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Compound Detail

CHEMBL1921916

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C[C@@](C(=O)O[C@H]1C[N+]2(CCCc3ccccc3)CCC1CC2)(c1ccccc1)N1CCCCC1

Basic Information

ChEMBL ID CHEMBL1921916
Phase Preclinical
Structure Type MOL
InChI Key OZXJKDPJLLASGG-GFDKVKMOSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

461.7
MW (Da)
5.17
ALogP
3
HBA
0
HBD
29.5
PSA (Ų)
0.40
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H41N2O2+
MW 461.67
Aromatic Rings 2
Heavy Atoms 34
NP-Likeness 0.11

Activity Summary

Kd 1 meas. best 9.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Kd 9.8 9.8 0.2 1

Pharmacokinetic Data

Parameter Value Units Species
CL 86.0 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 = 0.1585 nM 9.8 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