Cloprostenol

Cloprostenol
Clinical data
Trade names	Cyclomate, Estrumate
Routes of; administration	Intramuscular
ATCvet code	QG02AD90(WHO);
Pharmacokineticdata
Excretion	67%renal,25%fecal
Identifiers
	IUPAC name (5Z)-7-{(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-Chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl}-5-heptenoic acid;
CAS Number	40665-92-7;
PubChemCID	5311053;
ChemSpider	4470590;
UNII	4208238832;
CompTox Dashboard(EPA)	DTXSID50860575 DTXSID7048372, DTXSID50860575;
ECHA InfoCard	100.050.009
Chemical and physical data
Formula	C22H29ClO6
Molar mass	424.915
3D model (JSmol)	Interactive image;
	SMILES 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;
	InChI 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;

Cloprostenolis a synthetic analogue ofprostaglandin F_2α(PGF_2α).^[1]It is a potent luteolytic agent; this means that, within hours of administration, it causes thecorpus luteumto stop production ofprogesterone,and to reduce in size over several days.^[1]This effect is used in animals to induceestrusand to cause abortion.^[2]

References[edit]

^^a ^bCooper M (January 1981). "Prostaglandins in veterinary practice".In Practice.3(1): 30, 32–4.doi:10.1136/inpract.3.1.30.PMID 7346485.S2CID 6197103.
^Plumb DC (2015). "Cloprostenol Sodium".Plumb's Veterinary Drug Handbook(8th ed.). Wiley.ISBN 9781118911938.

Thisveterinary medicine–related article is astub.You can help Wikipedia byexpanding it.

[Cooper_1981-1] Cooper M (January 1981). "Prostaglandins in veterinary practice".In Practice.3(1): 30, 32–4.doi:10.1136/inpract.3.1.30.PMID 7346485.S2CID 6197103.

[Plumb_2015-2] Plumb DC (2015). "Cloprostenol Sodium".Plumb's Veterinary Drug Handbook(8th ed.). Wiley.ISBN 9781118911938.

[1]

[2]