Hydroxytertatolol

Hydroxytertatolol
Clinical data
Other names	4-Hydroxytertatolol
ATC code	None;
Identifiers
	IUPAC name 8-{2-Hydroxy-3-[(2-methyl-2-propanyl)amino]propoxy}-4-thiochromanol;
CAS Number	111897-93-9 ;
PubChem CID	163871 ;
ChemSpider	143721 ;
UNII	RKM76FBC3F ;
CompTox Dashboard (EPA)	DTXSID70920605 ;
Chemical and physical data
Formula	C16H25NO3S
Molar mass	311.44 g·mol−1
3D model (JSmol)	Interactive image ;
	SMILES OC(CNC(C)(C)C)COc2cccc1c2SCCC1O;
	InChI InChI=1S/C16H25NO3S/c1-16(2,3)17-9-11(18)10-20-14-6-4-5-12-13(19)7-8-21-15(12)14/h4-6,11,13,17-19H,7-10H2,1-3H3; Key:RVGKVEPDZHPSBE-UHFFFAOYSA-N;

Last updated January 03, 2026

Hydroxytertatolol is a beta blocker.^[1]^[2] It is a derivative of tertatolol.

References

↑ Lave T, Efthymiopoulos C, Christmann D, Koffel JC, Jung L (1995). "Determination of 4-Hydroxytertatolol Stereoisomers in Rat and Human Urine by High-Performance Liquid Chromatography". Journal of Liquid Chromatography. 18 (14): 2801–2812. doi:10.1080/10826079508009325.
↑ Bastian G, Urien S, Brée F, Jolliet P, Rocher I, Crambes O, Tillement JP (1992). "Stereoselective binding of tertatolol and of 4-hydroxytertatolol to human plasma proteins". European Journal of Drug Metabolism and Pharmacokinetics. 17 (3): 233–236. doi:10.1007/bf03190151. PMID 1362702. S2CID 28632918.

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[1] Lave T, Efthymiopoulos C, Christmann D, Koffel JC, Jung L (1995). "Determination of 4-Hydroxytertatolol Stereoisomers in Rat and Human Urine by High-Performance Liquid Chromatography". Journal of Liquid Chromatography. 18 (14): 2801–2812. doi:10.1080/10826079508009325.

[2] Bastian G, Urien S, Brée F, Jolliet P, Rocher I, Crambes O, Tillement JP (1992). "Stereoselective binding of tertatolol and of 4-hydroxytertatolol to human plasma proteins". European Journal of Drug Metabolism and Pharmacokinetics. 17 (3): 233–236. doi:10.1007/bf03190151. PMID 1362702. S2CID 28632918.

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