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Compound Detail

CHEMBL4168935

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CCC(CC)O[C@@H]1C=C(C(=O)O)[C@H](n2cc(C(O)CC)nn2)[C@H](NC(=N)N)[C@H]1NC(C)=O

Basic Information

ChEMBL ID CHEMBL4168935
Phase Preclinical
Structure Type MOL
InChI Key ANCDXOXUNZPPDW-FVAVCCDCSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

451.5
MW (Da)
0.22
ALogP
8
HBA
6
HBD
188.5
PSA (Ų)
0.21
QED
1
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H33N7O5
MW 451.53
Aromatic Rings 1
Heavy Atoms 32
NP-Likeness 0.39

Activity Summary

Ki 1 meas. best 8.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Neuraminidase
CHEMBL6015
Ki 8.4 8.4 4.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Neuraminidase Ki = 4.0 nM 8.4 Inhibition of Influenza A virus (H3N2) neuraminidase activity 29965752

Literature References

PubMed DOI Target Context # Activities
29965752 10.1021/acs.jmedchem.8b00929 Neuraminidase 2

Data from ChEMBL 36 via Core Engine