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Compound Detail

CHEMBL4166645

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O=C1C=CC2(C=C1)C(c1ccccc1)=CC(=O)N2C(C(=O)NC1CCCCC1)c1ccc(Cl)cc1

Basic Information

ChEMBL ID CHEMBL4166645
Phase Preclinical
Structure Type MOL
InChI Key VXBVYHBHIVARRK-UHFFFAOYSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

487.0
MW (Da)
5.19
ALogP
3
HBA
1
HBD
66.5
PSA (Ų)
0.63
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H27ClN2O3
MW 487.00
Aromatic Rings 2
Heavy Atoms 35
NP-Likeness -0.19

Activity Summary

EC50 2 meas. best 6.98

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
EC50 6.98 6.98 104.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
29704723 10.1016/j.ejmech.2018.04.020 Histamine H3 receptor 4
29704723 10.1016/j.ejmech.2018.04.020 5-hydroxytryptamine receptor 2C 2
29704723 10.1016/j.ejmech.2018.04.020 Histamine H1 receptor 2
29704723 10.1016/j.ejmech.2018.04.020 Histamine H2 receptor 2
29704723 10.1016/j.ejmech.2018.04.020 Histamine H4 receptor 2
29704723 10.1016/j.ejmech.2018.04.020 Luciferin 4-monooxygenase 1
29704723 10.1016/j.ejmech.2018.04.020 HEK-293T 1
29704723 10.1016/j.ejmech.2018.04.020 No relevant target 1

Data from ChEMBL 36 via Core Engine