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Compound Detail

CHEMBL5593156

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O=c1[nH]c2c(N3CCN(CCCc4c[nH]c5ccc(Cl)cc45)CC3)cccc2n1Cc1ccccc1

Basic Information

ChEMBL ID CHEMBL5593156
Phase Preclinical
Structure Type MOL
InChI Key LJIZVKWBEVEPDS-UHFFFAOYSA-N
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

500.1
MW (Da)
5.27
ALogP
4
HBA
2
HBD
60.1
PSA (Ų)
0.32
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H30ClN5O
MW 500.05
Aromatic Rings 5
Heavy Atoms 36
NP-Likeness -1.13

Activity Summary

Ki 2 meas. best 7.68
IC50 1 meas. best 5.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.68 7.2 21.0 2
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.6 5.6 2500.0 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