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Compound Detail

CHEMBL96553

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CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](/C=C/C(=O)n1ccc2ccccc21)CCC(N)=O

Basic Information

ChEMBL ID CHEMBL96553
Phase Preclinical
Structure Type MOL
InChI Key ZMWGEBIZZDWASN-AOXXHNHHSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

665.8
MW (Da)
4.66
ALogP
7
HBA
4
HBD
161.6
PSA (Ų)
0.13
QED
1
Ro5 Violations
16
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H43N5O6
MW 665.79
Aromatic Rings 4
Heavy Atoms 49
NP-Likeness -0.12

Activity Summary

EC50 2 meas. best 5.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
EC50 5.75 5.75 1800.0 1
rhinovirus B14
CHEMBL613759
EC50 5.75 5.75 1800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
9667970 10.1021/jm980068d HeLa 2
9667970 10.1021/jm980068d Human rhinovirus A protease 1
27996267 10.1021/acs.jmedchem.6b00788 Unchecked 1
27996267 10.1021/acs.jmedchem.6b00788 rhinovirus B14 1
27996267 10.1021/acs.jmedchem.6b00788 H1-HeLa 1

Data from ChEMBL 36 via Core Engine