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Compound Detail

CHEMBL255460

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O=C(Cn1c(=O)sc2ccc(Cl)cc21)N1CCCC(c2ccccc2)C1CN1CCOCC1

Basic Information

ChEMBL ID CHEMBL255460
Phase Preclinical
Structure Type MOL
InChI Key VWGHPHKDTXAJJF-UHFFFAOYSA-N
5
Targets
5
Activities
3
Assay Types
4
PK Parameters
6
Publications
0
Known Names

Molecular Properties

486.0
MW (Da)
3.82
ALogP
6
HBA
0
HBD
54.8
PSA (Ų)
0.55
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 C25H28ClN3O3S
MW 486.04
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness -1.43

Activity Summary

IC50 2 meas. best 6.17
Ki 2 meas. best 8.22
EC50 1 meas. best 5.1

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 6.17 6.17 680.0 1
Unchecked
CHEMBL612545
Ki 5.46 5.46 3500.0 1
Kappa-type opioid receptor
CHEMBL237
EC50 5.1 5.1 7900.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.1 5.1 8000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 130.0 mL.min-1.kg-1 Rattus norvegicus
Cmax 329.19 nM Rattus norvegicus
F 1.0 % Rattus norvegicus
T1/2 5.0 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