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Compound Detail

CHEMBL1088179

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CO[C@H]1C2C(=O)C=C3S[C@H]4C[C@]31C1=C(N4)C(=O)c3[nH]cc4c3C1=[N+]2CC4

Basic Information

ChEMBL ID CHEMBL1088179
Phase Preclinical
Structure Type MOL
InChI Key TYPMFNKWGPMUPQ-CHJBIQGWSA-O
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

366.4
MW (Da)
0.74
ALogP
5
HBA
2
HBD
74.2
PSA (Ų)
0.72
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C19H16N3O3S+
MW 366.42
Aromatic Rings 1
Heavy Atoms 26
NP-Likeness 3.39

Activity Summary

IC50 2 meas. best 5.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
K562
CHEMBL385
IC50 5.6 5.6 2500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
K562 IC50 = 2500.0 nM 5.6 Cytotoxicity against human K562 cells assessed as viable cells after 72 hrs by M... 20055495

Literature References

PubMed DOI Target Context # Activities
20055495 10.1021/np9005629 Sortase A 1
20055495 10.1021/np9005629 K562 1
20055495 10.1021/np9005629 Salmonella enterica 1
20055495 10.1021/np9005629 Proteus vulgaris 1
20055495 10.1021/np9005629 Escherichia coli 1
20055495 10.1021/np9005629 Staphylococcus aureus 1
20055495 10.1021/np9005629 Micrococcus luteus 1
20055495 10.1021/np9005629 Bacillus subtilis 1

Data from ChEMBL 36 via Core Engine