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Compound Detail

CHEMBL2059579

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CC(C)N(C)CC(O)CN1[C@@H]2CC[C@H]1C[C@@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2

Basic Information

ChEMBL ID CHEMBL2059579
Phase Preclinical
Structure Type MOL
InChI Key BGFSEKYXUQKOMR-CWNQJQRUSA-N
1
Targets
2
Activities
2
Assay Types
1
PK Parameters
5
Publications
0
Known Names

Molecular Properties

441.6
MW (Da)
3.04
ALogP
6
HBA
2
HBD
73.6
PSA (Ų)
0.66
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H39N5O2
MW 441.62
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -1.24

Activity Summary

EC50 1 meas. best 8.3
Ki 1 meas. best 8.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 4
CHEMBL1875
Ki 8.4 8.4 4.0 1
5-hydroxytryptamine receptor 4
CHEMBL1875
EC50 8.3 8.3 5.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.5 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22683222 10.1016/j.bmcl.2012.05.034 5-hydroxytryptamine receptor 4 3
22683222 10.1016/j.bmcl.2012.05.034 Unchecked 1
22683222 10.1016/j.bmcl.2012.05.034 Voltage-gated inwardly rectifying potassium channel KCNH2 1
22683222 10.1016/j.bmcl.2012.05.034 Liver microsomes 1
22683222 10.1016/j.bmcl.2012.05.034 Caco-2 1

Data from ChEMBL 36 via Core Engine