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Urapidil Референце Литература Spoljašnje veze Мени за навигацију34661-75​-1WHO56395437A78GF17HJS„The mechanism of the sympathoinhibitory action of urapidil: role of 5-HT1A receptors”1917978185513022894410.1016/0014-2999(79)90018-9609738010.1111/j.1440-1681.1984.tb00289.x298402310.1016/0014-2999(85)90725-31702490ууу

Фенолни етриПиперазиниПиримидини


simpatolitičkiantihipertenzivnilekantagonistα1-adrenergičkog receptoraα2-adrenergičkog receptoraantagonistaα1-adrenergičkog receptoraβ1-adrenoceptoruFDAEvropiMVASanathucalvhutlfizrazvnocosyvacongtumrsysieponprocC3C4C5C9










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Urapidil




Из Википедије, слободне енциклопедије






Иди на навигацију
Иди на претрагу





















Urapidil
Urapidil Structural Formulae V.1.svg

IUPAC ime
6-(3-[4-(2-methoxyphenyl)piperazin-1-yl]propylamino)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
Klinički podaci
Način primeneOralno
Pravni status
Pravni status

  • ℞ (Prescription only)

Identifikatori
CAS broj
34661-75​-1 ДаY
64887-14-5 (HCl)
ATC kod
C02CA06 (WHO)
PubChemCID 5639
ChemSpider5437
UNII
A78GF17HJS ДаY
Hemijski podaci
Formula
C20H29N5O3
Molarna masa387,48 g·mol−1



Urapidil je simpatolitički antihipertenzivni lek. On deluje kao antagonist α1-adrenergičkog receptora i agonist 5-HT1A receptora[1] Mada je jedan inicijalni izveštaj izneo da je urapidil takođe agonist α2-adrenergičkog receptora,[2] to nije potvrđeno u kasnijim studijama.[3] Za razliku od drugih antagonista α1-adrenergičkog receptora, urapidil ne izaziva refleks tahikardije, što može da bude posledica njegove slabe antagonističke aktivnosti na β1-adrenoceptoru,[4][5] kao i usled njegovog uticaja na srčani vagalni disk.[6] Urapidil trenutno nije odobren od strane FDA, ali je dostupan u Evropi.



Референце




  1. ^ Ramage AG (1991). „The mechanism of the sympathoinhibitory action of urapidil: role of 5-HT1A receptors”. Br. J. Pharmacol. 102 (4): 998—1002. PMC 1917978 Слободан приступ. PMID 1855130. 


  2. ^ Eltze M (1979). „Investigations on the mode of action of a new antihypertensive drug, urapidil, in the isolated vas deferens”. Eur. J. Pharmacol. 59 (1-2): 1—9. PMID 228944. doi:10.1016/0014-2999(79)90018-9. 


  3. ^ Verberne AJ, Rand MJ (1984). „Pharmacological activities of the antihypertensive drug urapidil in the rat”. Clin. Exp. Pharmacol. Physiol. 11: 407—412. PMID 6097380. doi:10.1111/j.1440-1681.1984.tb00289.x. 


  4. ^ Schoetensack W, Bruckschen EG, Zech K (1983). Urapidil. New Drugs Annual: Cardiovascular Drugs. стр. 19. 


  5. ^ Verberne AJ, Rand MJ (1985). „Effect of urapidil on β-adrenoceptors of rat atria”. Eur. J. Pharmacol. 108 (2): 193—196. PMID 2984023. doi:10.1016/0014-2999(85)90725-3. 


  6. ^ Ramage AG (1990). „Influence of 5-HT1A receptor agonists on sympathetic and parasympathetic nerve activity”. J. Cardiovasc. Pharmacol. 15: S75—S85. PMID 1702490. 



Литература



  • Schoetensack W, Bruckschen EG, Zech K (1983). Urapidil. New Drugs Annual: Cardiovascular Drugs. стр. 19. 


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