Basic Molecular Information

Basic Information

DICL ID
DICL_CP_0340507
PubChem CID
Molecular Formula
C16H20N2O2S2
Molecular Weight
336.482 g/mol
Synonyms/Alias
[MK6-83; 1062271-24-2; 5-methyl-N-(2-(piperidin-1-yl)phenyl)thiophene-2-sulfonamide; RE9JUR6NT4; 5-Methyl-N-[2-(1-piperidinyl)phenyl]-2-thiophenesulfonamide; 5-Methyl-N-(2-(1-piperidinyl)phenyl)-2-thi...
InChI Key
IRGYSXZCDAWOOC-UHFFFAOYSA-N
InChI
InChI=1S/C16H20N2O2S2/c1-13-9-10-16(21-13)22(19,20)17-14-7-3-4-8-15(14)18-11-5-2-6-12-18/h3-4,7-10,1...
IUPAC Name
5-methyl-N-(2-piperidin-1-ylphenyl)thiophene-2-sulfonamide
CAS Number
1062271-24-2

Structure Information

Chemical Structure Visualization

SMILES Notation
2D Molecular Drawing
Carbon (C)
Hydrogen (H)
Oxygen (O)
Nitrogen (N)
Sulfur (S)
SDF

42 44 0 0 0 0 0 0 0 0999 V2000
4.1115 -4.0147 -0.4066 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5428 -2.6766 -0.7398 C 0 0 0 0 0 0 0 0 0 0 0 0
2.4799 -2.441...

Experimental Data

Activity Data

Target Ion Channel
Transient receptor potential channel mucolipin 1 F465L
Uniprot Accession Number
Function
Activator
Species
Homo sapiens (Human)
IC50
N/A (Not available)
EC50
EC50: 100 nM
Ki
N/A (Not available)
Kd
N/A (Not available)
Inhibition
N/A (Not available)

Experimental Conditions

pH
pH 7.4
Holding Potential
−200 to 100 mV mV
Temperature
Room Temperature
Test Method
Patch-clamping
Test Species
HEK293 cell (Homo sapiens embryonic kidney 293 cell)

Binding Information

Binding Site
Extracellular domain
Binding Site Residue
F408Δ, F465L

Disease Information

Related Disease
Not specified

References

URL
N/A (Not available)
PMID
Patent
N/A (Not available)

Computed Properties

Heavy Atom Count
22
Rotatable Bonds
4
logP
3.8476
Complexity
92.3705
TPSA (Ų)
49.41
H-Bond Donors
1
H-Bond Acceptors
4
Ring Count
3
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