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Compound Detail

CHEMBL108374

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CCOC(=O)C1=C(c2ccccc2)N=C(C)/C(=C(/O)OCC)C1C(OC)OC

Basic Information

ChEMBL ID CHEMBL108374
Phase Preclinical
Structure Type MOL
InChI Key BPFFROYMJAEJNU-XDJHFCHBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

389.4
MW (Da)
3.48
ALogP
7
HBA
1
HBD
86.6
PSA (Ų)
0.42
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H27NO6
MW 389.45
Aromatic Rings 1
Heavy Atoms 28
NP-Likeness -0.41

Activity Summary

Ki 1 meas. best 4.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A3
CHEMBL256
Ki 4.82 4.82 15300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Adenosine receptor A3 Ki = 15300.0 nM 4.82 Binding affinity to human adenosine A3 receptor 18809334

Literature References

PubMed DOI Target Context # Activities
18809334 10.1016/j.bmc.2008.08.048 Transient receptor potential cation channel subfamily V member 1 3
18809334 10.1016/j.bmc.2008.08.048 Adenosine receptor A3 2
9703464 10.1021/jm980093j Adenosine receptor A1 1
9703464 10.1021/jm980093j Adenosine receptor A2a 1
9703464 10.1021/jm980093j Adenosine receptor A3 1
9703464 10.1021/jm980093j Unchecked 1

Data from ChEMBL 36 via Core Engine