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Compound Detail

CHEMBL5594446

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Cc1c(OCc2ccccc2)cccc1N1CCN(CCCc2c[nH]c3ccc(Cl)cc23)CC1

Basic Information

ChEMBL ID CHEMBL5594446
Phase Preclinical
Structure Type MOL
InChI Key YVRGVXHJDRBTTR-UHFFFAOYSA-N
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

474.1
MW (Da)
6.46
ALogP
3
HBA
1
HBD
31.5
PSA (Ų)
0.32
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H32ClN3O
MW 474.05
Aromatic Rings 4
Heavy Atoms 34
NP-Likeness -1.06

Activity Summary

Ki 2 meas. best 7.31
IC50 1 meas. best 4.87

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.31 6.97 49.0 2
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.87 4.87 13600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
38901106 10.1016/j.ejmech.2024.116601 5-hydroxytryptamine receptor 6 4
38901106 10.1016/j.ejmech.2024.116601 Adrenergic receptor alpha-1 1
38901106 10.1016/j.ejmech.2024.116601 Histamine H1 receptor 1
38901106 10.1016/j.ejmech.2024.116601 Muscarinic acetylcholine receptor M1 1
38901106 10.1016/j.ejmech.2024.116601 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine