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Compound Detail

CHEMBL3335488

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N=C(N)NCCC[C@H](NC(=O)c1ccccc1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL3335488
Phase Preclinical
Structure Type MOL
InChI Key FJEZTJJYGATLFV-VABKMULXSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

552.7
MW (Da)
-0.13
ALogP
6
HBA
8
HBD
218.3
PSA (Ų)
0.08
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H40N8O4
MW 552.68
Aromatic Rings 2
Heavy Atoms 40
NP-Likeness 0.01

Activity Summary

IC50 1 meas. best 4.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Genome polyprotein
CHEMBL3308998
IC50 4.92 4.92 11900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Genome polyprotein IC50 = 11900.0 nM 4.92 Inhibition of Dengue virus serotype 2 NS2B-NS3 protease by homogeneous fluorimet... 25221663

Literature References

PubMed DOI Target Context # Activities
25221663 10.1021/ml500245v Genome polyprotein 3
25221663 10.1021/ml500245v Prothrombin 1

Data from ChEMBL 36 via Core Engine