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Compound Detail

CHEMBL1947157

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O=c1[nH]c2c(O)ccc([C@@H](O)CNCCc3cccc(CNCCc4c(Cl)cccc4Cl)c3)c2s1

Basic Information

ChEMBL ID CHEMBL1947157
Phase Preclinical
Structure Type MOL
InChI Key MCZWBSFGGNTCLH-QHCPKHFHSA-N
4
Targets
5
Activities
2
Assay Types
3
PK Parameters
10
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 -0.44

Activity Summary

IC50 4 meas. best 9.7
EC50 1 meas. best 9.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Beta-2 adrenergic receptor
CHEMBL210
IC50 9.7 9.7 0.2 1
Beta-2 adrenergic receptor
CHEMBL210
EC50 9.3 9.3 0.5 1
Beta-1 adrenergic receptor
CHEMBL213
IC50 7.9 7.9 12.6 1
Alpha-1D adrenergic receptor
CHEMBL223
IC50 7.2 7.2 63.1 1
D(2) dopamine receptor
CHEMBL217
IC50 6.6 6.6 251.2 1

Pharmacokinetic Data

Parameter Value Units Species
CL 5.17 uL.min-1.(10^6cells)-1 Homo sapiens
CL 63.0 mL.min-1.g-1 Homo sapiens
CL 78.0 uL.min-1.(10^6cells)-1 Rattus norvegicus

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
- 10.6019/CHEMBL3301361 ADMET 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