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Compound Detail

CHEMBL215319

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CNC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C

Basic Information

ChEMBL ID CHEMBL215319
Phase Preclinical
Structure Type MOL
InChI Key MPTVYBQTBOJQJK-AGQYDFLVSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

431.5
MW (Da)
2.57
ALogP
7
HBA
1
HBD
111.9
PSA (Ų)
0.73
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 C23H29NO7
MW 431.49
Aromatic Rings 1
Heavy Atoms 31
NP-Likeness 2.73

Activity Summary

Ki 1 meas. best 5.86

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Kappa-type opioid receptor
CHEMBL237
Ki 5.86 5.86 1392.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Kappa-type opioid receptor Ki = 1392.0 nM 5.86 Inhibition of [3H]diprenorphine binding to human KOR expressed in CHO cells 16777411

Literature References

PubMed DOI Target Context # Activities
16777411 10.1016/j.bmcl.2006.05.093 Kappa-type opioid receptor 3

Data from ChEMBL 36 via Core Engine