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Compound Detail

CHEMBL5267153

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COC(=O)c1cc2c(c(OC)c1OC)[C@H](C)C[C@@H](OC(=O)Nc1ccc(C)cc1)[C@H]2[C@@H](C)CCC=C(C)C

Basic Information

ChEMBL ID CHEMBL5267153
Phase Preclinical
Structure Type MOL
InChI Key QVYBTGYBCREHCU-MZFMZNHHSA-N
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

523.7
MW (Da)
7.39
ALogP
6
HBA
1
HBD
83.1
PSA (Ų)
0.27
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H41NO6
MW 523.67
Aromatic Rings 2
Heavy Atoms 38
NP-Likeness 0.81

Activity Summary

IC50 3 meas. best 5.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Haemonchus contortus
CHEMBL613144
IC50 5.15 5.15 7100.0 1
Plasmodium falciparum
CHEMBL364
IC50 4.91 4.9 12200.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
36799121 10.1021/acs.jnatprod.2c01041 Haemonchus contortus 4
36799121 10.1021/acs.jnatprod.2c01041 Plasmodium falciparum 2
36799121 10.1021/acs.jnatprod.2c01041 ADMET 2
36799121 10.1021/acs.jnatprod.2c01041 Unchecked 1
36799121 10.1021/acs.jnatprod.2c01041 HEK293 1
36799121 10.1021/acs.jnatprod.2c01041 Human immunodeficiency virus 1 1

Data from ChEMBL 36 via Core Engine