(+) -Cloprostenol

• Description :

  (+) -Cloprostenol is a prostaglandin F2α (PGF2α) analogue, and shows selective agonistic activity at the prostaglandin receptor.

• Product Name Alternative :

  D-Cloprostenol

• UNSPSC :

  12352005

• Hazard Statement :

  H302

• Target :

  Prostaglandin Receptor

• Type :

  Reference compound

• Related Pathways :

  GPCR/G Protein

• Field of Research :

  Endocrinology

• Assay Protocol :

  https://www.medchemexpress.com/__addition__-Cloprostenol.html

• Purity :

  98.06

• Solubility :

  DMSO : 100 mg/mL (ultrasonic) |Ethanol : 50 mg/mL (ultrasonic)

• Smiles :

  OC(CCC/C=C\C[C@@H]1[C@H]([C@H](O)C[C@@H]1O)/C=C/[C@@H](O)COC2=CC(Cl)=CC=C2)=O

• Molecular Formula :

  C22H29ClO6

• Molecular Weight :

  424.92

• Precautions :

  H302

• References & Citations :

  [1]Manca R, et al. Intra-vesicle administration of D-cloprostenol for induction of abortion in mid-gestation bitches. Anim Reprod Sci. 2008 Jun;106 (1-2) :133-42. Epub 2007 Apr 21.|[2]Re G, et al. Specific binding of dl-cloprostenol and d-cloprostenol to PGF2 alpha receptors in bovine corpus luteum and myometrial cell membranes. J Vet Pharmacol Ther. 1994 Dec;17 (6) :455-8.

• Shipping Conditions :

  Room Temperature

• Storage Conditions :

  -20°C, 3 years; 4°C, 2 years (Powder)

• Scientific Category :

  Reference compound1

• Clinical Information :

  No Development Reported

• Isoform :

  FP

• CAS Number :

  [54276-21-0]