Methanesulfonamide,N-[4-[[1-[2-(6-methyl-2-pyridinyl)ethyl]-4-piperidinyl]carbonyl]phenyl]-,dihydrochloride


Chemical Name: Methanesulfonamide,N-[4-[[1-[2-(6-methyl-2-pyridinyl)ethyl]-4-piperidinyl]carbonyl]phenyl]-,dihydrochloride
CAS Number: 113559-13-0
Product Number: AG0008YW(AGN-PC-0P51DE)
Synonyms:
MDL No: MFCD00889193
Molecular Formula: C21H29Cl2N3O3S
Molecular Weight: 474.4443

Identification/Properties


Computed Properties
Molecular Weight:
474.441g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
7
Exact Mass:
473.131g/mol
Monoisotopic Mass:
473.131g/mol
Topological Polar Surface Area:
87.8A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
603
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



E-4031 is a potent and selective blocker of the rapid component of the delayed rectifier potassium current in cardiac cells. In chemical synthesis, E-4031 is often utilized as a pharmacological tool to study the role of potassium channels in various biological processes. Its ability to selectively inhibit the rapid delayed rectifier potassium current makes it a valuable compound for investigating the physiological and pathological functions of these channels. Furthermore, E-4031's specificity for the hERG channel has led to its widespread use in drug discovery and safety pharmacology studies to assess the potential cardiotoxic effects of new drug candidates.