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Compound Detail

CHEMBL4450993

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CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](C)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N2

Basic Information

ChEMBL ID CHEMBL4450993
Phase Preclinical
Structure Type MOL
InChI Key RERFKFYMYKTFND-DCTWAECPSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

1525.7
MW (Da)

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C71H92N14O20S2
MW 1525.73

Activity Summary

Ki 2 meas. best 9.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Chymotrypsin
CHEMBL4523987
Ki 9.38 9.38 0.4 1
Chymase
CHEMBL4068
Ki 8.77 8.77 1.7 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
31855419 10.1021/acs.jmedchem.9b01811 Chymase 1
31855419 10.1021/acs.jmedchem.9b01811 Cathepsin G 1
31855419 10.1021/acs.jmedchem.9b01811 Chymotrypsin 1

Data from ChEMBL 36 via Core Engine