SULFONTEROL HYDROCHLORIDE, (+)-

Details

Stereochemistry	UNKNOWN
Molecular Formula	C14H23NO4S.ClH
Molecular Weight	337.863
Optical Activity	( + )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of SULFONTEROL HYDROCHLORIDE, (+)-

Structure Search

SMILES

Cl.CC(C)(C)NCC(O)C1=CC=C(O)C(CS(C)(=O)=O)=C1

InChI

InChIKey=WRQNLSYJACCVQD-UHFFFAOYSA-N

InChI=1S/C14H23NO4S.ClH/c1-14(2,3)15-8-13(17)10-5-6-12(16)11(7-10)9-20(4,18)19;/h5-7,13,15-17H,8-9H2,1-4H3;1H

HIDE SMILES / InChI

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C14H23NO4S
Molecular Weight	301.402
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6109736 | https://www.ncbi.nlm.nih.gov/pubmed/239238

Sulfonterol is a benzenemethanol derivative patented by Smith Kline and French Laboratories as a bronchodilator. Sulfonterol acts as a β-adrenergic partial agonist.

Originator

Approval Year

PubMed

Title	Date	PubMed
Adrenergic agents. 3. Synthesis and adrenergic activity of some catecholamine analogs bearing a substituted sulfonyl or sulfonylalkyl group in the meta position.	1975-07	239238

Patents

Substance Class	Chemical Created by `admin` on `Tue Apr 01 16:31:39 GMT 2025` Edited by `admin` on `Tue Apr 01 16:31:39 GMT 2025`
Record UNII	6Z3D3DL7JC
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

BENZENEMETHANOL, .ALPHA.-(((1,1-DIMETHYLETHYL)AMINO)METHYL)-4-HYDROXY-3-((METHYLSULFONYL)METHYL)-, HYDROCHLORIDE, (+)-

Preferred Name

English

SULFONTEROL HYDROCHLORIDE, (+)-

Common Name

English

Code System Code Type Description

FDA UNII

6Z3D3DL7JC

Created by admin on Tue Apr 01 16:31:39 GMT 2025 , Edited by admin on Tue Apr 01 16:31:39 GMT 2025

PRIMARY

CAS

56490-85-8