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Compound Detail

CHEMBL2448522

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CC(C)C[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2ccc(O)cc2)NC(=O)CNC(=O)[C@@H](N)CSSC[C@@H](C(=O)O)NC1=O

Basic Information

ChEMBL ID CHEMBL2448522
Phase Preclinical
Structure Type BOTH
InChI Key PAWKGYIVQKIFDO-FADBTOOJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

683.9
MW (Da)
-1.03
ALogP
11
HBA
9
HBD
255.1
PSA (Ų)
0.11
QED
3
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H45N7O8S2
MW 683.85
Aromatic Rings 1
Heavy Atoms 46
NP-Likeness 1.15

Activity Summary

Ki 1 meas. best 4.9

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 4.9 4.9 12500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 12500.0 nM 4.9 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 Unchecked 3
22780881 10.1021/jm300655h No relevant target 1

Data from ChEMBL 36 via Core Engine