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홈 >> Lipids >> Prostaglandins

Prostaglandins

Products for  Prostaglandins

  1. Cat.No. 상품명 정보
  2. GC41431 δ12-Prostaglandin D2

    Δ12PGD2

     Prostaglandin D2 (PGD2) is one of the five primary enzymatic prostaglandins derived directly from PGH2. δ12-Prostaglandin D2 Chemical Structure
  3. GC41476 δ17-6-keto Prostaglandin F1α

    ω3 6keto PGF2α

     δ17-6-keto Prostaglandin F1α (δ17-6-keto PGF1α) is a cyclooxygenase (COX) product of eicosapentaenoic acid (EPA) in various tissues such as seminal vesicles, lung, Polymorphonuclear leukocytes, and ocular tissues. δ17-6-keto Prostaglandin F1α Chemical Structure
  4. GC49515 (±)-Ibuprofen-d3 (sodium salt)

    DL-Ibuprofen-d3

     An internal standard for the quantification of (±)-ibuprofen (±)-Ibuprofen-d3 (sodium salt) Chemical Structure
  5. GC41315 (±)-Ketoprofen Glucuronide

    rac-Ketoprofen Acyl-β-D-glucuronide, (R,S)-Ketoprofen Glucuronide

     (±)-Ketoprofen glucuronide is a phase II metabolite of the non-steroidal anti-inflammatory drug (NSAID) ketoprofen. (±)-Ketoprofen Glucuronide Chemical Structure
  6. GC45278 (±)-Ketoprofen-d3

    (R,S)-Ketoprofen-d3, 2-(3-benzoylphenyl)Propionic Acid-d3

       (±)-Ketoprofen-d3 Chemical Structure
  7. GC41685 (±)-WIN 55,212 (mesylate) (±)-WIN 55,212-2 is a potent aminoalkylindole cannabinoid (CB) receptor agonist with a Ki value of 62.3 and 3.3 nM for human recombinant central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors, respectively. (±)-WIN 55,212 (mesylate) Chemical Structure
  8. GC40270 (±)5(6)-DiHET

    (±)5,6-DiHETrE

    5(6)-DiHET is a fully racemic version of the enantiomeric forms biosynthesized from 5(6)-EET by epoxide hydrolases.

     (±)5(6)-DiHET Chemical Structure
  9. GC40281 (+)-15-epi Cloprostenol

    DCloprostenol, (+)15(S)Cloprostenol

     Cloprostenol is a synthetic prostaglandin F2α (PGF2α) analog and a potent FP receptor agonist. (+)-15-epi Cloprostenol Chemical Structure
  10. GC40282 (+)-5-trans Cloprostenol

    DCloprostenol, (+)5,6trans Cloprostenol, (+)5trans16mchlorophenoxy tetranor PGF2α, (+)5trans16mchlorophenoxy tetranor Prostaglandin F2α

     Cloprostenol is a synthetic derivative of prostaglandin F2α that is used in veterinary medicine as a luteolytic agent for the induction of estrus and in the treatment of reproductive disorders in cattle, swine, and horses. (+)-5-trans Cloprostenol Chemical Structure
  11. GC45260 (+)-Cloprostenol isopropyl ester

    (+)-5-cis Cloprostenol isopropyl ester, (+)16mchlorophenoxy tetranor Prostaglandin F2α isopropyl ester

     (+)-클로프로스테놀 이소프로필 에스테르, 프로스타글란딘 F2α 유사체는 (+)-클로프로스테놀의 중간체입니다. (+)-Cloprostenol isopropyl ester Chemical Structure
  12. GC45262 (+)-Cloprostenol methyl ester

    DCloprostenol methyl ester, (+)16mChlorophenoxy tetranor PGF2α methyl ester

     (+)-Cloprostenol is a synthetic analog of prostaglandin F2α (PGF2α). (+)-Cloprostenol methyl ester Chemical Structure
  13. GC40716 (R)-Butaprost

    (±)15deoxy16Rhydroxy17cyclobutyl PGE1 methyl ester, 15deoxy16Rhydroxy17cyclobutyl PGE1 methyl ester, TR 4978

     Butaprost is a structural analog of prostaglandin E2 (PGE2) with good selectivity for the EP2 receptor subtype. (R)-Butaprost Chemical Structure
  14. GC41714 (R)-Butaprost (free acid)

    (±)15deoxy16Rhydroxy17cyclobutyl PGE1, 15deoxy16Rhydroxy17cyclobutyl PGE1

     Butaprost is a structural analog of prostaglandin E2 (PGE2) with good selectivity for the EP2 receptor subtype. (R)-Butaprost (free acid) Chemical Structure
  15. GC49179 (S)-O-Desmethyl Naproxen

    (S)-6-Desmethyl Naproxen

     A metabolite of (S)-naproxen (S)-O-Desmethyl Naproxen Chemical Structure
  16. GC41761 1-(6-Methoxy-2-naphthyl)ethanol

    Naproxen Impurity K

     1-(6-Methoxy-2-naphthyl)ethanol is a potential impurity in commercial preparations of naproxen. 1-(6-Methoxy-2-naphthyl)ethanol Chemical Structure
  17. GC18235 1-O-Hexadecyl-sn-glycerol

    α-Chimyl Alcohol, (S)-(+)-Chimyl Alcohol

    1-O-Hexadecyl-sn-glycerol is a bioactive alkyl glyceryl ether.

     1-O-Hexadecyl-sn-glycerol Chemical Structure
  18. GC49366 1-Salicylate Glucuronide

    Salicyl Phenolic Glucuronide, Salicylic Acid Phenolic Glucuronide

     A metabolite of salicylic acid and aspirin 1-Salicylate Glucuronide Chemical Structure
  19. GC40577 11β-13,14-dihydro-15-keto Prostaglandin F2α

    11β13,14dihydro15keto PGF2α, 11-epi-13,14-dihydro-15-keto PGF2α

     11β-13,14-dihydro-15-keto Prostaglandin F2α (11β-13,14-dihydro-15-keto PGF2α) is a metabolite of Prostaglandin D2 (PGD2) in the 15-hydroxy PGDH pathway. 11β-13,14-dihydro-15-keto Prostaglandin F2α Chemical Structure
  20. GC41243 11β-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. 11β-Misoprostol Chemical Structure
  21. GC41410 11β-Prostaglandin E2

    11β-PGE2

     11β-프로스타글란딘 E2(11β-디노프로스톤), 프로스타노이드 유도체는 53.3nM의 Ki로 쥐의 시상하부 막에 대한 [3H]PGE2 결합을 억제합니다. 11β-Prostaglandin E2 Chemical Structure
  22. GC41432 11β-Prostaglandin F1β

    9β,11βPGF1α, 11βPGF1β, 11epi PGF1β

     11β-PGF1β is the stereoisomer of PGF1α with both C-9 and C-11 hydroxyls inverted. 11β-Prostaglandin F1β Chemical Structure
  23. GC41404 11β-Prostaglandin F2α Ethanolamide

    11-epi PGF2α-EA, 11β-PGF2α-EA, 11β-Prostamide F2α

     11β-Prostaglandin F2α ethanolamide (11β-PGF2α-EA) is the theoretical hepatic metabolite of PGD2-EA, produced during COX-2 metabolism of the endogenous cannabinoid AEA which is found in brain, liver, and other mammalian tissues. 11β-Prostaglandin F2α Ethanolamide Chemical Structure
  24. GC18634 11-deoxy Prostaglandin E1

    11deoxy PGE1

     11-deoxy Prostaglandin E1 (11-deoxy PGE1) is a synthetic analog of PGE1. 11-deoxy Prostaglandin E1 Chemical Structure
  25. GC41121 11-deoxy Prostaglandin E2

    11deoxy PGE2

     11-deoxy Prostaglandin E2 (11-deoxy PGE2) is a stable, synthetic analog of PGE2. 11-deoxy Prostaglandin E2 Chemical Structure
  26. GC41401 11-deoxy Prostaglandin F1α

    11deoxy PGF1α

     11-deoxy PGF1α is a synthetic analog of PGF1α. 11-deoxy Prostaglandin F1α Chemical Structure
  27. GC41402 11-deoxy Prostaglandin F1β

    9β,11deoxy PGF1α, 11deoxy PGF1β

     11-deoxy PGF1β is a synthetic analog of PGF1β. 11-deoxy Prostaglandin F1β Chemical Structure
  28. GC40274 11-deoxy Prostaglandin F2α

    11deoxy PGF2α

     11-deoxy PGF2α is a synthetic analog of PGF2α. 11-deoxy Prostaglandin F2α Chemical Structure
  29. GC40275 11-deoxy Prostaglandin F2β

    11deoxy PGF2β

     11-deoxy Prostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β. 11-deoxy Prostaglandin F2β Chemical Structure
  30. GC40335 11-deoxy-11-methylene Prostaglandin D2

    11deoxy11methylene PGD2

     Prostaglandin D2 is one of the five primary enzymatic prostaglandins derived directly from PGH2. 11-deoxy-11-methylene Prostaglandin D2 Chemical Structure
  31. GC41879 11-deoxy-11-methylene-15-keto Prostaglandin D2

    11deoxy11methylene15keto PGD2

     Prostaglandin D2 (PGD2) is one of the five primary enzymatic prostaglandins derived directly from PGH2. 11-deoxy-11-methylene-15-keto Prostaglandin D2 Chemical Structure
  32. GC40390 11-deoxy-16,16-dimethyl Prostaglandin E2

    11deoxy16,16dimethyl PGE2

     11-deoxy-16,16-dimethyl PGE2 is a stable synthetic analog of PGE2. 11-deoxy-16,16-dimethyl Prostaglandin E2 Chemical Structure
  33. GC41880 11-keto Fluprostenol

    Fluprostenol Prostaglandin D2

     11-keto Fluprostenol is an analog of prostaglandin D2 (PGD2) with structural modifications intended to give it a prolonged half-life and greater potency. 11-keto Fluprostenol Chemical Structure
  34. GC18617 11β-Prostaglandin E1

    11βPGE1, 11epi PGE1

     11β-Prostaglandin E1 (11β-PGE1) is an epimerized form of PGE1 at the C-11 position. 11β-Prostaglandin E1 Chemical Structure
  35. GC18637 11β-Prostaglandin F2α

    9α,11βPGF2α, 11βPGF2α, 11epi PGF2α

    11β-Prostaglandin F2α (11β-PGF2α) is the primary plasma metabolite of PGD2 in vivo.

     11β-Prostaglandin F2α Chemical Structure
  36. GC40745 13,14-dehydro-15-cyclohexyl Carbaprostacyclin 13,14-dehydro-15-cyclohexyl Carbaprostacyclin is a chemically stable analog of PGI2. 13,14-dehydro-15-cyclohexyl Carbaprostacyclin Chemical Structure
  37. GC41433 13,14-dihydro Prostaglandin E1

    PGE0, 13,14-dihydro PGE1

     13,14-dihydro Prostaglandin E1 (13,14-dihydro PGE1) is a biologically active metabolite of PGE1 with comparable potency to the parent compound. 13,14-dihydro Prostaglandin E1 Chemical Structure
  38. GC41902 13,14-dihydro Prostaglandin F1α

    PGFα, 13,14dihydro PGF1α

     13,14-dihydro PGF1α is a potential metabolite of PGF1α. 13,14-dihydro Prostaglandin F1α Chemical Structure
  39. GC41434 13,14-dihydro Prostaglandin F2α

    13,14-dihydro PGF2α

    13,14-dihydro Prostaglandin F2α (13,14-dihydro PGF2α) is the analog of PGF2α which has no unsaturation in the lower side chain.

     13,14-dihydro Prostaglandin F2α Chemical Structure
  40. GC41435 13,14-dihydro-15(R)-Prostaglandin E1

    13,14dihydro15(R)PGE1

     13,14-dihydro-15(R)-Prostaglandin E1 (13,14-dihydro-15(R)-PGE1) is an analog of 13,14-dihydro-PGE1 , which has the hydroxyl group at C-15 in the unnatural R configuration. 13,14-dihydro-15(R)-Prostaglandin E1 Chemical Structure
  41. GC41097 13,14-dihydro-15-keto Prostaglandin A2

    13,14-dihydro-15-keto PGA2

     PGE2 is metabolized rapidly to 13,14-dihydro-15-keto PGE2, which is present in the plasma of humans and other mammals. 13,14-dihydro-15-keto Prostaglandin A2 Chemical Structure
  42. GC40578 13,14-dihydro-15-keto Prostaglandin D1

    13,14dihydro15keto PGD1

     Prostaglandin D1 (PGD1) is the theoretical D-series metabolite of dihomo-γ-linolenic acid (DGLA), but to date it has not been isolated as a natural product. 13,14-dihydro-15-keto Prostaglandin D1 Chemical Structure
  43. GC41411 13,14-dihydro-15-keto Prostaglandin D2

    13,14-dihydro-15-keto PGD2

    13,14-dihydro-15-keto Prostaglandin D2 (13,14-dihydro-15-keto PGD2) is a metabolite of PGD2 which is formed through the 15-hydroxy PGDH pathway.

     13,14-dihydro-15-keto Prostaglandin D2 Chemical Structure
  44. GC18783 13,14-dihydro-15-keto Prostaglandin E1

    11α-Hydroxy-9,15-diketoprostanoic Acid, 15-keto-PGE0, 13,14-dihydro-15-keto PGE1, 15-keto-dihydro-PGE1, 15-keto Prostaglandin E0

     13,14-dihydro-15-keto Prostaglandin E1 (PGE1) is a metabolite of PGE1 with much reduced biological activity. 13,14-dihydro-15-keto Prostaglandin E1 Chemical Structure
  45. GC41413 13,14-dihydro-15-keto Prostaglandin E2

    13,14-dihydro-15-keto PGE2

    13,14-dihydro-15-keto Prostaglandin E2 (13,14-dihydro-15-keto PGE2) is the primary metabolite of PGE2 in plasma.

     13,14-dihydro-15-keto Prostaglandin E2 Chemical Structure
  46. GC41436 13,14-dihydro-15-keto Prostaglandin F1α

    13,14dihydro15keto PGF1α

     13,14-dihydro-15-keto Prostaglandin F1α (13,14-dihydro-15-keto PGF1α) is a metabolite of PGF1α that has been reported in the rat stomach. 13,14-dihydro-15-keto Prostaglandin F1α Chemical Structure
  47. GC40579 13,14-dihydro-15-keto Prostaglandin F2α

    13,14dihydro15keto PGF2α, PGFM

     13,14-dihydro-15-keto Prostaglandin F2α (13,14-dihydro-15-keto PGF2α) is the first prominent plasma metabolite of PGF2α in the 15-hydroxy PGDH pathway. 13,14-dihydro-15-keto Prostaglandin F2α Chemical Structure
  48. GC40625 13,14-dihydro-15-keto-tetranor Prostaglandin D2 A common metabolic pathway for several prostaglandins (PGs), including PGD2, involves the reduction of the double bond between C-13 and C-14 and oxidation of the hydroxyl group at C-15, producing 13,14-dihydro-15-keto PGs. 13,14-dihydro-15-keto-tetranor Prostaglandin D2 Chemical Structure
  49. GC40626 13,14-dihydro-15-keto-tetranor Prostaglandin E2

    13,14-dihydro-15-keto-tetranor PGE2

     A common metabolic pathway for several prostaglandins (PG), including PGE2, involves the reduction of the double bond between C-13 and C-14 and oxidation of the hydroxyl group at C-15, producing 13,14-dihydro-15-keto PGs. 13,14-dihydro-15-keto-tetranor Prostaglandin E2 Chemical Structure
  50. GC41903 13,14-dihydro-15-keto-tetranor Prostaglandin F1α

    5β, 7αdihydroxy11ketotetranorProstanoic Acid, 9β13,14dihydro15ketotetranor Prostaglandin F1α, 9β,11αdihydroxy15oxo2,3,4,5tetranorProstanoic Acid

     The metabolism of F series prostaglandins (PGs), including PGF1α and PGF2α, commonly begins with the reduction of the double bond between C-13 and C-14 and oxidation of the hydroxyl group at C-15, producing 13,14-dihydro-15-keto PGs. 13,14-dihydro-15-keto-tetranor Prostaglandin F1α Chemical Structure
  51. GC41904 13,14-dihydro-15-keto-tetranor Prostaglandin F1β

    5β, 7αdihydroxy11ketotetranorProstanoic Acid, 9β13,14dihydro15ketotetranor Prostaglandin F1α, 9β,11αdihydroxy15oxo2,3,4,5tetranorProstanoic Acid

     13,14-dihydro-15-keto tetranor-Prostaglandin F1β is a major urinary metabolite of PGE2 that is excreted in guinea pig urine at a concentration range of 1.34-2.74 μg/kg. 13,14-dihydro-15-keto-tetranor Prostaglandin F1β Chemical Structure
  52. GC41905 13,14-dihydro-16,16-difluoro Prostaglandin E1

    15hydroxy Lubiprostone

     Prostaglandin E1 (PGE1) is produced by the metabolism of dihomo-γ-linolenic acid (DGLA) by the cyclooxygenase pathway. 13,14-dihydro-16,16-difluoro Prostaglandin E1 Chemical Structure
  53. GC41472 15(R),19(R)-hydroxy Prostaglandin E2

    15(R),19(R)hydroxy PGE2

     19(R)-Hydroxylated prostaglandins occur in μg/ml concentrations in the semen of certain mammalian species, especially primates. 15(R),19(R)-hydroxy Prostaglandin E2 Chemical Structure
  54. GC40532 15(R),19(R)-hydroxy Prostaglandin F2α

    15(R),19(R)hydroxy PGF2α

     19(R)-Hydroxylated prostaglandins (PGs) occur in μg/ml concentrations in the semen of certain mammalian species, especially primates. 15(R),19(R)-hydroxy Prostaglandin F2α Chemical Structure
  55. GC41921 15(R)-15-methyl Prostaglandin A2

    15(R)15methyl PGA2

     Arbaprostil (15(R)-15-methyl prostaglandin E2) is a synthetic prostaglandin E2 (PGE2) analog developed for its cytoprotective activity. 15(R)-15-methyl Prostaglandin A2 Chemical Structure
  56. GC41164 15(R)-15-methyl Prostaglandin D2

    15(R)15methyl PGD2

     15(R)-15-methyl Prostaglandin D2 (15(R)-15-methyl PGD2) is a metabolically stable synthetic analog of PGD2. 15(R)-15-methyl Prostaglandin D2 Chemical Structure
  57. GC41165 15(R)-15-methyl Prostaglandin E2

    Arbaprostil, 15(R)15methyl PGE2

     15(R)-15-methyl Prostaglandin E2 (15(R)-15-methyl PGE2) is a prodrug for the potent PGE2 analog 15(S)-15-methyl PGE2. 15(R)-15-methyl Prostaglandin E2 Chemical Structure
  58. GC41440 15(R)-15-methyl Prostaglandin F2α

    15(R)15methyl PGF2α

     15(R)-15-methyl PGF2α is a metabolically stable analog of PGF2α. 15(R)-15-methyl Prostaglandin F2α Chemical Structure
  59. GC41244 15(R)-15-methyl Prostaglandin F2α methyl ester

    15(R)-Methyl carboprost, 15(R)15methyl PGF2α methyl ester

     15(R)-15-methyl Prostaglandin F2α methyl ester (15(R)-15-methyl PGF2α methyl ester) is a lipid soluble prodrug form of 15(R)-15-methyl PGF2α with increased membrane permeability. 15(R)-15-methyl Prostaglandin F2α methyl ester Chemical Structure
  60. GC40988 15(R)-17-phenyl trinor Prostaglandin F2α

    15epi Bimatoprost (free acid), 15(R)Bimatoprost (free acid), 15(R)17phenyl trinor PGF2α

     17-phenyl trinor Prostaglandin F2α N-ethyl amide (17-phenyl trinor PGF2α) is an F-series prostaglandin analog which has been approved for use as an ocular hypotensive drug, sold under the Allergan trade name 17-phenyl trinor PGF2α ethyl amide. 15(R)-17-phenyl trinor Prostaglandin F2α Chemical Structure
  61. GC40648 15(R)-17-phenyl trinor Prostaglandin F2α ethyl amide

    15(R)Bimatoprost, 15(R)17phenyl trinor PGF2α ethyl amide

     15(R)-17-phenyl trinor Prostaglandin F2α ethyl amide (15(R)-17-phenyl trinor PGF2α ethyl amide) is an isomer of bimatoprost, characterized by an inverted (β) hydroxyl group at C-15. 15(R)-17-phenyl trinor Prostaglandin F2α ethyl amide Chemical Structure
  62. GC41922 15(R)-17-phenyl trinor Prostaglandin F2α isopropyl ester

    15epi Bimatoprost isopropyl ester, 15(R)Bimatoprost isopropyl ester, 15(R)17phenyl trinor PGF2α isopropyl ester

     15(R)-17-phenyl trinor Prostaglandin F2α isopropyl ester (15(R)-17-phenyl trinor PGF2α isopropyl ester) is the latanoprost-related isomer containing both a double bond at 13,14 and an inverted (β) hydroxyl group at C-15. 15(R)-17-phenyl trinor Prostaglandin F2α isopropyl ester Chemical Structure
  63. GC41416 15(R)-Prostaglandin D2

    15(R)PGD2

     Many of the effects of prostaglandin D2 (PGD2) are transduced via a traditional 7-transmembrane GPCR, the DP1 receptor. 15(R)-Prostaglandin D2 Chemical Structure
  64. GC41417 15(R)-Prostaglandin E2

    15(R)PGE2, 15epi PGE2

     15(R)-Prostaglandin E2 (15(R)-PGE2) is the C-15 epimer of the naturally occurring 15(S)-PGE2. 15(R)-Prostaglandin E2 Chemical Structure
  65. GC46439 15(R)-Prostaglandin F1α

    15(R)-PGF1α, 15-epi PGF1α

     The C-15 epimer of PGF1α 15(R)-Prostaglandin F1α Chemical Structure
  66. GC40581 15(R)-Prostaglandin F2α

    15epi PGF2α

     15(R)-PGF2α is the C-15 epimer of the naturally occurring mammalian autacoid PGF2α. 15(R)-Prostaglandin F2α Chemical Structure
  67. GC41166 15(S)-15-methyl Prostaglandin D2

    15(S)15methyl PGD2

     15(S)-15-methyl Prostaglandin D2 (15(S)-15-methyl PGD2) is a metabolically stable synthetic analog of PGD2. 15(S)-15-methyl Prostaglandin D2 Chemical Structure
  68. GC18767 15(S)-15-methyl Prostaglandin E1

    15(S)15methyl PGE1

     15(S)-15-methyl Prostaglandin E1 (15(S)-15-methyl PGE1) is a metabolically stable synthetic analog of PGE1 . 15(S)-15-methyl Prostaglandin E1 Chemical Structure
  69. GC41167 15(S)-15-methyl Prostaglandin E2

    15(S)15methyl PGE2

     15(S)-15-methyl PGE2 is a potent, metabolically stable analog of PGE2. 15(S)-15-methyl Prostaglandin E2 Chemical Structure
  70. GC41924 15(S)-15-methyl Prostaglandin F2α isopropyl ester

    15(S)15methyl PGF2α isopropyl ester

     15(S)-15-methyl Prostaglandin F2α (15(S)-15-methyl PGF2α) has been shown to have potent uterine stimulant and abortifacient properties when administered intramuscularly to induce labor. 15(S)-15-methyl Prostaglandin F2α isopropyl ester Chemical Structure
  71. GC18372 15(S)-15-methyl Prostaglandin F2α methyl ester

    Methyl carboprost, 15(S)15methyl PGF2α methyl ester, U36384

     15(S)-15-methyl PGF2α methyl ester is a derivative of 15(S)-15-methyl PGF2α with increased membrane permeability. 15(S)-15-methyl Prostaglandin F2α methyl ester Chemical Structure
  72. GC41226 15(S)-acetate Prostaglandin A2 methyl ester

    15-acetyl PGA2 methyl ester, 15S-O-acetyl-PGA2 methyl ester, 15S-PGA2 methyl ester, 15-acetate

     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
  73. GC40283 15(S)-Fluprostenol (+)-15(R)-Fluprostenol isopropyl ester is a prodrug (Travoprost) which is converted by esterase enzymatic activity in the cornea to yield the corresponding free acid. 15(S)-Fluprostenol Chemical Structure
  74. GC41589 15(S)-Fluprostenol isopropyl ester

    15(S)FluIpr

     15(S)-Fluprostenol isopropyl ester (15(S)-Flu-Ipr) is the unnatural C-15 epimer of Travoprost. 15(S)-Fluprostenol isopropyl ester Chemical Structure
  75. GC41093 15(S)-Latanoprost

    15epi Latanoprost

     15(S)-Latanoprost is an analog of latanoprost in which the hydroxyl at carbon 15 is inverted relative to latanoprost. 15(S)-Latanoprost Chemical Structure
  76. GC49036 15-(6-nitroxyhexanoyl)-17-phenyl trinor Prostaglandin F2α

    15-(6-nitroxyhexanoyl)-17-phenyl trinor PGF2α, 15-(6-nitroxyhexanoyl)-Bimatoprost, NCX 470

     A nitric oxide-donating derivative of 17-phenyl trinor prostaglandin F2α 15-(6-nitroxyhexanoyl)-17-phenyl trinor Prostaglandin F2α Chemical Structure
  77. GC41168 15-cyclohexyl pentanor Prostaglandin F2α

    15cyclohexyl pentanor PGF2α

     15-cyclohexyl pentanor PGF2α is an analog of PGF2α with resistance to 15-hydroxy PGDH metabolism. 15-cyclohexyl pentanor Prostaglandin F2α Chemical Structure
  78. GC40375 15-deoxy-δ12,14-Prostaglandin A1

    15deoxyΔ12,14PGA1

     15-deoxy-δ12,14-Prostaglandin A1 (15-deoxy-δ12,14-PGA1) is a synthetic PGA1 analog. 15-deoxy-δ12,14-Prostaglandin A1 Chemical Structure
  79. GC40350 15-deoxy-δ12,14-Prostaglandin A2

    15deoxyΔ12,14PGA2

     15-deoxy-δ12,14-PGA2 is a synthetic analog of PGA2. 15-deoxy-δ12,14-Prostaglandin A2 Chemical Structure
  80. 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
  81. GC41125 15-epi Prostaglandin A1

    15epi PGA1

     15-epi PGA1 is the 15(R) stereoisomer of PGA1. 15-epi Prostaglandin A1 Chemical Structure
  82. GC41931 15-keto Cloprostenol isopropyl ester 15-keto Cloprostenol isopropyl ester is a potential impurity found in commercial cloprostenol isopropyl ester preparations. 15-keto Cloprostenol isopropyl ester Chemical Structure
  83. GC41933 15-keto Fluprostenol isopropyl ester

    15keto Travoprost

     15-케토 플루프로스테놀 이소프로필 에스테르(15-케토 플루프로스테놀 이소프로필 에스테르)는 트라보프로스트의 대사 산물입니다. 15-keto Fluprostenol isopropyl ester Chemical Structure
  84. GC41934 15-keto Latanoprost 15-Keto latanoprost는 안구 혈압 강하제인 Latanoprost의 대사 산물입니다. 15-keto Latanoprost Chemical Structure
  85. GC40989 15-keto Latanoprost (free acid) 15-keto Latanoprost is a potential metabolite of latanoprost when administered to animals. 15-keto Latanoprost (free acid) Chemical Structure
  86. GC41103 15-keto Prostaglandin A1

    15keto PGA1

     Prostaglandin A1 (PGA1) was first isolated as a dehydration product of the PGE1 compounds found in human semen. 15-keto Prostaglandin A1 Chemical Structure
  87. GC18320 15-keto Prostaglandin E1

    15keto PGE1

     15-keto PGE1 is the inactive metabolite of PGE1 produced by 15-hydroxy PGDH. 15-keto Prostaglandin E1 Chemical Structure
  88. GC40605 15-keto Prostaglandin E2

    15-keto PGE2

    15-keto Prostaglandin E2 (15-keto PGE2) is a metabolite of PGE2 formed by 15-hydroxy PGDH.

     15-keto Prostaglandin E2 Chemical Structure
  89. GC40582 15-keto Prostaglandin F1α

    15-keto PGF1α

     15-keto PGF1α is the initial metabolite of PGF1α via 15-hydroxy PGDH. 15-keto Prostaglandin F1α Chemical Structure
  90. GC41418 15-keto Prostaglandin F2α

    15-keto PGF2α

    15-keto Prostaglandin F2α (15-keto PGF2α) is the first metabolite of PGF2α.

     15-keto Prostaglandin F2α Chemical Structure
  91. GC41936 15-keto-17-phenyl trinor Prostaglandin F2α

    15keto17phenyl trinor PGF2α

     Bimatoprost is an F-series prostaglandin (PG) analog which has been approved for use as an ocular hypotensive drug. 15-keto-17-phenyl trinor Prostaglandin F2α Chemical Structure
  92. GC41159 16,16-dimethyl Prostaglandin D2

    16,16dimethyl PGD2

     16,16-dimethyl PGD2 is a metabolically stable synthetic analog of PGD2. 16,16-dimethyl Prostaglandin D2 Chemical Structure
  93. GC18777 16,16-dimethyl Prostaglandin E1

    16,16dimethyl PGE1

     16,16-dimethyl PGE1 is a metabolically stable synthetic analog of PGE1. 16,16-dimethyl Prostaglandin E1 Chemical Structure
  94. GC41943 16,16-dimethyl Prostaglandin E2 p-(p-acetamidobenzamido) phenyl ester

    16,16dimethyl PGE2 4(4acetamidobenzamido) phenyl ester

     The p-(p-acetamidobenzamido) phenyl ester is a crystalline derivative of 16,16-dimethyl PGE2 and a potential prodrug. 16,16-dimethyl Prostaglandin E2 p-(p-acetamidobenzamido) phenyl ester Chemical Structure
  95. GC18774 16,16-dimethyl Prostaglandin F2α

    16,16dimethyl PGF2α

     16,16-dimethyl PGF2α is a metabolically stable analog of PGF2α. 16,16-dimethyl Prostaglandin F2α Chemical Structure
  96. GC18803 16,16-dimethyl Prostaglandin F2β

    9β,16,16dimethyl PGF2α, 16,16dimethyl PGF2β

     16,16-dimethyl PGF2β is a metabolically stable analog of PGF2β. 16,16-dimethyl Prostaglandin F2β Chemical Structure
  97. GC40762 16-phenoxy Prostaglandin F2α ethyl amide

    16phenoxy PGF2α ethyl amide

     Prostaglandin F2α (PGF2α), acting through the FP receptor, causes smooth muscle contraction and exhibits potent luteolytic activity. 16-phenoxy Prostaglandin F2α ethyl amide Chemical Structure
  98. GC18785 16-phenoxy tetranor Prostaglandin A2

    16phenoxy tetranor PGA2

     16-phenoxy tetranor PGA2 is a minor metabolite found in human plasma after intravenous administration of sulprostone. 16-phenoxy tetranor Prostaglandin A2 Chemical Structure
  99. GC41447 16-phenoxy tetranor Prostaglandin E2

    16phenoxy tetranor PGE2

     16-phenoxy tetranor PGE2 is the free acid form of sulprostone formed by the hydrolysis of the methylsulfonamide bond. 16-phenoxy tetranor Prostaglandin E2 Chemical Structure
  100. GC41946 16-phenoxy tetranor Prostaglandin F2α

    16phenoxy tetranor PGF2α

     16-phenoxy PGF2α is a metabolically stable analog of PGF2α. 16-phenoxy tetranor Prostaglandin F2α Chemical Structure
  101. GC41947 16-phenoxy tetranor Prostaglandin F2α cyclopropyl methyl amide

    16phenoxy tetranor PGF2α cyclopropyl methyl amide

     The actions of many clinical F-series prostaglandins (PGs), including those used for estrous synchronization and for reduction of intraocular pressure (IOP), are mediated through the PGF2α (FP) receptor. 16-phenoxy tetranor Prostaglandin F2α cyclopropyl methyl amide Chemical Structure

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