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Compound Detail

CHEMBL1202156

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C[N+](C)(CC(=O)c1ccc(-c2ccc(C(=O)C[N+](C)(C)CC3CCCCO3)cc2)cc1)CC1CCCCO1.[Br-].[Br-]

Basic Information

ChEMBL ID CHEMBL1202156
Phase Preclinical
Structure Type MOL
InChI Key LITRVNJDVUELSA-UHFFFAOYSA-L
Parent Compound CHEMBL41975
Active Moiety CHEMBL41975
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

522.7
MW (Da)
5.01
ALogP
4
HBA
0
HBD
52.6
PSA (Ų)
0.31
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H46Br2N2O4
MW 682.54
Aromatic Rings 2
Heavy Atoms 38
NP-Likeness -0.12

Activity Summary

IC50 1 meas. best 5.16

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Acetylcholinesterase
CHEMBL4768
IC50 5.16 5.16 6900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Acetylcholinesterase IC50 = 6900.0 nM 5.16 Concentration required to inhibit hydrolytic activity of bovine erythrocyte acet... 2033583

Literature References

PubMed DOI Target Context # Activities
2033583 10.1021/jm00109a009 Mus musculus 2
2033583 10.1021/jm00109a009 Acetylcholinesterase 1

Data from ChEMBL 36 via Core Engine