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Compound Detail

CHEMBL2059316

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O=C1COc2ccccc2N1CCCN1CCC(n2c(=O)[nH]c3ncccc32)CC1

Basic Information

ChEMBL ID CHEMBL2059316
Phase Preclinical
Structure Type MOL
InChI Key GQELUVZMNVVOHX-UHFFFAOYSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

407.5
MW (Da)
2.18
ALogP
6
HBA
1
HBD
83.5
PSA (Ų)
0.70
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H25N5O3
MW 407.47
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness -1.46

Activity Summary

IC50 1 meas. best 4.66
Ki 1 meas. best 6.19

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
D(2) dopamine receptor
CHEMBL217
Ki 6.19 6.19 650.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.66 4.66 22000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22677319 10.1016/j.bmcl.2012.05.048 Muscarinic acetylcholine receptor M1 2
22677319 10.1016/j.bmcl.2012.05.048 Liver microsomes 1
22677319 10.1016/j.bmcl.2012.05.048 Voltage-gated inwardly rectifying potassium channel KCNH2 1
22677319 10.1016/j.bmcl.2012.05.048 D(2) dopamine receptor 1

Data from ChEMBL 36 via Core Engine