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Compound Detail

CHEMBL551613

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O=C(c1ccc(C2=CC3(CCNCC3)Oc3ccccc32)cc1)N1Cc2ccccc2C1

Basic Information

ChEMBL ID CHEMBL551613
Phase Preclinical
Structure Type MOL
InChI Key VWPKIYFLRDRFNX-UHFFFAOYSA-N
5
Targets
6
Activities
3
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

422.5
MW (Da)
4.79
ALogP
3
HBA
1
HBD
41.6
PSA (Ų)
0.65
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H26N2O2
MW 422.53
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -0.14

Activity Summary

Ki 3 meas. best 9.28
IC50 2 meas. best 5.75
EC50 1 meas. best 7.35

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Delta-type opioid receptor
CHEMBL236
Ki 9.28 9.28 0.5 1
Delta-type opioid receptor
CHEMBL236
EC50 7.35 7.35 45.0 1
Mu-type opioid receptor
CHEMBL233
Ki 6.35 6.35 450.0 1
Kappa-type opioid receptor
CHEMBL237
Ki 6.05 6.05 890.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.75 5.75 1800.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.46 5.46 3501.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19694468 10.1021/jm900773n Delta-type opioid receptor 2
19694468 10.1021/jm900773n Mu-type opioid receptor 1
19694468 10.1021/jm900773n Kappa-type opioid receptor 1
19694468 10.1021/jm900773n Voltage-gated inwardly rectifying potassium channel KCNH2 1
19694468 10.1021/jm900773n Cytochrome P450 2D6 1

Data from ChEMBL 36 via Core Engine