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Compound Detail

CHEMBL4203781

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CC[C@H]1OC(=O)[C@@](C)(F)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(OC)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCCCN=[N+]=[N-])C(=O)O[C@]12C

Basic Information

ChEMBL ID CHEMBL4203781
Phase Preclinical
Structure Type MOL
InChI Key TUXKKFMQIRGPGW-AXJWTBQKSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

727.9
MW (Da)
4.37
ALogP
12
HBA
1
HBD
189.9
PSA (Ų)
0.08
QED
2
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H58FN5O10
MW 727.87
Aromatic Rings 0
Heavy Atoms 51
NP-Likeness 1.19

Activity Summary

Kd 1 meas. best 8.68

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Bacterial 70S ribosome
CHEMBL2363135
Kd 8.68 8.68 2.1 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
31820982 10.1021/acs.jmedchem.9b01183 Bacterial 70S ribosome 2
30258539 10.1021/acsmedchemlett.8b00248 Staphylococcus aureus 1
31820982 10.1021/acs.jmedchem.9b01183 Streptococcus pneumoniae 1

Data from ChEMBL 36 via Core Engine