Pamatolol

Pamatolol
	200px
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other; This page is a soft redirect. Names #REDIRECTmw:Help:Magic words#Other; This page is a soft redirect.-	IUPAC name Methyl N-[2-[4-[2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]ethyl]carbamate
ChemSpider	39320
	InChI InChI=1S/C16H26N2O4/c1-12(2)18-10-14(19)11-22-15-6-4-13(5-7-15)8-9-17-16(20)21-3/h4-7,12,14,18-19H,8-11H2,1-3H3,(H,17,20); Key: UGENBJKPPGFFAT-UHFFFAOYSA-N; InChI=1/C16H26N2O4/c1-12(2)18-10-14(19)11-22-15-6-4-13(5-7-15)8-9-17-16(20)21-3/h4-7,12,14,18-19H,8-11H2,1-3H3,(H,17,20); Key: UGENBJKPPGFFAT-UHFFFAOYAH;
Jmol-3D images	Image
PubChem	Template:Chembox PubChem/format
	SMILES Template:Chembox SMILES/format;
Molar mass	Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Pamatolol is a beta adrenergic receptor antagonist.^[1]

References

^ Ban, T; Sada, S; Takahashi, Y; Sada, H; Fujita, T (1985). "Effects of para-substituted beta-adrenoceptor blocking agents and methyl-substituted phenoxypropanolamine derivatives on maximum upstroke velocity of action potential in guinea-pig papillary muscles". Naunyn-Schmiedeberg's archives of pharmacology 329 (1): 77–85. PMID 2582279. doi:10.1007/bf00695196.

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