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Compound Detail

CHEMBL3288092

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C=C(C)[C@@H]1CC[C@@]2(C)[C@H]1[C@H]1CC[C@@H]3[C@@]4(C)CC[C@H](OC(=O)CCCCC(=O)O)C(C)(C)[C@@H]4CC[C@@]3(C)[C@]1(C)C[C@@H]2OC(=O)CCCCC(=O)O

Basic Information

ChEMBL ID CHEMBL3288092
Phase Preclinical
Structure Type MOL
InChI Key WFDSSHLGLSSCAL-RNMYOVDNSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

699.0
MW (Da)
9.39
ALogP
6
HBA
2
HBD
127.2
PSA (Ų)
0.11
QED
2
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H66O8
MW 698.98
Aromatic Rings 0
Heavy Atoms 50
NP-Likeness 1.95

Activity Summary

IC50 1 meas. best 4.09

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cholinesterase
CHEMBL5763
IC50 4.09 4.09 80600.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cholinesterase IC50 = 80600.0 nM 4.09 Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate a... 24835788

Literature References

PubMed DOI Target Context # Activities
24835788 10.1016/j.bmc.2014.04.050 Acetylcholinesterase 2
24835788 10.1016/j.bmc.2014.04.050 Cholinesterase 2
24835788 10.1016/j.bmc.2014.04.050 Unchecked 1

Data from ChEMBL 36 via Core Engine