Dinoprost

• CAT Number: I004046
• CAS Number: 551-11-1
• Molecular Formula: C20H34O5
• Molecular Weight: 354.50
• Purity: ≥95%
• Synonyms: Dinoprost;PGF2α
• Solubility: 10 mM in water
• Storage: Store at -20°C
• IUPAC Name: (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]cyclopentyl]hept-5-enoic acid
• InChI: InChI=1S/C20H34O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-19,21-23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1
• InChIKey: PXGPLTODNUVGFL-YNNPMVKQSA-N
• SMILES: CCCCC[C@@H](/C=C/[C@H]1[C@@H](C[C@@H]([C@@H]1C/C=C\CCCC(=O)O)O)O)O

Dinoprost (Cat No.:I004046) is a naturally occurring prostaglandin used in veterinary and reproductive medicine. It induces uterine contractions and is primarily employed to manage reproductive functions, including estrus synchronization, luteolysis, and the induction of labor or abortion in livestock. Dinoprost mimics the natural hormone’s role in regulating the estrous cycle, enhancing fertility control in breeding programs. Additionally, it is used in certain medical conditions requiring uterine evacuation. Its reliable action on smooth muscles makes it an essential tool in animal reproductive health management.

Reference

[1]. Sharma I, et al. Role of 8-iso-prostaglandin F2alpha and 25-hydroxycholesterol in the pathophysiology of endometriosis. Fertil Steril. 2010 Jun;94(1):63-70.

[2]. Coulthard G, et al. Stereocontrolled organocatalytic synthesis of prostaglandin PGF2α in seven steps. Nature. 2012 Sep 13;489(7415):278-81.