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Compound Detail

CHEMBL583093

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CC[C@H]1OC(=O)[C@H](C)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)(O)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(C3CN([C@H](C)c4ccnc5ncccc45)C3)C(=O)O[C@]12C

Basic Information

ChEMBL ID CHEMBL583093
Phase Preclinical
Structure Type MOL
InChI Key WQQQUDROKZMYJS-SMXRDDNFSA-N
2
Targets
2
Activities
2
Assay Types
1
PK Parameters
7
Publications
0
Known Names

Molecular Properties

810.0
MW (Da)
3.92
ALogP
14
HBA
2
HBD
181.2
PSA (Ų)
0.30
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C43H63N5O10
MW 810.00
Aromatic Rings 2
Heavy Atoms 58
NP-Likeness 0.91

Activity Summary

IC50 1 meas. best 4.37
Ki 1 meas. best 8.28

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cytochrome P450 3A
CHEMBL2364675
Ki 8.28 8.28 5.3 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.37 4.37 43000.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 2.0 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19775168 10.1021/jm900729s Streptococcus pneumoniae 4
19775168 10.1021/jm900729s Haemophilus influenzae 2
19775168 10.1021/jm900729s ADMET 2
19775168 10.1021/jm900729s Streptococcus pyogenes 1
19775168 10.1021/jm900729s Liver microsomes 1
19775168 10.1021/jm900729s Voltage-gated inwardly rectifying potassium channel KCNH2 1
19775168 10.1021/jm900729s Cytochrome P450 3A 1

Data from ChEMBL 36 via Core Engine