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'''Amosulalol''' ([[International Nonproprietary Name|INN]]) is an anti-hypertensive drug. It has much higher affinity for alpha-1 adrenergic receptors than for beta adrenergic receptors.<ref>{{cite book |title=Pharmacology of Antihypertensive Therapeutics |url=https://archive.org/details/pharmacologyofan0093unse |url-access=registration |date=1990 |publisher=Springer |pages=[https://archive.org/details/pharmacologyofan0093unse/page/180 180]-183}}</ref>
'''Amosulalol''' ([[International Nonproprietary Name|INN]]) is an anti-hypertensive drug. It has much higher affinity for alpha-1 adrenergic receptors than for beta adrenergic receptors.<ref>{{cite book | vauthors = Sponer G, Bartsch W, Hooper RG | chapter = Drugs acting on multiple receptors: β-blockers with additional properties. | title = Pharmacology of antihypertensive therapeutics | date = 1990 | pages = 131–226 (183) | publisher = Springer | location = Berlin, Heidelberg | series = Handbook of Experimental Pharmacology | volume = 93 | doi = 10.1007/978-3-642-74209-5_5 | isbn = 978-3-642-74209-5 | chapter-url = https://archive.org/details/pharmacologyofan0093unse }}</ref>


It is not approved for use in the United States.
It is not approved for use in the United States.

Revision as of 07:44, 2 March 2021

Amosulalol
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • (RS)-5-[1-hydroxy-2-[2-(2-methoxyphenoxy)ethylamino]ethyl]-2-methylbenzenesulfonamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC18H24N2O5S
Molar mass380.46 g·mol−1
3D model (JSmol)
  • CC1=C(C=C(C=C1)C(CNCCOC2=CC=CC=C2OC)O)S(=O)(=O)N
  • InChI=1S/C18H24N2O5S/c1-13-7-8-14(11-18(13)26(19,22)23)15(21)12-20-9-10-25-17-6-4-3-5-16(17)24-2/h3-8,11,15,20-21H,9-10,12H2,1-2H3,(H2,19,22,23) checkY
  • Key:LVEXHFZHOIWIIP-UHFFFAOYSA-N checkY
  (verify)

Amosulalol (INN) is an anti-hypertensive drug. It has much higher affinity for alpha-1 adrenergic receptors than for beta adrenergic receptors.[1]

It is not approved for use in the United States.

References

  1. ^ Sponer G, Bartsch W, Hooper RG (1990). "Drugs acting on multiple receptors: β-blockers with additional properties.". Pharmacology of antihypertensive therapeutics. Handbook of Experimental Pharmacology. Vol. 93. Berlin, Heidelberg: Springer. pp. 131–226 (183). doi:10.1007/978-3-642-74209-5_5. ISBN 978-3-642-74209-5.