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Accueil >> Lipids

Lipids

Products for  Lipids

  1. Cat.No. Nom du produit Informations
  2. GC40816 α-Linolenoyl Ethanolamide α-Linolenoyl ethanolamide is an endocannabinoid containing α-linolenic acid in place of the arachidonate moiety of AEA. α-Linolenoyl Ethanolamide Chemical Structure
  3. GC14406 (±)-Acetylcarnitine chloride weak cholinergic agonist; intermediates in lipid metabolism (±)-Acetylcarnitine chloride Chemical Structure
  4. GC15834 (±)-Decanoylcarnitine chloride intermediate in lipid metabolism (±)-Decanoylcarnitine chloride Chemical Structure
  5. GC17351 (±)-Hexanoylcarnitine chloride

    intermédiaires importants dans le métabolisme des lipides

     (±)-Hexanoylcarnitine chloride Chemical Structure
  6. GC16427 (±)-Lauroylcarnitine chloride important intermediates in lipid metabolism (±)-Lauroylcarnitine chloride Chemical Structure
  7. GC10056 (±)-Myristoylcarnitine chloride cholinergic agonist; important intermediates in lipid metabolism (±)-Myristoylcarnitine chloride Chemical Structure
  8. GC13909 (±)-Octanoylcarnitine chloride homolog of acetylcarnitine chloride (±)-Octanoylcarnitine chloride Chemical Structure
  9. GC49510 (±)-Tuberonic Acid A derivative of jasmonic acid (±)-Tuberonic Acid Chemical Structure
  10. GC45269 (±)10(11)-DiHDPA (±)10(11)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid. (±)10(11)-DiHDPA Chemical Structure
  11. GC45270 (±)10(11)-EDP Ethanolamide (±)10(11)-EDP ethanolamide is an ω-3 endocannabinoid epoxide and cannabinoid (CB) receptor agonist (EC50s = 0.43 and 22.5 nM for CB1 and CB2 receptors, respectively). (±)10(11)-EDP Ethanolamide Chemical Structure
  12. GC41212 (±)10(11)-EpDPA Cytochrome P450 metabolism of polyunsaturated fatty acids produces numerous bioactive epoxide regioisomers. (±)10(11)-EpDPA Chemical Structure
  13. GC41213 (±)10-HDHA

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

     (±)10-HDHA Chemical Structure
  14. GC41214 (±)11-HDHA (±)11-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)11-HDHA Chemical Structure
  15. GC41648 (±)13(14)-DiHDPA (±)13(14)-DiHDPA is a metabolite of docosahexaenoic acid that is produced via oxidation by cytochrome P450 epoxygenases. (±)13(14)-DiHDPA Chemical Structure
  16. GC41191 (±)13(14)-EpDPA (M)13(14)-EpDPA (13,14-EpDPE) est le produit de la réaction de la cytochrome P-450 époxygénase avec l'acide docosahexaénoïque (DHA). (±)13(14)-EpDPA Chemical Structure
  17. GC41192 (±)13-HDHA (±)13-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)13-HDHA Chemical Structure
  18. GC41193 (±)14-HDHA (±)14-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)14-HDHA Chemical Structure
  19. GC41653 (±)16(17)-DiHDPA (±)16(17)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid. (±)16(17)-DiHDPA Chemical Structure
  20. GC41194 (±)16(17)-EpDPA

    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.

     (±)16(17)-EpDPA Chemical Structure
  21. GC41196 (±)16-HDHA (±)16-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)16-HDHA Chemical Structure
  22. GC41197 (±)17-HDHA (±)17-HDHA is an autoxidation product of docosahexaenoic acid in vitro. (±)17-HDHA Chemical Structure
  23. GC40388 (±)19(20)-DiHDTE (±)19(20)-DiHDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid. (±)19(20)-DiHDTE Chemical Structure
  24. GC41655 (±)19(20)-EDP Ethanolamide (±)19(20)-EDP ethanolamide is an ω-3 endocannabinoid epoxide and cannabinoid (CB) receptor agonist (EC50s = 108 and 280 nM for CB1 and CB2, respectively). (±)19(20)-EDP Ethanolamide Chemical Structure
  25. GC41199 (±)19(20)-EpDPA 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. (±)19(20)-EpDPA Chemical Structure
  26. GC40905 (±)19(20)-EpDTE (±)19(20)-EpDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid. (±)19(20)-EpDTE Chemical Structure
  27. GC41201 (±)4(5)-DiHDPA lactone (±)5(6)-DiHET lactone is a 1,5 cyclic ester derived from (±)5(6)-DiHET, which, in turn, is a potential derivative of epoxidation of arachidonic acid at the α-5 double bond. (±)4(5)-DiHDPA lactone Chemical Structure
  28. GC41660 (±)4(5)-EpDPA methyl ester (±)4(5)-EpDPA methyl ester is a derivative of (±)4(5)-EpDPA which is stable enough to ship and handle routinely. (±)4(5)-EpDPA methyl ester Chemical Structure
  29. GC41202 (±)4-HDHA (±)4-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)4-HDHA Chemical Structure
  30. GC46263 (±)5-iPF2α-VI-d11 An internal standard for the quantification of (±)5iPF2αVI (±)5-iPF2α-VI-d11 Chemical Structure
  31. GC41663 (±)7(8)-DiHDPA (±)7(8)-DiHDPA is a major metabolite of docosahexaenoic acid that is produced via oxidation by cytochrome P450 epoxygenases. (±)7(8)-DiHDPA Chemical Structure
  32. GC41203 (±)7(8)-EpDPA Docosahexaenoic acid is the most abundant ω-3 fatty acid in neural tissues, especially in the brain and retina. (±)7(8)-EpDPA Chemical Structure
  33. GC40906 (±)7(8)-EpDTE (±)7(8)-EpDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid. (±)7(8)-EpDTE Chemical Structure
  34. GC41664 (±)7-epi Jasmonic Acid

    (±)-7-epi Jasmonic acid is the major metabolite of the 12-oxo phytodienoic acid pathway of the metabolism of 13(S)-hydroperoxy linolenic acid in plants.

     (±)7-epi Jasmonic Acid Chemical Structure
  35. GC41204 (±)7-HDHA

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

     (±)7-HDHA Chemical Structure
  36. GC40421 (±)8(9)-EE-14(Z)-E (±)14(15)-EE-8(Z)-E is a potent vasodilator in bovine coronary arteries. (±)8(9)-EE-14(Z)-E Chemical Structure
  37. GC41205 (±)8-HDHA (±)8-HDHA is an autoxidation product of docosahexaenoic acid (DHA) in vitro. (±)8-HDHA Chemical Structure
  38. 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
  39. GC50004 (+/-)-Decanoylcarnitine chloride Intermediate in lipid metabolism (+/-)-Decanoylcarnitine chloride Chemical Structure
  40. GC40444 (5Z,11Z,15R)-15-Hydroxyeicosa-5,11-dien-13-ynoic Acid (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
  41. GC41709 (R)-(+)-Docosahexaenyl-1'-Hydroxy-2'-Propylamide N-Acyl ethanolamines (NAEs) have diverse biological actions that are strongly affected by the associated acyl group. (R)-(+)-Docosahexaenyl-1'-Hydroxy-2'-Propylamide Chemical Structure
  42. GC41712 (R)-3-hydroxy Myristic Acid Lipopolysaccharides (LPS) are components of the cell walls of Gram-negative bacteria. (R)-3-hydroxy Myristic Acid Chemical Structure
  43. GC46356 (Z)-9-Hexadecenol An unsaturated long-chain fatty alcohol with diverse biological activities (Z)-9-Hexadecenol Chemical Structure
  44. 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
  45. GC41857 1',4"-Sophorolactone 6',6"-diacetate 1',4"-Sophorolactone 6',6"-diacetate is a major glycolipid produced from fermentation of sugar by yeasts including C. 1',4
  46. GC18352 1,2-Dioleoyl-3-dimethylammonium-propane Le 1,2-dioléoyl-3-diméthylammonium-propane est un lipide cationique. 1,2-Dioleoyl-3-dimethylammonium-propane Chemical Structure
  47. GC45783 1,2-Dioleoyl-rac-glycerol-13C3 An internal standard for the quantification of 1,2-dioleoyl-rac-glycerol 1,2-Dioleoyl-rac-glycerol-13C3 Chemical Structure
  48. GC41817 1,2-Dioleyloxy-3-dimethylamino-propane Le 1,2-dioleyloxy-3-diméthylamino-propane, un lipide cationique, est utilisé pour la préparation de liposomes. 1,2-Dioleyloxy-3-dimethylamino-propane Chemical Structure
  49. GC45306 1,6-Diphenyl-1,3,5-hexatriene Le 1,6-diphényl-1,3,5-hexatriène est une sonde fluorescente. 1,6-Diphenyl-1,3,5-hexatriene Chemical Structure
  50. GC45317 1-Pyrenesulfonic Acid (sodium salt)   1-Pyrenesulfonic Acid (sodium salt) Chemical Structure
  51. GC40971 10(S),17(S)-DiHDHA La 10(S),17(S)-DiHDHA (également connue sous le nom de neuroprotectine D1 lorsqu'elle est produite dans les tissus neuronaux) est un acide gras dihydroxy dérivé du DHA qui présente de puissantes activités protectrices et anti-inflammatoires. 10(S),17(S)-DiHDHA Chemical Structure
  52. GC48802 10(S)-HOME An oxylipin 10(S)-HOME Chemical Structure
  53. GC40423 11(S)-HEDE 11(S)-HEDE is isolated by the chromatographic resolution of (±)11-HEDE. 11(S)-HEDE Chemical Structure
  54. 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
  55. GC40446 11(S)-HETE 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
  56. GC49317 11(Z)-Docosenoic Acid A 22-carbon monounsaturated fatty acid 11(Z)-Docosenoic Acid Chemical Structure
  57. GC41886 12-Doxylstearic Acid 12-Doxylstearic acid is a form of stearic acid that contains a (4,4-dimethyl-3-oxazolinyloxy (DOXYL) group, creating a hydrophobic spin label. 12-Doxylstearic Acid Chemical Structure
  58. GC18280 13(E)-Docosenoic Acid

    13(E)-Docosenoic acid is a 22-carbon monounsaturated fatty acid. It is the trans isomer of 13(Z)-docosenoic acid .

     13(E)-Docosenoic Acid Chemical Structure
  59. GC41901 13(Z)-Docosenoic Acid methyl ester 13(Z)-Docosenoic acid methyl ester is a fatty acid methyl ester that is a flavor-active, volatile, and aromatic compound found in cooked commercial shrimp waste. 13(Z)-Docosenoic Acid methyl ester Chemical Structure
  60. GC41910 13-Docosenamide 13-Docosenamide is the amide of docosenoic acid. 13-Docosenamide Chemical Structure
  61. GC41914 13-OxoODE

    13-oxoODE is produced from 13-HODE by a NAD+-dependent dehydrogenase present in rat colonic mucosa.

     13-OxoODE Chemical Structure
  62. GC41206 14(S)-HDHA La 14(S)-HDHA (14(S)-HDoHE) est un produit d'oxygénation de l'acide docosahexaénoÏque (DHA). 14(S)-HDHA Chemical Structure
  63. GC41320 14,15-Leukotriene A4 methyl ester 14,15-Leukotriene A4 (14,15-LTA4) methyl ester is an esterified form of 14,15-LTA4, a leukotriene isomer formed from arachidonic acid by 15-lipoxygenase (15-LO) that inhibits LTA4 hydrolase. 14,15-Leukotriene A4 methyl ester Chemical Structure
  64. GC40426 15(R)-HEDE 15(R)-HEDE is isolated by the chromatographic resolution of (±)15-HEDE. 15(R)-HEDE Chemical Structure
  65. GC41226 15(S)-acetate Prostaglandin A2 methyl ester 15(S)-acetate Prostaglandin A2 methyl ester is a 15-acetylated derivative of prostaglandin A2 methyl ester. 15(S)-acetate Prostaglandin A2 methyl ester Chemical Structure
  66. GC41930 15-hydroxy Pentadecanoic Acid methyl ester 15-hydroxy Pentadecanoic acid methyl ester is a hydroxylated fatty acid methyl ester that is a key intermediate in the synthesis of the musk-odored macrocyclic lactones cyclopentadecanolide and exaltolide. 15-hydroxy Pentadecanoic Acid methyl ester Chemical Structure
  67. GC41300 17β-hydroxy Exemestane 17β-hydroxy Exemestane is the primary active metabolite of exemestane. 17β-hydroxy Exemestane Chemical Structure
  68. GC41207 17(R)-HDHA 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
  69. GC49178 17(R)-Protectin D1 An aspirin-triggered epimer of protectin D1 17(R)-Protectin D1 Chemical Structure
  70. GC41951 17(R)-Resolvin D1

    Resolvins are a family of potent lipid mediators derived from both eicosapentaenoic acid and docosahexaenoic acid.

     17(R)-Resolvin D1 Chemical Structure
  71. GC41227 17(R)-Resolvin D1 methyl ester 17(R)-Resolvin D1 (17(R)-RvD1) is an aspirin-triggered epimer of RvD1 that reduces human polymorphonuclear leukocyte transendothelial migration, the earliest event in acute inflammation, with equipotency to RvD1 (EC50 = ~30 nM). 17(R)-Resolvin D1 methyl ester Chemical Structure
  72. GC45307 17(R)-Resolvin D3   17(R)-Resolvin D3 Chemical Structure
  73. GC41952 17(R)-Resolvin D4 17(R)-Resolvin D4 (17(R)-RvD4) is an aspirin-triggered epimer of RvD4 . 17(R)-Resolvin D4 Chemical Structure
  74. GC40975 17(S)-HpDHA 17(S)-HpDHA is a mono-oxygenation product of docosahexaenoic acid in human whole blood, human leukocytes, human glial cells, and mouse brain. 17(S)-HpDHA Chemical Structure
  75. GC41957 17-hydroxy Heptadecanoic Acid methyl ester 17-hydroxy Heptadecanoic acid methyl ester is a hydroxylated fatty acid methyl ester and substrate for lactonizing lipase from Pseudomonas nov. 17-hydroxy Heptadecanoic Acid methyl ester Chemical Structure
  76. GC41529 17-oxo-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-Docosahexaenoic Acid 17-oxo-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-Docosahexaenoic acid is a metabolite of lipoxygenase-mediated oxidation of DHA that is produced endogenously by aspirin-enhanced COX-2 activity. 17-oxo-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-Docosahexaenoic Acid Chemical Structure
  77. GC41209 17-oxo-7(Z),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid Docosapentaenoic acid (DPA) is a ω-3 fatty acid found in fish oils. 17-oxo-7(Z),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid Chemical Structure
  78. GC45324 2,5-dimethyl Celecoxib   2,5-dimethyl Celecoxib Chemical Structure
  79. GC42135 2-chloro Palmitic Acid L'acide 2-chloro palmitique, un médiateur lipidique inflammatoire, interfère avec la palmitoylation des protéines, induit des marqueurs de stress ER, réduit la teneur en ATP ER et active la transcription et la sécrétion d'IL-6 ainsi que d'IL-8.2-chloro L'acide palmitique perturbe la mitochondrie potentiel membranaire et induit le clivage de la procaspase-3 et de la PARP. L'acide palmitique 2-chloro peut traverser la barrière hémato-encéphalique (BBB) et compromettre les fonctions ER et mitochondriales dans la lignée cellulaire endothéliale du cerveau humain hCMEC/D3. 2-chloro Palmitic Acid Chemical Structure
  80. GC42136 2-chloro Stearic Acid 2-chloro Stearic acid is a bioactive fatty acid that accumulates in primary human monocytes and neutrophils as well as murine neutrophils stimulated with phorbol 12-myristate 13-acetate. 2-chloro Stearic Acid Chemical Structure
  81. GC42162 2-hydroxy Arachidic Acid methyl ester 2-hydroxy Arachidic acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in sediment samples from the Harney River and in petroleum ether extracts of I. 2-hydroxy Arachidic Acid methyl ester Chemical Structure
  82. GC18391 2-hydroxy Decanoic Acid

    2-hydroxy Decanoic acid is a fatty acid found in the lipophilic portion of the lipopolysaccharide fraction of P.

     2-hydroxy Decanoic Acid Chemical Structure
  83. GC40486 2-hydroxy Decanoic Acid methyl ester 2-hydroxy Decanoic acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in A. 2-hydroxy Decanoic Acid methyl ester Chemical Structure
  84. GC42163 2-hydroxy Docosanoic Acid L'acide 2-hydroxy docosanoïque a des activités antioxydantes, inhibitrices de la cholinestérase et antimicrobiennes. 2-hydroxy Docosanoic Acid Chemical Structure
  85. GC40472 2-hydroxy Docosanoic Acid methyl ester 2-hydroxy Docosanoic acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in ripe and unripe strawberry homogenates, Pseudosuberites and S. 2-hydroxy Docosanoic Acid methyl ester Chemical Structure
  86. GC40492 2-hydroxy Lauric Acid 2-hydroxy Lauric acid is a naturally occuring hydroxylated fatty acid that is found in Acinetobacter species. 2-hydroxy Lauric Acid Chemical Structure
  87. GC42164 2-hydroxy Lauric Acid methyl ester 2-hydroxy Lauric acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in coliform bacteria isolated from human sewage. 2-hydroxy Lauric Acid methyl ester Chemical Structure
  88. GC40473 2-hydroxy Lignoceric Acid 2-hydroxy Lignoceric acid is an α-hydroxy very long chain fatty acid that is normally present in the mammalian nervous system. 2-hydroxy Lignoceric Acid Chemical Structure
  89. GC42165 2-hydroxy Lignoceric Acid methyl ester 2-hydroxy Lignoceric acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in ripe and unripe strawberry homogenates, Pseudosuberites and S. 2-hydroxy Lignoceric Acid methyl ester Chemical Structure
  90. GC42167 2-hydroxy Myristic Acid methyl ester 2-hydroxy Myristic acid methyl ester is a rare hydroxylated fatty acid methyl ester that has been isolated from aquatic microbial sources. 2-hydroxy Myristic Acid methyl ester Chemical Structure
  91. GC42168 2-hydroxy Palmitic Acid L'acide 2-hydroxy palmitique est un intermédiaire du métabolisme de la phytosphingosine. 2-hydroxy Palmitic Acid Chemical Structure
  92. GC42169 2-hydroxy Palmitic Acid methyl ester 2-hydroxy Palmitic acid methyl ester is a naturally occuring hydroxy fatty acid methyl ester. 2-hydroxy Palmitic Acid methyl ester Chemical Structure
  93. GC42171 2-hydroxy Stearic Acid methyl ester 2-hydroxy Stearic acid is a hydroxylated fatty acid methyl ester that broadens phase transition in dimyristoylphosphatidylcholine (DMPC) lipid membranes. 2-hydroxy Stearic Acid methyl ester Chemical Structure
  94. GC18752 2-hydroxy Tricosanoic Acid 2-hydroxy Tricosanoic acid is a hydroxylated fatty acid that has been found in the inner bark of E. 2-hydroxy Tricosanoic Acid Chemical Structure
  95. GC18575 2-hydroxy Tricosanoic Acid methyl ester 2-hydroxy Tricosanoic acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in ripe and unripe strawberry homogenates, Pseudosuberites and S. 2-hydroxy Tricosanoic Acid methyl ester Chemical Structure
  96. GC49283 2-O-(α-D-Glucopyranosyl)glycerol A compatible solute 2-O-(α-D-Glucopyranosyl)glycerol Chemical Structure
  97. GC41387 20-hydroxy Arachidic Acid 20-hydroxy Arachidic acid is a hydroxylated fatty acid that has been found in the suberin component of silver birch (B. 20-hydroxy Arachidic Acid Chemical Structure
  98. GC42084 20-hydroxy Arachidic Acid methyl ester 20-hydroxy Arachidic acid methyl ester is a hydroxylated fatty acid methyl ester that has been found in P. 20-hydroxy Arachidic Acid methyl ester Chemical Structure
  99. GC42088 21-hydroxy Heneicosanoic Acid methyl ester 21-hydroxy Heneicosanoic acid methyl ester is a hydroxylated fatty acid methyl ester and substrate for lactonizing lipase from Pseudomonas nov. 21-hydroxy Heneicosanoic Acid methyl ester Chemical Structure
  100. GC41210 22-HDHA 22-HDHA is an oxidation product of docosahexaenoic acid. 22-HDHA Chemical Structure
  101. GC42089 22-hydroxy Docosanoic Acid 22-hydroxy Docosanoic acid is a hydroxylated fatty acid that has been found in the suberin component of silver birch (B. 22-hydroxy Docosanoic Acid Chemical Structure

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