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Compound Detail

CHEMBL4168288

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CC(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H]1C[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)NCCC(N)=O)N(CCCNC(=N)N)C1

Basic Information

ChEMBL ID CHEMBL4168288
Phase Preclinical
Structure Type MOL
InChI Key XEMUICZHJOJAME-ZOOWYRFPSA-N
7
Targets
10
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

1711.1
MW (Da)

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C72H131N35O14
MW 1711.07

Activity Summary

IC50 10 meas. best 8.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Pseudomonas aeruginosa
CHEMBL348
IC50 8.3 8.3 5.0 1
Staphylococcus epidermidis
CHEMBL353
IC50 7.85 7.85 14.0 1
Enterobacter sp.
CHEMBL612402
IC50 7.85 7.85 14.0 1
Escherichia coli
CHEMBL354
IC50 7.75 7.75 18.0 1
Staphylococcus aureus
CHEMBL352
IC50 7.64 7.64 23.0 1
Bacillus subtilis
CHEMBL359
IC50 7.35 7.35 45.0 1
Mycobacterium tuberculosis
CHEMBL360
IC50 5.96 5.7675 1100.0 4

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
29738954 10.1016/j.ejmech.2018.04.039 Mycobacterium tuberculosis 8
29738954 10.1016/j.ejmech.2018.04.039 Escherichia coli 2
29738954 10.1016/j.ejmech.2018.04.039 Pseudomonas aeruginosa 2
29738954 10.1016/j.ejmech.2018.04.039 Enterobacter sp. 2
29738954 10.1016/j.ejmech.2018.04.039 Bacillus subtilis 2
29738954 10.1016/j.ejmech.2018.04.039 Staphylococcus aureus 2
29738954 10.1016/j.ejmech.2018.04.039 Staphylococcus epidermidis 2
29738954 10.1016/j.ejmech.2018.04.039 HeLa 1

Data from ChEMBL 36 via Core Engine