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1 References  














Zinterol






تۆرکجه
فارسی
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From Wikipedia, the free encyclopedia
 


Zinterol
Names
IUPAC name

N-[5-[2-[(1,1-dimethyl-2-phenylethyl)amino]-1-hydroxyethyl]-2-hydroxyphenyl]methanesulfonamide

Identifiers

CAS Number

3D model (JSmol)

ChEMBL
ChemSpider
ECHA InfoCard 100.189.867 Edit this at Wikidata

IUPHAR/BPS

MeSH Zinterol

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C19H26N2O4S/c1-19(2,12-14-7-5-4-6-8-14)20-13-18(23)15-9-10-17(22)16(11-15)21-26(3,24)25/h4-11,18,20-23H,12-13H2,1-3H3 checkY

    Key: XJBCFFLVLOPYBV-UHFFFAOYSA-N checkY

  • InChI=1/C19H26N2O4S/c1-19(2,12-14-7-5-4-6-8-14)20-13-18(23)15-9-10-17(22)16(11-15)21-26(3,24)25/h4-11,18,20-23H,12-13H2,1-3H3

    Key: XJBCFFLVLOPYBV-UHFFFAOYAI

  • O=S(=O)(Nc1cc(ccc1O)C(O)CNC(C)(C)Cc2ccccc2)C

Properties

Chemical formula

C19H26N2O4S
Molar mass 378.49 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Zinterol is a beta-adrenergic agonist.[1]

Its structure is based on soterenol (antiarrhythmic) and phentermine.

References[edit]

  1. ^ Heubach JF, Graf EM, Molenaar P, et al. (May 2001). "Murine ventricular L-type Ca2+ current is enhanced by zinterol via β1-adrenoceptors, and is reduced in TG4 mice overexpressing the human β2-adrenoceptor". Br. J. Pharmacol. 133 (1): 73–82. doi:10.1038/sj.bjp.0704045. PMC 1572761. PMID 11325796.


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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Zinterol&oldid=900196357"

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    This page was last edited on 4 June 2019, at 02:12 (UTC).

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