Basic Molecular Information

Basic Information

DICL ID
DICL_CP_0316733
PubChem CID
Molecular Formula
C13H16N4O
Molecular Weight
244.298 g/mol
Synonyms/Alias
[CHEMBL598045; SCHEMBL4698915; BDBM50309870; 4-Oxazolo[5;4-c]pyridin-2-yl-1;4-diazabicyclo[3.2.2]nonane]
InChI Key
AJMDHGFXFDUETC-UHFFFAOYSA-N
InChI
InChI=1S/C13H16N4O/c1-4-14-9-12-11(1)15-13(18-12)17-8-7-16-5-2-10(17)3-6-16/h1,4,9-10H,2-3,5-8H2
IUPAC Name
2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-[1,3]oxazolo[5,4-c]pyridine
CAS Number
N/A (Not available)

Structure Information

Chemical Structure Visualization

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

34 37 0 0 0 0 0 0 0 0999 V2000
-1.2683 -1.6858 0.7040 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.3872 -1.7044 -0.3592 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.0259 -0.385...

Experimental Data

Activity Data

Target Ion Channel
5-hydroxytryptamine receptor 3A
Uniprot Accession Number
Function
Antagonist
Species
Mus musculus (Mouse)
IC50
N/A (Not available)
EC50
N/A (Not available)
Ki
Ki: 162 nM
Kd
N/A (Not available)
Inhibition
N/A (Not available)

Experimental Conditions

pH
pH 7.4
Holding Potential
Not specified
Temperature
37 °C
Test Method
Binding assay ([3H] LY-278584)
Test Species
HEK293 cell (Homo sapiens embryonic kidney 293 cell)

Binding Information

Binding Site
extracellular domain
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
18
Rotatable Bonds
1
logP
1.5072
Complexity
68.612
TPSA (Ų)
45.4
H-Bond Donors
0
H-Bond Acceptors
5
Ring Count
5
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