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Compound Detail

CHEMBL3741725

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N=C(N)NCCC[C@H](NC(=O)c1scc2c1OCCO2)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(N)=O)c1ccc(OCc2ccccc2)cc1

Basic Information

ChEMBL ID CHEMBL3741725
Phase Preclinical
Structure Type MOL
InChI Key IWYQELXFLIYYEX-OHSXHVKISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

708.8
MW (Da)
1.42
ALogP
10
HBA
8
HBD
246.0
PSA (Ų)
0.05
QED
2
Ro5 Violations
19
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H44N8O7S
MW 708.84
Aromatic Rings 3
Heavy Atoms 50
NP-Likeness -0.40

Activity Summary

IC50 1 meas. best 6.71

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.71 6.71 194.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 194.0 nM 6.71 Inhibition of Dengue virus serotype-2 NS2B-NS3 protease using 2-Abz-Nle-Lys-Arg-... 26562070

Literature References

PubMed DOI Target Context # Activities
26562070 10.1021/acs.jmedchem.5b01441 Unchecked 3
26562070 10.1021/acs.jmedchem.5b01441 Prothrombin 1

Data from ChEMBL 36 via Core Engine