(+) -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