Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL2022273

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
Clc1ccc2c(c1)N=C(N1CCN(C3CCCCC3)CC1)c1cccnc1O2

Basic Information

ChEMBL ID CHEMBL2022273
Phase Preclinical
Structure Type MOL
InChI Key VJUWCGANMBDVKL-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

396.9
MW (Da)
4.87
ALogP
5
HBA
0
HBD
41.0
PSA (Ų)
0.69
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H25ClN4O
MW 396.92
Aromatic Rings 2
Heavy Atoms 28
NP-Likeness -0.91

Activity Summary

Ki 4 meas. best 7.04

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 7.04 7.04 92.0 1
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 6.88 6.88 131.0 1
Alpha-2A adrenergic receptor
CHEMBL1867
Ki 6.38 6.38 412.0 1
D(4) dopamine receptor
CHEMBL219
Ki 6.1 6.1 798.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22268448 10.1021/jm2013419 D(4) dopamine receptor 1
22268448 10.1021/jm2013419 5-hydroxytryptamine receptor 1A 1
22268448 10.1021/jm2013419 5-hydroxytryptamine receptor 2A 1
22268448 10.1021/jm2013419 Alpha-2A adrenergic receptor 1
22268448 10.1021/jm2013419 No relevant target 1

Data from ChEMBL 36 via Core Engine