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Compound Detail

CHEMBL2337985

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CC[C@@H]1NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc2ccc(O)cc2)[C@@H](C)O)CSC(=O)[C@H](CCSC)NC(=O)[C@H]([C@@H](C)CC)NC(=O)[C@H](Cc2ccccc2)NC1=O

Basic Information

ChEMBL ID CHEMBL2337985
Phase Preclinical
Structure Type MOL
InChI Key BOWAMPLNHPWOMR-XONBHBSQSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

931.1
MW (Da)
-1.25
ALogP
14
HBA
11
HBD
307.5
PSA (Ų)
0.08
QED
3
Ro5 Violations
18
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H62N8O11S2
MW 931.15
Aromatic Rings 2
Heavy Atoms 64
NP-Likeness 0.78

Activity Summary

IC50 2 meas. best 8.55

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 8.55 7.705 2.8 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 2.8 nM 8.55 Inhibition of Staphylococcus aureus AgrC2 23294220
Unchecked IC50 = 137.0 nM 6.86 Inhibition of Staphylococcus aureus AgrC1 23294220

Literature References

PubMed DOI Target Context # Activities
23294220 10.1021/jm3014635 Unchecked 2

Data from ChEMBL 36 via Core Engine