Basic Molecular Information

Basic Information

DICL ID
DICL_CP_0326558
PubChem CID
Molecular Formula
C18H21N3O
Molecular Weight
295.386 g/mol
Synonyms/Alias
[CHEMBL432826; BDBM50081750; 1-[4-(1H-Imidazol-4-yl)-but-3-ynyl]-4-phenyl-piperidin-4-ol]
InChI Key
TWXXVWZCUMLSMF-UHFFFAOYSA-N
InChI
InChI=1S/C18H21N3O/c22-18(16-6-2-1-3-7-16)9-12-21(13-10-18)11-5-4-8-17-14-19-15-20-17/h1-3,6-7,14-15...
IUPAC Name
1-[4-(1H-imidazol-5-yl)but-3-ynyl]-4-phenylpiperidin-4-ol
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

43 45 0 0 0 0 0 0 0 0999 V2000
-1.8733 0.6871 -0.8890 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3720 0.9358 -0.6946 C 0 0 0 0 0 0 0 0 0 0 0 0
0.2674 -0.227...

Experimental Data

Activity Data

Target Ion Channel
Glutamate receptor ionotropic subunit NMDA 1 subunit 3A
Uniprot Accession Number
Function
Antagonist
Species
Homo sapiens (Human)
IC50
IC50: 8400 nM
EC50
N/A (Not available)
Ki
N/A (Not available)
Kd
N/A (Not available)
Inhibition
N/A (Not available)

Experimental Conditions

pH
pH 7.4
Holding Potential
−70 mV mV
Temperature
Room Temperature
Test Method
Patch-clamping
Test Species
Xenopus laevis oocyte

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
3
logP
2.1349
Complexity
86.0955
TPSA (Ų)
52.15
H-Bond Donors
2
H-Bond Acceptors
3
Ring Count
3
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