Basic Molecular Information

Basic Information

DICL ID
DICL_CP_0325602
PubChem CID
Molecular Formula
C18H16N2O2
Molecular Weight
292.338 g/mol
Synonyms/Alias
[CHEMBL75406; MLS000728638; HMS2270L14; BDBM50101422; SMR000470814; (R)-2-(1H-indol-3-yl)-2-oxo-N-(1-phenylethyl)acetamide; 2-(1H-Indol-3-yl)-2-oxo-N-(1-phenyl-ethyl)-acetamide]
InChI Key
JCQKMELKMGOGMR-GFCCVEGCSA-N
InChI
InChI=1S/C18H16N2O2/c1-12(13-7-3-2-4-8-13)20-18(22)17(21)15-11-19-16-10-6-5-9-14(15)16/h2-12,19H,1H3...
IUPAC Name
2-(1H-indol-3-yl)-2-oxo-N-[(1R)-1-phenylethyl]acetamide
CAS Number
355022-97-8

Structure Information

Chemical Structure Visualization

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

38 40 0 0 0 0 0 0 0 0999 V2000
-3.3750 0.7888 2.7692 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5386 0.9885 1.5012 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.2661 0.420...

Experimental Data

Activity Data

Target Ion Channel
Gamma-aminobutyric acid receptor subunit alpha-1/beta-2/gamma-2
Uniprot Accession Number
Function
Antagonist
Species
Bos taurus (Bovine)
IC50
N/A (Not available)
EC50
N/A (Not available)
Ki
Ki: 1150 nM
Kd
N/A (Not available)
Inhibition
N/A (Not available)

Experimental Conditions

pH
pH 7.4
Holding Potential
Not specified
Temperature
4 °C
Test Method
Binding assay ([3H] Ro15-1788)
Test Species
Bovine cerebral cortex

Binding Information

Binding Site
Not specified
Binding Site Residue
Not specified

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
3.228
Complexity
85.6289
TPSA (Ų)
61.96
H-Bond Donors
2
H-Bond Acceptors
2
Ring Count
3
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