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Compound Detail

CHEMBL1924051

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C[C@@](C(=O)O[C@H]1C[N+]2(CCc3cccc(F)c3)CCC1CC2)(c1cccs1)N1CCCCC1

Basic Information

ChEMBL ID CHEMBL1924051
Phase Preclinical
Structure Type MOL
InChI Key MZAVVLWULQNHMR-XRFQPOIASA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

471.7
MW (Da)
4.98
ALogP
4
HBA
0
HBD
29.5
PSA (Ų)
0.42
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 C27H36FN2O2S+
MW 471.66
Aromatic Rings 2
Heavy Atoms 33
NP-Likeness -0.44

Activity Summary

Kd 1 meas. best 9.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Kd 9.6 9.6 0.3 1

Pharmacokinetic Data

Parameter Value Units Species
CL 150.0 mL.min-1.g-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Kd = 0.2512 nM 9.6 Antagonist potency at M3 receptor in Dunkin Hartley guinea pig trachea assessed ... 22047691

Literature References

PubMed DOI Target Context # Activities
22047691 10.1016/j.bmcl.2011.10.002 Unchecked 1
22047691 10.1016/j.bmcl.2011.10.002 Plasma 1
22047691 10.1016/j.bmcl.2011.10.002 Liver microsomes 1
22047691 10.1016/j.bmcl.2011.10.002 Muscarinic acetylcholine receptor M3 1

Data from ChEMBL 36 via Core Engine