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Compound Detail

CHEMBL5281384

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COC(=O)c1cc2c(c(OC)c1OC)[C@H](C)C[C@@H](OC(=O)NS(=O)(=O)c1ccc(C)cc1)[C@H]2[C@@H](C)CCC=C(C)C

Basic Information

ChEMBL ID CHEMBL5281384
Phase Preclinical
Structure Type MOL
InChI Key GVJFNKNYGLKXOJ-MZFMZNHHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

587.7
MW (Da)
6.26
ALogP
8
HBA
1
HBD
117.2
PSA (Ų)
0.26
QED
2
Ro5 Violations
10
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H41NO8S
MW 587.74
Aromatic Rings 2
Heavy Atoms 41
NP-Likeness 0.71

Activity Summary

IC50 1 meas. best 5.21

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Haemonchus contortus
CHEMBL613144
IC50 5.21 5.21 6200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Haemonchus contortus IC50 = 6200.0 nM 5.21 Anthelmintic activity against third stage larvae of Haemonchus contortus assesse... 36799121

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 HEK293 1
36799121 10.1021/acs.jnatprod.2c01041 Human immunodeficiency virus 1 1

Data from ChEMBL 36 via Core Engine