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Compound Detail

CHEMBL2304055

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N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCCN)NC(=O)CNC(=O)[C@@H](N)CSSC[C@@H](C(=O)O)NC1=O

Basic Information

ChEMBL ID CHEMBL2304055
Phase Preclinical
Structure Type BOTH
InChI Key AUOVCRWLLASVMS-ADHGMGHFSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

719.9
MW (Da)
-4.50
ALogP
12
HBA
14
HBD
358.6
PSA (Ų)
0.04
QED
3
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H49N13O7S2
MW 719.90
Aromatic Rings 0
Heavy Atoms 48
NP-Likeness 0.80

Activity Summary

Ki 1 meas. best 5.46

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 5.46 5.46 3500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 3500.0 nM 5.46 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 2

Data from ChEMBL 36 via Core Engine