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Amperozide

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Amperozide
Clinical data
ATCvet code
Identifiers
  • 4-[4,4-bis(4-fluorophenyl)butyl]-N-ethylpiperazine-1-carboxamide
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC23H29F2N3O
Molar mass401.502 g·mol−1
3D model (JSmol)
  • CCNC(=O)N1CCN(CC1)CCCC(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F
  • InChI=1S/C23H29F2N3O/c1-2-26-23(29)28-16-14-27(15-17-28)13-3-4-22(18-5-9-20(24)10-6-18)19-7-11-21(25)12-8-19/h5-12,22H,2-4,13-17H2,1H3,(H,26,29) checkY
  • Key:NNAIYOXJNVGUOM-UHFFFAOYSA-N checkY
  (verify)

Amperozide is anatypical antipsychotic of thediphenylbutylpiperazine class which acts as anantagonist at the5-HT2Areceptor.[1] It does not blockdopamine receptors as with most antipsychotic drugs,[2] but does inhibit dopamine release,[3][4] and alters the firing pattern of dopaminergic neurons.[5] It was investigated for the treatment ofschizophrenia in humans,[6] but never adopted clinically. Its main use is instead inveterinary medicine, primarily in intensively farmed pigs, for decreasing aggression and stress and thereby increasing feeding and productivity.[7][8][9]

See also

[edit]

References

[edit]
  1. ^Svartengren J, Simonsson P (1990). "Receptor binding properties of amperozide".Pharmacology & Toxicology.66 (Suppl 1):8–11.doi:10.1111/j.1600-0773.1990.tb01599.x.PMID 2154737.
  2. ^Meltzer HY, Zhang Y, Stockmeier CA (May 1992). "Effect of amperozide on rat cortical 5-HT2 and striatal and limbic dopamine D2 receptor occupancy: implications for antipsychotic action".European Journal of Pharmacology.216 (1):67–71.doi:10.1016/0014-2999(92)90210-u.PMID 1388121.
  3. ^Eriksson E (1990). "Amperozide, a putative anti-psychotic drug: uptake inhibition and release of dopamine in vitro in the rat brain".Life Sciences.47 (23):2111–7.doi:10.1016/0024-3205(90)90310-n.PMID 1979998.
  4. ^Yamamoto BK, Meltzer HY (October 1992). "The effect of the atypical antipsychotic drug, amperozide, on carrier-mediated striatal dopamine release measured in vivo".The Journal of Pharmacology and Experimental Therapeutics.263 (1):180–5.PMID 1403783.
  5. ^Grenhoff J, Tung CS, Ugedo L, Svensson TH (1990). "Effects of amperozide, a putative antipsychotic drug, on rat midbrain dopamine neurons recorded in vivo".Pharmacology & Toxicology.66 (Suppl 1):29–33.doi:10.1111/j.1600-0773.1990.tb01603.x.PMID 2304893.
  6. ^Axelsson R, Nilsson A, Christensson E, Björk A (1991). "Effects of amperozide in schizophrenia. An open study of a potent 5-HT2 receptor antagonist".Psychopharmacology.104 (3):287–92.doi:10.1007/bf02246025.PMID 1924636.S2CID 2507927.
  7. ^Kyriakis SC, Martinsson K, Olsson NG, Bjork A (1990). "Thin sow syndrome (TSS): the effect of amperozide".The British Veterinary Journal.146 (5):463–7.doi:10.1016/0007-1935(90)90036-3.PMID 2224491.
  8. ^Kyriakis SC, Olsson NG, Martinsson K, Björk AK (September 1991). "Observations on the action of amperozide: are there social influences on sow-litter productivity?".Research in Veterinary Science.51 (2):169–73.doi:10.1016/0034-5288(91)90008-C.PMID 1788479.
  9. ^Papp I, Waller C, Biro O (October 1996). "[Practical experiences in the therapy of postweaning edema disease in piglets]".Berliner und Munchener Tierarztliche Wochenschrift.109 (10):385–7.PMID 8999770.
Typical
Disputed
Atypical
Others
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenylpiperazines
Benzylpiperazines
Naphthylpiperazines
Quinolinylpiperazines
Diphenylalkylpiperazines
Pyrimidinylpiperazines
Pyridinylpiperazines
Benzo(iso)thiazolylpiperazines
Tricyclic-linked piperazines
Others/uncategorized
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