(+)-<wbr/>Cloprostenol methyl amide

(+)-Cloprostenol methyl amide

CAT N°: 10010495
Price:

From 108.00 91.80

(+)-Cloprostenol is a synthetic analog of prostaglandin F2? (PGF2?). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters. It is 200 times and 100 times more potent than PGF2? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2?.{1182} Cloprostenol is also used in veterinary medicine as a luteolytic agent for the induction of estrus and the treatment of reproductive disorders in cattle, swine, and horses. (+)-Cloprostenol is a synthetic analog of prostaglandin F2? (PGF2?). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters. It is 200 times and 100 times more potent than PGF2? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2?.{1182} Cloprostenol is also used in veterinary medicine as a luteolytic agent for the induction of estrus and the treatment of reproductive disorders in cattle, swine, and horses. (+)-Cloprostenol methyl amide is a more lipid soluble form of (+)-cloprostenol. Amides of PGs may serve as prodrugs, under the condition they are hydrolyzed appropriately in certain tissues to generate the bioactive free acid.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • (+)-9?,11?,15R-trihydroxy-16-(3-chlorophenoxy)-17,18,19,20-tetranor-prosta-5Z,13E-dien-1-oic acid, methyl amide
  • Correlated keywords
    • analogs prosgaglandins PGs F2? PGF2? PGF2a PGF2alpha PGF2.alpha. F2a F2alpha F2.alpha. luteolytic luteolysis pregnancy abortion abortifacient estrus lipophilic synthetic FP agonist potent veterinary medicine vets agents treatments reporductiove disorders lipids free acids prodrugs pro-drugs pro drugs hydrolyzed tissues bioactive
  • Product Overview:
    (+)-Cloprostenol is a synthetic analog of prostaglandin F2? (PGF2?). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters. It is 200 times and 100 times more potent than PGF2? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2?.{1182} Cloprostenol is also used in veterinary medicine as a luteolytic agent for the induction of estrus and the treatment of reproductive disorders in cattle, swine, and horses. (+)-Cloprostenol is a synthetic analog of prostaglandin F2? (PGF2?). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters. It is 200 times and 100 times more potent than PGF2? in terminating pregnancy in hamsters and rats, respectively, without the side effects associated with PGF2?.{1182} Cloprostenol is also used in veterinary medicine as a luteolytic agent for the induction of estrus and the treatment of reproductive disorders in cattle, swine, and horses. (+)-Cloprostenol methyl amide is a more lipid soluble form of (+)-cloprostenol. Amides of PGs may serve as prodrugs, under the condition they are hydrolyzed appropriately in certain tissues to generate the bioactive free acid.

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