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Compound Detail

CHEMBL298788

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CC(C)C[C@H](NC(=O)[C@H](Cc1ccc(-c2ccccc2)cc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL298788
Phase Preclinical
Structure Type MOL
InChI Key WRNVKZZCUAPYRR-UVEJXLBHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

749.0
MW (Da)
6.14
ALogP
6
HBA
5
HBD
159.8
PSA (Ų)
0.08
QED
2
Ro5 Violations
18
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C45H56N4O6
MW 748.97
Aromatic Rings 4
Heavy Atoms 55
NP-Likeness 0.03

Activity Summary

IC50 1 meas. best 9.37

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus type 1 protease
CHEMBL243
IC50 9.37 9.37 0.4 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Human immunodeficiency virus type 1 protease IC50 = 0.43 nM 9.37 Inhibition of HIV-1 protease 1588552

Literature References

PubMed DOI Target Context # Activities
1588552 10.1021/jm00088a004 Human immunodeficiency virus type 1 protease 1

Data from ChEMBL 36 via Core Engine