Zinterol

Zinterol
Names
	IUPAC name N-2-(1,1-dimethyl-2-phenylethyl)amino-1-hydroxyethyl-2-hydroxyphenylmethanesulfonamide
Identifiers
CAS Number	37000-20-7 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL1243407 ;
ChemSpider	34825 ;
ECHA InfoCard	100.189.867
IUPHAR/BPS	3466;
MeSH	Zinterol
PubChem CID	37990;
UNII	7167N7AJJR ;
	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 Key: XJBCFFLVLOPYBV-UHFFFAOYSA-N ; 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). verify (what is ?) Infobox references

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

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

Referencesedit

^ 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.

This pharmacology-related article is a stub. You can help Wikipedia by expanding it.

Zdroj:https://en.wikipedia.org?pojem=Zinterol
Text je dostupný za podmienok Creative Commons Attribution/Share-Alike License 3.0 Unported; prípadne za ďalších podmienok. Podrobnejšie informácie nájdete na stránke Podmienky použitia.

[pmid11325796-1] 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.

[1]