1-(4-METHANESULFONAMIDOPHENOXY)-3-(N-METHYL-3,4-DICHLOROPHENYLETHYLAMINO)-2-PROPANOL

CN(CCC1=CC=C(Cl)C(Cl)=C1)CC(O)COC2=CC=C(NS(C)(=O)=O)C=C2

InChIKey=BQBSHJUQVIWEFM-UHFFFAOYSA-N

InChI=1S/C19H24Cl2N2O4S/c1-23(10-9-14-3-8-18(20)19(21)11-14)12-16(24)13-27-17-6-4-15(5-7-17)22-28(2,25)26/h3-8,11,16,22,24H,9-10,12-13H2,1-2H3

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

Targets

Primary Target	Pharmacology	Condition	Potency
delayed rectifier potassium channel activity 2 Target ID: GO:0005251 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1393293	Blocker 555

Substance Class	Chemical Created by `admin` on `Tue Apr 01 16:23:08 GMT 2025` Edited by `admin` on `Tue Apr 01 16:23:08 GMT 2025`
Record UNII	RV6721I4H5
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

METHANESULFONAMIDE, N-(4-(3-((2-(3,4-DICHLOROPHENYL)ETHYL)METHYLAMINO)-2-HYDROXYPROPOXY)PHENYL)-

Preferred Name

English

1-(4-METHANESULFONAMIDOPHENOXY)-3-(N-METHYL-3,4-DICHLOROPHENYLETHYLAMINO)-2-PROPANOL

Systematic Name

English

N-(4-(3-((2-(3,4-DICHLOROPHENYL)ETHYL)METHYLAMINO)-2-HYDROXYPROPOXY)PHENYL)METHANESULFONAMIDE

Systematic Name

English

Code System Code Type Description

PUBCHEM

2129

Created by admin on Tue Apr 01 16:23:08 GMT 2025 , Edited by admin on Tue Apr 01 16:23:08 GMT 2025

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EPA CompTox

DTXSID10928009

Created by admin on Tue Apr 01 16:23:08 GMT 2025 , Edited by admin on Tue Apr 01 16:23:08 GMT 2025

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FDA UNII

RV6721I4H5

Created by admin on Tue Apr 01 16:23:08 GMT 2025 , Edited by admin on Tue Apr 01 16:23:08 GMT 2025

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CAS

133229-23-9

Created by admin on Tue Apr 01 16:23:08 GMT 2025 , Edited by admin on Tue Apr 01 16:23:08 GMT 2025

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