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Aglepristone

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Aglepristone
Clinical data
Trade namesAlizin
Other namesRU-46534; RU-534; 11β-[4-(Dimethylamino)phenyl]-17β-hydroxy-17α-[(Z)-propenyl]estra-4,9-dien-3-one
Drug classAntiprogestogen;Antiglucocorticoid
ATC code
Identifiers
  • (8S,11R,13S,14S,17R)-11-[4-(dimethylamino)phenyl]-17-hydroxy-13-methyl-17-[(Z)-prop-1-enyl]-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.211.372Edit this at Wikidata
Chemical and physical data
FormulaC29H37NO2
Molar mass431.620g·mol−1
3D model (JSmol)
  • C/C=C\[C@@]1(CC[C@@H]2[C@@]1(C[C@@H](C3=C4CCC(=O)C=C4CC[C@@H]23)C5=CC=C(C=C5)N(C)C)C)O
  • InChI=1S/C29H37NO2/c1-5-15-29(32)16-14-26-24-12-8-20-17-22(31)11-13-23(20)27(24)25(18-28(26,29)2)19-6-9-21(10-7-19)30(3)4/h5-7,9-10,15,17,24-26,32H,8,11-14,16,18H2,1-4H3/b15-5-/t24-,25+,26-,28-,29-/m0/s1
  • Key:RTCKAOKDXNYXEH-FWSJOHTJSA-N

Aglepristone(INNTooltip International Nonproprietary Name) (brand nameAlizin;former developmental code namesRU-46534,RU-534) is asynthetic,steroidalantiprogestogenrelated tomifepristonewhich is marketed byVirbacin severalEuropeancountries for use inveterinary medicine.[1][2][3]It is specifically used as anabortifacientinpregnantanimals.[1][3][4]Aglepristone, similarly to mifepristone, also possesses someantiglucocorticoidactivity.[5][6]

See also

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References

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  1. ^abKaufman LK, Baldwin CJ (1 December 2013)."Pregnancy Loss in the Bitch and Queen".In Bonagura JD, Twedt DC (eds.).Kirk's Current Veterinary Therapy XV.Elsevier Health Sciences. pp. 3009–.ISBN978-0-323-22762-9.
  2. ^Squires EJ (2010)."Endocrine manipulation of reproduction.".Applied Animal Endocrinology.CABI. pp. 207–.ISBN978-1-84593-755-3.
  3. ^abPapich MC (3 November 2010)."Aglepristone".Saunders Handbook of Veterinary Drugs: Small and Large Animal.Elsevier Health Sciences. pp. 120–.ISBN978-1-4377-0192-0.
  4. ^Fieni F, Martal J, Marnet PG, Siliart B, Bernard F, Riou M, Bruyas JF, Tainturier D (2001). Concannon PW (ed.). "Hormonal variation in bitches after early or mid-pregnancy termination with aglepristone (RU534)".Journal of Reproduction and Fertility. Supplement.Advances in reproduction in dogs, cats and exotic carnivores: proceedings of the fourth International Symposium on Canine and Feline Reproduction, Oslo, Norway, 29 June-1 July 2000.57:243–8.ISBN978-0-906545-37-9.PMID11787157.
  5. ^Batista M, Reyes R, Santana M, Alamo D, Vilar J, González F, et al. (October 2011). "Induction of parturition with aglepristone in the Majorera goat".Reproduction in Domestic Animals = Zuchthygiene.46(5): 882–888.doi:10.1111/j.1439-0531.2011.01759.x.PMID21320179.
  6. ^Baan M, Taverne MA, de Gier J, Kooistra HS, Kindahl H, Dieleman SJ, Okkens AC (March 2008). "Hormonal changes in spontaneous and aglépristone-induced parturition in dogs".Theriogenology.69(4): 399–407.doi:10.1016/j.theriogenology.2007.10.008.PMID18054071.