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Compound Detail

CHEMBL4070637

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CC(C)C[C@H](NC(=O)OCc1ccc([N+](=O)[O-])cc1)C(=O)N[C@H](/C=C/S(=O)(=O)c1ccccc1)CCc1ccccc1

Basic Information

ChEMBL ID CHEMBL4070637
Phase Preclinical
Structure Type MOL
InChI Key KRUCDLDOLPAAJK-IQXDQLTMSA-N
4
Targets
4
Activities
3
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

593.7
MW (Da)
5.34
ALogP
7
HBA
2
HBD
144.7
PSA (Ų)
0.19
QED
2
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H35N3O7S
MW 593.70
Aromatic Rings 3
Heavy Atoms 42
NP-Likeness -0.42

Activity Summary

Ki 2 meas. best 7.85
EC50 1 meas. best 5.64
IC50 1 meas. best 5.88

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Rhodesain
CHEMBL4188
Ki 7.85 7.85 14.0 1
Procathepsin L
CHEMBL3837
Ki 6.6 6.6 250.0 1
Falcipain 2
CHEMBL5800
IC50 5.88 5.88 1320.0 1
Plasmodium falciparum
CHEMBL364
EC50 5.64 5.64 2310.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
28763614 10.1021/acs.jmedchem.7b00405 Rhodesain 3
28763614 10.1021/acs.jmedchem.7b00405 Procathepsin L 3
28763614 10.1021/acs.jmedchem.7b00405 Plasmodium falciparum 1
28763614 10.1021/acs.jmedchem.7b00405 Falcipain 2 1

Data from ChEMBL 36 via Core Engine