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Compound Detail

CHEMBL1645237

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CC1(C)[C@H](C(=O)[O-])N2C(=O)[C@@H]([C@@H](O)C(=O)N3CCCC3)[C@H]2S1(=O)=O.[Na+]

Basic Information

ChEMBL ID CHEMBL1645237
Phase Preclinical
Structure Type MOL
InChI Key XORTYTOHXGCONF-GHRKWLBTSA-M
Parent Compound CHEMBL1741067
Active Moiety CHEMBL1741067
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

360.4
MW (Da)
-1.59
ALogP
6
HBA
2
HBD
132.3
PSA (Ų)
0.58
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H19N2NaO7S
MW 382.37
Aromatic Rings 0
Heavy Atoms 24
NP-Likeness 0.08

Activity Summary

IC50 2 meas. best 6.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.8 6.775 160.0 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 160.0 nM 6.8 Inhibition of beta-lactamase PDC-3 21129961
Unchecked IC50 = 180.0 nM 6.75 Inhibition of beta-lactamase TEM-1 21129961

Literature References

PubMed DOI Target Context # Activities
21129961 10.1016/j.bmcl.2010.10.134 Unchecked 2

Data from ChEMBL 36 via Core Engine