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Compound Detail

CHEMBL4515559

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N=C(N)NCCC[C@@H]1NC(=O)CNC(=O)[C@H](CC(=O)O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N2

Basic Information

ChEMBL ID CHEMBL4515559
Phase Preclinical
Structure Type MOL
InChI Key BFQYCHQCQCZVFJ-APKGMPDHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

1605.9
MW (Da)

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C71H104N20O19S2
MW 1605.87

Activity Summary

Ki 1 meas. best 8.74

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasminogen
CHEMBL1801
Ki 8.74 8.74 1.8 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Plasminogen Ki = 1.8 nM 8.74 Inhibition of human plasmin using Ac-RM(O2)YR-pNA as substrate after 30 mins 30520638

Literature References

PubMed DOI Target Context # Activities
30520638 10.1021/acs.jmedchem.8b01139 Plasminogen 1

Data from ChEMBL 36 via Core Engine