Chemicals and Drugs

Cloprostenol

A synthetic prostaglandin F2alpha analog. The compound has luteolytic effects and is used for the synchronization of estrus in cattle.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

A synthetic prostaglandin F2alpha analog. The compound has luteolytic effects and is used for the synchronization of estrus in cattle.

Chemical Identity

Chemical Information

Molecular Formula
C22H29ClO6
Molecular Weight
424.9 g/mol
CAS Registry No.
40665-92-7
IUPAC Name
(Z)-7-[(1R,2R,3R,5S)-2-[(E,3R)-4-(3-chlorophenoxy)-3-hydroxybut-1-enyl]-3,5-dihydroxycyclopentyl]hept-5-enoic acid
InChIKey
VJGGHXVGBSZVMZ-QIZQQNKQSA-N
SMILES
C1[C@@H]([C@@H]([C@H]([C@@H]1O)/C=C/[C@H](COC2=CC(=CC=C2)Cl)O)C/C=C\CCCC(=O)O)O
MeSH Unique ID
D003008
Source
PubChem CID 5311053

MeSH Record

Classification

Narrower headings

Related Concepts

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Drug Class

Pharmacological Action

MeSH Record

Synonyms

10 entry terms
  • Cloprostenol Monosodium Salt
  • Cloprostenol Sodium
  • Estrumate
  • ICI-80,966
  • Oestrophan
  • ICI 80,966
  • ICI80,966
  • Monosodium Salt, Cloprostenol
  • Salt, Cloprostenol Monosodium
  • Sodium, Cloprostenol

MeSH Record

Aspects Covered

25 allowable subheadings

Indexed with the subheadings administration & dosage, adverse effects, agonists, analogs & derivatives, analysis, antagonists & inhibitors, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, economics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, urine.

MeSH Record

History Note

91(79); was see under PROSTAGLANDINS F, SYNTHETIC 1979-90

MeSH Record

Previous Indexing

  • Prostaglandins F (1975-1977)
  • Prostaglandins F, Synthetic (1978)

MeSH Hierarchy

Tree Numbers

AMA Style

References

  1. National Library of Medicine. Cloprostenol. Medical Subject Headings (MeSH). 2026. Unique ID D003008. http://id.nlm.nih.gov/mesh/2026/D003008
  2. Cloprostenol. In: Wikipedia. https://en.wikipedia.org/wiki/Cloprostenol
  3. Cloprostenol. In: Wikidata. https://www.wikidata.org/wiki/Q27076117
  4. Cloprostenol. In: PubChem Compound. CID 5311053. https://pubchem.ncbi.nlm.nih.gov/compound/5311053