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Compound Detail

CHEMBL2029899

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CONC(=O)CCCN(C)C(=O)c1ccc2c(c1)c1c(n2C)CC[C@@H](C2CCOCC2)C1

Basic Information

ChEMBL ID CHEMBL2029899
Phase Preclinical
Structure Type MOL
InChI Key OOVMTVFAEVACQP-GOSISDBHSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
6
Publications
0
Known Names

Molecular Properties

441.6
MW (Da)
3.24
ALogP
5
HBA
1
HBD
72.8
PSA (Ų)
0.67
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H35N3O4
MW 441.57
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -0.69

Activity Summary

EC50 1 meas. best 6.54

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cannabinoid receptor 1
CHEMBL218
EC50 6.54 6.54 291.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 36.0 mL.min-1.g-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22607668 10.1016/j.bmcl.2012.04.128 Cannabinoid receptor 1 2
22607668 10.1016/j.bmcl.2012.04.128 Liver microsomes 1
22607668 10.1016/j.bmcl.2012.04.128 Voltage-gated inwardly rectifying potassium channel KCNH2 1
22607668 10.1016/j.bmcl.2012.04.128 No relevant target 1
22607668 10.1016/j.bmcl.2012.04.128 Caco-2 1
22607668 10.1016/j.bmcl.2012.04.128 Nucleic Acid 1

Data from ChEMBL 36 via Core Engine