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Compound Detail

CHEMBL258251

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N#CCN(CC(=O)N1CCCC(c2ccccc2)C1CN1CCOCC1)c1ccc(Cl)c(Cl)c1

Basic Information

ChEMBL ID CHEMBL258251
Phase Preclinical
Structure Type MOL
InChI Key BFPVIFSFUVSFRI-UHFFFAOYSA-N
5
Targets
5
Activities
3
Assay Types
4
PK Parameters
6
Publications
0
Known Names

Molecular Properties

501.5
MW (Da)
4.43
ALogP
5
HBA
0
HBD
59.8
PSA (Ų)
0.53
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H30Cl2N4O2
MW 501.46
Aromatic Rings 2
Heavy Atoms 34
NP-Likeness -1.28

Activity Summary

IC50 2 meas. best 6.31
Ki 2 meas. best 8.22
EC50 1 meas. best 5.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Urotensin-2 receptor
CHEMBL3764
Ki 8.22 8.22 6.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 6.31 6.31 490.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.43 5.43 3700.0 1
Unchecked
CHEMBL612545
Ki 5.4 5.4 4000.0 1
Kappa-type opioid receptor
CHEMBL237
EC50 5.3 5.3 5000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 60.0 mL.min-1.kg-1 Rattus norvegicus
Cmax 737.85 nM Rattus norvegicus
F 7.0 % Rattus norvegicus
T1/2 2.6 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18502123 10.1016/j.bmcl.2008.05.027 Rattus norvegicus 5
18502123 10.1016/j.bmcl.2008.05.027 Urotensin-2 receptor 1
18502123 10.1016/j.bmcl.2008.05.027 Cytochrome P450 2D6 1
18502123 10.1016/j.bmcl.2008.05.027 Cytochrome P450 3A4 1
18502123 10.1016/j.bmcl.2008.05.027 Kappa-type opioid receptor 1
18502123 10.1016/j.bmcl.2008.05.027 Unchecked 1

Data from ChEMBL 36 via Core Engine