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Details

Stereochemistry RACEMIC
Molecular Formula C14H23NO4S
Molecular Weight 301.402
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFONTEROL

SMILES

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

InChI

InChIKey=RTLJQOLVPIGICL-UHFFFAOYSA-N
InChI=1S/C14H23NO4S/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

HIDE SMILES / InChI

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 ( + / - )

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

Approval Year

PubMed

PubMed

TitleDatePubMed
Adrenergic agents. 3. Synthesis and adrenergic activity of some catecholamine analogs bearing a substituted sulfonyl or sulfonylalkyl group in the meta position.
1975 Jul
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:52:59 GMT 2023
Edited
by admin
on Sat Dec 16 17:52:59 GMT 2023
Record UNII
Z540ZT2MI6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFONTEROL
INN  
INN  
Official Name English
.ALPHA.-(((1,1-DIMETHYLETHYL)AMINO)METHYL)-4-HYDROXY-3-((METHYLSULFONYL)METHYL)BENZENEMETHANOL
Common Name English
sulfonterol [INN]
Common Name English
BENZENEMETHANOL, .ALPHA.-(((1,1-DIMETHYLETHYL)AMINO)METHYL)-4-HYDROXY-3-((METHYLSULFONYL)METHYL)-
Systematic Name English
.ALPHA.-((TERT-BUTYLAMINO)METHYL)-4-HYDROXY-3-((METHYLSULFONYL)METHYL)BENZYL ALCOHOL
Systematic Name English
SK&F-53705A FREE BASE
Code English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
Code System Code Type Description
CAS
93913-97-4
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
SUPERSEDED
ChEMBL
CHEMBL2110716
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
CAS
42461-79-0
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
EVMPD
SUB10741MIG
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
INN
3608
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
MESH
C028820
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID10866098
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
FDA UNII
Z540ZT2MI6
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
PUBCHEM
170373
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
NCI_THESAURUS
C76549
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
SMS_ID
100000083786
Created by admin on Sat Dec 16 17:53:00 GMT 2023 , Edited by admin on Sat Dec 16 17:53:00 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY