Zinterol

Zinterol

Names
IUPAC name N-[5-[2-[(1,1-dimethyl-2-phenylethyl)amino]-1-hydroxyethyl]-2-hydroxyphenyl]methanesulfonamide
Identifiers
CAS Number	37000-20-7^N
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL1243407^N
ChemSpider	34825^Y
ECHA InfoCard	100.189.867
IUPHAR/BPS	3466
MeSH	Zinterol
PubChem CID	37990
UNII	7167N7AJJR^Y
CompTox Dashboard (EPA)	DTXSID70865845
InChI 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^Y Key: XJBCFFLVLOPYBV-UHFFFAOYSA-N^Y 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
SMILES 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 ^YN ?) Infobox references

Zinterol is a beta-adrenergic agonist.^[1]

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

References

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.