Structure
  50. GC42400 4-hydroperoxy 2-Nonenal 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
  51. GC40778 4-hydroxy Hexenal

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

     4-hydroxy Hexenal Chemical Structure
  52. GC46656 4-hydroxy Hexenal-d3 An internal standard for the quantification of 4-hydroxy hexenal 4-hydroxy Hexenal-d3 Chemical Structure
  53. GC42411 4-hydroxy Nonenal 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
  54. 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
  55. GC42464 4-oxo-2-Nonenal

    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
  56. GC40498 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
  57. GC46674 4-oxo-2-Nonenal-d3 An internal standard for the quantification of 4oxo-2nonenal 4-oxo-2-Nonenal-d3 Chemical Structure
  58. GC40053 5α,6α-epoxy Cholestanol An oxysterol and a metabolite of cholesterol produced by oxidation 5α,6α-epoxy Cholestanol Chemical Structure
  59. GC40693 5α-hydroxy-6-keto Cholesterol Cholesterol is the most abundant neutral lipid present in the surfactant of the lung epithelial lining fluid. 5α-hydroxy-6-keto Cholesterol Chemical Structure
  60. GC52413 5-Aminosalicylic Acid-d7 An internal standard for the quantification of 5-aminosalicylic acid 5-Aminosalicylic Acid-d7 Chemical Structure
  61. GC42563 5-methyl-2-HOBA (hydrochloride) 5-methyl-2-HOBA is an isoketal scavenger. 5-methyl-2-HOBA (hydrochloride) Chemical Structure
  62. GC45772 6(5H)-Phenanthridinone An inhibitor of PARP1 and 2 6(5H)-Phenanthridinone Chemical Structure
  63. GC40572 7-keto Cholesterol A bioactive sterol and a major oxysterol component of oxidized LDL 7-keto Cholesterol Chemical Structure
  64. GC46241 7-keto Cholesterol-d7

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

     7-keto Cholesterol-d7 Chemical Structure
  65. GC40587 8,12-iso-iPF2α-VI 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
  66. GC41138 8-iso Prostaglandin A1 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
  67. GC18781 8-iso Prostaglandin A2 Isoprostanes are prostaglandin (PG)-like compounds produced in vivo by free radical-catalyzed peroxidation of arachidonoyl-containing lipids. 8-iso Prostaglandin A2 Chemical Structure
  68. GC18737 8-iso Prostaglandin E1 Isoprostanes are a family of prostanoid molecules of non-cyclooxygenase origin. 8-iso Prostaglandin E1 Chemical Structure
  69. GC41425 8-iso Prostaglandin E2 8-iso PGE2 is one of several isoprostanes produced from arachidonic acid during lipid peroxidation. 8-iso Prostaglandin E2 Chemical Structure
  70. GC42629 8-iso Prostaglandin E2 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
  71. GC41437 8-iso Prostaglandin F1α 8-iso PGF1α is an isoprostane that was first identified in human semen. 8-iso Prostaglandin F1α Chemical Structure
  72. GC41438 8-iso Prostaglandin F1β 8-iso PGF1β is a potential autoxidation product of DGLA. 8-iso Prostaglandin F1β Chemical Structure
  73. GC46747 8-iso Prostaglandin F2α-d4 An internal standard for the quantification of 8iso prostaglandin F2α 8-iso Prostaglandin F2α-d4 Chemical Structure
  74. GC18829 8-iso Prostaglandin F3α

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

     8-iso Prostaglandin F3α Chemical Structure
  75. GC40588 8-iso-13,14-dihydro-15-keto Prostaglandin F2α 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
  76. GC41426 8-iso-15-keto Prostaglandin F2α 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
  77. GC41427 8-iso-15-keto Prostaglandin F2β 8-iso Prostaglandin F2β (8-iso PGF2β) is an isomer of PGF2α of non-enzymatic origin. 8-iso-15-keto Prostaglandin F2β Chemical Structure
  78. GC40332 8-iso-16-cyclohexyl-tetranor Prostaglandin E2 8-iso Prostaglandin E2 (8-iso PGE2) is one of several isoprostanes produced from polyunsaturated fatty acids during lipid peroxidation. 8-iso-16-cyclohexyl-tetranor Prostaglandin E2 Chemical Structure
  79. GC42634 9(R)-HODE cholesteryl ester 9(R)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. 9(R)-HODE cholesteryl ester Chemical Structure
  80. GC42635 9(S)-HODE cholesteryl ester 9(S)-HODE cholesteryl ester was originally extracted from atherosclerotic lesions. 9(S)-HODE cholesteryl ester Chemical Structure
  81. GC45960 9c(i472) 9c(i472) is a potent inhibitor of 15-LOX-1 (15-lipoxygenase-1) with an IC50 value of 0.19 μM. 9c(i472) Chemical Structure
  82. GC42658 A1-Phytoprostane-I A1-Phytoprostane-I is a cyclopentenone isoprostane produced by the action of reactive oxygen species on α-linolenic acid in plants. A1-Phytoprostane-I Chemical Structure
  83. GC19496 AAPH

    AAPH is a water-soluble azo compound

     AAPH Chemical Structure
  84. GC46821 Ajoene A disulfide with diverse biological activities Ajoene Chemical Structure
  85. GC49336 AMK (hydrochloride) An active metabolite of melatonin AMK (hydrochloride) Chemical Structure
  86. GC49419 Aniline-d5 An internal standard for the quantification of aniline Aniline-d5 Chemical Structure
  87. GC52332 Arimoclomol A co-inducer of heat shock proteins Arimoclomol Chemical Structure
  88. GC49103 Aromadendrene A sesquiterpene with diverse biological activities Aromadendrene Chemical Structure
  89. GC42890 Azelaoyl PAF Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPARγ. Azelaoyl PAF Chemical Structure
  90. GC52317 BCP-T.A. A ferroptosis inducer BCP-T.A. Chemical Structure
  91. GC42994 Butanoyl PAF Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes and activate polymorphonuclear leukocytes. Butanoyl PAF Chemical Structure
  92. GC49415 Capsorubin A carotenoid with diverse biological activities Capsorubin Chemical Structure
  93. GC52081 Chamazulene

    Chamazulene is a terpene that has been found in chamomile (M. recutita) flowers and has anti-inflammatory and antioxidant activities.

     Chamazulene Chemical Structure
  94. GC52278 Creatine Phosphate (sodium salt hydrate) A phosphorylated form of creatine Creatine Phosphate (sodium salt hydrate) Chemical Structure
  95. GC43329 Cu-ATSM The metallo-protein Cu/Zn-superoxide dismutase (SOD1) is a ubiquitous enzyme responsible for scavenging superoxide radicals. Cu-ATSM Chemical Structure
  96. GC49868 D-α-Tocopheryl Quinone An oxidative metabolite of vitamin E D-α-Tocopheryl Quinone Chemical Structure
  97. GC43504 D-myo-Inositol-1,2,3,4,5,6-hexaphosphate (sodium salt) Phytic acid (Inositol hexaphosphate) hexasodium is a phosphorus storage compound of seeds and cereal grains. D-myo-Inositol-1,2,3,4,5,6-hexaphosphate (sodium salt) Chemical Structure
  98. GC43382 DAz-2

    DAz-2 is a cell-permeable chemical probe used to detect cysteine oxidation in proteins.

     DAz-2 Chemical Structure
  99. GC45765 Deferiprone-d3 An internal standard for the quantification of deferiprone Deferiprone-d3 Chemical Structure
  100. GC45992 Diallyl Tetrasulfide An organosulfur compound with diverse biological activities Diallyl Tetrasulfide Chemical Structure
  101. GC45662 Dieugenol A neolignan with antioxidative and antiparasitic activities Dieugenol Chemical Structure

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