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Compound Detail

CHEMBL5556694

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COc1cc(C(=O)N2CCC(c3cccc([C@](O)(C(=O)OCC4CCN(Cc5ccccc5)CC4)c4ccccc4)c3)CC2)ccc1CNC[C@H](O)c1ccc(O)c2[nH]c(=O)ccc12

Basic Information

ChEMBL ID CHEMBL5556694
Phase Preclinical
Structure Type MOL
InChI Key PXFIGAQEXLTGJY-ZSXPQNSQSA-N
2
Targets
2
Activities
1
Assay Types
3
PK Parameters
3
Publications
0
Known Names

Molecular Properties

865.0
MW (Da)
6.78
ALogP
10
HBA
5
HBD
164.7
PSA (Ų)
0.07
QED
2
Ro5 Violations
15
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C52H56N4O8
MW 865.04
Aromatic Rings 6
Heavy Atoms 64
NP-Likeness -0.55

Activity Summary

Ki 2 meas. best 9.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Beta-2 adrenergic receptor
CHEMBL210
Ki 9.3 9.3 0.5 1
Muscarinic acetylcholine receptor M3
CHEMBL245
Ki 9.2 9.2 0.6 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 2.5 hr Homo sapiens
T1/2 2.5 hr Rattus norvegicus
T1/2 0.5833 hr Cavia porcellus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
38857426 10.1021/acs.jmedchem.4c00298 ADMET 5
38857426 10.1021/acs.jmedchem.4c00298 Muscarinic acetylcholine receptor M3 2
38857426 10.1021/acs.jmedchem.4c00298 Beta-2 adrenergic receptor 2

Data from ChEMBL 36 via Core Engine