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Compound Detail

CHEMBL3582485

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NC(=O)[C@@H]1CC(=O)NCCCC[C@@H](NC(=O)[C@@H](N)Cc2ccc(O)cc2)C(=O)N[C@@H](Cc2ccc(F)cc2F)C(=O)N[C@@H](Cc2ccccc2)C(=O)N1

Basic Information

ChEMBL ID CHEMBL3582485
Phase Preclinical
Structure Type BOTH
InChI Key RQLFTSFUIHSJFS-JZVHMONDSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

735.8
MW (Da)
0.14
ALogP
8
HBA
8
HBD
234.8
PSA (Ų)
0.15
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C37H43F2N7O7
MW 735.79
Aromatic Rings 3
Heavy Atoms 53
NP-Likeness 0.16

Activity Summary

EC50 2 meas. best 8.39
IC50 2 meas. best 9.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Mu-type opioid receptor
CHEMBL270
IC50 9.16 9.16 0.7 1
Kappa-type opioid receptor
CHEMBL3952
IC50 8.49 8.49 3.3 1
Mu-type opioid receptor
CHEMBL233
EC50 8.39 8.39 4.1 1
Kappa-type opioid receptor
CHEMBL237
EC50 8.12 8.12 7.6 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
26005537 10.1021/acsmedchemlett.5b00056 Kappa-type opioid receptor 3
26005537 10.1021/acsmedchemlett.5b00056 Mu-type opioid receptor 3
26005537 10.1021/acsmedchemlett.5b00056 Delta-type opioid receptor 2
26005537 10.1021/acsmedchemlett.5b00056 Brain 1

Data from ChEMBL 36 via Core Engine