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Compound Detail

CHEMBL496531

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O=C1c2cc3ccccc3n2CCN1CCCCN1CCN(c2cccc(Cl)c2Cl)CC1

Basic Information

ChEMBL ID CHEMBL496531
Phase Preclinical
Structure Type MOL
InChI Key DGKURWUVIVQHCD-UHFFFAOYSA-N
7
Targets
7
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

471.4
MW (Da)
5.01
ALogP
4
HBA
0
HBD
31.7
PSA (Ų)
0.47
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H28Cl2N4O
MW 471.43
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -1.38

Activity Summary

Ki 7 meas. best 9.98

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
D(3) dopamine receptor
CHEMBL234
Ki 9.98 9.98 0.1 1
5-hydroxytryptamine receptor 1A
CHEMBL273
Ki 8.03 8.03 9.3 1
Unchecked
CHEMBL612545
Ki 7.74 7.74 18.4 1
5-hydroxytryptamine receptor 2A
CHEMBL322
Ki 7.08 7.08 83.0 1
D(2) dopamine receptor
CHEMBL339
Ki 6.91 6.91 122.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 6.7 6.7 200.0 1
D(1A) dopamine receptor
CHEMBL265
Ki 5.36 5.36 4370.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19072656 10.1021/jm800689g Mus musculus 3
19072656 10.1021/jm800689g Voltage-gated inwardly rectifying potassium channel KCNH2 1
19072656 10.1021/jm800689g Unchecked 1
19072656 10.1021/jm800689g 5-hydroxytryptamine receptor 2A 1
19072656 10.1021/jm800689g 5-hydroxytryptamine receptor 1A 1
19072656 10.1021/jm800689g D(3) dopamine receptor 1
19072656 10.1021/jm800689g D(2) dopamine receptor 1
19072656 10.1021/jm800689g D(1A) dopamine receptor 1

Data from ChEMBL 36 via Core Engine