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Compound Detail

CHEMBL434900

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COC(=O)C1OC(SC2C=C[C@H]3[C@H]4Cc5ccc(OC(C)=O)c6c5[C@@]3(CCN4C)[C@H]2O6)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O

Basic Information

ChEMBL ID CHEMBL434900
Phase Preclinical
Structure Type MOL
InChI Key FDACUKQNARRBTL-CAOWVPONSA-N
1
Targets
3
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

659.7
MW (Da)
1.85
ALogP
14
HBA
0
HBD
153.2
PSA (Ų)
0.18
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H37NO12S
MW 659.71
Aromatic Rings 1
Heavy Atoms 46
NP-Likeness 1.27

Activity Summary

Ki 3 meas. best 4.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 4.0 4.0 100000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 100000.0 nM 4.0 Inhibition of [3H]DAMGO binding to Opioid receptor mu 1 15509180

Literature References

PubMed DOI Target Context # Activities
15509180 10.1021/jm049554t Unchecked 9
15509180 10.1021/jm049554t Opioid receptors; mu & delta 1
15509180 10.1021/jm049554t Opioid receptors; mu & kappa 1

Data from ChEMBL 36 via Core Engine