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Compound Detail

CHEMBL2448521

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C[C@@H]1NC(=O)[C@@H](CS)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCCN)NC(=O)CNC1=O

Basic Information

ChEMBL ID CHEMBL2448521
Phase Preclinical
Structure Type BOTH
InChI Key FNKIQVGOYIYPCY-GFJXEVPCSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

788.0
MW (Da)
-6.40
ALogP
13
HBA
15
HBD
367.0
PSA (Ų)
0.03
QED
3
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H57N13O9S
MW 787.95
Aromatic Rings 0
Heavy Atoms 54
NP-Likeness 1.01

Activity Summary

Ki 1 meas. best 5.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 5.66 5.66 2200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 2200.0 nM 5.66 Inhibition of Dengue Virus 2 NS2B-NS3 protease using Benzoyl-Nle-Lys-Arg-Arg-AMC... 22780881

Literature References

PubMed DOI Target Context # Activities
22780881 10.1021/jm300655h No relevant target 3
22780881 10.1021/jm300655h Unchecked 2

Data from ChEMBL 36 via Core Engine