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Compound Detail

CHEMBL5594193

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O=c1[nH]c2c(N3CCN(CCc4c[nH]c5ccc(Cl)cc45)CC3)cccc2n1Cc1ccccc1

Basic Information

ChEMBL ID CHEMBL5594193
Phase Preclinical
Structure Type MOL
InChI Key RYHBOPBYJJVUMX-UHFFFAOYSA-N
3
Targets
6
Activities
2
Assay Types
2
PK Parameters
7
Publications
0
Known Names

Molecular Properties

486.0
MW (Da)
4.88
ALogP
4
HBA
2
HBD
60.1
PSA (Ų)
0.36
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H28ClN5O
MW 486.02
Aromatic Rings 5
Heavy Atoms 35
NP-Likeness -1.15

Activity Summary

IC50 4 meas. best 5.98
Ki 2 meas. best 8.1

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 8.1 7.61 8.0 2
5-hydroxytryptamine receptor 6
CHEMBL3371
IC50 5.98 5.98 1042.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.4 5.4 4000.0 1
ADMET
CHEMBL612558
IC50 4.64 4.485 23000.0 2

Pharmacokinetic Data

Parameter Value Units Species
CL 115.5 mL.min-1.g-1 Rattus norvegicus
T1/2 1.0 hr Rattus norvegicus

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 5
38901106 10.1016/j.ejmech.2024.116601 ADMET 5
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
38901106 10.1016/j.ejmech.2024.116601 No relevant target 1

Data from ChEMBL 36 via Core Engine