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Compound Detail

CHEMBL583298

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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(Cc4c(O)cnc5ncccc45)C3)C(=O)O[C@]12C

Basic Information

ChEMBL ID CHEMBL583298
Phase Preclinical
Structure Type MOL
InChI Key KNDXCMQNZXPRGV-UIPKLHSNSA-N
1
Targets
2
Activities
2
Assay Types
1
PK Parameters
7
Publications
0
Known Names

Molecular Properties

812.0
MW (Da)
3.07
ALogP
15
HBA
3
HBD
201.4
PSA (Ų)
0.27
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 C42H61N5O11
MW 811.97
Aromatic Rings 2
Heavy Atoms 58
NP-Likeness 0.83

Activity Summary

IC50 1 meas.
Ki 1 meas. best 7.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cytochrome P450 3A
CHEMBL2364675
Ki 7.6 7.6 25.0 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 3
19775168 10.1021/jm900729s ADMET 2
19775168 10.1021/jm900729s Streptococcus pyogenes 1
19775168 10.1021/jm900729s Haemophilus influenzae 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