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Compound Detail

CHEMBL2059381

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O=C1/C(=C/c2ccc(F)cc2)C[C@@]2(O)[C@H]3Cc4ccc(O)c5c4[C@@]2(CCN3CC2CC2)[C@H]1O5

Basic Information

ChEMBL ID CHEMBL2059381
Phase Preclinical
Structure Type MOL
InChI Key AWAQOPSDMCQZAA-PMDSDZCYSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
7
Publications
0
Known Names

Molecular Properties

447.5
MW (Da)
3.36
ALogP
5
HBA
2
HBD
70.0
PSA (Ų)
0.71
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H26FNO4
MW 447.51
Aromatic Rings 2
Heavy Atoms 33
NP-Likeness 0.83

Activity Summary

Ki 3 meas. best 7.68
IC50 1 meas. best 4.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Mu-type opioid receptor
CHEMBL233
Ki 7.68 7.68 20.9 1
Delta-type opioid receptor
CHEMBL236
Ki 7.46 7.46 34.5 1
Kappa-type opioid receptor
CHEMBL237
Ki 6.97 6.97 108.0 1
Trichomonas vaginalis
CHEMBL612884
IC50 4.89 4.89 12800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22818080 10.1016/j.bmcl.2012.06.085 Glutathione reductase, putative 3
28662966 10.1016/j.bmc.2017.06.026 Trichomonas vaginalis 2
22818080 10.1016/j.bmcl.2012.06.085 Plasmodium chabaudi 1
26099536 10.1016/j.bmcl.2015.06.002 Trichomonas vaginalis 1
28662966 10.1016/j.bmc.2017.06.026 Mu-type opioid receptor 1
28662966 10.1016/j.bmc.2017.06.026 Delta-type opioid receptor 1
28662966 10.1016/j.bmc.2017.06.026 Kappa-type opioid receptor 1

Data from ChEMBL 36 via Core Engine