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Atiprosin

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Atiprosin
Clinical data
Other namesAY-28,228
Routes of
administration
Oral
ATC code
  • none
Identifiers
  • (4aR,12bS)-1-ethyl-12-methyl-4-(propan-2-yl)-1,2,3,4,4a,5,6,12b-octahydropyrazino[2',3':3,4]pyrido[1,2-a]indole
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC20H29N3
Molar mass311.473 g·mol−1
3D model (JSmol)
  • n23c1ccccc1c(c2[C@H]4N(CCN([C@@H]4CC3)C(C)C)CC)C
  • InChI=1S/C20H29N3/c1-5-21-12-13-22(14(2)3)18-10-11-23-17-9-7-6-8-16(17)15(4)19(23)20(18)21/h6-9,14,18,20H,5,10-13H2,1-4H3/t18-,20+/m1/s1 checkY
  • Key:WXNVFYIBELASJW-QUCCMNQESA-N checkY
 ☒NcheckY (what is this?)  (verify)

Atiprosin (developmental code nameAY-28,228) is anantihypertensiveagent which acts as aselectiveα1-adrenergic receptorantagonist.[1][2][3][4] It also possesses someantihistamine activity, though it is some 15-fold weaker in this regard than as analpha blocker.[3] It was never marketed.[1]

See also

[edit]

References

[edit]
  1. ^abDavid J. Triggle (1996).Dictionary of Pharmacological Agents. Boca Raton: Chapman & Hall/CRC.ISBN 0-412-46630-9.
  2. ^Jirkovsky I, Santroch G, Baudy R, Oshiro G (February 1987). "Octahydropyrazino[2',3':3,4]pyrido[1,2-a]indoles. A new class of potent antihypertensive agents".Journal of Medicinal Chemistry.30 (2):388–94.doi:10.1021/jm00385a022.PMID 3806618.
  3. ^abGrimes D, Rimele TJ, Henry DE, et al. (September 1987)."In vitro isolated tissue studies with atiprosin (AY-28,228): a new antihypertensive compound".Journal of Cardiovascular Pharmacology.10 (3):249–58.doi:10.1097/00005344-198709000-00001.PMID 2444771.S2CID 9361176.
  4. ^Oshiro G, Wojdan A, Klein M, Metcalf G (September 1987)."Antihypertensive and hypotensive actions of atiprosin (AY-28,228) in rats, dogs, and monkeys".Journal of Cardiovascular Pharmacology.10 (3):341–9.doi:10.1097/00005344-198709000-00014.PMID 2444784.S2CID 19086175.

External links

[edit]
  • Media related toAtiprosin at Wikimedia Commons
Sympatholytic (and closely related)antihypertensives (C02)
Sympatholytics
(antagonizeα-adrenergic
vasoconstriction)
Central
α2-Adrenergic receptor agonists
Adrenergic release inhibitors
Imidazoline receptor agonists
Ganglion-blocking/nicotinic antagonists
Peripheral
Indirect
Monoamine oxidase inhibitors
VMAT inhibitors
Tyrosine hydroxylase inhibitors
Direct
α1-Adrenergic receptor blockers
Non-selective α-adrenergic receptor blockers
Otherantagonists
Serotonin receptor antagonists
Endothelin receptor antagonists (forPHTooltip Pulmonary hypertension)
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
Others


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