Search Site
  • 0
    Mi cesta

    Click Here to Find How Many Items You Have Added:)

    image loader

    Adding item(s) to cart......

Inicio >> Lipids >> Reactive O2/N2 Pathways

Reactive O2/N2 Pathways

Products for  Reactive O2/N2 Pathways

  1. Cat.No. Nombre del producto Información
  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 importante producto metabólico del ácido araquidónico mediante catálisis 12-LOX, inhibe la apoptosis celular de forma dependiente de la dosis. (±)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 (ácido 13-hidroperoxilinoleico) es una mezcla racémica de hidroperóxidos, que se produce por la oxidación del ácido linoleico por la lipoxigenasa. (±)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 es un hidroperóxido lipídico de cadena larga, es un producto de la peroxidación del ácido linoleico. (±)9-HpODE 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. 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 estándar interno para la cuantificación de 1-palmitoil-2-arachidonoil-sn-glicero-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

     El 10-nitrooleato (CXA-10), un Ácido graso nitro, tiene efectos potenciales en estados patolÓgicos en los que el estrés oxidativo, la inflamaciÓn, la fibrosis y/o la toxicidad tisular directa juegan un papel importante. 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 metabolito activo del ácido araquidónico y 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

     An oxysterol and a metabolite of cholesterol produced by oxidation 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

     El colesterol 7-ceto, oxisterol tóxico, inhibe el paso limitante de la biosíntesis de ácidos biliares colesterol 7 alfa-hidroxilasa, así como también inhibe fuertemente la HMG-CoA reductasa (la enzima limitante de la biosíntesis del colesterol). 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 prostaglandina E2 (iPE2-III) es un miembro de la clase de prostanoides isoprostano. 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 isómero de PGF2α producido por la peroxidación radical libre del ácido araquidónico.

     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 es una mezcla de las moléculas de señalización lipíendde nitroalqueno 9-nitrooleato. 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

Artículos 1 al 100 de 116 totales

por página
  1. 1
  2. 2

Fijar Dirección Descendente