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Compound Detail

CHEMBL1807859

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C[C@H]1O[C@@H](n2cnc3c(N)nc(OC4CCCC4)nc32)[C@H](O)[C@@H]1OCc1ccc(Cl)c(Cl)c1

Basic Information

ChEMBL ID CHEMBL1807859
Phase Preclinical
Structure Type MOL
InChI Key MNVPSIWOEXVTDY-PTCKGGSZSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
5
Publications
0
Known Names

Molecular Properties

494.4
MW (Da)
3.90
ALogP
9
HBA
2
HBD
117.5
PSA (Ų)
0.53
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H25Cl2N5O4
MW 494.38
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness 0.34

Activity Summary

IC50 1 meas. best 6.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.89 6.89 130.0 1

Pharmacokinetic Data

Parameter Value Units Species
Fu - - Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 130.0 nM 6.89 Inhibition of Staphylococcus aureus LigA by FRET-based assay 21719282

Literature References

PubMed DOI Target Context # Activities
21719282 10.1016/j.bmcl.2011.05.128 Unchecked 2
21719282 10.1016/j.bmcl.2011.05.128 No relevant target 2
21719282 10.1016/j.bmcl.2011.05.128 Streptococcus pneumoniae 1
21719282 10.1016/j.bmcl.2011.05.128 Plasma 1
21719282 10.1016/j.bmcl.2011.05.128 Staphylococcus aureus 1

Data from ChEMBL 36 via Core Engine