55028-72-3
55028-72-3
Chemical Structure
Cloprostenol sodium salt
Synonym(s): ICI 80996 sodium salt
- CAS No.: 55028-72-3
- Formula:C22H28ClNaO6
- Molecular Weight:446.90
IUPAC Name: sodium (Z)-7-((1S,2S,3S,5R)-2-((S,E)-4-(3-chlorophenoxy)-3-hydroxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl)hept-5-enoate
InChIKey: IFEJLMHZNQJGQU-CAXRJTGMSA-M
SMILES: O=C(O[Na])CCC/C=C\C[C@H]1[C@H](/C=C/[C@H](O)COC2=CC=CC(Cl)=C2)[C@@H](O)C[C@H]1O
Biological Activity: Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent[1], and is a PGF2α receptor agonist[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Cloprostenol sodium salt | 99.84% | Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent, and is a PGF2α receptor agonist. | ||||||||||||||||||||
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Cloprostenol sodium salt (Standard) | ≥98% | Cloprostenol sodium salt (Standard) is the analytical standard of Cloprostenol sodium salt. This product is intended for research and analytical applications. Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent, and is a PGF2α receptor agonist. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 1.00
HY-107381A(+)-Cloprostenol sodium -
Similarity Score 0.92
HY-134009(+)-Cloprostenol methyl ester -
Similarity Score 0.91
HY-107381(+)-Cloprostenol -
Similarity Score 0.91
HY-120955(+)-5-trans Cloprostenol -
Similarity Score 0.91
HY-120982(+)-15-epi Cloprostenol -
Similarity Score 0.91
HY-121314Cloprostenol -
Similarity Score 0.89
HY-100571Cloprostenol isopropyl ester -
Similarity Score 0.80
HY-11852016-Phenoxy tetranor prostaglandin F2α methyl ester -
Similarity Score 0.78
HY-13906316-Phenoxy tetranor prostaglandin F2α -
Explore the MedChemAI to find more analogs
References
- [1]. Salazar H, et al. Luteolytic effects of a prostaglandin analogue, cloprostenol (ICI 80,996), in rats: ultrastructural and biochemical observations. Biol Reprod. 1976 May;14(4):458-72. [Content Brief]
- [2]. Pastel E, et al. Aldose reductases influence prostaglandin F2α levels and adipocyte differentiation in male mouse and human species. Endocrinology. 2015 May;156(5):1671-84. [Content Brief]
