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Compound Detail

CHEMBL5592733

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O=S(=O)(c1ccccc1)c1c[nH]c2c(C3CCN(CCc4c[nH]c5ccc(Cl)cc45)CC3)cccc12

Basic Information

ChEMBL ID CHEMBL5592733
Phase Preclinical
Structure Type MOL
InChI Key INMUONCZNWFUBD-UHFFFAOYSA-N
2
Targets
3
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

518.1
MW (Da)
6.56
ALogP
3
HBA
2
HBD
69.0
PSA (Ų)
0.27
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H28ClN3O2S
MW 518.08
Aromatic Rings 5
Heavy Atoms 36
NP-Likeness -1.01

Activity Summary

Ki 2 meas. best 7.51
IC50 1 meas. best 5.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.51 7.155 31.0 2
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.16 5.16 7000.0 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