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Compound Detail

CHEMBL3348525

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CC[C@@H](O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NS(=O)(=O)N1CCOCC1

Basic Information

ChEMBL ID CHEMBL3348525
Phase Preclinical
Structure Type MOL
InChI Key UXMAYVMTBZDBGV-MZBLVXSRSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

662.9
MW (Da)
1.19
ALogP
8
HBA
6
HBD
186.0
PSA (Ų)
0.15
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H50N6O7S
MW 662.85
Aromatic Rings 2
Heavy Atoms 46
NP-Likeness -0.16

Activity Summary

IC50 1 meas. best 8.96
Ki 1 meas. best 6.07

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Renin
CHEMBL286
IC50 8.96 8.96 1.1 1
Cathepsin E
CHEMBL3092
Ki 6.07 6.07 850.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Renin IC50 = 1.1 nM 8.96 Inhibitory activity against monkey renin 8410973
Cathepsin E Ki = 850.0 nM 6.07 Binding affinity against human cathepsin E 8410973

Literature References

PubMed DOI Target Context # Activities
8410973 10.1021/jm00070a004 Renin 1
8410973 10.1021/jm00070a004 Pepsin A 1
8410973 10.1021/jm00070a004 Gastricsin 1
8410973 10.1021/jm00070a004 Cathepsin D 1
8410973 10.1021/jm00070a004 Cathepsin E 1

Data from ChEMBL 36 via Core Engine