Basic Molecular Information

Basic Information

DICL ID
DICL_CP_0348963
PubChem CID
Molecular Formula
C15H17ClN2O2S2
Molecular Weight
356.9 g/mol
Synonyms/Alias
[746609-35-8; 5-chloro-N-(2-piperidin-1-ylphenyl)thiophene-2-sulfonamide; MLS000570381; 5-chloro-N-[2-(1-piperidinyl)phenyl]-2-thiophenesulfonamide; SMR000150436; 5-Chloro-N-(2-(piperidin-1-yl)phenyl)...
InChI Key
RXDWTDRPUXJDPY-UHFFFAOYSA-N
InChI
InChI=1S/C15H17ClN2O2S2/c16-14-8-9-15(21-14)22(19,20)17-12-6-2-3-7-13(12)18-10-4-1-5-11-18/h2-3,6-9,...
IUPAC Name
5-chloro-N-(2-piperidin-1-ylphenyl)thiophene-2-sulfonamide
CAS Number
746609-35-8

Structure Information

Chemical Structure Visualization

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

39 41 0 0 0 0 0 0 0 0999 V2000
-3.9507 1.6532 -1.5412 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5067 0.2282 -1.9481 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0361 -0.060...

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: 640 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
4.1926
Complexity
92.6435
TPSA (Ų)
49.41
H-Bond Donors
1
H-Bond Acceptors
4
Ring Count
3
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