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Compound Detail

CHEMBL5542534

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O=C(c1ccc(CNC[C@H](O)c2ccc(O)c3[nH]c(=O)ccc23)cc1)N1CC(COc2cccc([C@](O)(C(=O)OCC3CCN(Cc4ccccc4)CC3)c3ccccc3)c2)C1

Basic Information

ChEMBL ID CHEMBL5542534
Phase Preclinical
Structure Type MOL
InChI Key WXPDLMCIWWALOY-DYSCKZRXSA-N
2
Targets
2
Activities
1
Assay Types
3
PK Parameters
3
Publications
0
Known Names

Molecular Properties

837.0
MW (Da)
5.90
ALogP
10
HBA
5
HBD
164.7
PSA (Ų)
0.07
QED
2
Ro5 Violations
16
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C50H52N4O8
MW 836.99
Aromatic Rings 6
Heavy Atoms 62
NP-Likeness -0.62

Activity Summary

Ki 2 meas. best 9.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Beta-2 adrenergic receptor
CHEMBL210
Ki 9.0 9.0 1.0 1
Muscarinic acetylcholine receptor M3
CHEMBL245
Ki 8.9 8.9 1.3 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 2.5 hr Homo sapiens
T1/2 0.8333 hr Rattus norvegicus
T1/2 0.3167 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