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Compound Detail

CHEMBL1944689

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O=c1[nH]c2c(O)ccc([C@@H](O)CNCCc3ccc(CNCCc4c(Cl)cccc4Cl)cc3)c2s1

Basic Information

ChEMBL ID CHEMBL1944689
Phase Preclinical
Structure Type MOL
InChI Key GVRKTUGZYSOYMQ-QHCPKHFHSA-N
4
Targets
5
Activities
2
Assay Types
0
PK Parameters
9
Publications
0
Known Names

Molecular Properties

532.5
MW (Da)
4.80
ALogP
6
HBA
5
HBD
97.4
PSA (Ų)
0.18
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H27Cl2N3O3S
MW 532.49
Aromatic Rings 4
Heavy Atoms 35
NP-Likeness -0.46

Activity Summary

IC50 4 meas. best 8.4
EC50 1 meas. best 9.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Beta-2 adrenergic receptor
CHEMBL210
EC50 9.5 9.5 0.3 1
Beta-2 adrenergic receptor
CHEMBL210
IC50 8.4 8.4 4.0 1
Alpha-1D adrenergic receptor
CHEMBL223
IC50 7.1 7.1 79.4 1
Beta-1 adrenergic receptor
CHEMBL213
IC50 6.4 6.4 398.1 1
D(2) dopamine receptor
CHEMBL217
IC50 6.0 6.0 1000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22079756 10.1016/j.bmcl.2011.10.049 Beta-2 adrenergic receptor 3
22079756 10.1016/j.bmcl.2011.10.049 Beta-1 adrenergic receptor 1
22079756 10.1016/j.bmcl.2011.10.049 Alpha-1D adrenergic receptor 1
22079756 10.1016/j.bmcl.2011.10.049 D(2) dopamine receptor 1
22079756 10.1016/j.bmcl.2011.10.049 Voltage-gated inwardly rectifying potassium channel KCNH2 1
22079756 10.1016/j.bmcl.2011.10.049 Cytochrome P450 2D6 1
22079756 10.1016/j.bmcl.2011.10.049 Cytochrome P450 3A4 1
22079756 10.1016/j.bmcl.2011.10.049 No relevant target 1
- 10.6019/CHEMBL3301361 No relevant target 1

Data from ChEMBL 36 via Core Engine