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Compound Detail

CHEMBL3924503

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OC[C@H]1[C@H](O)[C@@H](O)[C@@H]2CS/C(=N/CCCCCCCc3ccccc3)N12

Basic Information

ChEMBL ID CHEMBL3924503
Phase Preclinical
Structure Type MOL
InChI Key KLZLUZLAMATWIA-VTOIPPNNSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

378.5
MW (Da)
2.05
ALogP
5
HBA
3
HBD
76.3
PSA (Ų)
0.57
QED
0
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H30N2O3S
MW 378.54
Aromatic Rings 1
Heavy Atoms 26
NP-Likeness 0.42

Activity Summary

IC50 1 meas. best 6.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.0 6.0 1000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1000.0 nM 6.0 Inhibition of Penicillium decumbens alpha-L-rhamnosidase using p-nitrophenyl-gly... 27789075

Literature References

PubMed DOI Target Context # Activities
27789075 10.1016/j.bmc.2016.10.015 Unchecked 8
27789075 10.1016/j.bmc.2016.10.015 Tissue alpha-L-fucosidase 1
27789075 10.1016/j.bmc.2016.10.015 Uncharacterized protein 1
27789075 10.1016/j.bmc.2016.10.015 Beta-galactosidase 1

Data from ChEMBL 36 via Core Engine