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Compound Detail

CHEMBL5556348

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COc1cc(CNC[C@H](O)c2ccc(O)c3[nH]c(=O)ccc23)c(Cl)cc1C(=O)NCCCOc1cccc([C@](O)(C(=O)O[C@@H]2CCCN(C)C2)c2ccccc2)c1

Basic Information

ChEMBL ID CHEMBL5556348
Phase Preclinical
Structure Type MOL
InChI Key QMXBUNNZUHZSQY-LLNIBVGPSA-N
2
Targets
2
Activities
1
Assay Types
3
PK Parameters
3
Publications
0
Known Names

Molecular Properties

799.3
MW (Da)
4.79
ALogP
11
HBA
6
HBD
182.7
PSA (Ų)
0.06
QED
3
Ro5 Violations
16
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H47ClN4O9
MW 799.32
Aromatic Rings 5
Heavy Atoms 57
NP-Likeness -0.45

Activity Summary

Ki 2 meas. best 10.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Beta-2 adrenergic receptor
CHEMBL210
Ki 10.0 10.0 0.1 1
Muscarinic acetylcholine receptor M3
CHEMBL245
Ki 9.8 9.8 0.2 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 2.5 hr Homo sapiens
T1/2 2.167 hr Rattus norvegicus
T1/2 2.5 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 1
38857426 10.1021/acs.jmedchem.4c00298 Beta-2 adrenergic receptor 1

Data from ChEMBL 36 via Core Engine