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Accueil >> Lipids >> Reactive O2/N2 Pathways

Reactive O2/N2 Pathways

Products for  Reactive O2/N2 Pathways

  1. Cat.No. Nom du produit Informations
  2. GC41213 (±)10-HDHA

    10hydroxy Docosahexaenoic Acid, (±)10HDoHE

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

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

    11hydroxy Docosahexaenoic Acid, (±)11-HDoHE

     (±)11-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)11-HDHA Chemical Structure
  4. 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
  5. GC40387 (±)11-HEPE (±)11-HEPE is produced by non-enzymatic oxidation of eicosapentaenoic acid. (±)11-HEPE Chemical Structure
  6. 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
  7. GC40359 (±)12-HEPE

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

     (±)12-HEPE Chemical Structure
  8. 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
  9. GC48738 (±)12-HETE-d8

    (±)12-Hydroxyeicosatetraenoic Acid-d8

     (±)12-HETE-d8 Chemical Structure
  10. 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
  11. GC41192 (±)13-HDHA

    13hydroxy Docosahexaenoic Acid, (±)13-HDoHE

     (±)13-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)13-HDHA Chemical Structure
  12. 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
  13. GC41193 (±)14-HDHA

    14hydroxy Docosahexaenoic Acid, (±)14-HDoHE

     (±)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-hydroxy Eicosapentaenoic Acid

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

     (±)15-HEPE Chemical Structure
  16. 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
  17. GC48739 (±)15-HETE-d8

    (±)15-Hydroxyeicosatetraenoic Acid-d8

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

    16hydroxy Docosahexaenoic Acid, (±)16-HDoHE

     (±)16-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)16-HDHA Chemical Structure
  19. 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
  20. 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
  21. GC40362 (±)18-HEPE (±)18-HEPE is produced by non-enzymatic oxidation of EPA. (±)18-HEPE Chemical Structure
  22. GC41202 (±)4-HDHA

    4hydroxy Docosahexaenoic Acid, (±)4HDoHE

     (±)4-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)4-HDHA Chemical Structure
  23. GC40364 (±)5-HEPE (±)5-HEPE is produced by non-enzymatic oxidation of EPA. (±)5-HEPE Chemical Structure
  24. 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
  25. 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
  26. 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
  27. 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
  28. GC41204 (±)7-HDHA

    7hydroxy Docosahexaenoic Acid, (±)7HDoHE

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

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

    8hydroxy Docosahexaenoic Acid, (±)8HDoHE

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

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

     (±)8-HEPE Chemical Structure
  31. GC40367 (±)9-HEPE (±)9-HEPE is produced by non-enzymatic oxidation of EPA. (±)9-HEPE Chemical Structure
  32. 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
  33. GC46268 (±)9-HETE-d8

    (±)9-Hydroxyeicosatetraenoic Acid-d8

     A neuropeptide with diverse biological activities (±)9-HETE-d8 Chemical Structure
  34. 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
  35. 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
  36. GC42023 1-Palmitoyl-2-Arachidonoyl-sn-glycero-3-PC

    1-Palmitoyl-2-Arachidonoyl-sn-glycero-3-Phosphocholine, PAPC, PC(16:0/20:4)

     1-Palmitoyl-2-arachidonoyl-sn-glycero-3-PC (PAPC) is a phospholipid containing palmitic acid (16:0) and arachidonic acid (20:4) at the sn-1 and sn-2 positions, respectively, that is found in biological membranes. 1-Palmitoyl-2-Arachidonoyl-sn-glycero-3-PC Chemical Structure
  37. GC90811 1-Palmitoyl-d9-2-Arachidonoyl-sn-glycero-3-PC

    Un standard interne pour la quantification de 1-palmitoyl-2-arachidonoyl-sn-glycéro-3-PC.

     1-Palmitoyl-d9-2-Arachidonoyl-sn-glycero-3-PC Chemical Structure
  38. GC42042 1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PE

    1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-phosphoethanolamine, 15(S)-HpETE-SAPE, 15(S)-hydroperoxyeicostetraenoic acid-SAPE

     1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PE is a phospholipid that contains stearic acid at the sn-1 position and 15(S)-HpETE at the sn-2 position. 1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PE Chemical Structure
  39. GC41868 10-Nitrooleate

    10Nitrooleic Acid, 10nitro9transOctadecenoic Acid

     Le 10-nitrooléate (CXA-10), un acide gras nitré, a des effets potentiels dans les états pathologiques dans lesquels le stress oxydatif, l'inflammation, la fibrose et/ou la toxicité tissulaire directe jouent un rÔle important. 10-Nitrooleate Chemical Structure
  40. GC46403 10-Nitrooleate-d17

    10Nitrooleic Acidd17, 10nitro9-trans-Octadecenoic Acidd17

     A neuropeptide with diverse biological activities 10-Nitrooleate-d17 Chemical Structure
  41. GC40368 11(R)-HEPE 11(R)-HEPE is produced by the oxidation of EPA by 11(R)-LO. 11(R)-HEPE Chemical Structure
  42. 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
  43. GC46420 13(S)-HODE-d4 An internal standard for the quantification of 13-HODE 13(S)-HODE-d4 Chemical Structure
  44. 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
  45. GC46441 15(S)-HEPE-d5

    15S-Hydroxyeicosapentaenoic Acid-d5

     A neuropeptide with diverse biological activities 15(S)-HEPE-d5 Chemical Structure
  46. 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
  47. GC41928 15-deoxy-δ12,14-Prostaglandin J2 Glutathione

    15deoxyΔ12,14PGJ2 Glutathione

     15-deoxy-δ12,14-Prostaglandin J2 Glutathione (15-deoxy-δ12,14-PGJ2 Glutathione) is a non-enzymatic adduct formed from 15-deoxy-δ12,14-PGJ2 and glutathione. 15-deoxy-δ12,14-Prostaglandin J2 Glutathione Chemical Structure
  48. GC40453 16(R)-HETE

    16(R)-Hydroxyeicosatetraenoic Acid

    Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites.

     16(R)-HETE Chemical Structure
  49. GC41207 17(R)-HDHA

    17(R)hydroxy Docosahexaenoic Acid, 17(R)HDoHE

     Resolvins are a group of polyhydroxylated metabolites of docosahexaenoic acid (DHA) found in the inflammatory exudates of aspirin-treated experimental animals. 17(R)-HDHA Chemical Structure
  50. 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
  51. GC41210 22-HDHA

    22-hydroxy Docosahexaenoic Acid, 22-OH DHA

     22-HDHA is an oxidation product of docosahexaenoic acid. 22-HDHA Chemical Structure
  52. 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
  53. 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
  54. GC46656 4-hydroxy Hexenal-d3

    4-HHE-d3

     An internal standard for the quantification of 4-hydroxy hexenal 4-hydroxy Hexenal-d3 Chemical Structure
  55. 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
  56. 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
  57. 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
  58. GC46660 4-hydroxy Nonenal Mercapturic Acid-d3 A neuropeptide with diverse biological activities 4-hydroxy Nonenal Mercapturic Acid-d3 Chemical Structure
  59. 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
  60. GC46674 4-oxo-2-Nonenal-d3

    4ONEd3

     An internal standard for the quantification of 4oxo-2nonenal 4-oxo-2-Nonenal-d3 Chemical Structure
  61. 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
  62. 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
  63. GC40459 5(R)-HETE

    5(R)-Hydroxyeicosatetraenoic Acid

     5(R)-HETE is a rare lipoxygenase product of arachidonic acid. 5(R)-HETE Chemical Structure
  64. GC46679 5(S)-HETE-d8

    5(S)-Hydroxyeicosatetraenoic Acid-d8

     An internal standard for the quantification of 5-HETE 5(S)-HETE-d8 Chemical Structure
  65. GC40201 7β-hydroxy Cholesterol-d7

    7α-hydroxycholesterol-d7

     7β-hydroxy Cholesterol-d7 is intended for use as an internal standard for the quantification of 7β-hydroxy cholesterol by GC- or LC-MS. 7β-hydroxy Cholesterol-d7 Chemical Structure
  66. 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
  67. 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
  68. 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
  69. 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
  70. GC41247 8-iso Misoprostol Misoprostol is a widely sold analog of prostaglandin E1 (PGE1) which has potent but relatively non-selective agonist activity with respect to the prostanoid EP receptor subgroup. 8-iso Misoprostol Chemical Structure
  71. 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
  72. 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
  73. 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
  74. 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
  75. 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
  76. 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
  77. GC46745 8-iso Prostaglandin E2-d4

    8epi PGE2d4, 8iso PGE2d4

     A neuropeptide with diverse biological activities 8-iso Prostaglandin E2-d4 Chemical Structure
  78. 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
  79. GC46746 8-iso Prostaglandin F1α-d9

    8epi PGF1αd9

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

    8epi9βPGF1α, 8iso PGF1β

     8-iso PGF1β is a potential autoxidation product of DGLA. 8-iso Prostaglandin F1β Chemical Structure
  81. 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
  82. 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
  83. 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
  84. 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
  85. 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
  86. 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
  87. GC40608 8-iso-15-keto Prostaglandin E2

    8epi15keto PGE2, 8iso15keto PGE2

     8-iso-15-keto Prostaglandin E2 (8-iso-15-keto PGE2) is an isoprostane, one member of a large family of biomarkers produced by the free radical peroxidative degradation of membrane lipids. 8-iso-15-keto Prostaglandin E2 Chemical Structure
  88. 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
  89. 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
  90. GC40332 8-iso-16-cyclohexyl-tetranor Prostaglandin E2

    8-iso-16-cyclohexyl-tetranor PGE2

     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
  91. GC40991 8-iso-17-phenyl trinor Prostaglandin F2α

    8-iso-17-phenyl PGF2β

     8-iso-17-phenyl trinor Prostaglandin F2α (8-iso-17-phenyl trinor PGF2α) is the C-8 epimer of bimatoprost (free acid), a metabolically stable analog of PGF2α. 8-iso-17-phenyl trinor Prostaglandin F2α Chemical Structure
  92. GC40992 8-iso-17-phenyl trinor Prostaglandin F2β

    8-iso-17-phenyl PGF2β

     Bimatoprost (free acid) is a metabolically stable analog of prostaglandin F2α (PGF2α) and a potent agonist for the FP receptor. 8-iso-17-phenyl trinor Prostaglandin F2β Chemical Structure
  93. GC92043 9(10)-Nitrooleate

    9(10)-Nitrooleic Acid; OA-NO2; 9(10)-nitro-9-trans-Octadecenoic Acid

     9(10)-Nitrooleate est un mélange des molécules de signalisation des lipides endogènes du nitroalkène 9-nitrooléate. 9(10)-Nitrooleate Chemical Structure
  94. GC46748 9(E),11(E)-12-nitro Conjugated Linoleic Acid

    9(E),11(E)-12-nitro CLA, 12-NO2-CLA

     A nitrated fatty acid 9(E),11(E)-12-nitro Conjugated Linoleic Acid Chemical Structure
  95. GC46749 9(E),11(E)-9-nitro Conjugated Linoleic Acid

    9E,11E-9-nitro CLA

     A nitrated fatty acid 9(E),11(E)-9-nitro Conjugated Linoleic Acid Chemical Structure
  96. GC46751 9(R)-HETE-d8

    9(R)-Hydroxyeicosatetraenoic Acid-d8

     A neuropeptide with diverse biological activities 9(R)-HETE-d8 Chemical Structure
  97. GC46755 9(S)-HODE-13C18

    (+)-α-Dimorphecolic Acid

     A neuropeptide with diverse biological activities 9(S)-HODE-13C18 Chemical Structure
  98. GC40250 9(S)-HODE-d4 MaxSpec® Standard 9(S)-HODE-d4 is intended for use as an internal standard for the quantification of 9(S)-HODE by GC- or LC-mass spectrometry. 9(S)-HODE-d4 MaxSpec® Standard Chemical Structure
  99. GC42649 9-Nitrooleate

    9Nitrooleic Acid, 9nitro9transOctadecenoic Acid

     Nitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate, cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. 9-Nitrooleate Chemical Structure
  100. GC46760 9-Nitrooleate-d17

    9Nitrooleic Acidd17, 9nitro9-trans-Octadecenoic Acidd17

     A neuropeptide with diverse biological activities 9-Nitrooleate-d17 Chemical Structure
  101. GC46761 9-Oxononanoic Acid

    Azelaaldehydic Acid

     An oxidized fatty acid 9-Oxononanoic Acid Chemical Structure

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